Surgical journey for participants (pts) in the MATTERHORN trial: A global, randomized, phase 3 study of durvalumab (D) plus 5-fluorouracil, leucovorin, oxaliplatin and docetaxel (FLOT) in resectable gastric/gastroesophageal junction (G/GEJ) adenocarcinoma.
Abstract
353 Background: In MATTERHORN (NCT04592913), perioperative D + FLOT significantly improved event-free survival (EFS) vs placebo (P) + FLOT in pts with resectable G/GEJ adenocarcinoma (Janjigian et al. N Engl J Med 2025). The surgical journey for pts in MATTERHORN is described. Methods: In this global, Phase 3, double-blind study, pts with resectable G/GEJ adenocarcinoma were randomized 1:1 to D 1500 mg or P every 4 weeks (Q4W; Day 1 of each cycle) + FLOT Q2W (Days 1 and 15 of each cycle) for 4 cycles (2 cycles each neoadjuvant / adjuvant), followed by D 1500 mg or P Q4W for 10 cycles. Surgery delays, adjuvant treatment (tx) initiation delays and EFS by surgical status were assessed in the full analysis set (randomized pts; FAS); surgical morbidities and mortalities were assessed in the safety analysis set (pts with ≥1 tx dose; SAS). Results: Of 948 pts randomized to D + FLOT (n=474) or P + FLOT (n=474), 90.9% vs 90.3% attempted surgery, 10.1% vs 10.8% had a surgery delay, and 86.9% vs 84.4% completed surgery. The most common surgery delay was <2 weeks for pts in the D + FLOT (5.9%) and P + FLOT (5.9%) arms. In the D + FLOT vs P + FLOT arms, 2.3% vs 4.6% of pts had an adjuvant tx initiation delay. Median (range) time from surgery to adjuvant tx initiation was 56 (29–152) vs 56 (31–186) days. Among pts in the SAS (D + FLOT [n=475] vs P + FLOT [n=469]), serious adverse events possibly related to surgery were 12.8% vs 13.0%. Of pts in the SAS who completed surgery (D + FLOT [n=413] vs P + FLOT [n=399]), mortality rates were 1.2% vs 1.5% within 30 days of surgery and 3.1% vs 2.0% within 90 days of surgery. Of pts in the FAS who completed surgery (D + FLOT [n=412] vs P + FLOT [n=400]), 91.5% vs 92.3% had an R0 resection, 5.6% vs 5.3% had an R1 resection, and 2.7% vs 2.5% had an R2 resection; 91.0% vs 93.3% had a D2 / D3 lymphadenectomy. Among pts randomized to D + FLOT vs P + FLOT, 35.4% vs 35.0% had a total gastrectomy and 26.8% vs 26.2% had a gastroesophagectomy. D + FLOT improved EFS vs P + FLOT in pts who completed surgery, regardless of tumor location, resection margin or type of lymphadenectomy (Table). Conclusions: In pts with resectable G / GEJ adenocarcinoma, the surgical journey did not differ with D + FLOT vs P + FLOT. EFS benefit with D + FLOT was observed irrespective of tumor location, resection margin or lymphadenectomy type. Clinical trial information: NCT04592913 . D + FLOT n P + FLOT n EFS hazard ratio vs P + FLOT(95% CI) Tumor location G 276 265 0.70 (0.52–0.94) GEJ 136 135 0.64 (0.43–0.95) Resection margin R0 377 369 0.67 (0.51–0.86) R1 23 21 0.58 (0.28–1.19) Type of lymphadenectomy D1 36 26 0.75 (0.33–1.70) D2 / D3 375 373 0.67 (0.52–0.86)
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Daniela Molena
Division of Thoracic Surgery, Memorial Sloan Kettering Cancer Center and Weill Cornell Medicine, New York
Woo Jin Hyung
Department of Surgery, Yonsei University College of Medicine, Seoul, South Korea
Zev A. Wainberg
Jonsson Comprehensive Cancer Center, University of California, Los Angeles, Los Angeles
Moishe Liberman
Centre Hospitalier de l’Université de Montréal, Montreal
Gunnar Folprecht
From Bielefeld University, Medical School and University Medical Center Ostwestfalen-Lippe, Campus Hospital Lippe, Detmold, Germany (J.H.); the Department of Radiation Oncology, Medical University of Graz, Graz, Austria (T.B.); the Clinical Trials Unit, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany (C.S.); the Institute of Surgical Pathology, University Medical Center Freiburg, Germany (P.B.); the Department of Surgery, University Medical Center Schleswig-Holstein–Campus Lübeck, Lübeck, Germany (B.K., T.K.); Comprehensive Cancer Center Augsburg, Faculty of Medicine, University of Augsburg, Augsburg, Germany (R.C.); the Department of General and Visceral Surgery, University Medical Center Freiburg, Freiburg, Germany (S.U.); the Department of General, Visceral, and Thoracic Surgery, University Medical Center Hamburg–Eppendorf, Hamburg, Germany (J.R.I.); the Department of Gastrointestinal Surgery, IRCCS San Raffaele Scientific Institute and San Raffaele Vita-Salute Universi...
Inmaculada Ales Diaz
Hospital Regional Universitario de Malaga, Malaga, Spain
Takaki Yoshikawa
National Cancer Center Hospital, Tokyo, Japan
Salah-Eddin Al-Batran
Krankenhaus Nordwest, University Cancer Center (UCT) Frankfurt, and Frankfurt Institute of Clinical Cancer Research (IKF), Frankfurt, Germany
Eric Van Cutsem
University Hospitals Gasthuisberg, Leuven, Belgium
Kei Muro
Department of Clinical Oncology, Aichi Cancer Center Hospital, Nagoya, Japan
Peter Philipp Grimminger
Department of General, Visceral, and Transplantation Surgery, University Medical Center of the Johannes Gutenberg-University Mainz, Mainz, Germany
Takeshi Omori
Department of Gastroenterological Surgery, Osaka International Cancer Institute, Osaka, Japan
Miguel Sotelo Lezama
Department of Medical Oncology, Hospital María Auxiliadora, Lima, Peru
István Sipocz
Aladár Petz County University Teaching Hospital, Győr, Hungary
Myriam Chalabi
Lin-Yang Cheng
Oncology R&D, Oncology Biometrics, AstraZeneca, Gaithersburg, MD
Eric Heilbron
Oncology R&D, Late-Stage Development, AstraZeneca, Gaithersburg, MD
Scott Robbins
Oncology R&D, Late-Stage Development, AstraZeneca, Gaithersburg, MD
Yelena Y. Janjigian
Memorial Sloan Kettering Cancer Center, New York
Josep Tabernero
Vall d’Hebron Hospital Campus, Barcelona