Thorax Institute Curie Montsouris, Institut Curie, Paris, France.
Radiotherapy Department, Institut Gustave Roussy, Villejuif, France.
Clin Lung Cancer. 2021 Sep;22(5):469-472. doi: 10.1016/j.cllc.2021.01.020. Epub 2021 Feb 4.
Thymomas are rare intrathoracic malignancies that may be aggressive and difficult to treat. Knowledge and level of evidence for treatment strategies are mainly based on retrospective studies or expert opinion. Currently there is no strong evidence that postoperative radiotherapy after complete resection of localized thymoma is associated with survival benefit in patients. RADIORYTHMIC is a phase III, randomized trial aiming at comparing postoperative radiotherapy versus surveillance after complete resection of Masaoka-Koga stage IIb/III thymoma. Systematic central pathologic review will be performed before patient enrollment as per the RYTHMIC network pathway.
Three hundred fourteen patients will be included; randomization 1:1 will attribute either postoperative radiotherapy (50-54 Gy to the mediastinum using intensity-modulated radiation therapy or proton beam therapy) or surveillance. Stratification criteria include histologic grading (thymoma type A, AB, B1 vs B2, B3), stage, and delivery of preoperative chemotherapy. Patient recruitment will be mainly made through the French RYTHMIC network of 15 expert centers participating in a nationwide multidisciplinary tumor board. Follow-up will last 7 years. The primary endpoint is recurrence-free survival. Secondary objectives include overall survival, assessment of acute and late toxicities, and analysis of prognostic and predictive biomarkers.
The first patient will be enrolled in January 2021, with results expected in 2028.
胸腺瘤是一种罕见的胸腔内恶性肿瘤,可能具有侵袭性且难以治疗。关于治疗策略的知识和证据水平主要基于回顾性研究或专家意见。目前,没有强有力的证据表明完全切除局部胸腺瘤后进行术后放疗会使患者的生存获益。RADIORYTHMIC 是一项 III 期随机试验,旨在比较完全切除 Masaoka-Koga 分期 IIb/III 胸腺瘤后,术后放疗与观察的疗效。在患者入组前,将按照 RYTHMIC 网络途径进行系统性中央病理审查。
将纳入 314 例患者;采用 1:1 随机分组,分别给予术后放疗(纵隔 50-54 Gy,采用调强放疗或质子束治疗)或观察。分层标准包括组织学分级(胸腺瘤 A、AB、B1 与 B2、B3)、分期和术前化疗的实施情况。患者招募主要通过参与全国多学科肿瘤委员会的 15 个专家中心的法国 RYTHMIC 网络进行。随访时间为 7 年。主要终点是无复发生存率。次要目标包括总生存率、急性和迟发性毒性的评估,以及预后和预测生物标志物的分析。
预计 2021 年 1 月将纳入首例患者,结果将于 2028 年公布。