Evidence map›Paper›PMID 31297962›Full record

SynthesisCancer medicine2019

Rational application of the first-line chemotherapy and immune checkpoint inhibitors in advanced nonsmall cell lung cancer: A meta-analysis.

Rui Cao, Jie-Tao Ma, Shu-Ling Zhang, Li Sun, Yang Liu, Xiang-Yan Zhang, Wei Jing, Le-Tian Huang, Cheng-Bo Han

Abstract readMeta-Analysis
In one paragraph

Synthesis in Cancer medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
–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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. 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

9 authors.

Rui CaoDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.ORCID https://orcid.org/0000-0002-2211-0652
Jie-Tao MaDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Shu-Ling ZhangDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Li SunDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Yang LiuDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Xiang-Yan ZhangDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Wei JingDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Le-Tian HuangDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.
Cheng-Bo HanDepartment of Oncology, Shengjing Hospital of China Medical University, Shenyang, China.

Funding

National Natural Science Foundation of China 81501990
6 · The paper itself

Abstract

objectiveTo compare the relative efficacy of immune checkpoint inhibitors (ICIs) or chemotherapy (CT) alone, or their combination modality in the first-line treatment of advanced nonsmall cell lung cancer (NSCLC).

methodsThis meta-analysis was performed on the eligible randomized controlled trials (RCTs) after searching web databases and meeting abstracts. The main research endpoints were the comparisons of median overall survival (mOS), the OS rate of 6 months (OSR6m), 1 year (OSR1y) and 2 years (OSR2y), median progression-free survival (mPFS), the PFS rate of 6 months (PFSR6m) and 1-year (PFSR1y), objective response rates (ORR), and treatment-related adverse events (TRAEs).

resultsEleven RCTs comprising 6278 cases were included. In the subgroup of programmed death-ligand 1 (PD-L1) ≥50%, compared with chemotherapy, the ICIs showed similar OSR6m (P > 0.05), but significantly improved efficacy in mOS, OSR1y, OSR2y, and ORR (all P < 0.05), also had less grade ≥ 3 TRAEs. Compared with pembrolizumab alone, pembrolizumab plus CT in the subgroup of PD-L1 ≥ 50% had similar mOS, OSR6m, OSR1y, and PFSR1y (all P > 0.05), but significantly improved mPFS, PFSR6m, and ORR (all P < 0.05 for interaction). Compared with the CT group, ICIs plus CT group with PD-L1 ≥ 50% or <1% showed significant benefit in OS, PFS, and ORR (all P < 0.05). However, in the ICIs plus CT group with 1% ≤ PD-L1 ≤ 49%, only PFS and ORR showed significant benefit compared with CT group (all P < 0.05), but not for results of OS.

conclusionsThe findings support the rationale for using pembrolizumab alone in the first-line treatment of PD-L1 ≥ 50% advanced NSCLC due to the similar OS and lower grade ≥ 3 TRAEs. However, the combination of ICIs and chemotherapy is strongly recommended in patients with PD-L1 ≤ 49% for significant survival benefit.

Indexed as

Molecular Targeted TherapyAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsBiomarkers, TumorCarcinoma, Non-Small-Cell LungClinical Trials, Phase II as TopicClinical Trials, Phase III as TopicHumansLung NeoplasmsPublication BiasRemission InductionTreatment OutcomeAntineoplastic Agents, ImmunologicalBiomarkers, Tumorchemotherapyimmunotherapymeta-analysisnonsmall cell lung cancerprogrammed death-ligand 1

Identifiers

PMID31297962
PMCPMC6718602

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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.