Evidence map›Paper›PMID 41252810›Full record

ArticleESMO open2025

Immunotherapy beyond progression combined with platinum-based chemotherapy after primary resistance to first-line immunotherapy in patients with advanced NSCLC and PD-L1 ≥50.

A De Giglio, L Zullo, A Di Federico, M Cani, M Aldea, D Soldato, F G Dall'Olio, F Mantuano, F Sperandi, V Favorito and 9 more

Abstract readMulticenter Study
In one paragraph

Article in ESMO open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Therapeutic vaccines for NSCLC: From mechanisms to clinical translation.Chinese medical journal pulmonary and critical care medicine · 2026
    Review
  2. Review
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

19 authors.

A De GiglioDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy; Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
L ZulloCancer Medicine Department, Gustave Roussy, Villejuif, France.
A Di FedericoDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy; Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
M CaniDepartment of Oncology, Azienda Ospedaliero-Universitaria S. Luigi Gonzaga Hospital, University of Turin, Orbassano, Italy.
M AldeaCancer Medicine Department, Gustave Roussy, Villejuif, France.
D SoldatoDepartment of Medical Oncology, U.O. Clinica di Oncologia Medica, IRCCS Ospedale Policlinico San Martino, Genoa, Italy.
F G Dall'OlioCancer Medicine Department, Gustave Roussy, Villejuif, France.
F MantuanoDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
F SperandiMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
V FavoritoDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy.
A SadowskaDepartment of Respiratory Medicine, Maastricht University Medical Centre, GROW Research Institute for Oncology and Reproduction, Maastricht, The Netherlands.
L E L HendriksDepartment of Respiratory Medicine, Maastricht University Medical Centre, GROW Research Institute for Oncology and Reproduction, Maastricht, The Netherlands.
T GorriaMedical Oncology Department, Hospital Clinic of Barcelona, Barcelona, Spain; Department of Medicine, University of Barcelona, Barcelona, Spain.
L MezquitaMedical Oncology Department, Hospital Clinic of Barcelona, Barcelona, Spain; Department of Medicine, University of Barcelona, Barcelona, Spain; Laboratory of Translational Genomics and Targeted Therapies in Solid Tumors, IDIBAPS, Barcelona, Spain.
F TabbòOncology Unit, Department of Medicine, Michele and Pietro Ferrero Hospital, Verduno, Italy.
S NovelloDepartment of Oncology, Azienda Ospedaliero-Universitaria S. Luigi Gonzaga Hospital, University of Turin, Orbassano, Italy.
F GelsominoMedical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy. Electronic address: francesco_gelsomino@aosp.bo.it.
B BesseCancer Medicine Department, Gustave Roussy, Villejuif, France.
A ArdizzoniDepartment of Medical and Surgical Sciences, University of Bologna, Bologna, Italy; Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrimary resistance to immune checkpoint inhibitors (ICIs) remains a major challenge in patients with advanced non-small-cell lung cancer (NSCLC) and programmed death-ligand 1 (PD-L1) expression ≥50%. The benefit of continuing ICIs beyond progression in combination with chemotherapy is unclear. PATIENTS AND

methodsThis multicenter retrospective study included patients with advanced NSCLC and PD-L1 ≥50% treated with first-line ICI monotherapy at five European centers. Primary resistance was defined as progressive disease as best response or stable disease lasting <6 months. Outcomes of second-line platinum-based chemotherapy alone or combined with ICI were compared. The primary endpoint was progression-free survival 2, defined as time from first-line ICI initiation to second-line progression or death.

resultsAmong 293 eligible patients, 119 (38%) showed primary resistance. Compared with those who did not develop primary resistance, patients with primary resistance more often had multisite progression (74% versus 42%) and less often oligoprogression (13% versus 54%) (P < 0.001). Second-line platinum-based chemotherapy was administered to 43.7% (52/119) of patients with primary resistance, 34.6% (18/52) of whom received ICI beyond progression. Baseline characteristics were comparable across treatment groups. Patients who received ICI beyond progression, compared with those who received only chemotherapy, had significantly longer median progression-free survival 2 (12.3 versus 7.0 months, P < 0.001) and OS (21.8 versus 10.1 months, P = 0.007), with similar overall response rate (66.7% versus 39.3%, P = 0.13). No relevant safety signals emerged.

conclusionIn patients with NSCLC and PD-L1 ≥50% showing primary resistance to first-line ICI, continuing immunotherapy beyond progression combined with chemotherapy may improve survival outcomes. These findings should be considered hypothesis-generating and warrant prospective confirmation.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsB7-H1 AntigenCarcinoma, Non-Small-Cell LungDrug Resistance, NeoplasmImmune Checkpoint InhibitorsImmunotherapyLung NeoplasmsAdultAgedAged, 80 and overDisease ProgressionFemaleHumansMaleMiddle AgedPlatinumB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsPlatinumchemo-immunotherapyimmune checkpoint inhibitorsnon-small cell lung cancerPD-L1 ≥50%primary resistancesecond-line treatment

Identifiers

PMID41252810
PMCPMC12666335

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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.