TY - JOUR
T1 - Incidence of fistula occurrence in patients with cervical cancer treated with bevacizumab
T2 - data from real-world clinical practice
AU - Sugiyama, Toru
AU - Katsumata, Noriyuki
AU - Toita, Takafumi
AU - Ura, Masako
AU - Shimizu, Ayaka
AU - Kamijima, Shuichi
AU - Aoki, Daisuke
N1 - Funding Information:
We would like to thank the patients, physicians, and medical institutions who participated in this survey, and Sheridan Henness, PhD, who wrote the first draft of this manuscript on behalf of inScience Communications, Springer Healthcare. This medical writing assistance was funded by Chugai Pharmaceutical Co, Ltd. We would also like to thank Hideyuki Hashimoto, Chiemi Yamagiwa, Haruna Nishimura, and Yuya Ueda from the Chugai Drug Safety Division for their input into clinical data extraction and analysis, Kosei Tajima from Chugai Clinical Development Division for his assistance with the statistics, and Kiyoko Ogino, Yue Zheng, Shinichi Funahashi, and Nobuhiko Ishizuka from the Chugai Medical Affairs Division for their assistance with manuscript development.
Funding Information:
Toru Sugiyama has received consultancy fees from Chugai Pharmaceutical Co., Ltd.; Noriyuki Katsumata has received consultancy fees from Nippon Zoki; Takafumi Toita has no conflicts of interest to declare; Masako Ura, Ayaka Shimizu, and Shuichi Kamijima are employees of Chugai Pharmaceutical Co., Ltd. and Daisuke Aoki has received research grants from Takeda, and consultancy fees and honoraria for speaking engagements from Takeda, Chugai Pharmaceutical Co., Ltd., AstraZeneca, and MSD.
Funding Information:
We would like to thank the patients, physicians, and medical institutions who participated in this survey, and Sheridan Henness, PhD, who wrote the first draft of this manuscript on behalf of inScience Communications, Springer Healthcare. This medical writing assistance was funded by Chugai Pharmaceutical Co, Ltd. We would also like to thank Hideyuki Hashimoto, Chiemi Yamagiwa, Haruna Nishimura, and Yuya Ueda from the Chugai Drug Safety Division for their input into clinical data extraction and analysis, Kosei Tajima from Chugai Clinical Development Division for his assistance with the statistics, and Kiyoko Ogino, Yue Zheng, Shinichi Funahashi, and Nobuhiko Ishizuka from the Chugai Medical Affairs Division for their assistance with manuscript development.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/9
Y1 - 2022/9
N2 - Background: This study aimed to determine the incidence of pelvic fistulas in cervical cancer patients treated with bevacizumab in Japanese clinical practice. Methods: A post-marketing surveillance (PMS) study was conducted between June 2016 and February 2018 to survey physicians who treated advanced or recurrent cervical cancer patients with bevacizumab (according to the product label). The clinical/treatment status of patients with pelvic fistulas was assessed in an additional retrospective case series study. Results: 142 patients were included in the PMS study (median age 51 years; 66.9% squamous cell carcinoma; 66.2% recurrent cervical cancer; 64.1% previous radiotherapy). Patients received a median of seven bevacizumab doses. Six patients, all of whom had a history of pelvic irradiation, developed seven fistulas (4.2%; 95% confidence interval, 1.56–8.96), and five patients had also undergone pelvic surgery. The case series study of the patients who developed fistulas indicated that three patients had high cumulative bladder and rectal doses of radiation, and two of them had undergone salvage re-irradiation for pelvic recurrence. The other three patients underwent both radical hysterectomy and adjuvant radiotherapy, but did not receive an excessive radiation dose to the bladder or rectum. Conclusions: This study found that the upper limit of the 95% confidence interval for pelvic fistula incidence did not exceed the incidence reported in the GOG 240 study. To ensure an adequate benefit-risk assessment of bevacizumab in cervical cancer patients, a comprehensive evaluation of prior treatment is essential and the possibility of unexpected fistulas, even after careful evaluation, should be considered.
AB - Background: This study aimed to determine the incidence of pelvic fistulas in cervical cancer patients treated with bevacizumab in Japanese clinical practice. Methods: A post-marketing surveillance (PMS) study was conducted between June 2016 and February 2018 to survey physicians who treated advanced or recurrent cervical cancer patients with bevacizumab (according to the product label). The clinical/treatment status of patients with pelvic fistulas was assessed in an additional retrospective case series study. Results: 142 patients were included in the PMS study (median age 51 years; 66.9% squamous cell carcinoma; 66.2% recurrent cervical cancer; 64.1% previous radiotherapy). Patients received a median of seven bevacizumab doses. Six patients, all of whom had a history of pelvic irradiation, developed seven fistulas (4.2%; 95% confidence interval, 1.56–8.96), and five patients had also undergone pelvic surgery. The case series study of the patients who developed fistulas indicated that three patients had high cumulative bladder and rectal doses of radiation, and two of them had undergone salvage re-irradiation for pelvic recurrence. The other three patients underwent both radical hysterectomy and adjuvant radiotherapy, but did not receive an excessive radiation dose to the bladder or rectum. Conclusions: This study found that the upper limit of the 95% confidence interval for pelvic fistula incidence did not exceed the incidence reported in the GOG 240 study. To ensure an adequate benefit-risk assessment of bevacizumab in cervical cancer patients, a comprehensive evaluation of prior treatment is essential and the possibility of unexpected fistulas, even after careful evaluation, should be considered.
KW - Bevacizumab
KW - Fistula
KW - Health surveys
KW - Uterine cervical neoplasms
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U2 - 10.1007/s10147-022-02196-8
DO - 10.1007/s10147-022-02196-8
M3 - Article
C2 - 35760943
AN - SCOPUS:85132938331
SN - 1341-9625
VL - 27
SP - 1517
EP - 1528
JO - International Journal of Clinical Oncology
JF - International Journal of Clinical Oncology
IS - 9
ER -