M. Pérol

ORCID: 0000-0002-3296-423X
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About
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Research Areas
  • Lung Cancer Treatments and Mutations
  • Lung Cancer Research Studies
  • Lung Cancer Diagnosis and Treatment
  • Cancer Immunotherapy and Biomarkers
  • Colorectal Cancer Treatments and Studies
  • Cancer Genomics and Diagnostics
  • HER2/EGFR in Cancer Research
  • Gastric Cancer Management and Outcomes
  • Pancreatic and Hepatic Oncology Research
  • Brain Metastases and Treatment
  • Cancer therapeutics and mechanisms
  • Multiple and Secondary Primary Cancers
  • Cancer Treatment and Pharmacology
  • Neuroendocrine Tumor Research Advances
  • Radiomics and Machine Learning in Medical Imaging
  • Hepatocellular Carcinoma Treatment and Prognosis
  • Economic and Financial Impacts of Cancer
  • Occupational and environmental lung diseases
  • Cancer Diagnosis and Treatment
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Neutropenia and Cancer Infections
  • Peptidase Inhibition and Analysis
  • PI3K/AKT/mTOR signaling in cancer
  • Ferroptosis and cancer prognosis

Centre Léon Bérard
2016-2025

Centre de Recherche en Cancérologie de Lyon
2016-2025

Université Claude Bernard Lyon 1
2012-2025

Dana-Farber Cancer Institute
2025

Université de Lyon
2023

National Cancer Center Hospital East
2023

AstraZeneca (Brazil)
2023

MSD (UK) Limited (United Kingdom)
2023

Boehringer Ingelheim (India)
2023

Daiichi Sankyo (United States)
2023

Alectinib, a highly selective inhibitor of anaplastic lymphoma kinase (ALK), has shown systemic and central nervous system (CNS) efficacy in the treatment ALK-positive non-small-cell lung cancer (NSCLC). We investigated alectinib as compared with crizotinib patients previously untreated, advanced NSCLC, including those asymptomatic CNS disease.In randomized, open-label, phase 3 trial, we randomly assigned 303 NSCLC to receive either (600 mg twice daily) or (250 daily). The primary end point...

10.1056/nejmoa1704795 article EN New England Journal of Medicine 2017-06-06

Human epidermal growth factor receptor 2 (HER2)-targeted therapies have not been approved for patients with non-small-cell lung cancer (NSCLC). The efficacy and safety of trastuzumab deruxtecan (formerly DS-8201), a HER2 antibody-drug conjugate, in

10.1056/nejmoa2112431 article EN New England Journal of Medicine 2021-09-18

We conducted a phase III study to compare the survival impact of concurrent versus sequential treatment with radiotherapy (RT) and chemotherapy (CT) in unresectable stage non-small-cell lung cancer (NSCLC).Patients were randomly assigned one two arms. In arm, patients received induction CT cisplatin (120 mg/m2) on days 1, 29, 57, vinorelbine (30 mg/m2/wk) from day 1 78, followed by thoracic RT at dose 66 Gy 33 fractions (2 per fraction 5 week). same was started cycles 20 mg/m2/d etoposide 50...

10.1200/jco.2005.03.070 article EN Journal of Clinical Oncology 2005-08-09

The ALEX study demonstrated significantly improved progression-free survival (PFS) with alectinib versus crizotinib in treatment-naive ALK-positive non-small-cell lung cancer (NSCLC) at the primary data cut-off (9 February 2017). We report mature PFS (cut-off: 30 November 2018) and overall (OS) up to 5 years 29 2019).Patients stage III/IV NSCLC were randomized receive twice-daily 600 mg (n = 152) or 250 151) until disease progression, toxicity, withdrawal death. Primary end point:...

10.1016/j.annonc.2020.04.478 article EN cc-by-nc-nd Annals of Oncology 2020-05-11

Purpose Comprehensive geriatric assessment (CGA) is recommended to assess the vulnerability of elderly patients, but its integration in cancer treatment decision making has never been prospectively evaluated. Here, patients with advanced non–small-cell lung (NSCLC), we compared a standard strategy chemotherapy allocation on basis performance status (PS) and age an experimental CGA. Patients Methods In multicenter, open-label, phase III trial, ≥ 70 years old PS 0 2 stage IV NSCLC were...

