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前列腺切除术后立体定向消融放疗耐受性:拓展超分割放疗的边界

SABR tolerance after prostatectomy: pushing the boundaries of ultrahypofractionation.

作者信息

Montero Angel, Hernando Ovidio, López Mercedes, Valero Jeannette, Ciérvide Raquel, Sánchez Emilio, Prado Alejandro, Zobec Helena B, Chen-Zhao Xin, Álvarez Beatriz, García-Aranda Mariola, Alonso Leyre, Alonso Rosa, Fernández-Letón Pedro, Rubio Carmen

机构信息

Department of Radiation Oncology, HM Hospitales, C/Oña 10, 28050, Madrid, Spain.

Universidad Camilo José Cela of Madrid, Madrid, Spain.

出版信息

Clin Transl Oncol. 2025 Jan 25. doi: 10.1007/s12094-025-03845-w.

Abstract

OBJECTIVE

To evaluate the feasibility and tolerance of ultra-hypofractionated SABR (stereotactic ablative radiation therapy) protocol following radical prostatectomy.

PATIENTS AND METHODS

We included patients undergoing adjuvant or salvage SABR between April 2019 and April 2023 targeting the surgical bed and pelvic lymph nodes up to a total dose of 36.25 Gy (7.25 Gy/fraction) and 26 Gy (5.2 Gy/fraction), respectively, in 5 fractions on alternate days with an urethra sparing protocol. Acute and late adverse effects were assessed using the CTCAE v5.0. Pearson's chi-square test for categorical variables was used to compare characteristics and possible associations among different subgroups.

RESULTS

Adjuvant radiation therapy (ART) was administered to 40 high-risk patients (detectable post-surgery PSA, Grade Group 4/5, nodal involvement, R1/R2 resection margin), while salvage radiotherapy (SRT) was delivered to 60 patients with rising PSA levels post-undetectable values. Elective nodal irradiation was performed in 57 patients, with 11 additional patients receiving a simultaneous integrated boost (total dose: 40 Gy in 5 fractions) for macroscopic nodal disease. Twenty-four high-risk patients underwent 24-months androgen deprivation therapy (ADT). Treatment was well-tolerated with minimal toxicity. The maximum grade of SABR-related toxicity observed was grade 3. Acute gastrointestinal (GI) toxicity included seven cases of grade 2 and one of grade 3, while acute genitourinary (GU) events were limited to grade 2 in eight patients. Early-late toxicity included two cases of grade 3 and seven of grade 2 for GI, and 11 cases of grade 2 for GU. No toxicity above grade 3 was reported. With a median follow-up of 24 months (6-60 months), 14 patients experienced disease recurrence.

CONCLUSIONS

Ultra-hypofractionated adjuvant/salvage SABR appears feasible and safe. Longer follow-up is needed to validate observed outcomes.

摘要

目的

评估前列腺癌根治术后超分割立体定向消融放疗(SABR)方案的可行性和耐受性。

患者与方法

我们纳入了2019年4月至2023年4月期间接受辅助或挽救性SABR治疗的患者,分别针对手术床和盆腔淋巴结,总剂量分别为36.25 Gy(7.25 Gy/分次)和26 Gy(5.2 Gy/分次),分5次隔日进行,采用保留尿道方案。使用CTCAE v5.0评估急性和晚期不良反应。采用Pearson卡方检验对分类变量进行分析,以比较不同亚组之间的特征和可能的关联。

结果

40例高危患者(术后可检测到PSA、分级组4/5、淋巴结受累、R1/R2切缘)接受了辅助放疗(ART),而60例PSA水平在不可检测值后升高的患者接受了挽救性放疗(SRT)。57例患者进行了选择性淋巴结照射,另外11例患者因肉眼可见的淋巴结疾病接受了同步整合加量放疗(总剂量:40 Gy,分5次)。24例高危患者接受了24个月的雄激素剥夺治疗(ADT)。治疗耐受性良好,毒性极小。观察到的与SABR相关的毒性最高级别为3级。急性胃肠道(GI)毒性包括7例2级和1例3级,而急性泌尿生殖系统(GU)事件仅限于8例2级患者。早晚期毒性包括GI方面2例3级和7例2级,GU方面11例2级。未报告3级以上毒性。中位随访24个月(6 - 60个月),14例患者出现疾病复发。

结论

超分割辅助/挽救性SABR似乎可行且安全。需要更长时间的随访来验证观察到的结果。

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