The examples and perspective in this article deal primarily with the United States and do not represent a worldwide view of the subject.(March 2018) |
Proton therapy | |
---|---|
Other names | Proton beam therapy |
ICD-10-PCS | Z92.3 |
In medicine, proton therapy, or proton radiotherapy, is a type of particle therapy that uses a beam of protons to irradiate diseased tissue, most often to treat cancer. The chief advantage of proton therapy over other types of external beam radiotherapy is that the dose of protons is deposited over a narrow range of depth; hence in minimal entry, exit, or scattered radiation dose to healthy nearby tissues.
When evaluating whether to treat a tumor with photon or proton therapy, physicians may choose proton therapy if it is important to deliver a higher radiation dose to targeted tissues while significantly decreasing radiation to nearby organs at risk. [1] The American Society for Radiation Oncology Model Policy for Proton Beam therapy says proton therapy is considered reasonable if sparing the surrounding normal tissue "cannot be adequately achieved with photon-based radiotherapy" and can benefit the patient. [2] Like photon radiation therapy, proton therapy is often used in conjunction with surgery and/or chemotherapy to most effectively treat cancer.
Proton therapy is a type of external beam radiotherapy that uses ionizing radiation. In proton therapy, medical personnel use a particle accelerator to target a tumor with a beam of protons. [4] [5] These charged particles damage the DNA of cells, ultimately killing them by stopping their reproduction and thus eliminating the tumor. Cancerous cells are particularly vulnerable to attacks on DNA because of their high rate of division and their limited ability to repair DNA damage. Some cancers with specific defects in DNA repair may be more sensitive to proton radiation. [6]
Proton therapy lets physicians deliver a highly conformal beam, i.e. delivering radiation that conforms to the shape and depth of the tumor and sparing much of the surrounding, normal tissue. [7] For example, when comparing proton therapy to the most advanced types of photon therapy—intensity-modulated radiotherapy (IMRT) and volumetric modulated arc therapy (VMAT)—proton therapy can give similar or higher radiation doses to the tumor with a 50%-60% lower total body radiation dose. [8] [1]
Protons can focus energy delivery to fit the tumor shape, delivering only low-dose radiation to surrounding tissue. As a result, the patient has fewer side effects. All protons of a given energy have a certain penetration range; very few protons penetrate beyond that distance. [9] Also, the dose delivered to tissue is maximized only over the last few millimeters of the particle's range; this maximum is called the spread out Bragg peak , often called the SOBP (see visual). [10]
To treat tumors at greater depth, one needs a beam with higher energy, typically given in MeV (mega electron volts). Accelerators used for proton therapy typically produce protons with energies of 70 to 250 MeV. Adjusting proton energy during the treatment maximizes the cell damage within the tumor. Tissue closer to the surface of the body than the tumor gets less radiation, and thus less damage. Tissues deeper in the body get very few protons, so the dose becomes immeasurably small. [9]
In most treatments, protons of different energies with Bragg peaks at different depths are applied to treat the entire tumor. These Bragg peaks are shown as thin blue lines in the figure in this section. While tissues behind (or deeper than) the tumor get almost no radiation, the tissues in front of (shallower than) the tumor get radiation dosage based on the SOBP.
Most installed proton therapy systems use isochronous cyclotrons. [11] [12] Cyclotrons are considered simple to operate, reliable and can be made compact, especially with use of superconducting magnets. [13] Synchrotrons can also be used, with the advantage of easier production at varying energies. [14] Linear accelerators, as used for photon radiation therapy, are becoming commercially available as limitations of size and cost are resolved. [15] Modern proton systems incorporate high-quality imaging for daily assessment of tumor contours, treatment planning software illustrating 3D dose distributions, and various system configurations, e.g. multiple treatment rooms connected to one accelerator. Partly because of these advances in technology, and partly because of the continually increasing amount of proton clinical data, the number of hospitals offering proton therapy continues to grow.
FLASH radiotherapy is a technique under development for photon and proton treatments, using very high dose rates (necessitating large beam currents). If applied clinically, it could shorten treatment time to just one to three 1-second sessions, and further reducing side effects. [16] [17] [18] [19]
The first suggestion that energetic protons could be an effective treatment was made by Robert R. Wilson in a paper published in 1946 [20] while he was involved in the design of the Harvard Cyclotron Laboratory (HCL). [21] The first treatments were performed with particle accelerators built for physics research, notably Berkeley Radiation Laboratory in 1954 and at Uppsala in Sweden in 1957. In 1961, a collaboration began between HCL and Massachusetts General Hospital (MGH) to pursue proton therapy. Over the next 41 years, this program refined and expanded these techniques while treating 9,116 patients [22] before the cyclotron was shut down in 2002. In the USSR a therapeutic proton beam with energies up to 200 MeV was obtained at the synchrocyclotron of JINR in Dubna in 1967. The ITEP center in Moscow, Russia, which began treating patients in 1969, is the oldest proton center still in operation. The Paul Scherrer Institute in Switzerland was the world's first proton center to treat eye tumors beginning in 1984. In addition, they invented pencil beam scanning in 1996, which became the state-of-the art form of proton therapy. [23]
The world's first hospital-based proton therapy center was a low energy cyclotron centre for eye tumors at Clatterbridge Centre for Oncology in the UK, opened in 1989, [24] followed in 1990 at the Loma Linda University Medical Center (LLUMC) in Loma Linda, California. Later, the Northeast Proton Therapy Center at Massachusetts General Hospital was brought online, and the HCL treatment program was transferred to it in 2001 and 2002. At the beginning of 2023, there were 41 proton therapy centers in the United States, [25] and a total of 89 worldwide. [26] As of 2020, six manufacturers make proton therapy systems: Hitachi, Ion Beam Applications, Mevion Medical Systems, ProNova Solutions, ProTom International and Varian Medical Systems.
