TY - JOUR
T1 - Impact of pegfilgrastim as primary prophylaxis for metastatic castration-resistant prostate cancer patients undergoing cabazitaxel treatment
T2 - An open-label study in Japan
AU - Kosaka, Takeo
AU - Uemura, Hiroji
AU - Sumitomo, Makoto
AU - Harada, Kenichi
AU - Sugimoto, Mikio
AU - Hayashi, Narihiko
AU - Yoshimura, Kazuhiro
AU - Fukasawa, Satoshi
AU - Ecstein-Fraisse, Evelyne
AU - Sunaga, Yoshinori
AU - Oya, Mototsugu
N1 - Funding Information:
This work was supported by Sanofi K.K. and Kyowa Hakko Kirin. Sanofi K.K. was involved in the study design; in the collection, analysis and interpretation of data; in the writing of the report; and in the decision to submit the article for publication. Kyowa Hakko Kirin provided the study drug (pegfilgrastim).
Funding Information:
This work was supported by Sanofi K.K. and Kyowa Hakko Kirin. Sanofi K.K. was involved in the study design; in the collection, analysis and interpretation of data; in the writing of the report; and in the decision to submit the article for publication. Kyowa Hakko Kirin provided the study drug (pegfilgrastim). The authors thank Kyowa Hakko Kirin for providing the study drug (pegfilgrastim) and Susan E Cottrell, PhD, of Edanz Medical Writing for providing medical writing support, which was funded by Sanofi K.K.
Funding Information:
The authors thank Kyowa Hakko Kirin for providing the study drug (pegfil-grastim) and Susan E Cottrell, PhD, of Edanz Medical Writing for providing medical writing support, which was funded by Sanofi K.K.
Funding Information:
H. Uemura received consultancy fees from Janssen Pharmaceutical K.K., Astellas Pharma Inc., Takeda Pharmaceutical Co., Ltd, Bayer Yakuhin, Ltd, and Daiichi Sankyo Co., Ltd; and lecture fees from AstraZeneca K.K., Sanofi K.K., Fujifilm Corporation, Kyowa Hakko Kirin Co., Ltd, and Kissei Pharmaceutical Co. M. Sumitomo received consultancy fees from Sanofi K.K., Janssen Pharmaceutical K.K., Ono Pharmaceutical Co., Ltd, Pfizer Japan Inc., Takeda Pharmaceutical Co., Ltd, and Kissei Pharmaceutical Co.; lecture fees from Sanofi K.K., Pfizer Japan Inc., Takeda Pharmaceutical Co., Ltd, and AstraZeneca K.K.; and research funding from Ono Pharmaceutical Co., Ltd, Sanofi K.K., Astellas Pharma Inc., AstraZeneca K.K., and Takeda Pharmaceutical Co., Ltd., M. Sugimoto received manuscript writing/editing fees from Janssen Pharmaceutical K.K., Astellas Pharma Inc., Takeda Pharmaceutical Co., Ltd, and AstraZeneca K.K. Y. Sunaga is an employee of Sanofi K.K. and owns stock of Sanofi K.K. M. Oya received consultancy fees from Astellas Pharma Inc.; lecture fees from Astellas Pharma Inc., Janssen Pharmaceutical K.K., AstraZeneca, Sanofi, and Takeda; research funding from Astellas Pharma Inc. and Takeda Pharmaceutical Co., Ltd. E. Ecstein-Fraisse is an employee of Sanofi.
Publisher Copyright:
© The Author(s) 2019. Published by Oxford University Press.
PY - 2019/8/1
Y1 - 2019/8/1
N2 - Background: Cabazitaxel is an efficacious treatment for patients with metastatic castration-resistant prostate cancer who have previously progressed on docetaxel, but febrile neutropenia during the first cycle is a frequent complication. Asian patients are at increased risk of febrile neutropenia. Although primary prophylaxis with granulocyte colony-stimulating factor can reduce the incidence, its efficacy has not been prospectively demonstrated in Japanese patients with cabazitaxel treatment. Methods: PEGAZUS, a prospective, single-arm study conducted at eight clinical sites in Japan, enrolled 21 heavily pretreated patients with metastatic castration-resistant prostate cancer. Patients received cabazitaxel 25 mg/m2 every 3 weeks, up to 10 cycles. Oral prednisolone 10 mg was taken daily. Pegfilgrastim 3.6 mg was administered at least 24 h after the cabazitaxel infusion. The primary endpoint was the incidence of febrile neutropenia in the first cycle. Results: The median number of treatment cycles was seven. The relative dose intensity of cabazitaxel was 67.4% (range, 53.2–91.3%). Two of 21 patients (9.5%) experienced febrile neutropenia in the first cycle. This rate was lower than the rate (43%) previously observed without prophylactic granulocyte colony-stimulating factor in a similar patient population. Six patients showed a prostate-specific antigen response (28.6%). Three of four patients evaluable for tumor response had stable disease and one had progressive disease. Grade ≥3 diarrhea was not observed. Primary prophylaxis with granulocyte colony-stimulating factor significantly reduced the incidence of febrile neutropenia in this study. Conclusions: Cabazitaxel plus granulocyte colony-stimulating factor is safe and effective for Japanese patients with metastatic castration-resistant prostate cancer who have previously progressed on docetaxel.
AB - Background: Cabazitaxel is an efficacious treatment for patients with metastatic castration-resistant prostate cancer who have previously progressed on docetaxel, but febrile neutropenia during the first cycle is a frequent complication. Asian patients are at increased risk of febrile neutropenia. Although primary prophylaxis with granulocyte colony-stimulating factor can reduce the incidence, its efficacy has not been prospectively demonstrated in Japanese patients with cabazitaxel treatment. Methods: PEGAZUS, a prospective, single-arm study conducted at eight clinical sites in Japan, enrolled 21 heavily pretreated patients with metastatic castration-resistant prostate cancer. Patients received cabazitaxel 25 mg/m2 every 3 weeks, up to 10 cycles. Oral prednisolone 10 mg was taken daily. Pegfilgrastim 3.6 mg was administered at least 24 h after the cabazitaxel infusion. The primary endpoint was the incidence of febrile neutropenia in the first cycle. Results: The median number of treatment cycles was seven. The relative dose intensity of cabazitaxel was 67.4% (range, 53.2–91.3%). Two of 21 patients (9.5%) experienced febrile neutropenia in the first cycle. This rate was lower than the rate (43%) previously observed without prophylactic granulocyte colony-stimulating factor in a similar patient population. Six patients showed a prostate-specific antigen response (28.6%). Three of four patients evaluable for tumor response had stable disease and one had progressive disease. Grade ≥3 diarrhea was not observed. Primary prophylaxis with granulocyte colony-stimulating factor significantly reduced the incidence of febrile neutropenia in this study. Conclusions: Cabazitaxel plus granulocyte colony-stimulating factor is safe and effective for Japanese patients with metastatic castration-resistant prostate cancer who have previously progressed on docetaxel.
KW - Asian
KW - Febrile neutropenia
KW - Pegylated granulocyte colony-stimulating factor
KW - Prostate-specific antigen
KW - Taxane
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U2 - 10.1093/jjco/hyz051
DO - 10.1093/jjco/hyz051
M3 - Article
C2 - 31329922
AN - SCOPUS:85074377582
SN - 0368-2811
VL - 49
SP - 766
EP - 771
JO - Japanese Journal of Clinical Oncology
JF - Japanese Journal of Clinical Oncology
IS - 8
ER -