Evidence map›Paper›PMID 32260561›Full record

ReviewInternational journal of molecular sciences2020

Current Insights into Combination Therapies with MAPK Inhibitors and Immune Checkpoint Blockade.

Min Hwa Shin, Jiyoung Kim, Siyoung A Lim, Jeongsoo Kim, Kyung-Mi Lee

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
4.7field-weighted citation impact, top 4% 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

50 citing papers in PubMed, 1 synthesis or guideline pooled it, 76 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Review
  6. Review
  7. Article
  8. Review
  9. Article
  10. JAK-STAT Signaling in Autoimmunity and Cancer.ImmunoTargets and therapy · 2025
    Review
  11. Article
  12. Anti-Inflammatory Effect of Extract fromJournal of microbiology and biotechnology · 2024
    Article
  13. Review
  14. Review
  15. Review
  16. Review
  17. Circular RNAs: characteristics, functions, mechanisms, and potential applications in thyroid cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Review
  18. Article
  19. Article
  20. Article
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

5 authors at 1 institution in 1 country.

Min Hwa ShinDepartment of Biochemistry and Molecular Biology, College of Medicine, Korea University, Seoul 02841, Korea.ORCID 0000-0001-8802-5760
Jiyoung KimDepartment of Biochemistry and Molecular Biology, College of Medicine, Korea University, Seoul 02841, Korea.
Siyoung A LimDepartment of Biochemistry and Molecular Biology, College of Medicine, Korea University, Seoul 02841, Korea.
Jeongsoo KimDepartment of Biochemistry and Molecular Biology, College of Medicine, Korea University, Seoul 02841, Korea.
Kyung-Mi LeeDepartment of Biochemistry and Molecular Biology, College of Medicine, Korea University, Seoul 02841, Korea.ORCID 0000-0002-5378-9258
Korea University · KR

Funding

Korea University Korea University GrantNational Research Foundation of Korea NRF-2016M3A9B6948342National Research Foundation of Korea NRF-2017R1A2B3004828National Research Foundation of Korea NRF-2018M3A9D3079285National Research Foundation of Korea NRF-2018M3A9D3079288National Research Foundation of Korea NRF-2018R1D1A1B07041442
6 · The paper itself

Abstract

The recent development of high-throughput genomics has revolutionized personalized medicine by identifying key pathways and molecular targets controlling tumor progression and survival. Mitogen-activated protein kinase (MAPK) pathways are examples of such targets, and inhibitors against these pathways have shown promising clinical responses in patients with melanoma, non-small-cell lung cancer, colorectal cancer, pancreatic cancer, and thyroid cancer. Although MAPK pathway-targeted therapies have resulted in significant clinical responses in a large proportion of cancer patients, the rate of tumor recurrence is high due to the development of resistance. Conversely, immunotherapies have shown limited clinical responses, but have led to durable tumor regression in patients, and complete responses. Recent evidence indicates that MAPK-targeted therapies may synergize with immune cells, thus providing rationale for the development of combination therapies. Here, we review the current status of ongoing clinical trials investigating MAPK pathway inhibitors, such as BRAF and MAPK/ERK kinase (MEK) inhibitors, in combination with checkpoint inhibitors targeting programmed death protein 1 (PD-1), programmed death-ligand 1 (PD-L1), and cytotoxic T cell associated antigen-4 (CTLA-4). A better understanding of an individual drug's mechanism of action, patterns of acquired resistance, and the influence on immune cells will be critical for the development of novel combination therapies.

Indexed as

AnimalsClinical Trials as TopicCombined Modality TherapyHumansImmune Checkpoint InhibitorsImmunotherapyMitogen-Activated Protein Kinase KinasesNeoplasmsProtein Kinase InhibitorsImmune Checkpoint InhibitorsMitogen-Activated Protein Kinase KinasesProtein Kinase InhibitorsBRAF inhibitorcombination therapyCTLA-4immune checkpoint inhibitorMAPK targeted therapyMEK inhibitorPD-1PD-L1

Identifiers

PMID32260561
PMCPMC7177307
OpenAlexW3014580064

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.