Evidence map›Paper›PMID 41291649›Full record

SynthesisBMC pulmonary medicine2025

Efficacy and safety of anlotinib combined with immune checkpoint inhibitors in the treatment of extensive-stage small cell lung cancer: a meta-analysis based on real-world data.

Yuying Yan, Xuebin Yang, Xu Yan, Xin Wang, Zhaoshuai Ji

Abstract readMeta-Analysis
In one paragraph

Synthesis in BMC pulmonary medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

5 authors.

Yuying YanDepartment of Pharmacy, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua Medicine, Tsinghua University, No. 168 Litang Road, Changping District, Beijing, 102218, China.
Xuebin YangDepartment of Pharmacy, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua Medicine, Tsinghua University, No. 168 Litang Road, Changping District, Beijing, 102218, China.
Xu YanDepartment of Pharmacy, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua Medicine, Tsinghua University, No. 168 Litang Road, Changping District, Beijing, 102218, China.
Xin WangDepartment of Pharmacy, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua Medicine, Tsinghua University, No. 168 Litang Road, Changping District, Beijing, 102218, China.
Zhaoshuai JiDepartment of Pharmacy, Beijing Tsinghua Changgung Hospital, School of Clinical Medicine, Tsinghua Medicine, Tsinghua University, No. 168 Litang Road, Changping District, Beijing, 102218, China. jzsa00270@btch.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThis research intended to ascertain the clinical efficacy and safety of anlotinib plus immune checkpoint inhibitors (ICIs) in patients suffering from extensive-stage small cell lung cancer (ES-SCLC).

methodsAcademic databases, encompassing PubMed, Embase, and the Cochrane Library, were retrieved to aggregate pertinent research, published up to March 5, 2025. The primary outcome measures covered progression-free survival (PFS), median PFS (mPFS), overall survival (OS), disease control rate (DCR), and objective response rate (ORR). Additionally, secondary outcome measures comprised partial response (PR), complete response (CR), stable disease (SD), and progressive disease (PD).

resultsData pooled from 18 distinct studies, including 1,698 individuals, were synthesized and analyzed. The results revealed a statistically meaningful increase in PFS and OS for patients who received anlotinib combined with ICIs, as opposed to those receiving chemotherapy alone. Furthermore, with regard to improving ORR and DCR, anlotinib plus ICIs was significantly more efficacious than anlotinib monotherapy and chemotherapy monotherapy (P < 0.05). In comparison to chemotherapy monotherapy, anlotinib plus ICIs exhibited a notably elevated risk of thrombocytopenia (OR: 1.7, 95% CI: 1.19–2.43, P = 0.0034). However, when compared with anlotinib monotherapy, anlotinib plus ICIs did not elevate the incidence of severe adverse events (≥ grade 3). Subgroup analysis results indicated that the Eastern Cooperative Oncology Group (ECOG) performance status (PS) served as an independent predictor influencing both PFS and OS outcomes in individuals with SCLC. In contrast, neither brain metastases nor liver metastases emerged as independent prognostic factors influencing PFS and OS.

conclusionThis investigation indicates that anlotinib plus ICIs can extend PFS, elevate ORR and DCR, and prolong OS in individuals with SCLC. This meta-analysis offers new insights into the treatment paradigm for SCLC, indicating that anlotinib plus ICIs can substantially ameliorate clinical outcomes in such patients.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsImmune Checkpoint InhibitorsIndolesLung NeoplasmsQuinolinesSmall Cell Lung CarcinomaHumansProgression-Free SurvivalTreatment OutcomeanlotinibImmune Checkpoint InhibitorsIndolesQuinolinesAnlotinibEfficacyImmune checkpoint inhibitorsMeta-analysisSafetySmall cell lung cancer

Identifiers

PMID41291649
PMCPMC12649059

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.