Department of Radiation Therapy and Oncology, Shin-Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan.
Lung Cancer. 2011 Aug;73(2):189-94. doi: 10.1016/j.lungcan.2010.12.007. Epub 2011 Jan 17.
Upfront tyrosine kinase inhibitor (TKI) has proved effective for selective advanced lung cancer patients in Taiwan. We hypothesized that early integration of radiotherapy during TKI treatment would decrease the chance of drug resistance and prolong progression-free survival (PFS).
This study included 25 patients with stage IIIb or IV non-squamous cell, non-small cell lung cancer (NSqCLC) who responded to upfront TKI treatment. Multi-target radiotherapy was administered during the TKI treatment course. Tomotherapy comprising a hypofractionated schedule with a dose of 40-50 Gy in 16-20 fractions was used for individual metastatic lesions.
The patients' median follow-up duration was 30 months (range, 9-62 months). Of the 23 patients who had stage IV disease, 9 had oligometastases (≤5 gross target volumes) and 14 were in the more advanced stages of the disease. Twelve patients received more than 1 cycle of radiotherapy (median, 3; range, 2-6) with TKI being the only systemic treatment before they were salvaged with chemotherapy. The overall response rate after radiotherapy was 84.0%, and the median PFS was 16 months. The 3-year overall survival rate was 62.5% (95% confidence interval [CI], 39.1-85.8%). Toxicities were generally tolerated but it is necessary to prevent radiation-induced pneumonitis.
We showed that combined first-line TKI therapy and early multi-target radiotherapy are very effective in selected patients that respond to TKI, when the status of mutations in the epidermal growth factor receptor (EGFR) are not known before the treatment. Our data may aid expansion of the effectiveness of TKI treatment through radiotherapy in Asian patients with stage IV NSqCLC.
upfront 酪氨酸激酶抑制剂 (TKI) 已被证明对台湾的选择性晚期肺癌患者有效。我们假设在 TKI 治疗过程中早期整合放疗将降低耐药的机会并延长无进展生存期 (PFS)。
这项研究包括 25 名接受 upfront TKI 治疗的 IIIb 期或 IV 期非鳞状细胞、非小细胞肺癌 (NSqCLC) 患者。在 TKI 治疗过程中进行多靶区放疗。针对个体转移病灶,采用 40-50 Gy 分 16-20 次分割的调强放疗。
患者的中位随访时间为 30 个月(范围 9-62 个月)。23 名患有 IV 期疾病的患者中,9 名患有寡转移(≤5 个大体肿瘤体积),14 名处于疾病的更晚期。12 名患者在接受化疗挽救治疗之前,接受了超过 1 个周期的放疗(中位数 3 个;范围 2-6 个),且 TKI 是唯一的全身治疗。放疗后的总体缓解率为 84.0%,中位 PFS 为 16 个月。3 年总生存率为 62.5%(95%置信区间 [CI],39.1-85.8%)。毒性通常可以耐受,但需要预防放射性肺炎。
我们表明,对于接受 TKI 治疗的选择患者,在治疗前不知道表皮生长因子受体 (EGFR) 突变状态时,联合一线 TKI 治疗和早期多靶区放疗非常有效。我们的数据可能有助于通过放疗扩大亚洲 IV 期 NSqCLC 患者 TKI 治疗的疗效。