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DOI 10.1093/jjco/hyae004

Медицинская библиотека · Japanese journal of clinical oncology · 2024

Determination of enzalutamide long-term safety and efficacy for castration-resistant prostate cancer patients after combined anti-androgen blockade followed by alternative anti-androgen therapy: a multicenter prospective DELC study.

Nagahara Akira, Uemura Motohide, Sato Mototaka, Nakata Wataru, Tsujihata Masao, Takao Tetsuya, Matsumura Soichi, Nishimura Kensaku, Takada Shingo, Iwanishi Toshichika, Kobayashi Yasuyuki, Ishizuya Yu, Takada Tsuyoshi, Okada Koichi, Inoue Hitoshi, Kato Taigo, Hatano Koji, Kawashima Atsunari, Ujike Takeshi, Fujita Kazutoshi, Nonomura Norio

СтатьяМногоцентровое исследованиеНаблюдательное исследованиеПеревод пока не подготовлен

Аннотация

BACKGROUND

Alternative anti-androgen therapy has been widely used as a first-line treatment for castration-resistant prostate cancer, and it may affect treatment outcome of subsequent agents targeting the androgen receptor axis. We conducted the prospective observational DELC (Determination of Enzalutamide Long-term safety and efficacy for Castration-resistant prostate cancer patients after combined anti-androgen blockade followed by alternative anti-androgen therapy) study to evaluate the efficacy of enzalutamide in patients with castration-resistant prostate cancer who underwent prior combined androgen blockade with bicalutamide and then alternative anti-androgen therapy with flutamide.

METHODS

The DELC study enrolled 163 Japanese patients with castration-resistant prostate cancer who underwent alternative anti-androgen therapy with flutamide following failure of initial combined androgen blockade with bicalutamide in multiple institutions between January 2016 and March 2019. Primary endpoint was overall survival. Administration of enzalutamide was started at 160 mg orally once daily in all patients.

RESULTS

The rate of decline of prostate-specific antigen by 50% or more was 72.2%, and median overall survival was 42.05 months. Multivariate analysis revealed that higher pretreatment serum levels of prostate-specific antigen (≥11.3 ng/mL; P = 0.004), neuron-specific enolase (P = 0.014) and interleukin-6 (≥2.15 pg/mL; P = 0.004) were independent risk factors for overall survival. Fatigue (30.0%), constipation (19.6%) and appetite loss (17.8%) were the most common clinically relevant adverse events. The enzalutamide dose was not reduced in any patient under the age of 70, but adherence was decreased in those over 70.

CONCLUSIONS

In the DELC study, the safety of enzalutamide was comparable to that in previous reports. Serum levels of neuron-specific enolase and interleukin-6 were suggested as prognostic factors for castration-resistant prostate cancer with potential clinical utility.

Для цитирования: Nagahara Akira, Uemura Motohide, Sato Mototaka, Nakata Wataru, Tsujihata Masao, Takao Tetsuya, Matsumura Soichi, Nishimura Kensaku, Takada Shingo, Iwanishi Toshichika, Kobayashi Yasuyuki, Ishizuya Yu, Takada Tsuyoshi, Okada Koichi, Inoue Hitoshi, Kato Taigo, Hatano Koji, Kawashima Atsunari, Ujike Takeshi, Fujita Kazutoshi, Nonomura Norio. Determination of enzalutamide long-term safety and efficacy for castration-resistant prostate cancer patients after combined anti-androgen blockade followed by alternative anti-androgen therapy: a multicenter prospective DELC study.. Japanese journal of clinical oncology. 2024. DOI: 10.1093/jjco/hyae004.

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