医学
内科学
奥拉帕尼
置信区间
中止
PARP抑制剂
不利影响
比例危险模型
危险系数
肿瘤科
卵巢癌
癌症
胃肠病学
外科
聚ADP核糖聚合酶
化学
基因
聚合酶
生物化学
作者
Katherine E. Francis,S.I. Kim,Michael Friedlander,Val Gebski,Isabelle Ray Coquard,Andrew R. Clamp,Richard T. Penson,A.M. Oza,Tamar Perri,Tomasz Huzarski,Cristina Martín-Lorente,Sabrina Chiara Cecere,Nicoletta Colombo,Beyhan Ataseven,Keiichi Fujiwara,Gabe S. Sonke,Ignace Vergote,Éric Pujade-Lauraine,J.-W. Kim,C.K. Lee
标识
DOI:10.1016/j.annonc.2022.02.222
摘要
Maintenance treatment with poly (ADP-ribose) polymerase (PARP) inhibitor is now the standard of care in patients with BRCA-mutated platinum-sensitive recurrent ovarian cancer following response to chemotherapy. In the SOLO2 trial, adverse event (AE)-associated olaparib interruption, dose reduction, and discontinuation occurred in 50%, 28%, and 17% of patients, respectively. We used data from the SOLO2 trial to evaluate the impact of dose alterations on survival outcomes and identified baseline characteristics associated with dose alteration.We computed relative dose intensity (RDI) defined as the received dose as a percentage of the standard dose (300 mg twice a day) during the first 12 weeks on treatment. Patients were categorized into RDI >98%, RDI 90%-98%, and RDI <90%. The association between RDI categories with progression-free survival (PFS) and overall survival (OS) were examined using a 12-week landmark Cox regression analysis. Logistic regression analysis was used to correlate baseline factors with RDI at 12 weeks.In patients on olaparib included in the landmark analysis (n = 185), the mean 12-week RDI was 91.4%. There was no significant difference across 12-week RDI >98% (n = 110), 90%-98% (n = 29), and <90% (n = 45) categories for PFS (median, 14.2 versus 19.3 versus 34.4 months; P = 0.37) and OS (median, 49.7 versus 49.5 versus 54.1 months; P = 0.84). Risk of RDI ≤90% increased with baseline performance status 1 [odds ratio (OR): 2.54; 95% confidence interval (CI): 1.11-5.82] any nausea (OR: 3.17; 95% CI: 0.9-11.23), and with body weight ≤70 kg (OR: 1.86; 95% CI: 0.92-3.76).Dose reduction and interruption for the management of olaparib-associated AEs during the first 12 weeks did not impact on PFS and OS. When counselling patients requiring dose reductions or interruptions due to AEs, the results of this study will help assure patients that their outcomes will not be adversely affected.
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