Published April 2019 | Version v1
Journal article

Efficacy and safety of cabazitaxel for castration-resistant prostate cancer in patients with > 10 cycles of docetaxel chemotherapy: a multi-institutional study

  • 1. Kyushu University, Department of Urology, Graduate School of Medical Sciences (Japan)
  • 2. National Hospital Organization Kyushu Cancer Center, Department of Urology (Japan)
  • 3. Harasanshin Hospital, Division of Urology (Japan)
  • 4. Oita Prefectural Hospital, Department of Urology (Japan)
  • 5. National Hospital Organization Kyushu Medical Center, Department of Urology (Japan)
  • 6. Kyushu Central Hospital, Department of Urology (Japan)
  • 7. Kitakyushu Municipal Medical Center, Department of Urology (Japan)
  • 8. Japanese Red Cross Fukuoka Hospital, Department of Urology (Japan)
  • 9. JCHO Kyushu Hospital, Department of Urology (Japan)
  • 10. Miyazaki Prefectural Miyazaki Hospital, Department of Urology (Japan)

Description

This multi-institutional study aimed to investigate the efficacy and safety profiles of cabazitaxel after prior docetaxel chemotherapy in patients with castration-resistant prostate cancer (CRPC). This study included 63 Japanese patients with CRPC who were treated with cabazitaxel from 2014 to 2017. The oncological outcomes and adverse events (AEs) were documented, and prognostic factors for oncological outcomes and predictive factors for AEs were analysed. PSA decline was observed in 68.3% of patients, including 25.4% who achieved a ≥ 50% decline. The median progression-free survival, treatment failure-free survival, and overall survival were 4.3, 4.1, and 9.0 months, respectively. More cycles of prior docetaxel therapy was identified as common favourable prognostic factors for progression-free survival, treatment failure-free survival, and overall survival. Severe neutropenia, febrile neutropenia, and severe non-haematological AEs were observed in 73.0%, 33.3%, and 23.8% of patients, respectively. However, > 10 cycles of docetaxel was not associated with increased incidence of AEs. In conclusion, cabazitaxel chemotherapy was still active in Japanese CRPC patients treated with > 10 cycles of docetaxel chemotherapy, with an acceptable risk of AE burden. Treatment with cabazitaxel after > 10 cycles of docetaxel may be an appropriate option when it can be administered.

Additional details

Identifiers

Publishing Information

Journal Title
Medical Oncology (Online)
Journal Volume
36
Journal Issue
4
Journal Page Range
p. 1-7
ISSN
1559-131X

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
51102492
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
CASTRATION; CHEMOTHERAPY; NEOPLASMS; PATIENTS; PROSTATE; SAFETY
Descriptors DEC
BODY; DISEASES; GLANDS; MALE GENITALS; MEDICINE; ORGANS; SURGERY; THERAPY

Optional Information

Copyright
Copyright (c) 2019 Springer Science+Business Media, LLC, part of Springer Nature
Notes
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