Low Incidence of Corticosteroid-associated Adverse Events on Long-term Exposure to Low-dose Prednisone Given with Abiraterone Acetate to Patients with Metastatic Castration-resistant Prostate Cancer

被引:25
作者
Fizazi, Karim [1 ]
Chi, Kim N. [2 ]
de Bono, Johann S. [3 ,4 ]
Gomella, Leonard G. [5 ]
Miller, Kurt [6 ]
Rathkopf, Dana E. [7 ,8 ]
Ryan, Charles J. [9 ]
Scher, Howard I. [7 ,8 ]
Shore, Neal D. [10 ]
De Porre, Peter [11 ]
Londhe, Anil [12 ]
McGowan, Tracy [13 ]
Pelhivanov, Nonko [14 ]
Charnas, Robert [15 ]
Todd, Mary B. [16 ]
Montgomery, Bruce [17 ]
机构
[1] Univ Paris 11, Inst Gustave Roussy, Villejuif, France
[2] BC Canc Agcy, Vancouver, BC, Canada
[3] Inst Canc Res, Sutton, Surrey, England
[4] Royal Marsden Hosp, Sutton, Surrey, England
[5] Thomas Jefferson Univ, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[6] Charite, Berlin, Germany
[7] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[8] Weill Cornell Med Coll, New York, NY USA
[9] Univ Calif San Francisco, Helen Diller Family Comprehens Canc Ctr, San Francisco, CA 94143 USA
[10] Atlantic Urol Clin, Carolina Urol Res Ctr, Myrtle Beach, SC USA
[11] Janssen Res & Dev, Beerse, Belgium
[12] Janssen Res & Dev, Horsham, PA USA
[13] Janssen Sci Affairs, Horsham, PA USA
[14] Janssen Res & Dev, Raritan, NJ USA
[15] Janssen Res & Dev, Los Angeles, CA USA
[16] Janssen Global Serv, Raritan, NJ USA
[17] Univ Washington, Seattle, WA 98195 USA
关键词
Adverse events; Corticosteroids; Glucocorticoid; Long term; Metastatic castration-resistant prostate cancer; Tolerability; PLACEBO-CONTROLLED PHASE-3; STEROIDAL INHIBITORS; SURVIVAL ANALYSIS; DOUBLE-BLIND; CHEMOTHERAPY; MEN;
D O I
10.1016/j.eururo.2016.02.035
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Background: Abiraterone acetate (AA) is the prodrug of abiraterone, which inhibits CYP17A1 and testosterone synthesis and prolongs the survival of patients with metastatic castration-resistant prostate cancer (mCRPC). AA plus prednisone (P) (AA + P) is approved for the treatment of patients with mCRPC. Objective: To investigate whether long-term use of low-dose P with or without AA leads to corticosteroid-associated adverse events (CA-AEs) in mCRPC patients. Design, setting, and participants: The study included 2267 patients in COU-AA-301 and COU-AA-302. We used an inclusive Standardized MedDRA Queries-oriented approach to identify 112 preferred terms for known CA-AEs, and assessed the incidence of CA-AEs during 3-mo exposure intervals and across all P exposure levels. Intervention: All 2267 patients received 5 mg of P twice daily, and 1333/2267 received AA (1 g) plus P. Results and limitations: The CA-AE incidence after any P exposure was 25%, 26%, and 23% for any grade, and 5%, 5%, and 4% for grade >= 3 CA-AEs for all patients and the AA + P and P alone groups, respectively. The most common any-grade CA-AEs were hyperglycemia (7.4%, 7.8%, and 6.9% for all patients, AA + P, and P alone, respectively) and weight increase (4.3%, 3.9%, and 4.8%, respectively). When assessed by duration of exposure (3-mo intervals up to >= 30 mo), no discernable trend was observed for CA-AEs, including hyperglycemia and weight increase. The investigator-reported study discontinuation rate due to CA-AEs was 11/2267 (0.5%), and one patient had a CA-AE resulting in death. Conclusions: Low-dose P given with or without AA is associated with low overall incidence of CA-AEs. The frequency of CA-AEs remained low with increased duration of exposure to P. Patient summary: We assessed adverse events in patients with metastatic castration resistant prostate cancer during long-term treatment with a low dose of a corticosteroid. We found that long-term treatment with this low-dose corticosteroid is safe and tolerable. (C) 2016 European Association of Urology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:438 / 444
页数:7
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