Department of Radiation Oncology, Yonsei Cancer Center, Heavy Ion Therapy Research Institute, Yonsei University College of Medicine, Seoul, Korea.
Division of Medical Oncology, Department of Internal Medicine, Yonsei Cancer Center, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
Cancer Res Treat. 2024 Jan;56(1):115-124. doi: 10.4143/crt.2023.600. Epub 2023 Aug 29.
This study aimed to determine the role of local ablative radiotherapy (LART) in oligometastatic/oligoprogressive lung adenocarcinoma.
Patients (n=176) with oligometastatic lung adenocarcinoma treated with LART were identified, and those treated with LART at the initial diagnosis of synchronous oligometastatic disease (OMD group) or treated with LART when they presented with repeat oligoprogression (OPD group) were included.
In the OMD group (n=54), the 1- and 3-year progression-free survival (PFS) were 50.9% and 22.5%, respectively, whereas the 1- and 3-year overall survival in the OPD group were 75.9% and 58.1%, respectively. Forty-one patients (75.9%) received LART at all gross disease sites. Tyrosine kinase inhibitor (TKI) use and all-metastatic site LART were significant predictors of higher PFS (p=0.018 and p=0.046, respectively). In patients treated with TKIs at the time of LART (n=23) and those treated with all-metastatic site LART, the 1-year PFS was 86.7%, while that of patients not treated with all-metastatic site LART was 37.5% (p=0.006). In the OPD group (n=122), 67.2% of the patients (n=82) maintained a systemic therapy regimen after LART. The cumulative incidence of changing systemic therapy was 39.6%, 62.9%, and 78.5% at 6 months, 1 year, and 2 years after LART, respectively.
Aggressive LART can be an option to improve survival in patients with oligometastatic disease. Patients with synchronous oligometastatic disease receiving TKI and all-metastatic site LART may have improved PFS. In patients with repeat oligoprogression, LART might potentially extend survival by delaying the need to change the systemic treatment regimen.
本研究旨在探讨局部消融放疗(LART)在寡转移/寡进展性肺腺癌中的作用。
本研究纳入了 176 例接受 LART 治疗的寡转移肺腺癌患者,包括初始诊断为同步寡转移疾病(OMD 组)时接受 LART 治疗或出现重复寡进展(OPD 组)时接受 LART 治疗的患者。
在 OMD 组(n=54)中,1 年和 3 年无进展生存率(PFS)分别为 50.9%和 22.5%,而 OPD 组的 1 年和 3 年总生存率分别为 75.9%和 58.1%。41 例(75.9%)患者在所有大体疾病部位均接受了 LART 治疗。酪氨酸激酶抑制剂(TKI)的使用和所有转移部位的 LART 是 PFS 更高的显著预测因素(p=0.018 和 p=0.046)。在接受 LART 时使用 TKI 的患者(n=23)和接受所有转移部位 LART 的患者中,1 年 PFS 为 86.7%,而未接受所有转移部位 LART 的患者为 37.5%(p=0.006)。在 OPD 组(n=122)中,67.2%(n=82)的患者在 LART 后维持了系统治疗方案。在 LART 后 6 个月、1 年和 2 年,改变系统治疗的累积发生率分别为 39.6%、62.9%和 78.5%。
积极的 LART 是改善寡转移疾病患者生存的一种选择。接受 TKI 和所有转移部位 LART 的同步寡转移疾病患者可能有更好的 PFS。对于重复寡进展的患者,LART 可能通过延迟改变系统治疗方案来延长生存时间。