TY - JOUR
T1 - Investigation of the management and risk of febrile neutropenia associated with chemotherapy in the urological field
T2 - A multicenter, retrospective analysis
AU - Wada, Koichiro
AU - Tanimoto, Ryuta
AU - Nose, Hiroyuki
AU - Uehara, Shinya
AU - Watanabe, Toyohiko
AU - Hayami, Hiroshi
AU - Nagai, Shingo
AU - Yasuda, Mitsuru
AU - Deguchi, Takashi
AU - Shigeta, Keisuke
AU - Yazawa, Satoshi
AU - Kikuchi, Eiji
AU - Oya, Mototsugu
AU - Hashimoto, Jiro
AU - Uehara, Teruhisa
AU - Kurimura, Yuichiro
AU - Hiyama, Yoshiki
AU - Takahashi, Satoshi
AU - Tsukamoto, Taiji
AU - Sho, Takehiko
AU - Hamasuna, Ryoichi
AU - Miyazaki, Jun
AU - Togo, Yoshikazu
AU - Taoka, Rikiya
AU - Nakao, Atsushi
AU - Yamamoto, Shingo
AU - Kobayashi, Kanao
AU - Matsubara, Akio
AU - Ishikawa, Kiyohito
AU - Kumon, Hiromi
AU - Matsumoto, Tetsuro
N1 - Copyright:
Copyright 2014 Elsevier B.V., All rights reserved.
PY - 2014/5
Y1 - 2014/5
N2 - In Japan, chemotherapy for urogenital malignant diseases is commonly performed by urologists and febrile neutropenia (FN) is one of the major adverse events associated with chemotherapy, however, few reports exist from the urological field about FN. In this present study, a total of 883 courses of chemotherapy (326 patients) performed from 2010 to 2011 at 10 University Hospitals were retrospectively reviewed. The regimens were GC (gemcitabine and cisplatin), GCP (gemcitabine, cisplatin and paclitaxel) and M-VAC (methotrexate, vinblastine, doxorubicin, cisplatin) for urothelial carcinoma, and EP (etoposide and cisplatin) and BEP (bleomycin, etoposide and cisplatin) for testicular cancer. In 81 courses (9.2%, 66 patients; 20.2%) including FN, antimicrobials and granulocyte-colony stimulating factor (G-CSF) were administered in 69 courses (85.2%) and in 77 courses (95.1%), respectively. The MASCC risk-index score was evaluated in no more than 51 courses (63.0%) and 1 patient with 18 points on the MASCC score died due to myelotoxicity and infections. According to statistical investigations, FN is significantly more frequent in GCP and M-VAC than in GC (p = 0.0073, <0.0001) and in a similar manner in BEP than in EP (p = 0.0405). In patients with afebrile neutropenia (AN), observed in 232 courses (26.3%), antimicrobials and G-CSF were administered in 5 courses (2.2%) and in 144 courses (62.1%), respectively. Further evidence from the urological field is required to investigate the treatment and risk of FN for management of patients with urogenital malignancies.
AB - In Japan, chemotherapy for urogenital malignant diseases is commonly performed by urologists and febrile neutropenia (FN) is one of the major adverse events associated with chemotherapy, however, few reports exist from the urological field about FN. In this present study, a total of 883 courses of chemotherapy (326 patients) performed from 2010 to 2011 at 10 University Hospitals were retrospectively reviewed. The regimens were GC (gemcitabine and cisplatin), GCP (gemcitabine, cisplatin and paclitaxel) and M-VAC (methotrexate, vinblastine, doxorubicin, cisplatin) for urothelial carcinoma, and EP (etoposide and cisplatin) and BEP (bleomycin, etoposide and cisplatin) for testicular cancer. In 81 courses (9.2%, 66 patients; 20.2%) including FN, antimicrobials and granulocyte-colony stimulating factor (G-CSF) were administered in 69 courses (85.2%) and in 77 courses (95.1%), respectively. The MASCC risk-index score was evaluated in no more than 51 courses (63.0%) and 1 patient with 18 points on the MASCC score died due to myelotoxicity and infections. According to statistical investigations, FN is significantly more frequent in GCP and M-VAC than in GC (p = 0.0073, <0.0001) and in a similar manner in BEP than in EP (p = 0.0405). In patients with afebrile neutropenia (AN), observed in 232 courses (26.3%), antimicrobials and G-CSF were administered in 5 courses (2.2%) and in 144 courses (62.1%), respectively. Further evidence from the urological field is required to investigate the treatment and risk of FN for management of patients with urogenital malignancies.
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M3 - Article
AN - SCOPUS:84902342121
SN - 1340-7007
VL - 62
SP - 374
EP - 381
JO - Japanese Journal of Chemotherapy
JF - Japanese Journal of Chemotherapy
IS - 3
ER -