Evidence map›Paper›PMID 33740125›Full record

ArticleCancer immunology, immunotherapy : CII2021

Efficacy and safety of anti-PD-1-based therapy in combination with PARP inhibitors for patients with advanced solid tumors in a real-world setting.

Zhaozhen Wu, Haitao Tao, Sujie Zhang, Xiao Wang, Junxun Ma, Ruixin Li, Zhefeng Liu, Jinliang Wang, Pengfei Cui, Shixue Chen and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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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

14 authors at 3 institutions in 2 countries.

Zhaozhen WuDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.ORCID https://orcid.org/0000-0001-8962-5741
Haitao TaoDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Sujie ZhangDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Xiao WangSchool of Medicine, Oregon Health & Science University, Oregon, 97239-3098, USA.
Junxun MaDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Ruixin LiDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Zhefeng LiuDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Jinliang WangDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Pengfei CuiDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Shixue ChenDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Huang DiDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Ziwei HuangDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Xuan ZhengDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China.
Yi HuDepartment of Medical Oncology, Chinese PLA General Hospital, Beijing, 100853, China. huyi301zlxb@sina.com.ORCID https://orcid.org/0000-0001-9319-5692
Chinese PLA General Hospital · CNNankai University · CNOregon Health & Science University · US

Funding

National Basic Research Program of China (973 Program) 2017YFC0907904
6 · The paper itself

Abstract

backgroundRationale exists for combining immune checkpoint inhibitors and PARP inhibitors (PARPi), and results of clinical trials in ovarian cancer are promising, but data in other cancers are limited.

methodEfficacy and safety of PARPi/anti-PD-1 in advanced solid tumors were retrospectively analyzed. The efficacy measures included objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS) and overall survival (OS).

resultsThis retrospective study included data from 40 patients. The ORR was 27.5% (95% CI, 13.0-42.0%), with a DCR of 85.0% (95% CI, 73.4-96.6%). Except four patients in first-line treatment (three with PR and one with SD), the ORR of ≥second-line treatment, non-small cell lung cancer (NSCLC) and small cell lung cancer (SCLC) was 22.2%, 23.1% and 28.6%, and the DCR was 83.3%, 84.6% and 71.4%, separately. The median PFS of all patients, ≥second-line treatment, NSCLC and SCLC was 4.6 m, 4.2 m, 4.5 m and 3.7 m. The median OS was 9.4 m, 11.4 m, 12.7 m and 5.4 m, respectively. Multivariable analysis revealed that BRCA1/2 mutation was positively correlated with ORR (P = 0.008), and LDH≥250U/L was negatively correlated with lowered DCR (P = 0.018), while lymphocyte number, ECOG and LDH significantly influenced both PFS and OS. We found that the possible resistant mechanisms were sarcomatous degeneration and secondary mutation, including BRCA2 truncation mutation, A2M, JAK1,T790M, KEAP1 and mTOR mutation. 37.5% patients had ≥grade 3 adverse events.

conclusionPARPi/anti-PD-1 is an effective and tolerable method for patients with advanced solid tumors, and BRCA1/2 is a potential biomarker.

Indexed as

AdultAgedAged, 80 and overHumansImmune Checkpoint InhibitorsMiddle AgedNeoplasmsPoly(ADP-ribose) Polymerase InhibitorsRetrospective StudiesSurvival AnalysisImmune Checkpoint InhibitorsPoly(ADP-ribose) Polymerase InhibitorsAnti-PD-1EfficacyPARP inhibitorsSafetyTumors

Identifiers

PMID33740125
PMCPMC8423634
OpenAlexW3137779807

What OpenQuestion holds

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LicenceCC BY
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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.