Evidence map›Paper›PMID 33737855›Full record

ReviewClinical Medicine Insights. Oncology2021

The Synergistic Effect of PARP Inhibitors and Immune Checkpoint Inhibitors.

Zhaozhen Wu, Pengfei Cui, Haitao Tao, Sujie Zhang, Junxun Ma, Zhefeng Liu, Jinliang Wang, Yuanyu Qian, Shixue Chen, Ziwei Huang and 3 more

Abstract readReview
In one paragraph

Review in Clinical Medicine Insights. Oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
53citing 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

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

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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

13 authors.

Zhaozhen WuDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.ORCID https://orcid.org/0000-0001-8962-5741
Pengfei CuiDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Haitao TaoDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Sujie ZhangDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Junxun MaDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Zhefeng LiuDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Jinliang WangDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Yuanyu QianDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Shixue ChenDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Ziwei HuangDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Xuan ZhengDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Di HuangDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.
Yi HuDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, China.ORCID https://orcid.org/0000-0003-4740-0290

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Poly (ADP-ribose) polymerase (PARP) inhibitors have demonstrated great promise for treating cancers with homologous recombination (HR) defects, such as germline BRCA1/2 mutation. Further studies suggest that PARP inhibitors (PARPi) can also exhibit efficacy in HR-competent cancers, by amplifying the DNA damage and inducing immunogenic cell death, and PARPi lead to increasing tumor neoantigen, upregulation of interferons and PD-L1, and modulation of the tumor microenvironment, which may facilitate a more profound antitumor immune response. Immune checkpoint inhibitors (ICIs) targeting PD-1/PD-L1 or CTLA-4 have achieved impressive success in the treatment of different malignancies. However, only a subset of populations derive clinical benefit, and the biomarkers and resistance mechanisms are not fully understood. Therefore, given that PARPi could potentiate the therapeutic effect of ICIs, PARPi combined with ICIs are becoming an alternative for patients who cannot benefit from ICI monotherapy. In this review, we focus on the mechanisms and immune role of PARPi and discuss the rationale and clinical studies of this combined regimen.

Indexed as

BRCAcancerDNA damage responseimmune checkpoint inhibitorsPARP inhibitors

Identifiers

PMID33737855
PMCPMC7934064

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Registered trials

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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.