TY - JOUR
T1 - A comparison by mismatch repair status of real-world characteristics and outcomes in patients with stage II/III rectal cancer in the Netherlands
AU - Lunenberg, Renee A.
AU - Franken, Ingrid A.
AU - van der Baan, Frederieke H.
AU - Sijtsma, Femke P.C.
AU - Vink, Geraldine R.
AU - Braat, Manon N.G.J.A.
AU - Moons, Leon M.G.
AU - Lacle, Miangela M.
AU - Elferink, Marloes A.G.
AU - Boklage, Susan
AU - Intven, Martijn P.W.
AU - Garside, Jamie
AU - Koopman, Miriam
AU - van Wuijtswinkel, Rob
AU - Roodhart, Jeanine M.L.
N1 - Publisher Copyright:
© 2025 The Author(s). International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.
PY - 2026/2/15
Y1 - 2026/2/15
N2 - A subset of rectal cancer (RC), <5%, exhibits mismatch repair deficiency (dMMR); the remaining are classified as proficient (pMMR). Reported evidence on differences between dMMR and pMMR RC is limited. In this nationwide Dutch study, we compared patients with dMMR and pMMR stage II/III RC based on patient and tumor characteristics, treatment patterns, and associated outcomes. Patients diagnosed between 2015 and 2022 with known mismatch repair status were selected from the Netherlands Cancer Registry. Demographic, tumor, and treatment characteristics were compared in the total cohort. Subsequently, dMMR patients were matched 1:2 to pMMR patients on age, year of diagnosis, clinical tumor stage, and node stage. Overall survival (OS) and event-free survival (EFS) were analyzed using Kaplan–Meier estimates and Cox proportional hazard models. Among 7937 eligible patients, 182 (2.3%) had dMMR RC. These patients were younger and had more poorly differentiated tumors, more variation in histology, more advanced clinical stages, and more B-RAF proto-oncogene serine/threonine kinase mutations. In the total cohort, OS was better for dMMR compared with pMMR (hazard ratio [HR] = 0.62 [95% confidence interval [CI] 0.43–0.91]). In the matched cohort, dMMR continued to exhibit improved OS (HR = 0.54 [95% CI 0.33–0.88]), and demonstrated improved EFS (HR = 0.43 [95% CI 0.29–0.63]) after adjustment for potential confounders. dMMR RC is a rare entity associated with younger age and more advanced stages. Although patients with dMMR RC had significantly improved OS and EFS compared with patients with pMMR RC, immunotherapy may further enhance outcomes. This real-world study provides a basis for future investigations aimed at optimizing therapeutic strategies for patients with dMMR RC.
AB - A subset of rectal cancer (RC), <5%, exhibits mismatch repair deficiency (dMMR); the remaining are classified as proficient (pMMR). Reported evidence on differences between dMMR and pMMR RC is limited. In this nationwide Dutch study, we compared patients with dMMR and pMMR stage II/III RC based on patient and tumor characteristics, treatment patterns, and associated outcomes. Patients diagnosed between 2015 and 2022 with known mismatch repair status were selected from the Netherlands Cancer Registry. Demographic, tumor, and treatment characteristics were compared in the total cohort. Subsequently, dMMR patients were matched 1:2 to pMMR patients on age, year of diagnosis, clinical tumor stage, and node stage. Overall survival (OS) and event-free survival (EFS) were analyzed using Kaplan–Meier estimates and Cox proportional hazard models. Among 7937 eligible patients, 182 (2.3%) had dMMR RC. These patients were younger and had more poorly differentiated tumors, more variation in histology, more advanced clinical stages, and more B-RAF proto-oncogene serine/threonine kinase mutations. In the total cohort, OS was better for dMMR compared with pMMR (hazard ratio [HR] = 0.62 [95% confidence interval [CI] 0.43–0.91]). In the matched cohort, dMMR continued to exhibit improved OS (HR = 0.54 [95% CI 0.33–0.88]), and demonstrated improved EFS (HR = 0.43 [95% CI 0.29–0.63]) after adjustment for potential confounders. dMMR RC is a rare entity associated with younger age and more advanced stages. Although patients with dMMR RC had significantly improved OS and EFS compared with patients with pMMR RC, immunotherapy may further enhance outcomes. This real-world study provides a basis for future investigations aimed at optimizing therapeutic strategies for patients with dMMR RC.
KW - microsatellite stability
KW - mismatch repair deficiency
KW - real-world
KW - rectal cancer
UR - https://www.scopus.com/pages/publications/105015495674
U2 - 10.1002/ijc.70127
DO - 10.1002/ijc.70127
M3 - Article
C2 - 40920070
AN - SCOPUS:105015495674
SN - 0020-7136
VL - 158
SP - 963
EP - 976
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 4
ER -