Evidence map›Paper›PMID 39415113›Full record

SynthesisBMC cancer2024

Network meta-analysis on the efficacy and safety of management for resectable stage IIIA-N2 non-small cell lung cancer.

Qiduo Yu, Haoshuai Yang, Fei Xiao, Zihan Wang, Zhenrong Zhang, Qianli Ma, Hongxiang Feng, Zhoujunyi Tian, Jin Zhang, Chaoyang Liang

Abstract readSystematic ReviewNetwork Meta-Analysis
In one paragraph

Synthesis in BMC cancer, 2024. 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

10 authors.

Qiduo Yu *Department of Thoracic Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
Haoshuai Yang *Department of Thoracic Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
Fei XiaoDepartment of Thoracic Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
Zihan WangInstitute of Clinical Medicine, China-Japan Friendship Hospital, Beijing, 100029, China.
Zhenrong ZhangDepartment of Thoracic Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
Qianli MaDepartment of Thoracic Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
Hongxiang FengDepartment of Thoracic Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
Zhoujunyi TianDepartment of Thoracic Surgery, China-Japan Friendship Hospital, Beijing, 100029, China.
Jin ZhangDepartment of Thoracic Surgery, China-Japan Friendship Hospital, Beijing, 100029, China. jinzhang08@126.com.
Chaoyang LiangDepartment of Thoracic Surgery, China-Japan Friendship Hospital, Beijing, 100029, China. liangchaoyang@zryhyy.com.cn.

Funding

National High Level Hospital Clinical Research Funding 2023-NHLHCRF-BQ-38National High Level Hospital Clinical Research Funding No. 2022-NHLHCRF-YS-04-01National High Level Hospital Clinical Research Funding No. 2022-NHLHCRF-YS-04-04
6 · The paper itself

Abstract

backgroundThere is controversy regarding the optimal treatment for stage IIIA-N2 non-small cell lung cancer (NSCLC). We aimed to address this crucial issue through a frequentist network meta-analysis.

methodsWe conducted a literature database search for randomized controlled trials comparing the following treatment modalities before March 1st, 2023: surgery, radiotherapy, chemotherapy, targeted therapy, immunotherapy, and various combinations of these treatments. Summary data on overall survival (OS) and treatment-related deaths (trDeath) were analyzed using frequentist methods.

resultsTwenty-two randomized controlled trials (RCTs) with 3269 participants were included, covering 17 treatment regimens. In terms of overall survival, surgery followed by adjuvant targeted therapy (S-T), neoadjuvant targeted therapy followed by surgery and adjuvant targeted therapy (T-S-T), and neoadjuvant chemotherapy followed by surgery and adjuvant chemotherapy (C-S-C) were relatively more advantageous than other treatment regimens. Overall, S-T is the most likely treatment option to prolong OS, with a 59.8% likelihood, while immunotherapy plus chemotherapy followed by surgery and adjuvant chemotherapy (IC-S-C) demonstrates good safety.

conclusionS-T and T-S-T treatments have the greatest potential to be the optimal overall survival treatments for stage IIIA-N2 NSCLC patients with positive driver genes, demonstrating significant clinical application prospects. While for patients with negative driver genes, C-S-C treatments benefit the most. The protocol was registered in the Prospective Register of Systematic Reviews, PROSPERO (CRD42022372711).

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsChemotherapy, AdjuvantCombined Modality TherapyHumansImmunotherapyNeoadjuvant TherapyNeoplasm StagingRandomized Controlled Trials as TopicTreatment OutcomeIIIA-N2Network meta-analysisNon-small cell lung cancerOverall survival

Identifiers

PMID39415113
PMCPMC11484310

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.