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局部进展期肝癌新辅助调强放疗的Ⅱ期临床研究:一项非随机对照研究。

Phase 2 Evaluation of Neoadjuvant Intensity-Modulated Radiotherapy in Centrally Located Hepatocellular Carcinoma: A Nonrandomized Controlled Trial.

机构信息

Department of Hepatobiliary Surgery, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Department of Radiation Oncology, National Cancer Center, National Clinical Research Center for Cancer, Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

出版信息

JAMA Surg. 2022 Dec 1;157(12):1089-1096. doi: 10.1001/jamasurg.2022.4702.

Abstract

IMPORTANCE

Centrally located hepatocellular carcinoma (HCC) is a special type of HCC whose outcome is unsatisfactory when treated with surgery alone. No standard adjuvant or neoadjuvant treatment for this disease has been established that improves clinical outcomes.

OBJECTIVE

To evaluate the effectiveness and safety of adding neoadjuvant intensity-modulated radiotherapy (IMRT) before surgery in patients with centrally located HCC.

DESIGN, SETTING, AND PARTICIPANTS: This phase 2, single-center, single-group prospective nonrandomized controlled trial was conducted between December 16, 2014, and January 29, 2019, at the Cancer Institute and Hospital of the Chinese Academy of Medical Sciences in Beijing, China. The last follow-up was on July 30, 2021. Patients with centrally located HCC who underwent neoadjuvant IMRT and surgery were included in the analysis.

INTERVENTIONS

Neoadjuvant IMRT followed by hepatectomy.

MAIN OUTCOMES AND MEASURES

The primary end point was 5-year overall survival (OS). The secondary end points were tumor response to IMRT, 5-year disease-free survival (DFS), and treatment-related adverse events.

RESULTS

Thirty-eight patients (mean [SD] age, 55.6 [9.3] years; 35 male [92.1%] individuals) completed the prescribed neoadjuvant IMRT without interruption. Radiographic tumor response to IMRT before surgery included partial response (16 [42.1%]) and stable disease (22 [57.9%]). Thirteen patients (34.2%) achieved major pathological response, of which 5 (13.2%) achieved pathologic complete response. With a median follow-up of 45.8 months, the median OS was not reached, and the OS rates were 94.6% at 1 year, 75.4% at 3 years, and 69.1% at 5 years. The median DFS was 45.8 months, and DFS rates were 70.3% at 1 year, 54.1% at 3 years, and 41.0% at 5 years. Radiotherapy-related grade 3 adverse events were observed in 3 patients (7.9%). Nineteen operative complications developed in 13 patients (34.2%), including grade I to II complications in 12 patients (31.6%) and grade IIIa complication in 1 patient (2.6%). No grade IIIb or higher operative complications were observed.

CONCLUSIONS AND RELEVANCE

Results of this trial suggest that neoadjuvant IMRT plus surgery is effective and well-tolerated in patients with centrally located HCC. These data may inform a future randomized clinical trial of this new treatment strategy.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT02580929.

摘要

重要性

中央型肝细胞癌(HCC)是一种特殊类型的 HCC,单独手术治疗的效果并不理想。目前尚未确定可改善临床结局的针对该疾病的标准辅助或新辅助治疗方法。

目的

评估新辅助调强放疗(IMRT)在中央型 HCC 患者中的有效性和安全性。

设计、地点和参与者:这是一项 2014 年 12 月 16 日至 2019 年 1 月 29 日在中国北京中国医学科学院肿瘤医院进行的单中心、单组前瞻性非随机对照临床试验。最后一次随访时间为 2021 年 7 月 30 日。分析了接受新辅助 IMRT 加手术的中央型 HCC 患者。

干预措施

新辅助 IMRT 加肝切除术。

主要终点和次要终点

主要终点是 5 年总生存率(OS)。次要终点包括 IMRT 治疗的肿瘤反应、5 年无病生存率(DFS)和治疗相关的不良事件。

结果

38 例患者(平均年龄[标准差]55.6[9.3]岁;35 例男性[92.1%])顺利完成了预定的新辅助 IMRT 治疗,没有中断。手术前 IMRT 对肿瘤的放射学反应包括部分缓解(16 例[42.1%])和稳定疾病(22 例[57.9%])。13 例(34.2%)患者获得主要病理缓解,其中 5 例(13.2%)获得病理完全缓解。中位随访 45.8 个月,中位 OS 未达到,OS 率分别为 1 年时 94.6%、3 年时 75.4%和 5 年时 69.1%。中位 DFS 为 45.8 个月,DFS 率分别为 1 年时 70.3%、3 年时 54.1%和 5 年时 41.0%。3 例(7.9%)患者出现与放疗相关的 3 级不良事件。13 例患者(34.2%)发生 19 例手术并发症,其中 12 例(31.6%)为 1 级至 2 级并发症,1 例(2.6%)为 3a 级并发症。未观察到 3b 级或更高级别的手术并发症。

结论和相关性

这项试验的结果表明,新辅助 IMRT 加手术对中央型 HCC 患者有效且耐受良好。这些数据可能为这种新治疗策略的未来随机临床试验提供信息。

试验注册

ClinicalTrials.gov 标识符:NCT02580929。

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