The newest form of proton therapy, pencil beam scanning, gives therapy by sweeping a proton beam laterally over the target so that it gives the required dose while closely conforming to shape of the targeted tumor. Before the use of pencil beam scanning, oncologists used a scattering method to direct a wide beam toward the tumor. [27]
The first commercially available proton delivery systems used a scattering process, or passive scattering, to deliver the therapy. With scattering proton therapy the proton beam is spread out by scattering devices, and the beam is then shaped by putting items such as collimators and compensators in the path of the protons. The collimators were custom made for the patient with milling machines. [28] Passive scattering gives homogeneous dose along the target volume. Therefore, passive scattering gives more limited control over dose distributions proximal to target. Over time many scattering therapy systems have been upgraded to deliver pencil beam scanning. Because scattering therapy was the first type of proton therapy available, most clinical data available on proton therapy—especially long-term data as of 2020—were acquired via scattering technology.
A newer and more flexible delivery method is pencil beam scanning, using a beam that sweeps laterally over the target so that it delivers the needed dose while closely conforming to the tumor's shape. This conformal delivery is achieved by shaping the dose through magnetic scanning of thin beamlets of protons without needing apertures and compensators. Multiple beams are delivered from different directions, and magnets in the treatment nozzle steer the proton beam to conform to the target volume layer as the dose is painted layer by layer. This type of scanning delivery provides greater flexibility and control, letting the proton dose conform more precisely to the shape of the tumor. [28]
Delivery of protons via pencil beam scanning, in use since 1996 at the Paul Scherrer Institute, [28] allows for the most precise type of proton delivery: intensity-modulated proton therapy (IMPT). IMPT is to proton therapy what IMRT is to conventional photon therapy—treatment that more closely conforms to the tumor while avoiding surrounding structures. [29] Virtually all new proton systems provide pencil beam scanning exclusively. A study led by Memorial Sloan Kettering Cancer Center suggests that IMPT can improve local control when compared to passive scattering for patients with nasal cavity and paranasal sinus malignancies. [30]
It was estimated that by the end of 2019, a total of ~200,000 patients had been treated with proton therapy. Physicians use protons to treat conditions in two broad categories:
Two prominent examples are pediatric neoplasms (such as medulloblastoma) and prostate cancer.
Irreversible long-term side effects of conventional radiation therapy for pediatric cancers are well documented and include growth disorders, neurocognitive toxicity, ototoxicity with subsequent effects on learning and language development, and renal, endocrine and gonadal dysfunctions. Radiation-induced secondary malignancy is another very serious adverse effect that has been reported. As there is minimal exit dose when using proton radiation therapy, dose to surrounding normal tissues can be significantly limited, reducing the acute toxicity which positively impacts the risk for these long-term side effects. Cancers requiring craniospinal irradiation, for example, benefit from the absence of exit dose with proton therapy: dose to the heart, mediastinum, bowel, bladder and other tissues anterior to the vertebrae is eliminated, hence a reduction of acute thoracic, gastrointestinal and bladder side effects. [36] [37] [38]
Proton therapy for eye tumors is a special case since this treatment requires only relatively low energy protons (~70 MeV). Owing to this low energy, some particle therapy centers only treat eye tumors. [22] Proton, or more generally, hadron therapy of tissue close to the eye affords sophisticated methods to assess the alignment of the eye that can vary significantly from other patient position verification approaches in image guided particle therapy. [39] Position verification and correction must ensure that the radiation spares sensitive tissue like the optic nerve to preserve the patient's vision.
For ocular tumors, selecting the type of radiotherapy depends on tumor location and extent, tumor radioresistance (calculating the dose needed to eliminate the tumor), and the therapy's potential toxic side effects on nearby critical structures. [40] For example, proton therapy is an option for retinoblastoma [41] and intraocular melanoma. [42] The advantage of a proton beam is that it has the potential to effectively treat the tumor while sparing sensitive structures of the eye. [43] Given its effectiveness, proton therapy has been described as the "gold standard" treatment for ocular melanoma. [44] [45] The implementation of momentum cooling technique in proton therapy for eye treatment can significantly enhance its effectiveness. [46] This technique aids in reducing the radiation dose administered to healthy organs while ensuring that the treatment is completed within a few seconds. Consequently, patients experience improved comfort during the procedure.
When receiving radiation for skull base tumors, side effects of the radiation can include pituitary hormone dysfunction and visual field deficit—after radiation for pituitary tumors—as well as cranial neuropathy (nerve damage), radiation-induced osteosarcoma (bone cancer), and osteoradionecrosis, which occurs when radiation causes part of the bone in the jaw or skull base to die. [47] Proton therapy has been very effective for people with base of skull tumors. [48] Unlike conventional photon radiation, protons do not penetrate beyond the tumor. Proton therapy lowers the risk of treatment-related side effects from when healthy tissue gets radiation. Clinical studies have found proton therapy to be effective for skull base tumors. [49] [50] [51]
Proton particles do not deposit exit dose, so proton therapy can spare normal tissues far from the tumor. This is particularly useful for head and neck tumors because of the anatomic constraints found in nearly all cancers in this region. The dosimetric advantage unique to proton therapy translates into toxicity reduction. For recurrent head and neck cancer requiring reirradiation, proton therapy is able to maximize a focused dose of radiation to the tumor while minimizing dose to surrounding tissues, hence a minimal acute toxicity profile, even in patients who got multiple prior courses of radiotherapy. [52]
When breast cancer — especially in the left breast — is treated with conventional radiation, the lung and heart, which are near the left breast, are particularly susceptible to photon radiation damage. Such damage can eventually cause lung problems (e.g. lung cancer) or various heart problems. Depending on location of the tumor, damage can also occur to the esophagus, or to the chest wall (which can potentially lead to leukemia). [53] One recent study showed that proton therapy has low toxicity to nearby healthy tissues and similar rates of disease control compared with conventional radiation. [54] Other researchers found that proton pencil beam scanning techniques can reduce both the mean heart dose and the internal mammary node dose to essentially zero. [55]
