作者
David M. O'Malley,Amit M. Oza,Domenica Lorusso,Carol Aghajanian,Ana Oaknin,Andrew Dean,Nicoletta Colombo,Johanne I Weberpals,Andrew R Clamp,Giovanni Scambia,Alexandra Leary,Robert G. Holloway,Margarita Amenedo Gancedo,Peter C.C. Fong,Jeffrey C. Goh,Deborah K. Armstrong,Susana Banerjee,Jesús García-Donas,Elizabeth M. Swisher,Terri Cameron,Lara Maloney,Sandra Goble,Kevin K. Lin,Jonathan A. Ledermann,Robert L. Coleman
摘要
Objective: In the ARIEL3 study (NCT01968213), rucaparib maintenance treatment significantly improved progression-free survival (PFS) versus placebo in all predefined, nested cohorts (BRCA mutant; BRCA mutant + wildtype BRCA/high loss of heterozygosity; and intent-to-treat population). Here we analyzed postprogression outcomes to evaluate the durability of the clinical benefit of rucaparib maintenance treatment following disease progression in the subgroup of patients with tumors associated with a mutation in a prespecified, non-BRCA, homologous recombination repair (HRR) gene.