10.1200/jco.2015.63.5839 article EN Journal of Clinical Oncology 2016-02-17

Immunotherapy is becoming a standard of care for many cancers. Immune-checkpoint inhibitors (ICI) can generate immune-related adverse events. Interstitial lung disease (ILD) has been identified as rare but potentially severe event. Between December 2015 and April 2016, we conducted retrospective study in centres experienced ICI use. We report the main features ICI–ILD with focus on clinical presentation, radiological patterns therapeutic strategies. 64 (3.5%) out 1826 cancer patients...

10.1183/13993003.00050-2017 article EN European Respiratory Journal 2017-08-01

BackgroundThe phase III ALEX study in patients with treatment-naive advanced anaplastic lymphoma kinase mutation-positive (ALK+) non-small-cell lung cancer (NSCLC) met its primary end point of improved progression-free survival (PFS) alectinib versus crizotinib. Here, we present detailed central nervous system (CNS) efficacy data from ALEX.Patients and methodsOverall, 303 aged ≥18 years underwent 1:1 randomization to receive twice-daily doses 600 mg or crizotinib 250 mg. Brain imaging was...

10.1093/annonc/mdy405 article EN cc-by-nc Annals of Oncology 2018-09-11

In approximately 60% of patients with NSCLC who are receiving EGFR tyrosine kinase inhibitors, resistance develops through the acquisition T790M mutation. We aimed to demonstrate that a highly sensitive and quantitative next-generation sequencing analysis mutations from urine plasma specimens is feasible.Short footprint mutation enrichment assays were used interrogate activating in or enrolled TIGER-X (NCT01526928), phase 1/2 clinical study rociletinib previously treated mutant-positive...

10.1016/j.jtho.2016.05.035 article EN cc-by-nc-nd Journal of Thoracic Oncology 2016-07-25

IntroductionImmune-checkpoint inhibitor (ICI) efficacy in patients with NSCLC harboring molecular alterations remains poorly elucidated. This study was undertaken to determine ICI against BRAF-, HER2-, MET-, and RET-NSCLC a real-world setting.MethodsIn this retrospective, multicenter ICI-treated MET- or RET-NSCLCs, we analyzed clinical characteristics outcomes: ICI-treatment duration, progression-free survival (PFS), objective response rate, duration of response, overall (OS).ResultsThere...

10.1016/j.jtho.2019.12.129 article EN cc-by-nc-nd Journal of Thoracic Oncology 2020-01-13

This phase III study investigated whether continuation maintenance with gemcitabine or switch erlotinib improves clinical outcome compared observation in patients advanced non-small-cell lung cancer (NSCLC) whose disease was controlled after cisplatin-gemcitabine induction chemotherapy.Four hundred sixty-four stage IIIB/IV NSCLC without tumor progression four cycles of were randomly assigned to (1,250 mg/m(2) days 1 and 8 a 3-week cycle) daily (150 mg/day) arms. On progression, all three...

10.1200/jco.2011.39.9782 article EN Journal of Clinical Oncology 2012-09-05

The phase II prospective, noncomparative BRAIN study (NCT00800202) investigated efficacy and safety of bevacizumab in chemotherapy-naïve or pretreated patients with non-small cell lung cancer (NSCLC) asymptomatic untreated brain metastases to provide data this previously unexplored subgroup.Patients stage IV nonsquamous NSCLC, Eastern Cooperative Oncology Group performance status 0-1, untreated, received first-line (15 mg/kg) plus carboplatin (area under the curve ×6) paclitaxel (200...

10.1158/1078-0432.ccr-14-2082 article EN Clinical Cancer Research 2015-01-23

Selpercatinib, a highly selective potent and brain-penetrant RET inhibitor, was shown to have efficacy in patients with advanced fusion–positive non–small-cell lung cancer (NSCLC) nonrandomized phase 1–2 study. Download PDF of the Research Summary. In randomized 3 trial, we evaluated safety first-line selpercatinib as compared control treatment that consisted platinum-based chemotherapy or without pembrolizumab at investigator's discretion. The primary end point progression-free survival...

