TY - JOUR
T1 - The impact of mismatch repair status in colorectal cancer on the decision to treat with adjuvant chemotherapy
T2 - an Australian population-based multicenter study
AU - He, Emily Y.J.
AU - Hawkins, Nicholas J.
AU - Mak, Gabriel
AU - Roncolato, Felicia
AU - Goldstein, David
AU - Liauw, Winston
AU - Clingan, Philip
AU - Chin, Melvin
AU - Ward, Robyn L.
N1 - Publisher Copyright:
© AlphaMed Press 2016.
PY - 2016/3/23
Y1 - 2016/3/23
N2 - Background. Testing for mismatch repair (MMR) status in colorectal cancer (CRC) may provide useful prognostic and predictive information. We evaluated the impact of such testing on real world practice regarding adjuvant chemotherapy for patients with resected CRC. Patients and Methods. A total of 175 patients with stage II and III mismatch repair-deficient (MMRD) CRC were identified from an Australian population-based study of incident CRCs. Their treatment decisions were compared with those for a cohort of 773 stage-matched patients with mismatch repair-proficient (MMRP) CRCs. The effect of MMR status, age, and pathologic characteristics on treatment decisions was determined using multiple regression analysis. Results. Overall, 32% of patients in stage II and 71% of patients in stage III received adjuvant chemotherapy. Among the stage II patients, those with MMRD cancer were less likely to receive chemotherapy than were MMRP cases (15%vs.38%;p <. 0001). In this group, the treatment decision was influenced by age, tumor location, and T stage. MMR status influenced the treatment decision such that its impact diminished with increasing patient age. Among patients with stage III tumors, no difference was found in the chemotherapy rates between the MMRD and MMRP cases. In this group, age was the only significant predictor of the treatment decision. Conclusion. The findings of this study suggest that knowledge of the MMR status of sporadic CRC influences treatment decisions for stage II patients, in an era when clear recommendations as to how these findings should influence practice are lacking.
AB - Background. Testing for mismatch repair (MMR) status in colorectal cancer (CRC) may provide useful prognostic and predictive information. We evaluated the impact of such testing on real world practice regarding adjuvant chemotherapy for patients with resected CRC. Patients and Methods. A total of 175 patients with stage II and III mismatch repair-deficient (MMRD) CRC were identified from an Australian population-based study of incident CRCs. Their treatment decisions were compared with those for a cohort of 773 stage-matched patients with mismatch repair-proficient (MMRP) CRCs. The effect of MMR status, age, and pathologic characteristics on treatment decisions was determined using multiple regression analysis. Results. Overall, 32% of patients in stage II and 71% of patients in stage III received adjuvant chemotherapy. Among the stage II patients, those with MMRD cancer were less likely to receive chemotherapy than were MMRP cases (15%vs.38%;p <. 0001). In this group, the treatment decision was influenced by age, tumor location, and T stage. MMR status influenced the treatment decision such that its impact diminished with increasing patient age. Among patients with stage III tumors, no difference was found in the chemotherapy rates between the MMRD and MMRP cases. In this group, age was the only significant predictor of the treatment decision. Conclusion. The findings of this study suggest that knowledge of the MMR status of sporadic CRC influences treatment decisions for stage II patients, in an era when clear recommendations as to how these findings should influence practice are lacking.
KW - Adjuvant chemotherapy
KW - Colorectal cancer
KW - Microsatellite instability
KW - Mismatch repair deficiency
KW - Treatment decisions
UR - http://www.scopus.com/inward/record.url?scp=84966318670&partnerID=8YFLogxK
U2 - 10.1634/theoncologist.2015-0530
DO - 10.1634/theoncologist.2015-0530
M3 - Article
C2 - 27009937
AN - SCOPUS:84966318670
SN - 1083-7159
VL - 21
SP - 618
EP - 625
JO - Oncologist
JF - Oncologist
IS - 5
ER -