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晚期 EGFR 突变或 ALK 重排的非小细胞肺癌患者生存超过五年——这些患者的生存曲线是否存在“尾部平台”?

Survival past five years with advanced, EGFR-mutated or ALK-rearranged non-small cell lung cancer-is there a "tail plateau" in the survival curve of these patients?

机构信息

Department of Respiratory Medicine, Graduate School of Medicine, Juntendo University, 3-1-3 Hongo, Bunkyo-Ku, Tokyo, 113-8421, Japan.

出版信息

BMC Cancer. 2022 Mar 25;22(1):323. doi: 10.1186/s12885-022-09421-7.

DOI:10.1186/s12885-022-09421-7
PMID:35337281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8953392/
Abstract

BACKGROUND

The prognosis of patients with NSCLC harboring oncogenic driver gene alterations, such as EGFR gene mutations or ALK fusion, has improved dramatically with the advent of corresponding molecularly targeted drugs. As patients were followed up for about five years in most clinical trials, the long-term outcomes beyond 5 years are unclear. The objectives of this study are to explore the clinical course beyond five years of chemotherapy initiation and to investigate factors that lead to long-term survival.

METHODS

One hundred and seventy-seven patients with advanced, EGFR-mutated or ALK-rearranged NSCLC who received their first chemotherapy between December 2008 and September 2015 were included. Kaplan Meier curves were drawn for the total cohort and according to subgroups of patients' characteristics.

RESULTS

Median OS in the total cohort was 40.6 months, the one-year survival rate was 89%, the three-year survival rate was 54%, and the five-year survival rate was 28%. Median OS was 36.9 months in EGFR-mutated patients and 55.4 months in ALK-rearranged patients. The OS curve seemed to plateau after 72 months, and most of the patients who were still alive after more than five years are on treatment. Female sex, age under 75 years, an ECOG PS of 0 to 1, ALK rearrangement, postoperative recurrence, and presence of brain metastasis were significantly associated with longer OS.

CONCLUSIONS

A tail plateau was found in the survival curves of patients with advanced, EGFR-mutated and ALK-rearranged NSCLC, but most were on treatment, especially with EGFR-mutated NSCLC.

摘要

背景

随着针对特定驱动基因改变的分子靶向药物的出现,携有 EGFR 基因突变或 ALK 融合等致癌驱动基因改变的 NSCLC 患者的预后有了显著改善。由于大多数临床试验中患者的随访时间约为 5 年,因此 5 年以上的长期结果尚不清楚。本研究的目的是探索化疗开始后 5 年以上的临床过程,并探讨导致长期生存的因素。

方法

共纳入 177 例接受第一代化疗的晚期 EGFR 突变或 ALK 重排 NSCLC 患者,化疗开始时间为 2008 年 12 月至 2015 年 9 月。根据患者特征的亚组,分别绘制总队列和各亚组的 Kaplan-Meier 生存曲线。

结果

总队列的中位 OS 为 40.6 个月,1 年生存率为 89%,3 年生存率为 54%,5 年生存率为 28%。EGFR 突变患者的中位 OS 为 36.9 个月,ALK 重排患者的中位 OS 为 55.4 个月。OS 曲线在 72 个月后似乎趋于平稳,5 年以上仍存活的大多数患者仍在接受治疗。女性、年龄<75 岁、ECOG PS 0-1、ALK 重排、术后复发、脑转移与 OS 延长显著相关。

结论

晚期 EGFR 突变和 ALK 重排 NSCLC 患者的生存曲线出现尾部平台,但大多数患者仍在接受治疗,尤其是 EGFR 突变型 NSCLC。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1ec/8953392/4dd6ee8e44c5/12885_2022_9421_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1ec/8953392/58448658dfd5/12885_2022_9421_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1ec/8953392/c78bd10e5884/12885_2022_9421_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1ec/8953392/4dd6ee8e44c5/12885_2022_9421_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1ec/8953392/58448658dfd5/12885_2022_9421_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1ec/8953392/c78bd10e5884/12885_2022_9421_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e1ec/8953392/4dd6ee8e44c5/12885_2022_9421_Fig3_HTML.jpg

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