A cross-sectional analysis from a real-world cohort of patients with microsatellite instability colorectal cancer (MSI-CRC) with localized disease from the Spanish RETUD registry.
Abstract
173 Background: Microsatellite instability (MSI) localized colorectal cancer (CRC) constitutes a subgroup of patients (pts) with different clinical and molecular characteristics and prognosis compared to microsatellite stable (MSS) disease. Here, we present our real world data regarding the management and clinical outcomes of a cohort of MSI-h localized CRC patients included in the Spanish Group of Treatment of Digestive Tumors (TTD) Registry (RETUD). Methods: RETUD is a national, multicenter registry for gastrointestinal tumors from the Spanish TTD Group. In this cross-sectional analysis we evaluated a real-world cohort of MSI-h localized CRC pts diagnosed from 1 st January 2017 to 29 th April 2024. Baseline characteristics and neo/adjuvant treatments are descriptively presented. Disease-free survival (DFS) and overall survival (OS) analyzed by Kaplan-Meier method are presented along with 95% confidence intervals (CI). Results: Five hundred and sixty-one (561) evaluable pts out of 679 MSI-CRC included in RETUD had a localized disease as initial diagnosis. Pts had a median age of 73.1 years and were predominantly Caucasian (97.7%) and female (52.6%). Fifty (12.4%) pts had Lynch Syndrome. Main tumor baseline characteristics are described (Table). Local-locoregional therapeutic procedures were: primary tumor resection in 531 (99.1%) pts and radiotherapy in 18 (3.2%) pts. A total of 198 (35.3%) pts received systemic therapy, mostly chemotherapy (n=165 83.3%) but 18 (9.1%) were treated with pembrolizumab due to unresectable disease. At database cut-off, 123 (21.9%) patients died, mostly due to not related intercurrent illness, and 96 (17.1%) pts developed metastasis. After a median follow up period of 28.5 months, the median (95% CI) OS was not reached and DFS was 78.2 (55.4-NA) months. The impact of adjuvant systemic therapy (chemotherapy vs. non-chemotherapy) for both stage II and stage III pts is under evaluation. Conclusions: Our work provides valuable real-world data from a cohort of MSI-h localized CRC pts treated under clinical practice conditions in Spain, reiterating the good disease prognosis exhibited by this subset of pts in contrast to MSS pts. Main tumor characteristics. Stage at initial diagnosis, n (%) I/II n (%) 55 (9.8) / 258 (46.0) III, n (%) 248 (44.2) Location of primary tumor a , n (%) right colon /left colon /rectum 447 (78.4) / 82 (14.4) / 41 (7.2) Type histological b , n (%) Intestinal 271 (48.9) Mucinous (colloid) adenocarcinoma (>50% mucinous) 115 (20.8) Signet ring cell carcinoma (>50% signet ring) 14 (2.5) Medullary carcinoma 18 (3.2) a Pts with more than 1 primary tumor; the percentage may be over 100%. b Unknown histology in 132 (23.8%) pts and missing data in 7 pts.
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Ana Fernandez Fernandez Montes
Department of Medical Oncology, Complejo Hospitalario Universitario de Ourense, Ourense, Spain
Carolina Muriel Lopez
Medical Oncology Department. Málaga University Regional Hospital, Malaga, Spain
Sandra Lopez
2MD Anderson Cancer Center, Department of Lymphoma Myeloma, Houston, United States
Candela Ferriol Martinez
Medical Oncology Department. Consorcio Hospital General Universitario de Valencia, Valencia, Spain
David Paez
Medical Oncology Department, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain
Belén de Frutos González
Department of Medical Oncology, Ramón y Cajal University Hospital, IRYCIS, CIBERONC, Madrid, Spain
Maria Auxiliadora Gomez Espana
Department of Medical Oncology, Reina Sofía University Hospital, University of Córdoba, CIBERONC, Córdoba, Spain
Carmé García-Benito
Medical Oncology Department, Complejo Hospitalario Universitario de Ourense, Ourense, Spain
Rosario Vidal-Tocino
Medical Oncology Department, Hospital Universitario de Salamanca, IBSAL, Salamanca, Spain
Marcos Melian Sosa
Department of Medical Oncology, Instituto Valenciano de Oncología, Valencia, Spain
Javier Sastre Valera
Department of Medical Oncology, Hospital Clínico San Carlos, Madrid, Spain
Pilar García-Alfonso
Medical Oncology Department, Hospital Universitario Gregorio Marañón, Madrid, Spain
Ismael Ghanem
Department of Medical Oncology Hospital Universitario La Paz, Madrid, Spain
Adelaida La Casta
Medical Oncology Department, Hospital Universitario de Donostia, San Sebastián, Spain
Javier Gallego
Eva Martínez de Castro
Department of Medical Oncology, Hospital Universitario Marqués de Valdecilla, Santander, Spain
Helena Verdaguer
Medical Oncology Department, Hospital Universitario de Granollers, Barcelona, Spain
Cristina Santos
Laboratory of Cancer Metabolism, ONCOBELL Program, Bellvitge Biomedical Research Institute
Encarnacion Jimenez
Medical Oncology Department, Hospital Universitario de Jerez, Jerez De La Frontera, Spain
Cristina Gravalos
Hospital Universitario 12 De Octubre, Madrid, Spain