Evidence map›Paper›PMID 40323324›Full record

ArticleDiscover oncology2025

Evaluating the safety and efficacy of combination immune checkpoint inhibitors and chemotherapy treatment in extensive-stage small cell lung cancer.

Yalin Xie, Xiang Li, Hongxu Lu, An Lei, Lei Li, Yun Jin, Yanyang Li, Wenchang Cen, Weifeng Zou, Ning Su and 1 more

Abstract read
In one paragraph

Article in Discover oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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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

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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

1 citing paper in PubMed.

  1. 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

11 authors.

Yalin Xie *State Key Laboratory of Respiratory Disease, Department of Oncology, Guangzhou Chest Hospital, Guangzhou Medical University, Guangdong, 510095, People's Republic of China.
Xiang Li *Department of Pharmacy, Guangzhou Chest Hospital, Guangzhou Medical University, Guangdong, 510095, People's Republic of China.
Hongxu Lu *State Key Laboratory of Respiratory Disease, Department of Oncology, Guangzhou Chest Hospital, Guangzhou Medical University, Guangdong, 510095, People's Republic of China.
An LeiState Key Laboratory of Respiratory Disease, Department of Oncology, Guangzhou Chest Hospital, Guangzhou Medical University, Guangdong, 510095, People's Republic of China.
Lei LiState Key Laboratory of Respiratory Disease, Department of Oncology, Guangzhou Chest Hospital, Guangzhou Medical University, Guangdong, 510095, People's Republic of China.
Yun JinState Key Laboratory of Respiratory Disease, Department of Oncology, Guangzhou Chest Hospital, Guangzhou Medical University, Guangdong, 510095, People's Republic of China.
Yanyang LiState Key Laboratory of Respiratory Disease, Department of Oncology, Guangzhou Chest Hospital, Guangzhou Medical University, Guangdong, 510095, People's Republic of China.
Wenchang CenState Key Laboratory of Respiratory Disease, Department of Oncology, Guangzhou Chest Hospital, Guangzhou Medical University, Guangdong, 510095, People's Republic of China.
Weifeng ZouDepartment of Respiratory and Critical Care, Guangzhou Chest Hospital, Guangzhou Medical University, Guangdong, 510095, People's Republic of China.
Ning SuState Key Laboratory of Respiratory Disease, Department of Oncology, Guangzhou Chest Hospital, Guangzhou Medical University, Guangdong, 510095, People's Republic of China. snxkyy@gzhmu.edu.cn.
Jizhen LiangDepartment of Oncology, Guangzhou Red Cross Hospital, Jinan University, Guangdong, 510095, People's Republic of China. liangjz1023@163.com.

Funding

Guangzhou Science and Technology Program 2023A03J0534Guangzhou Science and Technology Program 2023A03J0539Guangzhou Science and Technology Program 2023A03J0992Guangzhou Science and Technology Program 2024A03J0577"Tianshan Yingcai" Medical and Health Care High-level Talent Training Program Project TSYC202301B123
6 · The paper itself

Abstract

objectiveThis research effort was designed to retrospectively analyze the safety and efficacy of immune checkpoint inhibitors (ICIs) deployed in combination with chemotherapy in extensive-stage small cell lung cancer (ES-SCLC).

methodsES-SCLC patients diagnosed at Guangzhou Chest Hospital from January 1, 2018, through June 30, 2022, were divided into two groups: an IEP group (administered ICIs with etoposide and platinum-based chemotherapy) and an EP group (chemotherapy only). Median overall survival (OS) and progression-free survival (PFS) served as the primary endpoints for analysis, while secondary endpoints that were assessed included objective response rate (ORR), 1- and 2-year OS, and safety. Subgroup analyses explored sites of metastatic progression and ICI types.

resultsIn total, 102 patients were enrolled, including 33 in the IEP group and 69 in the EP group. The median OS was significantly longer in the IEP group (14.3 vs. 10.8 months, P = 0.028), while the median PFS showed no significant difference (5.9 vs. 5.3 months, P = 0.746). In subgroup analyses, those patients with brain metastases were found to have derived benefit from IEP treatment (median OS 15.9 vs. 8.3 months, hazard ratio [HR], 0.266 [95% CI, 0.087 to 0.817], P = 0.014). The PFS of patients administered PD-L1 inhibitors was longer than that of those administered PD-1 inhibitors (median 7.0 vs. 3.5 months; HR, 0.342 [95% CI, 0.141 to 0.832], P = 0.014). The safety profile of the IEP regimen was favorable, although these patients were more likely to experience immune-related pneumonia (12.1% vs. 1.4%, P = 0.020). Subgroups analyses showed that patients with a history of smoking (HR = 0.54, 95% CI: 0.31-0.94) and brain metastases (HR = 0.27, 95% CI: 0.09-0.82) were more likely to benefit from IEP treatment.

conclusionThe combination of ICIs and chemotherapy can afford better survival outcomes for ES-SCLC patients, especially in individuals suffering from brain metastases, and they should thus be considered as promising first-line treatment options. However, careful management of immune-related adverse events is crucial.

Indexed as

Brain metastasisChemotherapyImmune checkpoint inhibitorsPD-L1/PD-1Small cell lung cancer

Identifiers

PMID40323324
PMCPMC12052614

What OpenQuestion holds

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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.