TY - JOUR
T1 - Survival outcomes of metastatic breast cancer patients by germline BRCA1/2 status in a large multicenter real-world database
AU - Mailliez, Audrey
AU - D'Hondt, Veronique
AU - Lusque, Amelie
AU - Caron, Olivier
AU - Cabel, Luc
AU - Goncalves, Anthony
AU - Debled, Marc
AU - Gladieff, Laurence
AU - Ferrero, Jean Marc
AU - Petit, Thierry
AU - Mouret-Reynier, Marie Ange
AU - Eymard, Jean Christophe
AU - Levy, Christelle
AU - Uwer, Lionel
AU - Leheurteur, Marianne
AU - Desmoulins, Isabelle
AU - Bachelot, Thomas
AU - Frenel, Jean Sebastien
AU - de la Motte Rouge, Thibault
AU - Simon, Gaëtane
AU - Jacot, William
AU - Delaloge, Suzette
N1 - Publisher Copyright:
© 2022 The Authors. International Journal of Cancer published by John Wiley & Sons Ltd on behalf of UICC.
PY - 2023/3/1
Y1 - 2023/3/1
N2 - The outcomes and best treatment strategies for germline BRCA1/2 mutation (gBRCAm) carriers with metastatic breast cancer (MBC) remain uncertain. We compared the overall survival and the first line progression free survival (PFS1) of patients with a gBRCAm identified at initiation of first-line treatment with those of BRCA wild-type (WT) and not-tested (NT) individuals in the ESME real-world database of MBC patients between 2008 and 2016 (NCT03275311). Among the 20 624 eligible patients, 325 had a gBRCAm, 1138 were WT and 19 161 NT. Compared with WT, gBRCAm carriers were younger, and had more aggressive diseases. At a median follow-up of 50.5 months, median OS was 30.6 (95%CI: 21.9-34.3), 35.8 (95%CI: 32.2-37.8) and 39.3 months (95% CI: 38.3-40.3) in the gBRCAm, WT and NT subgroups, respectively. Median PFS1 was 7.9 (95%CI: 6.6-9.3), 7.8 (95%CI: 7.3-8.5) and 9.7 months (95%CI, 9.5-10.0). In the multivariable analysis conducted in the whole cohort, gBRCAm status had however no independent prognostic impact on OS and PFS1. Though, in the triple-negative subgroup, gBRCAm patients had better OS and PFS1 (HR vs WT = 0.76; 95%CI: 0.60-0.97; P =.027 and 0.69; 95% CI: 0.55-0.86; P =.001, respectively). In contrast, in patients with HR+/HER2 negative cancers, PFS1 appeared significantly and OS non significantly lower for gBRCAm carriers (PFS1: HR vs WT = 1.23; 95%CI: 1.03-1.46; P =.024; OS:HR = 1.22, 95% CI: 0.97-1.52, P =.089). In conclusion, gBRCA1/2 status appears to have divergent survival effects in MBC according to IHC subtype.
AB - The outcomes and best treatment strategies for germline BRCA1/2 mutation (gBRCAm) carriers with metastatic breast cancer (MBC) remain uncertain. We compared the overall survival and the first line progression free survival (PFS1) of patients with a gBRCAm identified at initiation of first-line treatment with those of BRCA wild-type (WT) and not-tested (NT) individuals in the ESME real-world database of MBC patients between 2008 and 2016 (NCT03275311). Among the 20 624 eligible patients, 325 had a gBRCAm, 1138 were WT and 19 161 NT. Compared with WT, gBRCAm carriers were younger, and had more aggressive diseases. At a median follow-up of 50.5 months, median OS was 30.6 (95%CI: 21.9-34.3), 35.8 (95%CI: 32.2-37.8) and 39.3 months (95% CI: 38.3-40.3) in the gBRCAm, WT and NT subgroups, respectively. Median PFS1 was 7.9 (95%CI: 6.6-9.3), 7.8 (95%CI: 7.3-8.5) and 9.7 months (95%CI, 9.5-10.0). In the multivariable analysis conducted in the whole cohort, gBRCAm status had however no independent prognostic impact on OS and PFS1. Though, in the triple-negative subgroup, gBRCAm patients had better OS and PFS1 (HR vs WT = 0.76; 95%CI: 0.60-0.97; P =.027 and 0.69; 95% CI: 0.55-0.86; P =.001, respectively). In contrast, in patients with HR+/HER2 negative cancers, PFS1 appeared significantly and OS non significantly lower for gBRCAm carriers (PFS1: HR vs WT = 1.23; 95%CI: 1.03-1.46; P =.024; OS:HR = 1.22, 95% CI: 0.97-1.52, P =.089). In conclusion, gBRCA1/2 status appears to have divergent survival effects in MBC according to IHC subtype.
KW - germline BRCA mutation
KW - metastatic breast cancer
KW - real world
KW - survival
UR - http://www.scopus.com/inward/record.url?scp=85139719745&partnerID=8YFLogxK
U2 - 10.1002/ijc.34304
DO - 10.1002/ijc.34304
M3 - Article
C2 - 36161271
AN - SCOPUS:85139719745
SN - 0020-7136
VL - 152
SP - 921
EP - 931
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 5
ER -