Efficacy of cisplatin-based neoadjuvant chemotherapy and risk factors for residual extravesical disease in muscle-invasive bladder cancer: insights from a nationwide cohort.
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Saito Ryoichi, Taoka Rikiya, Miki Jun, Fukuokaya Wataru, Matsui Yoshiyuki, Hatakeyama Shingo, Kawahara Takashi, Matsuda Ayumu, Kawai Taketo, Sazuka Tomokazu, Kato Minoru, Sano Takeshi, Urabe Fumihiko, Kashima Soki, Naito Hirohito, Murakami Yoji, Miyake Makito, Daizumoto Kei, Matsushita Yuto, Hayashi Takuji, Inokuchi Junichi, Sugino Yusuke, Shiga Kenichiro, Yamaguchi Noriya, Yamamoto Shingo, Yasue Keiji, Abe Takashige, Nakanishi Shotaro, Hashine Katsuyoshi, Fujii Masato, Nishihara Kiyoaki, Matsumoto Hiroaki, Tatarano Shuichi, Wada Koichiro, Sekito Sho, Maruyama Ryo, Nishiyama Naotaka, Nishiyama Hiroyuki, Kitamura Hiroshi, Kinoshita Hidefumi, Japan Urological Oncology Group
Аннотация
METHODS: Clinical data from 1474 patients who underwent radical cystectomy for cStage II-IIIA urothelial carcinoma were collected from 36 institutions of the Japanese Urological Oncology Group. Overall survival (OS) and non-urinary tract recurrence-free survival (NUT-RFS) were compared between the NAC-RC and upfront RC groups using the Kaplan-Meier method adjusted by inverse probability of treatment weighting. Logistic regression was used to identify independent risk factors for RED.
RESULTS: Pathological complete response (pT0N0) was achieved in 33.1 and 20.2% of cStage II and IIIA patients in the NAC-RC group, respectively, compared with 16.3 and 4.5% in the RC group. NAC significantly improved the OS and NUT-RFS in the IPTW-adjusted cohort. BCG-unresponsiveness, low serum albumin levels, and a high neutrophil-to-lymphocyte ratio were independent predictors of RED in the NAC-RC cohort. Squamous differentiation was associated with worse prognosis but a favorable response to NAC in some tumors.
CONCLUSIONS: Cisplatin-based NAC improves outcomes in patients with cStage II-IIIA MIBC, including some tumors with squamous differentiation; however, its benefits may be limited in BCG-unresponsive cases. Given the biological heterogeneity of urothelial cancer, individualized treatment planning that integrates biological features and treatment history is needed for patients with MIBC.