Small studies have found that, compared to conventional photon radiation, proton therapy delivers minimal toxic dose to healthy tissues [56] and specifically decreased dose to the heart and lung. [57] Large-scale trials are underway to examine other potential benefits of proton therapy to treat breast cancer. [58]
Though chemotherapy is the main treatment for lymphoma, consolidative radiation is often used in Hodgkin lymphoma and aggressive non-Hodgkin lymphoma, while definitive treatment with radiation alone is used in a small fraction of lymphoma patients. Unfortunately, treatment-related toxicities caused by chemotherapy agents and radiation exposure to healthy tissues are major concerns for lymphoma survivors. Advanced radiation therapy technologies such as proton therapy may offer significant and clinically relevant advantages such as sparing important organs at risk and decreasing the risk for late normal tissue damage while still achieving the primary goal of disease control. This is especially important for lymphoma patients who are being treated with curative intent and have long life expectancy following therapy. [59]
In prostate cancer cases, the issue is less clear. Some published studies found a reduction in long term rectal and genito-urinary damage when treating with protons rather than photons (meaning X-ray or gamma ray therapy). Others showed a small difference, limited to cases where the prostate is particularly close to certain anatomical structures. [60] [61] The relatively small improvement found may be the result of inconsistent patient set-up and internal organ movement during treatment, which offsets most of the advantage of increased precision. [61] [62] [63] One source suggests that dose errors around 20% can result from motion errors of just 2.5 mm (0.098 in).[ citation needed ] and another that prostate motion is between 5–10 mm (0.20–0.39 in). [64]
The number of cases of prostate cancer diagnosed each year far exceeds those of the other diseases referred to above, and this has led some, but not all, facilities to devote most of their treatment slots to prostate treatments. For example, two hospital facilities devote ~65% [65] and 50% [66] of their proton treatment capacity to prostate cancer, while a third devotes only 7.1%. [67]
Worldwide numbers are hard to compile, but one example says that in 2003 ~26% of proton therapy treatments worldwide were for prostate cancer. [68]
A growing amount of data shows that proton therapy has great potential to increase therapeutic tolerance for patients with GI malignancy. The possibility of decreasing radiation dose to organs at risk may also help facilitate chemotherapy dose escalation or allow new chemotherapy combinations. Proton therapy will play a decisive role for ongoing intensified combined modality treatments for GI cancers. The following review presents the benefits of proton therapy in treating hepatocellular carcinoma, pancreatic cancer and esophageal cancer. [69]
Post-treatment liver decompensation, and subsequent liver failure, is a risk with radiotherapy for hepatocellular carcinoma, the most common type of primary liver cancer. Research shows that proton therapy gives favorable results related to local tumor control, progression-free survival, and overall survival. [70] [71] [72] [73] Other studies, which examine proton therapy compared with conventional photon therapy, show that proton therapy gives improved survival and/or fewer side effects; hence proton therapy could significantly improve clinical outcomes for some patients with liver cancer. [74] [75]
For patients who get local or regional recurrences after their initial radiation therapy, physicians are limited in their treatment options due to their reluctance to give additional photon radiation therapy to tissues that have already been irradiated. Re-irradiation is a potentially curative treatment option for patients with locally recurrent head and neck cancer. In particular, pencil beam scanning may be ideally suited for reirradiation. [76] Research shows the feasibility of using proton therapy with acceptable side effects, even in patients who have had multiple prior courses of photon radiation. [77] [78] [79]
A large study on comparative effectiveness of proton therapy was published by teams of the University of Pennsylvania and Washington University in St. Louis in JAMA Oncology, assessing if proton therapy in the setting of concurrent chemoradiotherapy is associated with fewer 90-day unplanned hospitalizations and overall survival compared with concurrent photon therapy and chemoradiotherapy. [80] The study included 1483 adult patients with nonmetastatic, locally advanced cancer treated with concurrent chemoradiotherapy with curative intent and concluded, "proton chemoradiotherapy was associated with significantly reduced acute adverse events that caused unplanned hospitalizations, with similar disease-free and overall survival". A significant number of randomized controlled trials is recruiting, but only a limited number have been completed as of August 2020. A phase III randomized controlled trial of proton beam therapy versus radiofrequency ablation (RFA) for recurrent hepatocellular carcinoma organized by the National Cancer Center in Korea showed better 2-year local progression-free survival for the proton arm and concluded that proton beam therapy (PBT) is "not inferior to RFA in terms of local progression-free survival and safety, denoting that either RFA or PBT can be applied to recurrent small HCC patients". [70] A phase IIB randomized controlled trial of proton beam therapy versus IMRT for locally advanced esophageal cancer organized by University of Texas MD Anderson Cancer Center concluded that proton beam therapy reduced the risk and severity of adverse events compared with IMRT while maintaining similar progression free survival. [81] Another Phase II Randomized Controlled Trial comparing photons versus protons for Glioblastoma concluded that patients at risk of severe lymphopenia could benefit from proton therapy. [82] A team from Stanford University assessed the risk of secondary cancer after primary cancer treatment with external beam radiation using data from the National Cancer Database for 9 tumor types: head and neck, gastrointestinal, gynecologic, lymphoma, lung, prostate, breast, bone/soft tissue, and brain/central nervous system. [83] The study included a total of 450,373 patients and concluded that proton therapy was associated with a lower risk of second cancer.
The issue of when, whether, and how best to apply this technology is still under discussion by physicians and researchers. One recently introduced method, 'model-based selection', uses comparative treatment plans for IMRT and IMPT in combination with normal tissue complication probability (NTCP) models to identify patients who may benefit most from proton therapy. [84] [85]
Clinical trials are underway to examine the comparative efficacy of proton therapy (vs photon radiation) for the following:
The figure at the right of the page shows how beams of X-rays (IMRT; left frame) and beams of protons (right frame), of different energies, penetrate human tissue. A tumor with a sizable thickness is covered by the IMRT spread out Bragg peak (SOBP) shown as the red lined distribution in the figure. The SOBP is an overlap of several pristine Bragg peaks (blue lines) at staggered depths.
