Evidence map›Paper›PMID 35427835›Full record

SynthesisESMO open2022

Efficacy and safety of first-line checkpoint inhibitors-based treatments for non-oncogene-addicted non-small-cell lung cancer: a systematic review and meta-analysis.

M A Siciliano, G Caridà, D Ciliberto, M d'Apolito, C Pelaia, D Caracciolo, C Riillo, P Correale, A Galvano, A Russo and 3 more

Abstract readSystematic ReviewNetwork Meta-Analysis
In one paragraph

Synthesis in ESMO open, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 3 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

26 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Comparison of efficacy and safety of PD-1/PD-L1 combination therapy in first-line treatment of advanced NSCLC: an updated systematic review and network meta-analysis.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
    Pooled it
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  10. Molecular and clonal evolution of primary lesionsTranslational lung cancer research · 2025
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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

13 authors.

M A SicilianoDepartment of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.
G CaridàDepartment of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.
D CilibertoMater Domini University Hospital, Catanzaro, Italy.
M d'ApolitoDepartment of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.
C PelaiaDepartment of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.
D CaraccioloDepartment of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.
C RiilloDepartment of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.
P CorrealeUnit of Medical Oncology, Oncology Department, Grand Metropolitan Hospital 'Bianchi Melacrino-Morelli', Reggio Calabria, Italy.
A GalvanoDepartment of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, Palermo University Hospital, Palermo, Italy.
A RussoDepartment of Surgical, Oncological and Oral Sciences, Section of Medical Oncology, Palermo University Hospital, Palermo, Italy.
V BarbieriUnit of Medical Oncology, Oncology Department, 'Pugliese-Ciaccio' Hospital, Catanzaro, Italy.
P TassoneDepartment of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy.
P TagliaferriDepartment of Experimental and Clinical Medicine, Magna Græcia University, Catanzaro, Italy. Electronic address: tagliaferri@unicz.it.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFrontline immune checkpoint inhibitors (ICI)-based regimens in non-oncogene-addicted non-small-cell lung cancer (NSCLC) have been deeply investigated. To rank the available therapeutic options, we carried out a systematic review and Bayesian meta-analysis.

methodsA comprehensive search for randomized controlled trials (RCTs) of ICI regimens, and a pairwise and a network meta-analysis (NMA) with an all-comers and a stratified strategy were conducted. Endpoints were overall survival (OS), progression-free survival (PFS), objective response rate (ORR) and treatment-related adverse events (TRAEs).

resultsNineteen RCTs involving 17 treatment regimens were included. For the all-comers population, pembrolizumab/chemotherapy (CT) and cemiplimab were most likely the best treatments. For programmed death-ligand 1 (PD-L1) <1% nivolumab/ipilimumab with/without CT, for PD-L1 >1% and 1%-49% pembrolizumab/CT and for PD-L1 >50% cemiplimab ranked first for OS. In non-squamous (NSQ), pembrolizumab with/without CT ranked first for OS; cemiplimab ranked worse than the unselected population. In squamous (SQ), pooled hazard ratio (HR) showed a better chance in improving efficacy for combination strategy, while monotherapy did not, except for cemiplimab that ranked second. Atezolizumab/CT/bevacizumab ranked first in most subgroups for PFS. Direct comparison showed a non-statistically significant benefit of ICI regimens for the liver metastases cohort in OS, with a good ranking for pembrolizumab/CT and atezolizumab/bevacizumab/CT. Regarding brain metastases, all ICI regimens demonstrated an improvement in OS and PFS compared to CT. Nivolumab/ipilimumab/CT ranked better in this subset.

conclusionsOur meta-analysis updated on the most recent findings demonstrates that different ICI treatments rank differently in specific NSCLC settings (histology, biomarker and clinical presentation) offering a novel challenging scenario for clinical decision making and research planning.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungLung NeoplasmsB7-H1 AntigenBevacizumabHumansIpilimumabNivolumabAntineoplastic Agents, ImmunologicalB7-H1 AntigenBevacizumabIpilimumabNivolumabcheckpoints inhibitorsfrontline therapynetwork meta-analysisnon-small-cell lung cancersystematic review

Identifiers

PMID35427835
PMCPMC9271478

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.