Donovan Elysia K, Lo Simon S, Beriwal Sushil, Chen Hanbo, Cheung Patrick, Keller Andrew, Nwachukwu Chika, Mantz Constantine, Pond Gregory R, Schnarr Kara, Swaminath Anand, Albuquerque Kevin, Leung Eric
Department of Oncology, Division of Radiation Oncology, Escarpment Cancer Research Institute, McMaster University, Hamilton, Ontario, Canada.
Department of Radiation Oncology, University of Washington School of Medicine, Seattle.
JAMA Oncol. 2024 Jul 1;10(7):941-948. doi: 10.1001/jamaoncol.2024.1796.
The role of stereotactic ablative radiotherapy (SABR) for gynecologic malignant tumors has yet to be clearly defined despite recent clinical uptake.
To evaluate the outcomes of SABR in patients with oligometastatic and oligoprogressive gynecologic cancers.
DESIGN, SETTING, AND PARTICIPANTS: In this retrospective pooled analysis, patients with oligometastatic and oligoprogressive gynecologic cancers receiving SABR at 5 institutions from Canada and the US were studied. Data were collected from January 2011 to December 2020, and data were analyzed from January to December 2023.
Stereotactic ablative radiotherapy.
Cumulative incidence of local and distant recurrence, chemotherapy-free survival (CFS), and overall survival (OS) probabilities after SABR were calculated using Kaplan-Meier methods. Univariable and multivariable analysis was conducted using Cox regression methods.
A total of 215 patients with 320 lesions meeting criteria were included in the analysis; the median (range) age at primary diagnosis was 59 (23-86) years. The median (range) follow-up from SABR was 18.5 (0.1-124.5) months. The primary site included the endometrium (n = 107), ovary (n = 64), cervix (n = 30), and vulva or vagina (n = 14). Local cumulative incidence of recurrence was 13.7% (95% CI, 9.4-18.9) and 18.5% (95% CI, 13.2-24.5) at 1 and 5 years, respectively. Distant cumulative incidence of recurrence was 48.5% (95% CI, 41.4-55.1) and 73.1% (95% CI, 66.0-79.0) at 1 and 5 years, respectively. OS was 75.7% (95% CI, 69.2-81.1) and 33.1% (95% CI, 25.3-41.1) at 1 and 5 years, respectively. The median CFS was 21.7 months (95% CI, 15.4-29.9). On multivariable analysis, local recurrence was significantly associated with nodal metastasis, lesion size, biologically effective dose, treatment indication, institution, and primary disease type. Distant progression-free survival was associated with nodal targets and lesion size. OS and CFS were significantly associated with lesion size.
In this study, SABR appeared to have excellent local control with minimal toxic effects in this large patient group, and certain patients may achieve durable distant control and OS as well. It may be possible to delay time to chemotherapy in select patient subtypes and therefore reduce associated toxic effects. Prospective multicenter trials will be critical to establish which characteristics procure the greatest benefit from SABR use and to define the ideal time to implement SABR with other oncologic treatments.
尽管立体定向消融放疗(SABR)最近在临床上有所应用,但其在妇科恶性肿瘤中的作用尚未明确界定。
评估SABR在寡转移和寡进展性妇科癌症患者中的治疗效果。
设计、背景和参与者:在这项回顾性汇总分析中,研究了来自加拿大和美国5家机构接受SABR治疗的寡转移和寡进展性妇科癌症患者。数据收集时间为2011年1月至2020年12月,数据分析时间为2023年1月至12月。
立体定向消融放疗。
使用Kaplan-Meier方法计算SABR后局部和远处复发的累积发生率、无化疗生存期(CFS)和总生存期(OS)概率。使用Cox回归方法进行单变量和多变量分析。
共有215例患者的320个病灶符合纳入标准,分析中包括;初次诊断时的中位(范围)年龄为59(23 - 86)岁。SABR后的中位(范围)随访时间为18.5(0.1 - 124.5)个月。原发部位包括子宫内膜(n = 107)、卵巢(n = 64)、宫颈(n = 30)以及外阴或阴道(n = 14)。1年和5年时局部复发的累积发生率分别为13.7%(95%CI,9.4 - 18.9)和18.5%(95%CI,13.2 - 24.5)。1年和5年时远处复发的累积发生率分别为48.5%(95%CI,41.4 - 55.1)和73.1%(95%CI,66.0 - 79.0)。1年和5年时的OS分别为75.7%(95%CI,69.2 - 81.1)和33.1%(95%CI,25.3 - 41.1)。中位CFS为21.7个月(95%CI,15.4 - 29.9)。多变量分析显示,局部复发与淋巴结转移、病灶大小、生物等效剂量、治疗指征、机构以及原发疾病类型显著相关。远处无进展生存期与淋巴结靶区和病灶大小相关。OS和CFS与病灶大小显著相关。
在本研究中,SABR在这个大型患者群体中似乎具有良好的局部控制效果且毒性极小,部分患者可能也能实现持久的远处控制和OS。在特定患者亚型中可能可以延迟化疗时间,从而减少相关毒性。前瞻性多中心试验对于确定哪些特征能从SABR的使用中获得最大益处以及确定与其他肿瘤治疗联合实施SABR的理想时间至关重要。