Megavoltage X-ray therapy has less "skin sparing potential" than proton therapy: X-ray radiation at the skin, and at very small depths, is lower than for proton therapy. One study estimates that passively scattered proton fields have a slightly higher entrance dose at the skin (~75%) compared to therapeutic megavoltage (MeV) photon beams (~60%). [3] X-ray radiation dose falls off gradually, needlessly harming tissue deeper in the body and damaging the skin and surface tissue opposite the beam entrance. The differences between the two methods depends on:
The X-ray advantage of less harm to skin at the entrance is partially counteracted by harm to skin at exit point.
Since X-ray treatments are usually done with multiple exposures from opposite sides, each section of skin is exposed to both entering and exiting X-rays. In proton therapy, skin exposure at the entrance point is higher, but tissues on the opposite side of the body to the tumor get no radiation. Thus, X-ray therapy causes slightly less damage to skin and surface tissues, and proton therapy causes less damage to deeper tissues in front of and beyond the target. [5]
An important consideration in comparing these treatments is whether the equipment delivers protons via the scattering method (historically, the most common) or a spot scanning method. Spot scanning can adjust the width of the SOBP on a spot-by-spot basis, which reduces the volume of normal (healthy) tissue inside the high dose region. Also, spot scanning allows for intensity modulated proton therapy (IMPT), which determines individual spot intensities using an optimization algorithm that lets the user balance the competing goals of irradiating tumors while sparing normal tissue. Spot scanning availability depends on the machine and the institution. Spot scanning is more commonly known as pencil-beam scanning and is available on IBA, Hitachi, Mevion (known as HYPERSCAN [107] which became US FDA approved in 2017) and Varian.
Physicians base the decision to use surgery or proton therapy (or any radiation therapy) on tumor type, stage, and location. Sometimes surgery is superior (such as cutaneous melanoma), sometimes radiation is superior (such as skull base chondrosarcoma), and sometimes are comparable (for example, prostate cancer). Sometimes, they are used together (e.g., rectal cancer or early stage breast cancer).
The benefit of external beam proton radiation is in the dosimetric difference from external beam X-ray radiation and brachytherapy in cases where use of radiation therapy is already indicated, rather than as a direct competition with surgery. [31] In prostate cancer, the most common indication for proton beam therapy, no clinical study directly comparing proton therapy to surgery, brachytherapy, or other treatments has shown any clinical benefit for proton beam therapy. Indeed, the largest study to date showed that IMRT compared with proton therapy was associated with less gastrointestinal morbidity. [108]
Proton therapy is a type of external beam radiotherapy, and shares risks and side effects of other forms of radiation therapy. The dose outside of the treatment region can be significantly less for deep-tissue tumors than X-ray therapy, because proton therapy takes full advantage of the Bragg peak. Proton therapy has been in use for over 40 years, and is a mature technology. As with all medical knowledge, understanding of the interaction of radiations with tumor and normal tissue is still imperfect. [109]
Historically, proton therapy has been expensive. An analysis published in 2003 found that the cost of proton therapy is ~2.4 times that of X-ray therapies. [110] Newer, less expensive, and dozens more proton treatment centers are driving costs down and they offer more accurate three-dimensional targeting. Higher proton dosage over fewer treatments sessions (1/3 fewer or less) is also driving costs down. [111] [112] Thus the cost is expected to reduce as better proton technology becomes more widely available. An analysis published in 2005 determined that the cost of proton therapy is not unrealistic and should not be the reason for denying patients access to the technology. [113] In some clinical situations, proton beam therapy is clearly superior to the alternatives. [114] [115]
A study in 2007 expressed concerns about the effectiveness of proton therapy for prostate cancer, [116] but with the advent of new developments in the technology, such as improved scanning techniques and more precise dose delivery ('pencil beam scanning'), this situation may change considerably. [117] Amitabh Chandra, a health economist at Harvard University, said, "Proton-beam therapy is like the Death Star of American medical technology... It's a metaphor for all the problems we have in American medicine." [118] Proton therapy is cost-effective for some types of cancer, but not all. [119] [120] In particular, some other treatments offer better overall value for treatment of prostate cancer. [119]
As of 2018, the cost of a single-room particle therapy system is US$40 million, with multi-room systems costing up to US$200 million. [121] [122]
As of August 2020, there are over 89 particle therapy facilities worldwide, [123] with at least 41 others under construction. [124] As of August 2020, there are 34 operational proton therapy centers in the United States. As of the end of 2015 more than 154,203 patients had been treated worldwide. [125]
One hindrance to universal use of the proton in cancer treatment is the size and cost of the cyclotron or synchrotron equipment necessary. Several industrial teams are working on development of comparatively small accelerator systems to deliver the proton therapy to patients. [126] Among the technologies being investigated are superconducting synchrocyclotrons (also known as FM Cyclotrons), ultra-compact synchrotrons, dielectric wall accelerators, [126] and linear particle accelerators. [112]
Proton treatment centers in the United States as of 2024 [update] (in chronological order of first treatment date) include: [24] [127]
Institution | Location | Year of first treatment | Comments |
---|---|---|---|
Loma Linda University Medical Center [128] | Loma Linda, CA | 1990 | First hospital-based facility in USA; uses Spread Out Bragg's Peak (SOBP) |
Crocker Nuclear Laboratory [129] | Davis, CA | 1994 | Ocular treatments only (low energy accelerator); at University of California, Davis |
Francis H. Burr Proton Center | Boston, MA | 2001 | At Massachusetts General Hospital and formerly known as NPTC; continuation of Harvard Cyclotron Laboratory/MGH treatment program that began in 1961; Manufactured by Ion Beam Applications [130] |
University of Florida Health Proton Therapy Institute-Jacksonville [131] | Jacksonville, FL | 2006 | The UF Health Proton Therapy Institute is a part of a non-profit academic medical research facility affiliated with the University of Florida College of Medicine-Jacksonville. It is the first treatment center in the Southeast U.S. to offer proton therapy. Manufactured by Ion Beam Applications [130] |
