Combination therapy

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Combination therapy or polytherapy is therapy that uses more than one medication or modality. Typically, the term refers to using multiple therapies to treat a single disease, and often all the therapies are pharmaceutical (although it can also involve non-medical therapy, such as the combination of medications and talk therapy to treat depression). 'Pharmaceutical' combination therapy may be achieved by prescribing/administering separate drugs, or, where available, dosage forms that contain more than one active ingredient (such as fixed-dose combinations).

Contents

Polypharmacy is a related term, referring to the use of multiple medications (without regard to whether they are for the same or separate conditions/diseases). Sometimes "polymedicine" is used to refer to pharmaceutical combination therapy. Most of these kinds of terms lack a universally consistent definition, so caution and clarification are often advisable.

Uses

Conditions treated with combination therapy include tuberculosis, leprosy, cancer, malaria, and HIV/AIDS. One major benefit of combination therapies is that they reduce development of drug resistance since a pathogen or tumor is less likely to have resistance to multiple drugs simultaneously. Artemisinin-based monotherapies for malaria are explicitly discouraged to avoid the problem of developing resistance to the newer treatment.

Combination therapy may seem costlier than monotherapy in the short term, but when it is used appropriately, it causes significant savings: lower treatment failure rate, lower case-fatality ratios, fewer side-effects than monotherapy, slower development of resistance, and thus less money needed for the development of new drugs. [1]

In oncology

Combination therapy has gained momentum in oncology in recent years, with various studies demonstrating higher response rates with combinations of drugs compared to monotherapies, [2] [3] and the FDA recently approving therapeutic combination regimens that demonstrated superior safety and efficacy to monotherapies. [4] In a recent study about solid cancers, Martin Nowak, Bert Vogelstein, and colleagues showed that in most clinical cases, combination therapies are needed to avoid the evolution of resistance to targeted drugs. Furthermore, they find that the simultaneous administration of multiple targeted drugs minimizes the chance of relapse when no single mutation confers cross-resistance to both drugs. [1]

Various systems biology methods must be used to discover combination therapies to overcome drug resistance in select cancer types. [5] [6] Recent precision medicine approaches have focused on targeting multiple biomarkers found in individual tumors by using combinations of drugs. [7] [8] However, with 300 FDA-approved cancer drugs on the market, there almost 45,000 possible two-drug combinations and almost 4.5 million three-drug combinations for to choose from. [9] That level of complexity is one of the primary impediments to the growth of combination therapy in oncology. [7]

The National Cancer Institute has recently highlighted combination therapy as a top research priority in oncology. [10]

Bacterial infections

Combination therapy with two or more antibiotics are often used in an effort to treat multi-drug resistant Gram-negative bacteria. [11]

Contrast to monotherapy

Monotherapy, or the use of a single therapy, can be applied to any therapeutic approach, but it is most commonly used to describe the use of a single medication. Normally, monotherapy is selected because a single medication is adequate to treat the medical condition. However, monotherapies may also be used because of unwanted side effects or dangerous drug interactions. [12]

See also

Related Research Articles

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<span class="mw-page-title-main">Cancer immunotherapy</span> Artificial stimulation of the immune system to treat cancer

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<span class="mw-page-title-main">Dasatinib</span> Chemical compound

Dasatinib, sold under the brand name Sprycel among others, is a targeted therapy medication used to treat certain cases of chronic myelogenous leukemia (CML) and acute lymphoblastic leukemia (ALL). Specifically it is used to treat cases that are Philadelphia chromosome-positive (Ph+). It is taken by mouth.

<span class="mw-page-title-main">Ipilimumab</span> Pharmaceutical drug

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Pazopanib, sold under the brand name Votrient, is an anti-cancer medication marketed worldwide by Novartis. It is a potent and selective multi-targeted receptor tyrosine kinase inhibitor that blocks tumour growth and inhibits angiogenesis. It has been approved for renal cell carcinoma and soft tissue sarcoma by numerous regulatory administrations worldwide.

<span class="mw-page-title-main">PARP inhibitor</span> Pharmacological enzyme inhibitors of poly (ADP-ribose) polymerases

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A CDK inhibitor is any chemical that inhibits the function of CDKs. They are used to treat cancers by preventing overproliferation of cancer cells. The US FDA approved the first drug of this type, palbociclib (Ibrance), a CDK4/6 inhibitor, in February 2015, for use in postmenopausal women with breast cancer that is estrogen receptor positive and HER2 negative. While there are multiple cyclin/CDK complexes regulating the cell cycle, CDK inhibitors targeting CDK4/6 have been the most successful, with 4 CDK4/6 inhibitors haven been FDA approved. No inhibitors targeting other CDKs have been FDA approved, but several compounds are in clinical trials.

