Evidence map›Paper›PMID 38601759›Full record

ArticleFrontiers in oncology2024

A real-world retrospective, observational study of first-line pembrolizumab plus chemotherapy for metastatic non-squamous non-small cell lung cancer with PD-L1 tumor proportion score < 50% (PEMBROREAL).

Alessandro Cafaro, Flavia Foca, Oriana Nanni, Marco Chiumente, Marina Coppola, Paolo Baldo, Sabrina Orzetti, Fiorenza Enrico, Vito Ladisa, Rosa Lerose and 14 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 12% of its field
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, 7 citations in OpenAlex.

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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

24 authors at 15 institutions in 1 country.

Alessandro CafaroPharmacy Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Flavia FocaUnit of Biostatistics and Clinical Trials, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Oriana NanniUnit of Biostatistics and Clinical Trials, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Marco ChiumenteScientific Direction, Società Italiana di Farmacia Clinica e Terapia (SIFaCT), Turin, Italy.
Marina CoppolaPharmacy Unit, IRCCS Istituto Oncologico Veneto (IOV), Padova, Italy.
Paolo BaldoPharmacy Unit, CRO Aviano IRCCS, National Cancer Institute, Aviano, Italy.
Sabrina OrzettiPharmacy Unit, CRO Aviano IRCCS, National Cancer Institute, Aviano, Italy.
Fiorenza EnricoHospital Pharmacy, Candiolo Cancer Institute, FPO-IRCCS, Candiolo, Turin, Italy.
Vito LadisaHospital Pharmacy, IRCCS National Cancer Institute Foundation, Milan, Italy.
Rosa LeroseHospital Pharmacy, IRCCS-CROB Referral Cancer Center of Basilicata, Rionero in Vulture, PZ, Italy.
Patrizia NardulliPharmacy Unit, National Cancer Research Center Istituto Tumori "Giovanni Paolo II", Bari, Italy.
Piera MaiolinoPharmacy Unit, Istituto Nazionale Tumori "Fondazione G. Pascale", IRCCS, Naples, Italy.
Federica GradelliniPharmacy Unit, Azienda USL-IRCCS di Reggio Emilia, Reggio Emilia, Italy.
Anna Rita GasbarroPharmacy Unit, University Hospital Policlinico, Bari, Italy.
Gisella CarrucciuPharmacy Unit, Azienda Ospedaliera Brotzu, Cagliari, Italy.
Riccardo ProvasiPharmacy Unit, Azienda Sanitaria Universitaria Giuliano Isontina, Trieste, Italy.
Paola Cristina CappellettoHospital Pharmacy, Hospital of Bolzano (SABES-ASDAA), Bolzano, Italy.
Alessandra PasqualiniPharmacy Unit, S.Chiara Hospital, Trento, Italy.
Stefano VecchiaPharmacy Unit, Hospital Guglielmo da Saliceto, Piacenza, Italy.
Marianna VeraldiProtesic and Pharmaceutical Assistance sector n. 3, Department of Health Protection and Health Service Calabria Region, Catanzaro, Italy.
Adele Emanuela De FrancescoPharmacy Unit, Mater Domini Hospital, Catanzaro, Italy.
Lucio CrinòThoracic Oncology Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Angelo DelmonteThoracic Oncology Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Carla MasiniPharmacy Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Istituti di Ricovero e Cura a Carattere Scientifico · ITCentro di Riferimento Oncologico · ITAzienda Ospedaliera G. Brotzu · ITAzienda Ospedaliero Universitario Mater Domini · ITAzienda Sanitaria Unità Locale di Reggio Emilia · ITAzienda Sanitaria Universitaria Integrata di Trieste · ITCandiolo Cancer Institute · ITCentro di Riferimento Oncologico della Basilicata · ITGuglielmo da Saliceto Hospital · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITIstituto Oncologico Veneto · ITIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITIstituto Tumori Bari · ITOspedale di Bolzano · ITOspedale Santa Chiara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The phase III Keynote-189 trial established a first-line treatment combining pembrolizumab with pemetrexed and platinum as a standard treatment for patients with stage IV non-small cell lung cancer (NSCLC) without known Methods: PEMBROREAL is a retrospective, observational study on patients with NSCLC who started pembrolizumab combined with pemetrexed and platinum within the reimbursability time window, considered as December 2019 to December 2020. The primary endpoints were to assess progression-free survival (PFS) and overall survival (OS; using the Kaplan-Meier method), response to therapy, and tolerability. Results: Until February 2022, 279 patients (median follow-up: 19.7 months) have been observed. The median PFS was 8.0 months (95% confidence interval: 6.5-9.2). OS was not reached, but we can estimate a 12- to 24-month survival rate for the combined treatment: 66.1% and 52.5%, respectively. PD-L1 expression and Eastern Cooperative Group (ECOG) Performance Status were both associated with PFS and OS. Overall, only 44.4% of patients reported an adverse event, whereas toxicity led to a 5.4% discontinuation rate. Conclusion: The results of the PEMBROREAL study have shown that the combined treatment of pembrolizumab with pemetrexed and platinum is effective for metastatic non-squamous NSCLC, even for patients with PD-L1 levels below 50%, despite the differences in patient demographics and pathological features compared to the Keynote-189 study. The adverse events reported during the study were more typical of chemotherapy treatment rather than immunotherapy, and physicians were able to manage them easily.

Indexed as

immunotherapynon-small cell lung cancerobservational studypembrolizumabreal-world data

Identifiers

PMID38601759
PMCPMC11004281
OpenAlexW4393229344

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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.