University of Texas MD Anderson Cancer Center [132] | Houston, TX | ||
Oklahoma Proton Center [133] | Oklahoma City, OK | 2009 | 4 treatment rooms, Proteus PLUS system manufactured by Ion Beam Applications [130] |
Northwestern Medicine Chicago Proton Center | Warrenville, IL | 2010 | 4 treatment rooms, Proteus PLUS system manufactured by Ion Beam Applications [130] |
Roberts Proton Therapy Center [134] | Philadelphia, PA | The largest proton therapy center in the world, the Roberts Proton Therapy Center, which is a part of Penn's Abramson Cancer Center, University of Pennsylvania Health System; 5 treatment rooms, Proteus PLUS system manufactured by Ion Beam Applications [130] | |
Hampton University Proton Therapy Institute | Hampton, VA | 5 treatment rooms, Proteus PLUS system manufactured by Ion Beam Applications [130] | |
ProCure Proton Therapy Center [135] | Somerset, NJ | 2012 | 4 treatment rooms, Proteus PLUS system manufactured by Ion Beam Applications [130] |
SCCA Proton Therapy Center | Seattle, WA | 2013 | At Seattle Cancer Care Alliance; part of Fred Hutchinson Cancer Research Center; 4 treatment rooms, Proteus PLUS system manufactured by Ion Beam Applications [130] |
Siteman Cancer Center [111] | St. Louis, MO | First of the new single suite, ultra-compact, superconducting synchrocyclotron, [136] lower cost facilities to treat a patient using the Mevion Medical System's S250. [137] | |
Provision Proton Therapy Center [138] | Knoxville, TN | 2014 | 3 treatment rooms, Proteus PLUS system manufactured by Ion Beam Applications [130] |
California Protons Cancer Therapy Center [139] | San Diego, CA | 5 treatment rooms, manufactured by Varian Medical Systems [140] | |
Ackerman Cancer Center | Jacksonville, FL | 2015 | Ackerman Cancer Center is the world's first private, physician-owned practice to provide proton therapy, in addition to conventional radiation therapy and on-site diagnostic services. |
The Laurie Proton Therapy Center | New Brunswick, NJ | The Laurie Proton Therapy Center, part of Robert Wood Johnson University Hospital, is home to the world's third MEVION S250 Proton Therapy System. | |
Texas Center for Proton Therapy | Dallas Fort Worth, TX | A collaboration by "Texas Oncology and The US Oncology Network, supported by McKesson Specialty Health, and Baylor Health Enterprises"; three pencil beam rooms and cone beam CT imaging. [141] 3 treatment rooms, Proteus PLUS system manufactured by Ion Beam Applications [130] | |
Mayo Clinic Jacobson Building | Rochester, MN | 4 treatment rooms. [142] Manufactured by Hitachi. [143] | |
St. Jude Red Frog Events Proton Therapy Center | Memphis, TN | 3 treatment rooms | |
Mayo Clinic Cancer Center | Phoenix, AZ | 2016 | 4 treatment rooms. [144] Manufactured by Hitachi. [145] |
The Marjorie and Leonard Williams Center for Proton Therapy | Orlando, FL | http://www.ufhealthcancerorlando.com/centers/proton-therapy-center | |
Cancer and Blood Diseases Institute | Liberty Township, OH | Collaboration of University of Cincinnati Cancer Institute and Cincinnati Children's Hospital Medical Center, [146] [147] manufactured by Varian Medical Systems | |
Maryland Proton Treatment Center | Baltimore, MD | 5 treatment rooms, affiliated with the University of Maryland Greenebaum Comprehensive Cancer Center, manufactured by Varian Medical Systems. | |
Proton Therapy Center at University Hospitals Seidman Cancer Center | Cleveland, OH | Only proton therapy center in Northern Ohio. One treatment room with the Mevion S250 Proton Therapy System. Part of the NCI-designated Case Comprehensive Cancer Center, University Hospitals Seidman Cancer Center is one of the nation's leading freestanding cancer hospitals. | |
Miami Cancer Institute | Miami, FL | 2017 | 3 treatment rooms, all using pencil-beam scanning [148] Manufactured by Ion Beam Applications [130] |
Beaumont Proton Therapy Center | Royal Oak, MI | Single treatment room, Proteus ONE system manufactured by Ion Beam Applications [130] | |
Emory Proton Therapy Center Archived 2018-03-07 at the Wayback Machine | Atlanta, GA | 2018 | Five treatment rooms, ProBeam Superconducting Cyclotron [149] manufactured by Varian Medical Systems |
Provision CARES Proton Therapy Center | Nashville, TN | Three treatment rooms, Two Gantries and One Fixed Beam, All Pencil Beam Scanning, manufactured by ProNova Solutions, LLC | |
McLaren Proton Therapy Center | Flint, MI | The McLaren Proton Therapy System uses the industry's highest energy 330 MeV proton synchrotron to accelerate and deliver proton beam to two treatment rooms, with an opportunity to extend into a planned third room. Both operating treatment rooms are equipped with proton pencil beam scanning, cone beam computed tomography for image guidance, patient positioning system with 6-degrees of freedom that coupled with 180-degree partial gantry allows for complete flexibility of treatment angles. | |
New York Proton Center | New York, NY | 2019 | A partnership between Memorial Sloan Kettering, Montefiore Health, and Mount Sinai Health System. 4 treatment rooms, manufactured by Varian Medical Systems |
Johns Hopkins Proton Therapy Center | Washington, DC | 3 treatment rooms and 1 research gantry. Manufactured by Hitachi. | |
South Florida Proton Therapy Institute | Delray Beach, FL | One treatment room, manufactured by Varian Medical Systems | |
UAB Proton Therapy Center | Birmingham, AL | 2020 | One treatment room, manufactured by Varian Medical Systems |
Dwoskin PTC - University of Miami | Miami, FL | One treatment room, manufactured by Varian Medical Systems | |
The Inova Mather Proton Therapy Center | Fairfax, VA | Two treatment rooms, manufactured by Ion Beam Applications | |
The University of Kansas Cancer Center | Kansas City, KS | 2022 | Announced Feb 2019 [150] |
Penn Medicine Lancaster General Health Ann B. Barshinger Cancer Institute | Lancaster, PA | One treatment room, manufactured by Varian Medical Systems | |
Penn Medicine Virtua Health | Voorhees, NJ | One treatment room, manufactured by Varian Medical Systems | |
Ohio State, Nationwide Children's Hospital | Columbus, OH | 2023 | Three treatment rooms, manufactured by Varian Medical Systems |
Kansas City Proton Institute | Overland Park, KS | 2023 | One treatment room, multidisciplinary practice providing proton therapy, conventional radiation therapy and diagnostic services. |
OSF Healthcare | Peoria, IL | 2024 | One treatment room, manufactured by Varian Medical Systems |
Froedtert Hospital | Wauwatosa, WI | 2024 (Estimated) | Announced May 2022 [151] |
Mayo Clinic Florida | Jacksonville, FL | 2025 (Estimated) | Announced June 2019 [152] |
Stanford University Medical Center | Stanford, CA | 2025 (Estimated) | One treatment room, manufactured by Mevion Medical Systems. Announced April 2024. [153] |
The Indiana University Health Proton Therapy Center in Bloomington, Indiana opened in 2004 and ceased operations in 2014.
