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早期ALK重排非小细胞肺癌的治疗模式与转归

Treatment patterns and outcomes in early-stage ALK-rearranged non-small cell lung cancer.

作者信息

Schmid Sabine, Garcia Miguel, Cheng Sierra, Zhan Luna, Chotai Simren, Balaratnam Karmugi, Khan Khaleeq, Patel Devalben, Catherine Brown M, Sachdeva Robin, Xu Wei, Shepherd Frances A, Sacher Adrian, Leighl Natasha B, Bradbury Penelope, Moriarty Patrick, Sara Kuruvilla M, Liu Geoffrey

机构信息

Princess Margaret Cancer Centre, University Health Network, Toronto, Canada; Cantonal Hospital St. Gallen, St. Gallen, Switzerland.

Princess Margaret Cancer Centre, University Health Network, Toronto, Canada.

出版信息

Lung Cancer. 2022 Apr;166:58-62. doi: 10.1016/j.lungcan.2022.01.020. Epub 2022 Feb 3.

Abstract

INTRODUCTION

We evaluated the baseline demographics, treatment patterns, and outcomes of patients with ALK-rearranged early stage (Stage I-III) non-small cell lung cancer (NSCLC). We also evaluated the efficacy and toxicity of durvalumab consolidation treatment in patients with ALK-rearranged unresectable stage III disease.

METHODS

Retrospective chart-review analysis of all patients with histologically confirmed stage I-III reflexively tested ALK-rearranged NSCLC managed with curative intent at two Canadian Centers.

RESULTS

Of 48 patients, 19 (40%) were stage I, 5 (10%) were stage II and 24 (50%) were stage-III. Median progression-free survival (PFS) was 27.6 months overall (95%CI: 20.5-51.4) and 144.4 months in stage-I, 27.6 months in stage-II and 14.9 months in stage III patients. Of 20 patients with unresectable stage-III disease treated with chemoradiation (9 also received durvalumab consolidation), 18/90% have relapsed. Median PFS was 10.9 months (95%CI:5.9-22.5). A non-significant trend toward improved PFS was seen in patients receiving additional durvalumab compared to patients treated with chemoradiation alone (median PFS, 12.5 vs 5.9 months, p = 0.16). Toxicity-related treatment modifications on subsequent first ALK-TKI at time of metastatic disease were needed in three (33%) patients who had received chemoradiation alone and two (29%) patients with consolidation durvalumab; no relevant pulmonary or hepato-toxicity was observed overall.

CONCLUSION

Treatment strategies and PFS of patients with Stage I-III ALK-rearranged NSCLC are similar to patients without molecular driver alterations. Durvalumab consolidation treatment appears generally safe in patients with unresectable stage III ALK-rearranged disease; however, the degree of benefit of such an approach remains unclear.

摘要

引言

我们评估了间变性淋巴瘤激酶(ALK)重排的早期(I - III期)非小细胞肺癌(NSCLC)患者的基线人口统计学特征、治疗模式和预后。我们还评估了度伐利尤单抗巩固治疗在ALK重排的不可切除III期疾病患者中的疗效和毒性。

方法

对加拿大两个中心所有组织学确诊为I - III期且经反射性检测为ALK重排的NSCLC患者进行回顾性病历审查分析,这些患者接受了根治性治疗。

结果

48例患者中,19例(40%)为I期,5例(10%)为II期,24例(50%)为III期。总体中位无进展生存期(PFS)为27.6个月(95%置信区间:20.5 - 51.4),I期患者为144.4个月,II期患者为27.6个月,III期患者为14.9个月。20例接受放化疗的不可切除III期疾病患者中(9例还接受了度伐利尤单抗巩固治疗),18例(90%)复发。中位PFS为10.9个月(95%置信区间:5.9 - 22.5)。与单纯接受放化疗的患者相比,接受额外度伐利尤单抗治疗的患者PFS有改善的趋势,但差异无统计学意义(中位PFS,12.5个月对5.9个月,p = 0.16)。在单纯接受放化疗的3例(33%)患者和接受度伐利尤单抗巩固治疗的2例(29%)患者中,转移性疾病时后续首次使用ALK酪氨酸激酶抑制剂(ALK - TKI)治疗时需要进行与毒性相关的治疗调整;总体未观察到相关的肺部或肝毒性。

结论

I - III期ALK重排的NSCLC患者的治疗策略和PFS与无分子驱动改变的患者相似。度伐利尤单抗巩固治疗在ALK重排的不可切除III期疾病患者中似乎总体安全;然而,这种方法的获益程度仍不清楚。

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