Evidence map›Paper›PMID 39656678›Full record

Observational studyJapanese journal of clinical oncology2025

Real-world data of first-line treatment with pembrolizumab for NSCLC with high PD-L1 expression in elderly patients: a subgroup analysis of HOT/NJLCG2001.

Kazunari Tateishi, Hidenori Mizugaki, Yasuyuki Ikezawa, Ryo Morita, Keiki Yokoo, Toshiyuki Sumi, Mari Aso, Hajime Kikuchi, Atsushi Nakamura, Motoki Sekikawa and 12 more

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Japanese journal of clinical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

22 authors.

Kazunari TateishiFirst Department of Internal Medicine, Shinshu University School of Medicine, Matsumoto, Japan.ORCID 0000-0003-4641-640X
Hidenori MizugakiDepartment of Respiratory Medicine, NHO Hokkaido Cancer Center, Sapporo, Japan.
Yasuyuki IkezawaDepartment of Respiratory Medicine, Oji General Hospital, Tomakomai, Japan.
Ryo MoritaDepartment of Respiratory Medicine, Akita Kousei Medical Center, Akita, Japan.
Keiki YokooDepartment of Respiratory Medicine, Teine Keijinkai Hospital, Sapporo, Japan.
Toshiyuki SumiDepartment of Respiratory Medicine, Hakodate Goryoukaku Hospital, Hakodate, Japan.ORCID 0000-0002-2540-5878
Mari AsoDepartment of Respiratory Medicine, Yamagata Prefectural Central Hospital, Yamagata, Japan.
Hajime KikuchiDepartment of Respiratory Medicine, Obihiro-Kousei General Hospital, Obihiro, Japan.
Atsushi NakamuraDepartment of Pulmonary Medicine, Sendai Kousei Hospital, Sendai, Japan.
Motoki SekikawaDepartment of Respiratory Medicine, Steel Memorial Muroran Hospital, Muroran, Japan.
Fumiaki YoshiikeDepartment of Respiratory Medicine, Nagano Municipal Hospital, Nagano, Japan.
Yasuo KitamuraDepartment of Respiratory Medicine, Kushiro City General Hospital, Kushiro, Japan.
Nozomu KimuraDepartment of Respiratory Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
Tsutomu HachiyaDepartment of Respiratory Medicine, Japanese Red Cross Suwa Hospital, Suwa, Japan.
Kyoji TsurumiDepartment of Respiratory Medicine, Miyagi Cancer Center, Natori, Japan.
Toshihiko AgatsumaDepartment of Respiratory Medicine, Shinshu Ueda Medical Center, Ueda, Japan.
Furuta MegumiDepartment of Respiratory Medicine, Faculty of Medicine, Hokkaido University, Sapporo, Japan.
Keiichi NakamuraDepartment of Respiratory Medicine, National Hospital Organization Asahikawa Medical Center, Asahikawa, Japan.
Daisuke JinguDepartment of Respiratory Medicine, Saka General Hospital, Shiogama, Japan.
Hiroshi YamamotoDepartment of Respiratory Medicine, Iida Municipal Hospital, Iida, Japan.
Makoto KosakaCenter of Infectious Diseases, Nagano Prefectural Shinshu Medical Center, Suzaka, Japan.
Hiroshi YokouchiDepartment of Respiratory Medicine, NHO Hokkaido Cancer Center, Sapporo, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn the first-line treatment of elderly patients with advanced-stage non-small cell lung cancer (NSCLC) with high programmed death-ligand 1 (PD-L1) expression (tumor proportion score ≥ 50%), this study aimed to determine whether pembrolizumab monotherapy (MONO) or pembrolizumab plus platinum-based chemotherapy (COMB) should be selected.

methodsWe performed a retrospective multicenter study (sub-analysis of the HOT/NJLCG2001 trial) of 299 patients with NSCLC with high PD-L1 expression who received MONO or COMB as the first-line treatment between December 2018 and January 2020. We selected patients aged 75 years and older and assessed the clinical efficacy and toxicity.

resultsIn total, 81 (median age: 79 years) and 19 (median age: 76 years) patients received MONO and COMB, respectively. Twenty patients with a performance status (PS) score of 2-3 were enrolled in the MONO group. The median progression-free survival (PFS) was 7.8 and 8.9 months in the MONO and COMB groups, respectively. The median overall survival (OS) was 14.6 and 20.3 months, and the 2-year survival rates were 38.8 and 49.9%, respectively. Furthermore, 29.6% and 26.3% of patients discontinued treatment due to adverse events, respectively. In MONO, patients with PS 0-1 had a longer PFS (10.5 months) and OS (21.7 months) than those with PS 2-3 (0.7 and 1.6 months, respectively).

conclusionSome elderly patients with NSCLC and high PD-L1 expression might benefit from COMB; however, MONO is considered the preferred treatment. MONO may not be an effective or feasible treatment for patients with PS 2-3, even with high PD-L1 expression.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalAntineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenCarcinoma, Non-Small-Cell LungLung NeoplasmsAgedAged, 80 and overFemaleHumansMaleRetrospective StudiesAntibodies, Monoclonal, HumanizedAntineoplastic Agents, ImmunologicalB7-H1 AntigenCD274 protein, humanpembrolizumabchemotherapyelderly patientslung cancernon-small cell lung cancerPD-L1

Identifiers

PMID39656678
PMCPMC11882503

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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.