Evidence map›Paper›PMID 29370105›Full record

ReviewCancers2018

Tackling Cancer Resistance by Immunotherapy: Updated Clinical Impact and Safety of PD-1/PD-L1 Inhibitors.

Shifaa M Abdin, Dana M Zaher, El-Shaimaa A Arafa, Hany A Omar

Abstract readReview
In one paragraph

Review in Cancers, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

29 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  4. Article
  5. Review
  6. Current status ofRSC advances · 2023
    Review
  7. Review
  8. Review
  9. Article
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  15. Monoclonal Antibodies in Cancer Therapy.Antibodies (Basel, Switzerland) · 2020
    Review
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  18. Review
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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

4 authors.

Shifaa M AbdinCollege of Pharmacy, University of Sharjah, Sharjah 27272, UAE. U00044748@sharjah.ac.ae.
Dana M ZaherSharjah Institute for Medical Research, University of Sharjah, Sharjah 27272, UAE. U17105878@sharjah.ac.ae.ORCID 0000-0001-5814-0784
El-Shaimaa A ArafaDepartment of Pharmacology and Toxicology, College of Pharmacy and Health Sciences, Ajman University, Ajman 346, UAE. e.arafa@ajman.ac.ae.ORCID 0000-0002-9034-6624
Hany A OmarCollege of Pharmacy, University of Sharjah, Sharjah 27272, UAE. hanyomar@sharjah.ac.ae.ORCID 0000-0002-4670-8149

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cancer therapy has been constantly evolving with the hope of finding the most effective agents with the least toxic effects to eradicate tumors. Cancer immunotherapy is currently among the most promising options, fulfilling this hope in a wide range of tumors. Immunotherapy aims to activate immunity to fight cancer in a very specific and targeted manner; however, some abnormal immune reactions known as immune-related adverse events (IRAEs) might occur. Therefore, many researchers are aiming to define the most proper protocols for managing these complications without interfering with the anticancer effect. One of these targeted approaches is the inhibition of the interaction between the checkpoint protein, programmed death-receptor 1 (PD-1), and its ligand, programmed death-ligand 1 (PD-L1), via a class of antibodies known as PD-1/PD-L1 inhibitors. These antibodies achieved prodigious success in a wide range of malignancies, including those where optimal treatment is not yet fully identified. In this review, we have critically explored and discussed the outcome of the latest PD-1 and PD-L1 inhibitor studies in different malignancies compared to standard chemotherapeutic alternatives with a special focus on the clinical efficacy and safety. The approval of the clinical applications of nivolumab, pembrolizumab, atezolizumab, avelumab, and durvalumab in the last few years clearly highlights the hopeful future of PD-1/PD-L1 inhibitors for cancer patients. These promising results of PD-1/PD-L1 inhibitors have encouraged many ongoing preclinical and clinical trials to explore the extent of antitumor activity, clinical efficacy and safety as well as to extend their applications.

Indexed as

atezolizumabavelumabcancercheckpoint inhibitorsdurvalumabimmunotherapynivolumabPD-1PD-L1pembrolizumabpidilizumab

Identifiers

PMID29370105
PMCPMC5836064

What OpenQuestion holds

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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.