<span class="mw-page-title-main">ALK inhibitor</span>

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<span class="mw-page-title-main">Palbociclib</span> Medication for HR+ HER2− breast cancer

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<span class="mw-page-title-main">Ceritinib</span> ALK inhibitor for treatment of non-small-cell lung cancer

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<span class="mw-page-title-main">Osimertinib</span> Chemical compound, used as a medication to treat lung cancer

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Phenotypic response surfaces (PRS) is an artificial intelligence-guided personalized medicine platform that relies on combinatorial optimization principles to quantify drug interactions and efficacies to develop optimized combination therapies to treat a broad spectrum of illnesses.

References

  1. 1 2 Bozic; Reiter; Allen; et al. (June 25, 2013). "Evolutionary dynamics of cancer in response to targeted combination therapy". eLife. 2:e00747: e00747. doi: 10.7554/eLife.00747 . PMC   3691570 . PMID   23805382.
  2. Janku, Filip; Hong, David S.; Fu, Siqing; Piha-Paul, Sarina A.; Naing, Aung; Falchook, Gerald S.; Tsimberidou, Apostolia M.; Stepanek, Vanda M.; Moulder, Stacy L. (2014-01-30). "Assessing PIK3CA and PTEN in early-phase trials with PI3K/AKT/mTOR inhibitors". Cell Reports. 6 (2): 377–387. doi:10.1016/j.celrep.2013.12.035. ISSN   2211-1247. PMC   4409143 . PMID   24440717.
  3. Musgrove, Elizabeth A.; Caldon, C. Elizabeth; Barraclough, Jane; Stone, Andrew; Sutherland, Robert L. (2011-07-07). "Cyclin D as a therapeutic target in cancer". Nature Reviews. Cancer. 11 (8): 558–572. doi:10.1038/nrc3090. ISSN   1474-1768. PMID   21734724. S2CID   29093377.
  4. "Novartis receives FDA approval for first-of-its-kind Kisqali® Femara® Co-Pack for initial treatment of HR+/HER2- advanced or metastatic breast cancer | Novartis US". www.pharma.us.novartis.com. Archived from the original on 2017-10-04. Retrieved 2017-10-03.
  5. Korkut, A; Wang, W; Demir, E; Aksoy, BA; Jing, X; Molinelli, EJ; Babur, Ö; Bemis, DL; Onur Sumer, S; Solit, DB; Pratilas, CA; Sander, C (18 August 2015). "Perturbation biology nominates upstream-downstream drug combinations in RAF inhibitor resistant melanoma cells". eLife. 4. doi: 10.7554/elife.04640 . PMC   4539601 . PMID   26284497.
  6. Lee, MJ; Ye, AS; Gardino, AK; Heijink, AM; Sorger, PK; MacBeath, G; Yaffe, MB (11 May 2012). "Sequential application of anticancer drugs enhances cell death by rewiring apoptotic signaling networks". Cell. 149 (4): 780–94. doi:10.1016/j.cell.2012.03.031. PMC   3501264 . PMID   22579283.
  7. 1 2 "Drug Combinations to Overcome Treatment Resistance". National Cancer Institute. 2016-12-21. Retrieved 2017-10-03.
  8. Li, Xubin; Dowling, Elisabeth K.; Yan, Gonghong; Dereli, Zeynep; Bozorgui, Behnaz; Imanirad, Parisa; Elnaggar, Jacob H.; Luna, Augustin; Menter, David G.; Pilié, Patrick G.; Yap, Timothy A. (2022-05-02). "Precision Combination Therapies Based on Recurrent Oncogenic Coalterations". Cancer Discovery. 12 (6): OF1–OF18. doi:10.1158/2159-8290.CD-21-0832. ISSN   2159-8274. PMC   9524464 . PMID   35412613.
  9. Culjat, M (2017-05-11). "By the Numbers: Combination Therapy in Oncology | CureMatch". CureMatch Blog. Retrieved 2017-10-03.
  10. "Combination Therapies for Cancer - Annual Plan". National Cancer Institute. Archived from the original on 2017-10-05. Retrieved 2017-10-03.
  11. Tamma, P. D.; Cosgrove, S. E.; Maragakis, L. L. (2012-07-01). "Combination Therapy for Treatment of Infections with Gram-Negative Bacteria". Clinical Microbiology Reviews. 25 (3): 450–470. doi:10.1128/CMR.05041-11. ISSN   0893-8512. PMC   3416487 . PMID   22763634.
  12. "Glossary". Archived from the original on 2008-09-07. Retrieved 2008-04-02. Monotherapy: The treatment of epilepsy with a single medication rather than a combination. Monotherapy has advantages over combining medications in many patients, including absence of drug-drug interactions, fewer side effects, simpler dosing, and lower cost. However, not all patients can be controlled with monotherapy.