Evidence map›Paper›PMID 32759236›Full record

ArticleJournal for immunotherapy of cancer2020

Efficacy of immunotherapy in lung cancer with co-occurring mutations in NOTCH and homologous repair genes.

Marco Mazzotta, Marco Filetti, Mario Occhipinti, Daniele Marinelli, Stefano Scalera, Irene Terrenato, Francesca Sperati, Matteo Pallocca, Francesco Rizzo, Alain Gelibter and 18 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

17 citing papers in PubMed, 20 citations in OpenAlex.

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  12. Roles of Notch Signaling in the Tumor Microenvironment.International journal of molecular sciences · 2022
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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

28 authors at 6 institutions in 4 countries.

Marco MazzottaDivision of Medical Oncology 2, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Marco FilettiDepartment of Clinical and Molecular Medicine, Oncology Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy.
Mario OcchipintiMedical Oncology Unit B, Policlinico Umberto I, Sapienza University of Rome, Rome, Italy.
Daniele MarinelliDepartment of Clinical and Molecular Medicine, Oncology Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy.
Stefano ScaleraSAFU Laboratory, Department of Research, Advanced Diagnostic, and Technological Innovation, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Irene TerrenatoBiostatistics-Scientific Direction, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Francesca SperatiBiostatistics Unit, San Gallicano Dermatological Institute IRCCS, Rome, Italy.
Matteo PalloccaSAFU Laboratory, Department of Research, Advanced Diagnostic, and Technological Innovation, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Francesco RizzoDepartment of Clinical and Molecular Medicine, Oncology Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy.
Alain GelibterMedical Oncology Unit B, Policlinico Umberto I, Sapienza University of Rome, Rome, Italy.
Andrea BotticelliMedical Oncology Unit B, Policlinico Umberto I, Sapienza University of Rome, Rome, Italy.
Giorgia ScafettaDepartment of Clinical and Molecular Medicine, Pathology Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy.
Arianna Di NapoliDepartment of Clinical and Molecular Medicine, Pathology Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy.
Eriseld KrasniqiDivision of Medical Oncology 2, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Laura PizzutiDivision of Medical Oncology 2, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Maddalena BarbaDivision of Medical Oncology 2, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Silvia CarpanoDivision of Medical Oncology 2, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Patrizia ViciDivision of Medical Oncology 2, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Maurizio FanciulliSAFU Laboratory, Department of Research, Advanced Diagnostic, and Technological Innovation, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Francesca De NicolaSAFU Laboratory, Department of Research, Advanced Diagnostic, and Technological Innovation, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Ludovica CiuffredaSAFU Laboratory, Department of Research, Advanced Diagnostic, and Technological Innovation, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Frauke GoemanOncogenomic and Epigenetic Unit, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Ruggero De MariaInstitute of General Pathology, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome, Italy.
Andrea VecchioneDepartment of Clinical and Molecular Medicine, Pathology Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy.
Raffaele GiustiMedical Oncology Unit, Sant'Andrea Hospital, Rome, Italy.
Gennaro CilibertoScientific Direction, IRCCS Regina Elena National Cancer Institute, Rome, Italy.
Paolo MarchettiDepartment of Clinical and Molecular Medicine, Oncology Unit, Sant'Andrea Hospital, Sapienza University of Rome, Rome, Italy.
Marcello Maugeri-SaccàDivision of Medical Oncology 2, IRCCS Regina Elena National Cancer Institute, Rome, Italy maugeri.marcello@gmail.com.ORCID 0000-0003-2287-9581
National Cancer Institute · MYCTO Andrea Alesini · ITPoliclinico Umberto I · ITCancer Research And Biostatistics · USMRC Biostatistics Unit · GBUniversità Cattolica del Sacro Cuore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) provide significant survival benefits in non-small cell lung cancer (NSCLC). Nevertheless, while some patients obtain a prolonged benefit, a non-negligible fraction of patients experiences an ultrarapid disease progression. Identifying specific molecular backgrounds predicting opposite outcomes is instrumental to optimize the use of these agents in clinical practice.

methodsWe carried out an observational study with prospective design envisioning targeted next-generation sequencing (NGS) with an approved assay in 55 patients with metastatic NSCLC (Rome cohort), of whom 35 were treated with ICIs. Data from three clinically comparable datasets were collected and combined into a metadataset containing 779 patients. The datasets were related to the Memorial Sloan Kettering Cancer Center (MSKCC) cohort (tissue-based NGS) and the randomized phase II and III POPLAR and OAK trials (blood-based NGS).

resultsIn patients treated with ICIs in the Rome cohort, co-occurring mutations in NOTCH1-3 and homologous repair (HR) genes were associated with durable clinical benefit. Using the MSKCC/POPLAR/OAK metadaset, we confirmed the relationship between the NOTCH

conclusionsCo-occurring mutations in the NOTCH and HR pathways are associated with increased efficacy of immunotherapy in advanced NSCLC. This genomic predictor deserves further investigation to fully assess its potential in informing therapeutic decisions.

Indexed as

AdultAgedFemaleHumansImmunotherapyLung NeoplasmsMaleMiddle AgedMutationReceptors, NotchReceptors, Notchimmunotherapylung neoplasmstumor biomarkers

Identifiers

PMID32759236
PMCPMC7409965
OpenAlexW3047062181

What OpenQuestion holds

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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.