TY - JOUR
T1 - Fluorouracil, Leucovorin, and Irinotecan Plus Cetuximab Versus Cetuximab as Maintenance Therapy in First-Line Therapy for RAS and BRAF Wild-Type Metastatic Colorectal Cancer: Phase III ERMES Study
AU - Pinto, C.
AU - Orlandi, A.
AU - Normanno, N.
AU - Maiello, E.
AU - Calegari, M. A.
AU - Antonuzzo, L.
AU - Bordonaro, R.
AU - Zampino, M. G.
AU - Pini, S.
AU - Bergamo, F.
AU - Tonini, G.
AU - Avallone, A.
AU - Latiano, T. P.
AU - Rosati, G.
AU - Cogoni, A. A.
AU - Ballestrero, A.
AU - Zaniboni, A.
AU - Roselli, M.
AU - Tamberi, S.
AU - Barone, C.
PY - 2024
Y1 - 2024
N2 - PURPOSEThe intensity of anti-EGFR-based first-line therapy for RAS/BRAF wild-type (wt) metastatic colorectal cancer (mCRC), once disease control is achieved, is controversial. A de-escalation strategy with anti-EGFR monotherapy represents a potential option to maintain efficacy while reducing cytotoxicity.METHODSIn this multicenter, open-label, phase III trial, patients with untreated RAS/BRAF wt mCRC were randomly assigned to receive either fluorouracil, leucovorin, and irinotecan/cetuximab (FOLFIRI/Cet) until disease progression (arm A) or FOLFIRI/Cet for eight cycles followed by Cet alone (arm B). The coprimary end points were a noninferior progression-free survival (PFS) in the modified per-protocol (mPP) population (>eight cycles) and a lower incidence of grade (G) 3-4 adverse events (AEs) for arm B compared with arm A.RESULTSOverall, 606 patients were randomly assigned, with 300 assigned to arm A and 306 to arm B. The median follow-up was 22.3 months. In the mPP population, 291 events occurred with a PFS of 10 versus 12.2 months for arms B and A, respectively (P of noninferiority =.43). In the intention-to-treatment (ITT, ≥one cycle) population, 503 events occurred with a PFS of 9 versus 10.7 months (P =.39). The overall survival was 35.7 versus 30.7 months (P =.119) and 31.0 versus 25.2 months (P =.32) in the mPP and ITT population, respectively. Arm B had lower G3-4 AEs during the maintenance period than arm A (20.2% v 35.1%).CONCLUSIONThe ERMES study did not demonstrate noninferiority of maintenance with Cet alone. Despite a more favorable safety profile, maintenance with single-agent Cet after induction with FOLFIRI/Cet cannot be recommended for all patients but could represent an option in selected cases.
AB - PURPOSEThe intensity of anti-EGFR-based first-line therapy for RAS/BRAF wild-type (wt) metastatic colorectal cancer (mCRC), once disease control is achieved, is controversial. A de-escalation strategy with anti-EGFR monotherapy represents a potential option to maintain efficacy while reducing cytotoxicity.METHODSIn this multicenter, open-label, phase III trial, patients with untreated RAS/BRAF wt mCRC were randomly assigned to receive either fluorouracil, leucovorin, and irinotecan/cetuximab (FOLFIRI/Cet) until disease progression (arm A) or FOLFIRI/Cet for eight cycles followed by Cet alone (arm B). The coprimary end points were a noninferior progression-free survival (PFS) in the modified per-protocol (mPP) population (>eight cycles) and a lower incidence of grade (G) 3-4 adverse events (AEs) for arm B compared with arm A.RESULTSOverall, 606 patients were randomly assigned, with 300 assigned to arm A and 306 to arm B. The median follow-up was 22.3 months. In the mPP population, 291 events occurred with a PFS of 10 versus 12.2 months for arms B and A, respectively (P of noninferiority =.43). In the intention-to-treatment (ITT, ≥one cycle) population, 503 events occurred with a PFS of 9 versus 10.7 months (P =.39). The overall survival was 35.7 versus 30.7 months (P =.119) and 31.0 versus 25.2 months (P =.32) in the mPP and ITT population, respectively. Arm B had lower G3-4 AEs during the maintenance period than arm A (20.2% v 35.1%).CONCLUSIONThe ERMES study did not demonstrate noninferiority of maintenance with Cet alone. Despite a more favorable safety profile, maintenance with single-agent Cet after induction with FOLFIRI/Cet cannot be recommended for all patients but could represent an option in selected cases.
KW - colorectal
KW - colorectal
UR - https://publicatt.unicatt.it/handle/10807/312258
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85184432145&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85184432145&origin=inward
U2 - 10.1200/JCO.23.01021
DO - 10.1200/JCO.23.01021
M3 - Article
SN - 0732-183X
VL - 42
SP - 1278
EP - 1287
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 11
ER -