Evidence map›Paper›PMID 34297160›Full record

SynthesisCancer immunology, immunotherapy : CII2022

Efficacy and safety of PD-L1 inhibitors versus PD-1 inhibitors in first-line treatment with chemotherapy for extensive-stage small-cell lung cancer.

Hui Yu, Ping Chen, Xiuyu Cai, Chen Chen, Xuanye Zhang, Lina He, Yixin Zhou, Shaodong Hong, Bei Zhang

Open access · greenAbstract readMeta-Analysis
In one paragraph

Synthesis in Cancer immunology, immunotherapy : CII, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 9 pooled it
3.3field-weighted citation impact, top 5% 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

42 citing papers in PubMed, 9 syntheses or guidelines pooled it, 50 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

9 authors at 1 institution in 1 country.

Hui Yu *State Key Laboratory of Oncology in South China, Guangzhou, China.
Ping Chen *State Key Laboratory of Oncology in South China, Guangzhou, China.
Xiuyu Cai *State Key Laboratory of Oncology in South China, Guangzhou, China.
Chen ChenState Key Laboratory of Oncology in South China, Guangzhou, China.
Xuanye ZhangState Key Laboratory of Oncology in South China, Guangzhou, China.
Lina HeState Key Laboratory of Oncology in South China, Guangzhou, China.
Yixin ZhouState Key Laboratory of Oncology in South China, Guangzhou, China. zhouyx@sysucc.org.cn.
Shaodong HongState Key Laboratory of Oncology in South China, Guangzhou, China. hongshd@sysucc.org.cn.ORCID http://orcid.org/0000-0002-5632-6857
Bei ZhangState Key Laboratory of Oncology in South China, Guangzhou, China. zhangbei@sysucc.org.cn.
Sun Yat-sen University · CN

Funding

Medical Scientific Research Foundation of Guangdong Province C2019110National Natural Science Funds of China 81903176Science and Technology Program of Guangdong Province 2019A1515011596
6 · The paper itself

Abstract

objectivesProgrammed cell death-ligand 1 inhibitors plus chemotherapy (PD-L1 + Chemo) have achieved substantial progress in extensive-stage small-cell lung cancer (ES-SCLC). However, evidence about programmed cell death 1 inhibitors plus chemotherapy (PD-1 + Chemo) in SCLC is relatively lacking. Whether PD-1 inhibitors differ from PD-L1 inhibitors in their clinical outcomes remains controversial. MATERIALS AND

methodsWe performed a meta-analysis to compare efficacy and safety of PD-L1 + Chemo vs PD-1 + Chemo in ES-SCLC by searching PubMed, Embase, the Cochrane Library, and major oncology conferences. We examined overall survival (OS) as the primary outcome. Secondary outcomes included progression-free survival (PFS), objective response rate (ORR), and treatment-related adverse events (AEs).

resultsWe included four randomized trials (IMpower133, CASPIAN, KEYNOTE-604, and EA5161) with a total of 1553 patients. Direct comparison showed that PD-L1 + Chemo (PFS: hazard ratio [HR] 0.79; OS: HR 0.75) and PD-1 + Chemo (PFS: HR 0.72; OS: HR 0.77) significantly prolonged survival time compared with chemotherapy alone. But PD-L1 + Chemo (relative risk [RR]: 1.07) and PD-1 + Chemo (RR: 1.13) were not superior to chemotherapy alone in terms of ORR. Indirect comparison showed no significant difference in clinical efficacy between PD-L1 + Chemo and PD-1 + Chemo (OS: HR 0.99; PFS: HR 1.10; ORR: RR 0.95). We further stratified patients according to subgroups in terms of OS. In the subgroup of patients with brain metastasis, PD-L1 + Chemo tended to prolong OS (HR: 0.61, 0.28 to 1.32). There were no significant differences between PD-L1 + Chemo and PD-1 + Chemo regarding safety analyses. However, PD-L1 + Chemo exhibited a better safety profile in reducing the risk of treatment discontinuation due to AEs (RR: 0.43, 0.19 to 0.95) and pneumonia (pneumonia of any grade, RR: 0.59, 0.24 to 1.42; pneumonia of grade ≥ 3, RR: 0.37, 0.10 to 1.39).

conclusionsPD-L1 + Chemo and PD-1 + Chemo provided a significant survival benefit relative to chemotherapy alone for ES-SCLC. The efficacy and safety of PD-L1 + Chemo and PD-1 + Chemo were similar based on current evidence.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenDisease ManagementDisease SusceptibilityHumansImmune Checkpoint InhibitorsLung NeoplasmsMolecular Targeted TherapyNeoplasm MetastasisNeoplasm StagingOdds RatioPrognosisProgrammed Cell Death 1 ReceptorSmall Cell Lung CarcinomaTreatment OutcomeB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsPDCD1 protein, humanProgrammed Cell Death 1 ReceptorEfficacyFirst-line therapyPD-1 inhibitorsPD-L1 inhibitorsSmall-cell lung cancer

Identifiers

PMID34297160
PMCPMC10992902
OpenAlexW3183217190

What OpenQuestion holds

Textmetadata
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.