Institution | Maximum energy (MeV) | Year of first treatment | Location |
---|---|---|---|
Paul Scherrer Institute | 250 | 1984 | Villigen, Switzerland |
Clatterbridge Cancer Centre NHS Foundation Trust, low-energy for ocular [154] | 62 | 1989 | Liverpool, United Kingdom |
Centre de protonthérapie de l'Institut Curie | 235 | 1991 | Orsay, France |
Centre Antoine Lacassagne | 63 | 1991 | Nice, France |
Research Center for Charged Particle Therapy | 350–400 | 1994 | Chiba, Japan |
TRIUMF [155] | 74 | 1995 | Vancouver, Canada |
Helmholtz-Zentrum Berlin | 72 | 1998 | Berlin, Germany |
Proton Medical Research Center University of Tsukuba | 250 | 2001 | Tsukuba, Japan |
Centro di adroterapia oculare | 60 | 2002 | Catania, Italy |
Wanjie Proton Therapy Center | 230 | 2004 | Zibo, China |
Proton Therapy Center, Korea National Cancer Center | 230 | 2007 | Seoul, Korea |
Heidelberg Ion-Beam Therapy Center (HIT) | 230 | 2009 | Heidelberg, Germany |
Medipolis Proton Therapy and Research Center | 235 | 2011 | Kagoshima, Japan |
Instytut Fizyki Jądrowej | 230 | 2011 | Kraków, Poland |
Centro Nazionale di Adroterapia Oncologica | 250 | 2011 | Pavia, Italy |
Protonové centrum v Praze (PTC, Prague) | 230 | 2012 | Prague, Czech Republic |
Westdeutsches Protonentherapiezentrum Essen | 230 | 2013 | Essen, Germany |
PTC Uniklinikum Dresden | 230 | 2014 | Dresden, Germany |
Centro di Protonterapia, APSS Trento [156] | 230 | 2014 | Trento, Italy |
Shanghai Proton and Heavy Ion Center | 230 | 2014 | Shanghai, China |
Centrum Cyklotronowe Bronowice | 230 | 2015 | Kraków, Poland |
Samsung Medical Center Proton Therapy Center | 230 | 2015 | Seoul, Korea |
Proton and Radiation Therapy Center, Linkou Chang Gung Memorial Hospital | 230 | 2015 | Taipei, Taiwan |
Yung-Ching Proton Center, Kaohsiung Chang Gung Memorial Hospital [157] | 230 | 2018 | Kaohsiung, Taiwan |
Skandionkliniken [158] | 230 | 2015 | Uppsala, Sweden |
A. Tsyb Medical Radiological Research Centre | 250 | 2016 | Obninsk, Russia |
MedAustron | 250 | 2016 | Wiener Neustadt, Austria |
Clinical Proton Therapy Center Dr. Berezin Medical Institute [159] | 250 | 2017 | Saint-Petersburg, Russia |
Holland Proton Therapy Center [160] | 250 | 2018 | Delft, Netherlands |
UMC Groningen Protonen Therapie Centrum [161] | 230 | 2018 | Groningen, Netherlands |
The Christie [162] | 250 | 2018 | Manchester, United Kingdom |
Danish Centre for Particle Therapy [163] | 250 | 2019 | Aarhus, Denmark |
Apollo Proton Cancer Centre [164] | 230 | 2019 | Chennai, India |
MAASTRO Clinic Proton Therapy [165] | 230 | 2019 | Maastricht, Netherlands |
Clínica Universidad de Navarra | 230 | 2019 | Madrid, Spain |
Centro de Protonterapia de Quirónsalud [166] | 230 | 2019 | Madrid, Spain |
King Chulalongkorn Memorial Hospital [167] | 250 | 2021 | Bangkok, Thailand |
University College London Hospitals [168] | 250 | 2021 | London, United Kingdom |
Hefei Ion Medical Center [169] | 250 | 2022 | Hefei, China |
Proton Clinical Research Center of the Shandong Cancer Hospital | 250 | 2022 | Jinan, China |
Gleneagles Hospital Singapore [170] | 2023 | Singapore | |
Singapore Institute of Advanced Medicine Holdings - Proton Therapy SG [171] | 250 | 2023 | Singapore |
Mount Elizabeth Proton Therapy Centre [172] | 230 | 2023 | Singapore |
National Cancer Centre Singapore - Goh Cheng Liang Proton Therapy Centre [173] | 2023 | Singapore | |
Parkway Cancer Centre [174] | 2023 | Singapore | |
Hong Kong Sanatorium & Hospital - HKSH Proton Therapy Centre [175] [176] [177] | 2023 | Hong Kong, China | |
Central Japan International Medical Center [178] | 230 | 2024 | Minokamo, Japan |
Cancer Hospital Chinese Academy of Medical Sciences, Shenzhen Center [179] | 2024 | Shenzhen, China | |
Australian Bragg Centre for Proton Therapy & Research [180] [181] | 330 | 2023–2025 | Adelaide, Australia |
Heyou International Hospital [182] | 2026 [183] | Foshan, China |
In July 2020, construction began for "SAHMRI 2", the second building for the South Australian Health and Medical Research Institute. The building will house the Australian Bragg Centre for Proton Therapy & Research, a A$500+ million addition to the largest health and biomedical precinct in the Southern Hemisphere, Adelaide's BioMed City. The proton therapy unit is being supplied by ProTom International, which will install its Radiance 330 proton therapy system, the same system used at Massachusetts General Hospital. When in full operation, it will have the ability to treat approximately 600-700 patients per year with around half of these expected to be children and young adults. The facility is expected to be completed in late 2023, with its first patients treated in 2025. [181] In 2024 the South Australian government expressed concerns about the delivery of the project. [184]
Apollo Proton Cancer Centre (APCC) in Chennai, Tamil Nadu, a unit under Apollo Hospitals, is a Cancer specialty hospital. [185] APCC is the only cancer hospital in India with Joint Commission International accreditation. [186]
In January 2020, it was announced that a proton therapy center would be built in Ichilov Hospital, at the Tel Aviv Sourasky Medical Center. The project's construction was fully funded by donations. It will have two treatment rooms. [187] According to a newspaper report in 2023, it should be ready in three to four years. The report also mentions that "Proton therapy for cancer treatment has arrived in Israel and the Middle East with a clinical trial underway that sees Hadassah Medical Center partnering with P-Cure, an Israeli company that has developed a unique system designed to fit into existing hospital settings". [188]
