来自印度多中心癌症登记处的 ALK 阳性非小细胞肺癌治疗结果的真实世界数据

IF 0.6 Q4 ONCOLOGY South Asian Journal of Cancer Pub Date : 2023-11-21 DOI:10.1055/s-0043-1776290
L. Moharana, S. Panda, S. Devaraj, Ghanashyam Biswas, G.C. Subudhi, Prasanta Kumar Parida, Sourav Kumar Mishra, Jogamaya Pattnaik, Sambit K Mohanty, Sukanya Karunanidhi, Sandhya Lakshmi Singuluri, S. Saju, K. Rathnam, A. Sehrawat, Shikha Mudgal, S. Cyriac, Ashwin Philips, Anil Kumar Jose, Prasanth Ganesan
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This retrospective, multi-institutional study was conducted under the Network of Oncology Clinical Trials India and included a total of 67 ALK-positive metastatic lung cancer patients from 10 institutes across India, with a median follow-up of 23 months. In the first line setting, the objective response rate (ORR) with ALKi was 63.6% (crizotinib: 60.7%, ceritinib: 70%, alectinib: 66.6%, p  = 0.508), while with chemotherapy, it was 26.1%. The median progression-free survival (mPFS) for the first line ALKi group was significantly higher than that for chemotherapy (19 vs. 9 months, p  = 0.00, hazard ratio [HR] = 0.30, 95% confidence interval [CI]: 0.17–0.54). The mPFS for crizotinib, alectinib, and ceritinib was 17, 22, and 19 months, respectively ( p  = 0.48). Patients who received ALKi upfront or after 1 to 3 cycles of chemotherapy or after 4 or more cycles of chemotherapy had mPFS of 16, 22, and 23 months, respectively ( p  = 0.47). ALKi showed superior mPFS compared to chemotherapy in the second line (14 vs. 5 months; p  = 0.002) and the third line (20 vs. 4 months; p  = 0.009). The median overall survival (OS) was significantly better in patients who received ALKi in any line of therapy (44 vs. 14 months, p  < 0.001, HR = 0.10, 95% CI: 0.04–0.23). Brain progression was higher among those who did not receive ALKi (69.2 vs. 31.5%). In conclusion, the use of ALKi as first line treatment for ALK-positive metastatic NSCLC patients resulted in improved PFS. PFS and ORR did not significantly differ between patients who received ALKi upfront or after initiating chemotherapy. Notably, patients who received ALKi in second or later lines demonstrated significantly better outcomes compared to those receiving chemotherapy. 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引用次数: 0

摘要

Lalatendu Moharana 无性淋巴瘤激酶抑制剂(ALKi)是治疗 EML4-ALK 重排的转移性非小细胞肺癌(NSCLC)患者的标准疗法。目前有多种 ALKi 药物可供选择,但由于各种原因,并非所有符合条件的患者都能接受这些药物的治疗。鉴于我国现有的真实世界数据有限,我们旨在通过多中心合作评估治疗效果。这项回顾性、多机构研究是在印度肿瘤临床试验网络(Network of Oncology Clinical Trials India)下进行的,共纳入了来自印度10家机构的67名ALK阳性转移性肺癌患者,中位随访时间为23个月。在一线治疗中,ALKi的客观反应率(ORR)为63.6%(克唑替尼:60.7%,色瑞替尼:70%,阿来替尼:66.6%,P = 0.508),而化疗的客观反应率为26.1%。一线ALKi组的中位无进展生存期(mPFS)明显高于化疗组(19个月对9个月,P = 0.00,危险比[HR] = 0.30,95%置信区间[CI]:0.17-0.54):0.17-0.54).克唑替尼、阿来替尼和色瑞替尼的mPFS分别为17、22和19个月(P = 0.48)。先接受ALKi治疗或接受1至3个周期化疗或接受4个或更多周期化疗的患者的mPFS分别为16、22和23个月(P = 0.47)。在二线(14 个月对 5 个月;p = 0.002)和三线(20 个月对 4 个月;p = 0.009),ALKi 的 mPFS 优于化疗。在任何一线治疗中接受ALKi治疗的患者的中位总生存期(OS)明显更好(44个月对14个月,P<0.001,HR=0.10,95% CI:0.04-0.23)。未接受ALKi治疗的患者脑进展率更高(69.2%对31.5%)。总之,将ALKi作为ALK阳性转移性NSCLC患者的一线治疗可改善患者的PFS。前期或开始化疗后接受ALKi治疗的患者的PFS和ORR没有明显差异。值得注意的是,与接受化疗的患者相比,在二线或二线以上接受ALKi治疗的患者的疗效明显更好。在任何一线治疗中使用ALKi都与明显延长的OS有关。
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Real-World Data on Treatment Outcome of ALK-Positive Non-Small Cell Lung Cancer from an Indian Multicentric Cancer Registry
Abstract Lalatendu Moharana The Anaplastic lymphoma kinase inhibitors (ALKi) represent the standard of care for metastatic non-small cell lung cancer (NSCLC) patients with EML4-ALK rearrangements. Various ALKi agents are available; however, not all eligible patients receive treatment with them due to various reasons. Given the limited real-world data available in our country, we aimed to assess treatment outcomes through a multicenter collaboration. This retrospective, multi-institutional study was conducted under the Network of Oncology Clinical Trials India and included a total of 67 ALK-positive metastatic lung cancer patients from 10 institutes across India, with a median follow-up of 23 months. In the first line setting, the objective response rate (ORR) with ALKi was 63.6% (crizotinib: 60.7%, ceritinib: 70%, alectinib: 66.6%, p  = 0.508), while with chemotherapy, it was 26.1%. The median progression-free survival (mPFS) for the first line ALKi group was significantly higher than that for chemotherapy (19 vs. 9 months, p  = 0.00, hazard ratio [HR] = 0.30, 95% confidence interval [CI]: 0.17–0.54). The mPFS for crizotinib, alectinib, and ceritinib was 17, 22, and 19 months, respectively ( p  = 0.48). Patients who received ALKi upfront or after 1 to 3 cycles of chemotherapy or after 4 or more cycles of chemotherapy had mPFS of 16, 22, and 23 months, respectively ( p  = 0.47). ALKi showed superior mPFS compared to chemotherapy in the second line (14 vs. 5 months; p  = 0.002) and the third line (20 vs. 4 months; p  = 0.009). The median overall survival (OS) was significantly better in patients who received ALKi in any line of therapy (44 vs. 14 months, p  < 0.001, HR = 0.10, 95% CI: 0.04–0.23). Brain progression was higher among those who did not receive ALKi (69.2 vs. 31.5%). In conclusion, the use of ALKi as first line treatment for ALK-positive metastatic NSCLC patients resulted in improved PFS. PFS and ORR did not significantly differ between patients who received ALKi upfront or after initiating chemotherapy. Notably, patients who received ALKi in second or later lines demonstrated significantly better outcomes compared to those receiving chemotherapy. The use of ALKi in any line of therapy was associated with significantly prolonged OS.
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