Efficacy of Perioperative Pembrolizumab in Mismatch Repair Deficient/Microsatellite Unstable Localized Colorectal Cancers: Results of the Phase II Trial IMHOTEP
Abstract
PURPOSE Mismatch repair deficiency (dMMR) or microsatellite instability (MSI) represents a distinct phenotype among solid tumors resulting in the generation of highly immunogenic neoantigens. Pembrolizumab has been approved in first-line unresectable or metastatic dMMR/MSI colorectal cancers (CRC). We aimed to assess efficacy and tolerance of perioperative pembrolizumab in dMMR/MSI CRC. PATIENTS AND METHODS The prospective multicenter phase II trial IMHOTEP enrolled patients with localized resectable dMMR/MSI CRC to receive one or two cycles of IV pembrolizumab 400 mg once every 6 weeks before surgery and 1-year total duration thereafter. The primary end point was pathologic complete response (pCR) rate (ypT0N0). Secondary objectives included safety, event-free survival, and overall survival. RESULTS IMHOTEP enrolled 81 patients with dMMR/MSI CRC who received at least one cycle of pembrolizumab from November 26, 2021, to February 22, 2023: median age was 66 (21-89) years, 46 (52%) were women, and 63 (71%) had clinical stage III disease at baseline. Out of the 72 patients included in the efficacy population, 38 patients (52.7% [95% CI, 41.4 to 63.9]) achieved a pCR. The exploratory post hoc analysis showed a pCR rate increased from 46% (23/50) after one cycle to 68.2% (15/22) after two cycles of neoadjuvant pembrolizumab ( P = .0125). With a median follow-up of 24.5 (95% CI, 23.3 to 25.6) months, three disease recurrences occurred. Grade ≥3 immune-related toxicities were reported in 14 (15.7%) patients including one grade 5 (myasthenia). CONCLUSION The IMHOTEP trial showed promising results, with pCR achieved after one or two cycles of neoadjuvant pembrolizumab in 53% of patients with dMMR/MSI CRC. To our knowledge, this prospective study is the first to demonstrate the feasibility and the safety of perioperative pembrolizumab.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Christelle de la Fouchardière
Centre Leon Berard, Lyon, France
Aziz Zaanan
Department of Gastroenterology and Digestive Oncology, Paris-Cité University, Paris
Aymeric de Montfort
Romain Cohen
Sorbonne University; Department of Medical Oncology, Saint-Antoine Hospital, AP-HP, INSERM 938, SIRIC CURAMUS, Paris, France
Samuel Le Sourd
Department of Medical Oncology, Centre Eugène-Marquis, Rennes, France
David Tougeron
Department of Hepatology and Gastroenterology, Poitiers University Hospital, Poitiers, France
Emilie Soularue
Department of Oncology, Institute Mutualiste Montsouris, Paris, France
Olivier Dubreuil
Department of Digestive Oncology, Groupe Hospitalier Diaconesses Croix Saint Simon, Paris, France
Nicolas Williet
Emmanuelle Samalin-Scalzi
Department of Medical Oncology, Institut Régional du Cancer de Montpellier (ICM), Université Montpellier, Montpellier, France
Guillaume Piessen
Vincent Hautefeuille
Department of Hepato-Gastroenterology and Gastrointestinal Oncology, CHU d'Amiens, Amiens, France
Marine Jary
University Hospital of Besançon, Clinical Investigational Center, CIC-1431, University Hospital of Besançon, Besançon, France
Meher Ben Abdelghani
Medical Oncology Department, ICANS, Strasbourg, France
Ludovic Evesque
Department of Medical Oncology, Lacassagne Center, Nice, France
Philippe Rochigneux
Medical Oncology Department, Paoli-Calmettes Institute, Aix-Marseille University, Marseille, France
Ellen Blanc
Department of Clinical Research and Innovation, Centre Léon Bérard, Lyon, France
David Pérol
Centre Léon Bérard, Lyon, France
Frédéric Bibeau
Clélia Coutzac
Centre Leon Berard, Lyon, France