Lee Tae Hoon, Pyo Hongryull, Yoo Gyu Sang, Jeon Seong Soo, Seo Seong Il, Jeong Byong Chang, Jeon Hwang Gyun, Sung Hyun Hwan, Kang Minyong, Song Wan, Chung Jae Hoon, Bae Bong Kyung, Park Won
Department of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Department of Radiation Oncology, Chungbuk National University Hospital, Cheongju, Republic of Korea.
Radiat Oncol J. 2024 Jun;42(2):139-147. doi: 10.3857/roj.2024.00080. Epub 2024 Jun 25.
This study aimed to analyze the treatment outcomes of combined definitive radiation therapy (RT) and androgen deprivation therapy (ADT) for clinically node-positive prostate cancer.
Medical records of 60 patients with clinically suspected metastatic lymph nodes on radiological examination were retrospectively analyzed. Eight patients (13.3%) were suspected to have metastatic common iliac or para-aortic lymph nodes. All patients underwent definitive RT with a dose fractionation of 70 Gy in 28 fractions. ADT was initiated 2-3 months before RT and continued for at least 2 years. Biochemical failure rate (BFR), clinical failure rate (CFR), overall survival (OS), and prostate cancer-specific survival (PCSS) were calculated, and genitourinary and gastrointestinal adverse events were recorded.
The median follow-up period was 5.47 years. The 5-year BFR, CFR, OS, and PCSS rates were 19.1%, 11.3%, 89.0%, and 98.2%, respectively. The median duration of ADT was 2.30 years. BFR and CFR increased after 3 years, and 11 out of 14 biochemical failures occurred after the cessation of ADT. Grade 2 and beyond late genitourinary and gastrointestinal toxicity rates were 5.0% and 13.3%, respectively. However, only two grade 3 adverse events were reported, and no grade 4-5 adverse events were reported. Patients with non-regional lymph node metastases did not have worse BFR, CFR, or adverse event rates.
This study reported the efficacy and tolerable toxicity of hypofractionated definitive RT combined with ADT for clinically node-positive prostate cancer. Additionally, selected patients with adjacent non-regional lymph node metastases might be able to undergo definitive RT combined with ADT.
本研究旨在分析确定性放疗(RT)联合雄激素剥夺治疗(ADT)对临床淋巴结阳性前列腺癌的治疗效果。
回顾性分析60例经影像学检查临床怀疑有转移性淋巴结的患者的病历。8例患者(13.3%)怀疑有转移性髂总或腹主动脉旁淋巴结。所有患者均接受了70 Gy分28次的确定性放疗。ADT在放疗前2 - 3个月开始,并持续至少2年。计算生化失败率(BFR)、临床失败率(CFR)、总生存率(OS)和前列腺癌特异性生存率(PCSS),并记录泌尿生殖系统和胃肠道不良事件。
中位随访期为5.47年。5年BFR、CFR、OS和PCSS率分别为19.1%、11.3%、89.0%和98.2%。ADT的中位持续时间为2.30年。3年后BFR和CFR升高,14例生化失败中有11例发生在ADT停止后。2级及以上晚期泌尿生殖系统和胃肠道毒性率分别为5.0%和13.3%。然而,仅报告了2例3级不良事件,未报告4 - 5级不良事件。非区域淋巴结转移患者的BFR、CFR或不良事件发生率并无更差。
本研究报告了大分割确定性放疗联合ADT治疗临床淋巴结阳性前列腺癌的疗效和可耐受的毒性。此外,部分有相邻非区域淋巴结转移的患者可能能够接受确定性放疗联合ADT。