Evidence map›Paper›PMID 40910565›Full record

ArticleImmunotherapy2025

First-line pembrolizumab for metastatic NSCLC in lower-middle-income countries: bridging the efficacy-effectiveness gap.

Ullas Batra, Mansi Sharma, Alexis Andrew Miller, Kundan Singh Chufal, Irfan Ahmad, Abhinav Dewan, Sabeena Chowdhary, B P Amrith, Rashi Sachdeva, Vanshika Batra and 10 more

Abstract read
In one paragraph

Article in Immunotherapy, 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
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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

20 authors.

Ullas BatraDepartment of Medical Oncology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Mansi SharmaDepartment of Medical Oncology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Alexis Andrew MillerDepartment of Radiation Oncology, Illawarra Cancer Care Centre, New South Wales, Australia.
Kundan Singh ChufalDepartment of Radiation Oncology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Irfan AhmadDepartment of Radiation Oncology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.ORCID 0000-0003-2944-6797
Abhinav DewanDepartment of Medical Oncology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Sabeena ChowdharyDepartment of Medical Oncology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
B P AmrithDepartment of Medical Oncology, HCG Malnad Hospital & Institute of Oncology, Shimoga, India.
Rashi SachdevaDepartment of Research - Medical Unit 5, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Vanshika BatraM.B.B.S. Intern, SGT Medical College, Gurugram, India.
Preetha UmeshDepartment of Radiation Oncology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Kratika BhatiaDepartment of Radiation Oncology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Shrinidhi NathanyDepartment of Pathology and Molecular Oncology, Fortis Memorial Research Institute, Gurugram, India.
Anurag MehtaDepartment of Pathology and Molecular Oncology, Rajiv Gandhi Cancer Institute & Research Centre, Delhi, India.
Paulo Nunes FilhoDepartment of Medical Oncology, Fortrea Inc., Durham, NC, USA.
Khaled TolbaDepartment of Medical Oncology, Fortrea Inc., Durham, NC, USA.
Isagani M ChicoDepartment of Medical Oncology, Fortrea Inc., Durham, NC, USA.
Laura Vidal BoixaderDepartment of Medical Oncology, Fortrea Inc., Durham, NC, USA.
Luca CantiniDepartment of Medical Oncology, Fortrea Inc., Durham, NC, USA.
Kamal S SainiDepartment of Medical Oncology, Fortrea Inc., Durham, NC, USA.ORCID 0000-0001-6301-3309

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPembrolizumab is a standard first-line therapy for advanced/metastatic non-small cell lung cancer (a/mNSCLC) lacking actionable mutations. Data from lower-middle-income countries (LMICs) remain scarce.

methodsFrom January 2019 to June 2024, we prospectively analyzed 78 a/mNSCLC patients receiving pembrolizumab-based first-line therapy. Endpoints included overall survival (OS), progression-free survival (PFS), disease control rate (DCR), and conditional survival probabilities.

resultsWith a median follow-up of 27 months, median OS was 21 months (95% CI: 12.2-30.8) and median PFS 6.3 months (95% CI: 5.5-10.1). At first response evaluation (2 months), partial response was seen in 47.4% (37/78), stable disease in 16.7% (13/78). Next-generation sequencing (85% tested) revealed non-actionable mutations in 70%; notably, 4 of 6 long-term survivors harbored KRAS mutations. PD-L1 TPS ≥ 50% significantly lowered progression and mortality risk. Age, performance status (ECOG), and disease response significantly influenced the OS. The conditional survival probability for an additional 6 months after surviving the first 6 months was 78.1% (90% in patients with controlled disease).

conclusionReal-world LMIC data demonstrated comparable effectiveness of pembrolizumab-based therapy in a/mNSCLC despite a higher proportion of adverse prognostic factors. More studies in diverse clinical settings are needed to provide a reliable estimate of benefit.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungLung NeoplasmsAdultAgedAged, 80 and overDeveloping CountriesFemaleHumansMaleMiddle AgedMutationNeoplasm MetastasisProspective StudiesTreatment OutcomeAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalpembrolizumabComparative effectivenessimmunotherapynon-small cell lung cancerpembrolizumabreal-world data

Identifiers

PMID40910565
PMCPMC12427484

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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.