In October 2021, the Amancio Ortega Foundation arranged with the Spanish government and several autonomous communities to donate 280 million euros to install ten proton accelerators in the public health system. [189]
In 2013 the British government announced that £250 million had been budgeted to establish two centers for advanced radiotherapy: The Christie NHS Foundation Trust (the Christie Hospital) in Manchester, which opened in 2018; and University College London Hospitals NHS Foundation Trust, which opened in 2021. These offer high-energy proton therapy, and other types of advanced radiotherapy, including intensity-modulated radiotherapy (IMRT) and image-guided radiotherapy (IGRT). [190] In 2014, only low-energy proton therapy was available in the UK, at Clatterbridge Cancer Centre NHS Foundation Trust in Merseyside. But NHS England has paid to have suitable cases treated abroad, mostly in the US. Such cases rose from 18 in 2008 to 122 in 2013, 99 of whom were children. The cost to the National Health Service averaged ~£100,000 per case. [191]
Radiation therapy or radiotherapy is a treatment using ionizing radiation, generally provided as part of cancer therapy to either kill or control the growth of malignant cells. It is normally delivered by a linear particle accelerator. Radiation therapy may be curative in a number of types of cancer if they are localized to one area of the body, and have not spread to other parts. It may also be used as part of adjuvant therapy, to prevent tumor recurrence after surgery to remove a primary malignant tumor. Radiation therapy is synergistic with chemotherapy, and has been used before, during, and after chemotherapy in susceptible cancers. The subspecialty of oncology concerned with radiotherapy is called radiation oncology. A physician who practices in this subspecialty is a radiation oncologist.
External beam radiation therapy (EBRT) is a form of radiotherapy that utilizes a high-energy collimated beam of ionizing radiation, from a source outside the body, to target and kill cancer cells. A radiotherapy beam is composed of particles which travel in a consistent direction; each radiotherapy beam consists of one type of particle intended for use in treatment, though most beams contain some contamination by other particle types.
Brachytherapy is a form of radiation therapy where a sealed radiation source is placed inside or next to the area requiring treatment. Brachy is Greek for short. Brachytherapy is commonly used as an effective treatment for cervical, prostate, breast, esophageal and skin cancer and can also be used to treat tumours in many other body sites. Treatment results have demonstrated that the cancer-cure rates of brachytherapy are either comparable to surgery and external beam radiotherapy (EBRT) or are improved when used in combination with these techniques. Brachytherapy can be used alone or in combination with other therapies such as surgery, EBRT and chemotherapy.
A radioligand is a microscopic particle which consists of a therapeutic radioactive isotope and the cell-targeting compound - the ligand. The ligand is the target binding site, it may be on the surface of the targeted cancer cell for therapeutic purposes. Radioisotopes can occur naturally or be synthesized and produced in a cyclotron/nuclear reactor. The different types of radioisotopes include Y-90, H-3, C-11, Lu-177, Ac-225, Ra-223, In-111, I-131, I-125, etc. Thus, radioligands must be produced in special nuclear reactors for the radioisotope to remain stable. Radioligands can be used to analyze/characterize receptors, to perform binding assays, to help in diagnostic imaging, and to provide targeted cancer therapy. Radiation is a novel method of treating cancer and is effective in short distances along with being unique/personalizable and causing minimal harm to normal surrounding cells. Furthermore, radioligand binding can provide information about receptor-ligand interactions in vitro and in vivo. Choosing the right radioligand for the desired application is important. The radioligand must be radiochemically pure, stable, and demonstrate a high degree of selectivity, and high affinity for their target.
Radiosurgery is surgery using radiation, that is, the destruction of precisely selected areas of tissue using ionizing radiation rather than excision with a blade. Like other forms of radiation therapy, it is usually used to treat cancer. Radiosurgery was originally defined by the Swedish neurosurgeon Lars Leksell as "a single high dose fraction of radiation, stereotactically directed to an intracranial region of interest".
The Bragg peak is a pronounced peak on the Bragg curve which plots the energy loss of ionizing radiation during its travel through matter. For protons, α-rays, and other ion rays, the peak occurs immediately before the particles come to rest. It is named after William Henry Bragg, who discovered it in 1903 using alpha particles from radium, and wrote the first empirical formula for ionization energy loss per distance with Richard Kleeman.
Fast neutron therapy utilizes high energy neutrons typically between 50 and 70 MeV to treat cancer. Most fast neutron therapy beams are produced by reactors, cyclotrons (d+Be) and linear accelerators. Neutron therapy is currently available in Germany, Russia, South Africa and the United States. In the United States, one treatment center is operational, in Seattle, Washington. The Seattle center uses a cyclotron which produces a proton beam impinging upon a beryllium target.
