A phase II randomized trial of metastasis-directed therapy with alpha emitter radium-223 in men with oligometastatic castration-resistant prostate cancer (MEDAL)
Soichiro Yoshida,
Taro Takahara,
Yuki Arita,
Masaya Ito,
Sara Hayakawa,
Tomohiko Oguchi,
Yoshinobu Komai,
Noboru Numao,
Takeshi Yuasa,
Masaharu Inoue,
Hiroki Ushijima,
Shigehiro Kudo,
Yasumasa Shimano,
Yuki Nakamura,
Yusuke Uchida,
Sho Uehara,
Hajime Tanaka,
Hiroshi Yaegashi,
Kouji Izumi,
Minato Yokoyama,
Yoh Matsuoka,
Yasuo Yoshioka,
Koji Konishi,
Katsuyuki Nakanishi,
Akira Nagahara,
Akihiro Hirakawa,
Ryuji Koike,
Fumitaka Koga,
Kazuo Nishimura,
Atsushi Mizokami,
Junji Yonese,
Yukio Kageyama,
Ryoichi Yoshimura,
Yasuhisa Fujii
Affiliations
Soichiro Yoshida
Department of Urology, Tokyo Medical and Dental University
Taro Takahara
Department of Biomedical Engineering, Tokai University School of Engineering
Yuki Arita
Department of Radiology, Keio University School of Medicine
Masaya Ito
Department of Urology, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital
Sara Hayakawa
Department of Radiation Oncology, Department of Radiology, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital
Tomohiko Oguchi
Department of Genitourinary Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research
Yoshinobu Komai
Department of Genitourinary Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research
Noboru Numao
Department of Genitourinary Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research
Takeshi Yuasa
Department of Genitourinary Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research
Masaharu Inoue
Department of Urology, Saitama Cancer Center
Hiroki Ushijima
Department of Radiation Oncology, Saitama Cancer Center
Shigehiro Kudo
Department of Radiation Oncology, Saitama Cancer Center
Yasumasa Shimano
Department of Radiation Oncology, Saitama Cancer Center
Yuki Nakamura
Department of Urology, Tokyo Medical and Dental University
Yusuke Uchida
Department of Urology, Tokyo Medical and Dental University
Sho Uehara
Department of Urology, Tokyo Medical and Dental University
Hajime Tanaka
Department of Urology, Tokyo Medical and Dental University
Hiroshi Yaegashi
Department of Integrative Cancer Therapy and Urology, Kanazawa University Graduate School of Medical Science
Kouji Izumi
Department of Integrative Cancer Therapy and Urology, Kanazawa University Graduate School of Medical Science
Minato Yokoyama
Department of Urology, Tokyo Medical and Dental University
Yoh Matsuoka
Department of Urology, Tokyo Medical and Dental University
Yasuo Yoshioka
Radiation Oncology Department, Cancer Institute Hospital of Japanese Foundation for Cancer Research
Koji Konishi
Department of Radiation Oncology, Osaka International Cancer Institute
Katsuyuki Nakanishi
Department of Diagnostic and Interventional Radiology, Osaka International Cancer Institute
Akira Nagahara
Department of Urology, Osaka International Cancer Institute
Akihiro Hirakawa
Department of Clinical Biostatistics, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University
Ryuji Koike
Department of Medical Innovation Promotion Center, Tokyo Medical and Dental University
Fumitaka Koga
Department of Urology, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital
Kazuo Nishimura
Department of Urology, Osaka International Cancer Institute
Atsushi Mizokami
Department of Integrative Cancer Therapy and Urology, Kanazawa University Graduate School of Medical Science
Junji Yonese
Department of Genitourinary Oncology, Cancer Institute Hospital of Japanese Foundation for Cancer Research
Yukio Kageyama
Department of Urology, Saitama Cancer Center
Ryoichi Yoshimura
Department of Radiation Therapeutics and Oncology, Tokyo Medical and Dental University
Yasuhisa Fujii
Department of Urology, Tokyo Medical and Dental University
Abstract Background The significance of metastasis-directed therapy for oligometastatic prostate cancer has been widely discussed, and targeted therapy for progressive sites is a feasible option as a multidisciplinary treatment for castration-resistant prostate cancer (CRPC). When oligometastatic CRPC with only bone metastases progresses after targeted therapy, it tends to progress as multiple bone metastases. The progression of oligometastatic CRPC after targeted therapy may be due in part to the presence of micrometastatic lesions that, though undetected on imaging, were present prior to targeted therapy. Thus the systemic treatment of micrometastases in combination with targeted therapy for progressive sites is expected to enhance the therapeutic effect. Radium-223 dichloride (radium-223) is a radiopharmaceutical that selectively binds to sites of increased bone turnover and inhibits the growth of adjacent tumor cells by emitting alpha rays. Therefore, for oligometastatic CRPC with only bone metastases, radium-223 may enhance the therapeutic effect of radiotherapy for active metastases. Methods This phase II, randomized trial of Metastasis-Directed therapy with ALpha emitter radium-223 in men with oligometastatic CRPC (MEDAL) is designed to assess the utility of radium-223 in combination with metastasis-directed radiotherapy in patients with oligometastatic CRPC confined to bone. In this trial, patients with oligometastatic CRPC with three or fewer bone metastases on whole-body MRI with diffusion-weighted MRI (WB-DWI) will be randomized in a 1:1 ratio to receive radiotherapy for active metastases plus radium-223 or radiotherapy for active metastases alone. The prior use of androgen receptor axis-targeted therapy and prostate-specific antigen doubling time will be used as allocation factors. The primary endpoint will be radiological progression-free survival against progression of bone metastases on WB-DWI. Discussion This will be the first randomized trial to evaluate the effect of radium-223 in combination with targeted therapy in oligometastatic CRPC patients. The combination of targeted therapy for macroscopic metastases with radiopharmaceuticals targeting micrometastasis is expected to be a promising new therapeutic strategy for patients with oligometastatic CRPC confined to bone. Trial registration Japan Registry of Clinical Trials (jRCT) (jRCTs031200358); Registered on March 1, 2021, https://jrct.niph.go.jp/latest-detail/jRCTs031200358