Evidence map›Paper›PMID 28410237›Full record

SynthesisOncotarget2017

Combination therapy in combating cancer.

Reza Bayat Mokhtari, Tina S Homayouni, Narges Baluch, Evgeniya Morgatskaya, Sushil Kumar, Bikul Das, Herman Yeger

Open access · diamondAbstract readSystematic Review
In one paragraph

Synthesis in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1,132 papers.

0numbers the graph read from it
0cells of the map it votes in
1,132citing papers in PubMed
49.1field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1,132 citing papers in PubMed, 2,440 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Optimal Designs for Identifying Effective Doses in Drug Combination Studies.Biometrical journal. Biometrische Zeitschrift · 2026
    Article
  7. Topotecan Synergizes with SP141 in the Management of Uveal Melanoma.bioRxiv : the preprint server for biology · 2026
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Immunotherapy for Cancer: Current Advances and Future Directions.International journal of molecular sciences · 2026
    Review
  20. Article

1,072 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Reza Bayat MokhtariDevelopmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Tina S HomayouniDevelopmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Narges BaluchDepartment of Pathology and Molecular Medicine, Queen's University, Kingston, Ontario, Canada.
Evgeniya MorgatskayaDevelopmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Sushil KumarDevelopmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Bikul DasDepartment of Immunology and Infectious Diseases, The Forsyth Institute, Cambridge, Massachusetts, USA.
Herman YegerDevelopmental and Stem Cell Biology, The Hospital for Sick Children, Toronto, Ontario, Canada.
Hospital for Sick Children · CANovant Health Forsyth Medical Center · USQueen's University · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Combination therapy, a treatment modality that combines two or more therapeutic agents, is a cornerstone of cancer therapy. The amalgamation of anti-cancer drugs enhances efficacy compared to the mono-therapy approach because it targets key pathways in a characteristically synergistic or an additive manner. This approach potentially reduces drug resistance, while simultaneously providing therapeutic anti-cancer benefits, such as reducing tumour growth and metastatic potential, arresting mitotically active cells, reducing cancer stem cell populations, and inducing apoptosis. The 5-year survival rates for most metastatic cancers are still quite low, and the process of developing a new anti-cancer drug is costly and extremely time-consuming. Therefore, new strategies that target the survival pathways that provide efficient and effective results at an affordable cost are being considered. One such approach incorporates repurposing therapeutic agents initially used for the treatment of different diseases other than cancer. This approach is effective primarily when the FDA-approved agent targets similar pathways found in cancer. Because one of the drugs used in combination therapy is already FDA-approved, overall costs of combination therapy research are reduced. This increases cost efficiency of therapy, thereby benefiting the "medically underserved". In addition, an approach that combines repurposed pharmaceutical agents with other therapeutics has shown promising results in mitigating tumour burden. In this systematic review, we discuss important pathways commonly targeted in cancer therapy. Furthermore, we also review important repurposed or primary anti-cancer agents that have gained popularity in clinical trials and research since 2012.

Indexed as

Antineoplastic AgentsCarbonic Anhydrase InhibitorsHumansNeoplasmsSurvival RateAntineoplastic AgentsCarbonic Anhydrase Inhibitorscarbonic anhydrase 9 (CAIX)carbonic anhydrase inhibitor (CAI)HIF-1alphahistone deacetylase inhibitor (HDACi)Nrf2-Keap1

Identifiers

PMID28410237
PMCPMC5514969
OpenAlexW2600452401

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.