阿列克替尼
肺癌
医学
内科学
肿瘤科
性能状态
置信区间
克里唑蒂尼
存活率
间变性淋巴瘤激酶
总体生存率
恶性胸腔积液
作者
Eiji Iwama,Yasushi Goto,Haruyasu Murakami,Shinsuke Tsumura,Hiroyuki Sakashita,Yoshiaki Mori,Noriaki Nakagaki,Yuka Fujita,Masahiro Seike,Akihiro Bessho,Manabu Ono,Masaru Nishitsuji,Hiroaki Akamatsu,Ryotaro Morinaga,Takanori Akagi,Takayuki Shimose,Shoji Tokunaga,Nobuyuki Yamamoto,Yoichi Nakanishi,Kenji Sugio,Isamu Okamoto
出处
期刊:Oncologist
[Wiley]
日期:2019-10-30
卷期号:25 (4): 306-e618
被引量:11
标识
DOI:10.1634/theoncologist.2019-0728
摘要
Abstract Lessons Learned Alectinib confers a pronounced survival benefit in patients with ALK rearrangement-positive non-small cell lung cancer and a poor performance status. Survival benefit of alectinib for patients with a poor performance status was consistent regardless of the presence of central nervous system metastases. Background We previously reported a marked objective response rate (ORR) and safety for alectinib treatment in patients with ALK rearrangement-positive non-small cell lung cancer (NSCLC) and a poor performance status (PS) in the Lung Oncology Group in Kyushu (LOGiK) 1401 study. It remained unclear, however, whether alectinib might also confer a long-term survival benefit in such patients. Methods Eighteen patients with ALK rearrangement-positive advanced NSCLC and a PS of 2, 3, or 4 (n = 12, 5, and 1, respectively) were enrolled in LOGiK1401 between September 2014 and December 2015 and received alectinib. We have now updated the survival data for the study. Results The median follow-up time for all patients was 27.3 months. The median progression-free survival (PFS) was 16.2 months (95% confidence interval [CI], 7.1–30.8 months), and the median survival time (MST) and the 3-year overall survival rate were 30.3 months (95% CI, 11.5 months to not reached) and 43.8% (95% CI, 20.8–64.7%), respectively. This survival benefit was similarly manifest in patients with a PS of 2 (MST, 20.5 months) and those with a PS of ≥3 (MST, not reached). PFS did not differ between patients with or without central nervous system (CNS) metastases at baseline (median of 17.5 and 16.2 months, respectively, p = .886). Conclusion Alectinib showed a pronounced survival benefit for patients with ALK rearrangement-positive NSCLC and a poor PS regardless of the presence of CNS metastases, a patient population for which chemotherapy is not indicated.
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