In radiotherapy, radiation treatment planning (RTP) is the process in which a team consisting of radiation oncologists, radiation therapist, medical physicists and medical dosimetrists plan the appropriate external beam radiotherapy or internal brachytherapy treatment technique for a patient with cancer.
Tomotherapy is a type of radiation therapy treatment machine. In tomotherapy a thin radiation beam is modulated as it rotates around the patient, while they are moved through the bore of the machine. The name comes from the use of a strip-shaped beam, so that only one “slice” of the target is exposed at any one time by the radiation. The external appearance of the system and movement of the radiation source and patient can be considered analogous to a CT scanner, which uses lower doses of radiation for imaging. Like a conventional machine used for X-ray external beam radiotherapy, a linear accelerator generates the radiation beam, but the external appearance of the machine, the patient positioning, and treatment delivery is different. Conventional linacs do not work on a slice-by-slice basis but typically have a large area beam which can also be resized and modulated.
Intraoperative radiation therapy (IORT) is radiation therapy that is administered during surgery directly in the operating room.
Image-guided radiation therapy is the process of frequent imaging, during a course of radiation treatment, used to direct the treatment, position the patient, and compare to the pre-therapy imaging from the treatment plan. Immediately prior to, or during, a treatment fraction, the patient is localized in the treatment room in the same position as planned from the reference imaging dataset. An example of IGRT would include comparison of a cone beam computed tomography (CBCT) dataset, acquired on the treatment machine, with the computed tomography (CT) dataset from planning. IGRT would also include matching planar kilovoltage (kV) radiographs or megavoltage (MV) images with digital reconstructed radiographs (DRRs) from the planning CT.
Particle therapy is a form of external beam radiotherapy using beams of energetic neutrons, protons, or other heavier positive ions for cancer treatment. The most common type of particle therapy as of August 2021 is proton therapy.
Intraoperative electron radiation therapy is the application of electron radiation directly to the residual tumor or tumor bed during cancer surgery. Electron beams are useful for intraoperative radiation treatment because, depending on the electron energy, the dose falls off rapidly behind the target site, therefore sparing underlying healthy tissue.
Breast cancer management takes different approaches depending on physical and biological characteristics of the disease, as well as the age, over-all health and personal preferences of the patient. Treatment types can be classified into local therapy and systemic treatment. Local therapy is most efficacious in early stage breast cancer, while systemic therapy is generally justified in advanced and metastatic disease, or in diseases with specific phenotypes.
Brachytherapy is a type of radiotherapy, or radiation treatment, offered to certain cancer patients. There are two types of brachytherapy – high dose-rate (HDR) and low dose-rate (LDR). LDR brachytherapy is the one most commonly used to treat prostate cancer. It may be referred to as 'seed implantation' or it may be called 'pinhole surgery'.
Selective internal radiation therapy (SIRT), also known as transarterial radioembolization (TARE), radioembolization or intra-arterial microbrachytherapy is a form of radionuclide therapy used in interventional radiology to treat cancer. It is generally for selected patients with surgically unresectable cancers, especially hepatocellular carcinoma or metastasis to the liver. The treatment involves injecting tiny microspheres of radioactive material into the arteries that supply the tumor, where the spheres lodge in the small vessels of the tumor. Because this treatment combines radiotherapy with embolization, it is also called radioembolization. The chemotherapeutic analogue is called chemoembolization, of which transcatheter arterial chemoembolization (TACE) is the usual form.
Treatment for prostate cancer may involve active surveillance, surgery, radiation therapy – including brachytherapy and external-beam radiation therapy, proton therapy, high-intensity focused ultrasound (HIFU), cryosurgery, hormonal therapy, chemotherapy, or some combination. Treatments also extend to survivorship based interventions. These interventions are focused on five domains including: physical symptoms, psychological symptoms, surveillance, health promotion and care coordination. However, a published review has found only high levels of evidence for interventions that target physical and psychological symptom management and health promotion, with no reviews of interventions for either care coordination or surveillance. The favored treatment option depends on the stage of the disease, the Gleason score, and the PSA level. Other important factors include the man's age, his general health, and his feelings about potential treatments and their possible side-effects. Because all treatments can have significant side-effects, such as erectile dysfunction and urinary incontinence, treatment discussions often focus on balancing the goals of therapy with the risks of lifestyle alterations.
Nanobiotix is a biotechnology company that uses nanomedicine to develop new radiotherapy techniques for cancer patients. The company is headquartered in Paris, with additional corporate offices in New York and Massachusetts.
Neutron capture therapy (NCT) is a type of radiotherapy for treating locally invasive malignant tumors such as primary brain tumors, recurrent cancers of the head and neck region, and cutaneous and extracutaneous melanomas. It is a two-step process: first, the patient is injected with a tumor-localizing drug containing the stable isotope boron-10 (10B), which has a high propensity to capture low energy "thermal" neutrons. The neutron cross section of 10B is 1,000 times more than that of other elements, such as nitrogen, hydrogen, or oxygen, that occur in tissue. In the second step, the patient is radiated with epithermal neutrons, the sources of which in the past have been nuclear reactors and now are accelerators that produce higher energy epithermal neutrons. After losing energy as they penetrate tissue, the resultant low energy "thermal" neutrons are captured by the 10B atoms. The resulting decay reaction yields high-energy alpha particles that kill the cancer cells that have taken up enough 10B.
FLASH radiotherapy is an emerging form of radiotherapy which delivers a high dose of radiation to the patient in an ultra-short time frame which produces a tumour killing effect comparable to conventional radiotherapy but with less damage to surrounding healthy tissue. The treatment is in the early stages of development and is not yet widely available as a form of cancer therapy.
{{cite journal}}
: CS1 maint: multiple names: authors list (link)the beam then stops, resulting in virtually no radiation to the tissue beyond the target – or no 'exit dose'
Proton Patient Summary – Inception Through December 1998...Prostate...2591 64.3%
{{cite web}}
: CS1 maint: bot: original URL status unknown (link)