TY - JOUR
T1 - Rucaparib or Physician's Choice in Metastatic Prostate Cancer
AU - Fizazi, Karim
AU - Piulats, Josep M.
AU - Reaume, M. Neil
AU - Ostler, Peter
AU - Mcdermott, Ray
AU - Gingerich, Joel R.
AU - Pintus, Elias
AU - Sridhar, Srikala S.
AU - Bambury, Richard M.
AU - Emmenegger, Urban
AU - Lindberg, Henriette
AU - Morris, David
AU - Nolè, Franco
AU - Staffurth, John
AU - Redfern, Charles
AU - Sáez, María I.
AU - Abida, Wassim
AU - Daugaard, Gedske
AU - Heidenreich, Axel
AU - Krieger, Laurence
AU - Sautois, Brieuc
AU - Loehr, Andrea
AU - Despain, Darrin
AU - Heyes, Catherine A.
AU - Watkins, Simon P.
AU - Chowdhury, Simon
AU - Ryan, Charles J.
AU - Bryce, Alan H.
N1 - Publisher Copyright:
© 2023 Massachusetts Medical Society.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - Background: In a phase 2 study, rucaparib, an inhibitor of poly(ADP-ribose) polymerase (PARP), showed a high level of activity in patients who had metastatic, castration-resistant prostate cancer associated with a deleterious BRCA alteration. Data are needed to confirm and expand on the findings of the phase 2 study. Methods: In this randomized, controlled, phase 3 trial, we enrolled patients who had metastatic, castration-resistant prostate cancer with a BRCA1, BRCA2, or ATM alteration and who had disease progression after treatment with a second-generation androgen-receptor pathway inhibitor (ARPI). We randomly assigned the patients in a 2:1 ratio to receive oral rucaparib (600 mg twice daily) or a physician's choice control (docetaxel or a second-generation ARPI [abiraterone acetate or enzalutamide]). The primary outcome was the median duration of imaging-based progression-free survival according to independent review. Results: Of the 4855 patients who had undergone prescreening or screening, 270 were assigned to receive rucaparib and 135 to receive a control medication (intention-to-treat population); in the two groups, 201 patients and 101 patients, respectively, had a BRCA alteration. At 62 months, the duration of imaging-based progression-free survival was significantly longer in the rucaparib group than in the control group, both in the BRCA subgroup (median, 11.2 months and 6.4 months, respectively; hazard ratio, 0.50; 95% confidence interval [CI], 0.36 to 0.69) and in the intention-to-treat group (median, 10.2 months and 6.4 months, respectively; hazard ratio, 0.61; 95% CI, 0.47 to 0.80; P<0.001 for both comparisons). In an exploratory analysis in the ATM subgroup, the median duration of imaging-based progression-free survival was 8.1 months in the rucaparib group and 6.8 months in the control group (hazard ratio, 0.95; 95% CI, 0.59 to 1.52). The most frequent adverse events with rucaparib were fatigue and nausea. Conclusions: The duration of imaging-based progression-free survival was significantly longer with rucaparib than with a control medication among patients who had metastatic, castration-resistant prostate cancer with a BRCA alteration.
AB - Background: In a phase 2 study, rucaparib, an inhibitor of poly(ADP-ribose) polymerase (PARP), showed a high level of activity in patients who had metastatic, castration-resistant prostate cancer associated with a deleterious BRCA alteration. Data are needed to confirm and expand on the findings of the phase 2 study. Methods: In this randomized, controlled, phase 3 trial, we enrolled patients who had metastatic, castration-resistant prostate cancer with a BRCA1, BRCA2, or ATM alteration and who had disease progression after treatment with a second-generation androgen-receptor pathway inhibitor (ARPI). We randomly assigned the patients in a 2:1 ratio to receive oral rucaparib (600 mg twice daily) or a physician's choice control (docetaxel or a second-generation ARPI [abiraterone acetate or enzalutamide]). The primary outcome was the median duration of imaging-based progression-free survival according to independent review. Results: Of the 4855 patients who had undergone prescreening or screening, 270 were assigned to receive rucaparib and 135 to receive a control medication (intention-to-treat population); in the two groups, 201 patients and 101 patients, respectively, had a BRCA alteration. At 62 months, the duration of imaging-based progression-free survival was significantly longer in the rucaparib group than in the control group, both in the BRCA subgroup (median, 11.2 months and 6.4 months, respectively; hazard ratio, 0.50; 95% confidence interval [CI], 0.36 to 0.69) and in the intention-to-treat group (median, 10.2 months and 6.4 months, respectively; hazard ratio, 0.61; 95% CI, 0.47 to 0.80; P<0.001 for both comparisons). In an exploratory analysis in the ATM subgroup, the median duration of imaging-based progression-free survival was 8.1 months in the rucaparib group and 6.8 months in the control group (hazard ratio, 0.95; 95% CI, 0.59 to 1.52). The most frequent adverse events with rucaparib were fatigue and nausea. Conclusions: The duration of imaging-based progression-free survival was significantly longer with rucaparib than with a control medication among patients who had metastatic, castration-resistant prostate cancer with a BRCA alteration.
KW - Cancer
KW - Genetics
KW - Genitourinary Cancer
KW - Hematology/Oncology
KW - Treatments in Oncology
KW - Urology/Prostate Disease
KW - Urology/Prostate Disease General
UR - http://www.scopus.com/inward/record.url?scp=85148677731&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa2214676
DO - 10.1056/NEJMoa2214676
M3 - Article
C2 - 36795891
AN - SCOPUS:85148677731
SN - 0028-4793
VL - 388
SP - 719
EP - 732
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 8
ER -