10.1056/nejmoa2309457 article EN New England Journal of Medicine 2023-10-21

LBA9000 Background: EGFR TKIs are standard 1L therapy for metastatic NSCLC with sensitizing mutations; however, most patients (pts) ultimately experience PD. We report the protocol-specified final analysis (FA) from randomized, double-blind, phase 3 KEYNOTE-789 study of pemetrexed (pem) and platinum-based chemotherapy (chemo) or without pembrolizumab (pembro) as subsequent pts TKI-resistant, EGFR-mutant, nonsquamous (NCT03515837). Methods: Adults histologically cytologically confirmed stage...

10.1200/jco.2023.41.17_suppl.lba9000 article EN Journal of Clinical Oncology 2023-06-07

PURPOSE Epidermal growth factor receptor ( EGFR ) tyrosine kinase inhibitors (TKIs) are standard first-line therapy for -mutant, metastatic non–small cell lung cancer (NSCLC); however, most patients experience disease progression. We report results from the randomized, double-blind, phase III KEYNOTE-789 study of pemetrexed and platinum–based chemotherapy with or without pembrolizumab TKI-resistant, nonsquamous NSCLC (ClinicalTrials.gov identifier: NCT03515837 ). METHODS Adults...

10.1200/jco.23.02747 article EN Journal of Clinical Oncology 2024-08-22
Myung‐Ju Ahn Kentaro Tanaka Luís Paz-Ares Robin Cornelissen Nicolas Girard and 95 more Elvire Pons‐Tostivint David Vicente Baz Shunichi Sugawara Manuel Cobo M. Pérol Céline Mascaux Elena Poddubskaya Satoru Kitazono Hidetoshi Hayashi Min Hee Hong Enriqueta Felip Richard D. Hall Óscar Juan Daniel Brungs Shun Lü Marina Chiara Garassino Michael Chargualaf Yong Zhang Paul Howarth Deise Uema Aaron Lisberg Jacob Sands Gastón L. Martinengo Juan Puig Daniel Brungs Bo Gao Adnan Nagria Christos S. Karapetis Sagun Parakh Cheol Park Gaëtan Catala Frédéric Forget Sebahat Ocak Naveen S. Basappa Geoffrey Liu Ines B. Menjak Benjamin Shieh Shun Lü Feng Luo Hongmei Sun Jialei Wang Yu Yao Milada Zemanová Jaafar Bennouna Nicolas Girard Laurent Greillier Corinne Lamour H. Léna Céline Mascaux Julien Mazières Denis Moro‐Sibilot M. Pérol Elvire Pons‐Tostivint Virginie Westeel Akin Atmaca Christine Greil Niels Reinmuth Christian Schumann Thomas Wehler Juergen Wolf James Ho Csaba Böcskei Federico Cappuzzo Filippo de Marinis Claudia Proto Manlio Mencoboni Silvia Novello Stefania Salvagni Héctor Soto Parrà Haruko Daga Yasushi Goto Hidetoshi Hayashi Satoru Kitazono Kiyotaka Yoh Ryo Ko Masashi Kondo Toshiyuki Kozuki Takayasu Kurata Hideaki Mizutani Kadoaki Ohashi Satoshi Oizumi Isamu Okamoto Satoshi Sakaguchi H Ozasa Shunichi Sugawara Yuichi Tambo Motohiro Tamiya Hiroshi Tanaka Isamu Okamoto Froylán López-López Francisco Javier Ramirez Godinez Jerónimo Rafael Rodríguez Cid Robin Cornelissen Steven Gans Jos A. Stigt

PURPOSE The randomized, open-label, global phase III TROPION-Lung01 study compared the efficacy and safety of datopotamab deruxtecan (Dato-DXd) versus docetaxel in patients with pretreated advanced/metastatic non–small cell lung cancer (NSCLC). METHODS Patients received Dato-DXd 6 mg/kg or 75 mg/m 2 once every 3 weeks. Dual primary end points were progression-free survival (PFS) overall (OS). Objective response rate, duration response, secondary points. RESULTS In total, 299 305 randomly...

10.1200/jco-24-01544 article EN Journal of Clinical Oncology 2024-09-09
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