印度北部三级医院非鳞状非小细胞肺癌患者的流行病学、临床特征和治疗结果

V. Koyyala, M. Sharma, P. Goyal, Varun Goel, S. Bommera, Mohit Agrawal, K. Domadia, Krushna Choudhary, S. Bothra, A. Jajodia, B. Amrith, S. Joga, S. Pasricha, U. Batra
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引用次数: 0

摘要

背景:肺癌是印度和全球癌症相关死亡的最常见原因之一,有了更多的真实数据,更好地规划有限的肿瘤学资源是可能的。目的:本研究旨在评估本中心IV期肺腺癌患者的临床概况和治疗结果。材料与方法:对182例IV期肺腺癌患者进行前瞻性筛选分析,其中符合纳入标准的107例患者纳入最终分析。表皮生长因子受体(EGFR)和棘皮微管相关蛋白样4-间变性淋巴瘤激酶(EML4-ALK)基因组改变的患者使用酪氨酸激酶抑制剂治疗,其他患者按标准化疗方案治疗。测量缓解率(rr)、无进展生存期(PFS)和总生存期(OS)。结果:患者中位年龄为55.6岁(范围26-82岁),男女比例为1.23:1。104例(96.3%)患者可以分析EGFR和EML4-ALK的改变,分别在31.7%和8.7%的患者中检测到。整个队列的总RR为51.4%,而中位PFS和中位OS分别为6.9和13.7个月。egfr突变组和alk重排组的中位PFS分别为9.6个月和10.2个月,高于非egfr非alk患者。整个队列的中位生存期为13.7个月,而EGFR和ALK改变组的中位生存期未达到。结论:由于EGFR、ALK等驱动突变的患者预后优于无驱动突变的患者,因此每一位诊断为晚期非小细胞肺癌的患者都应进行突变分析。
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Epidemiological, clinical profile, and treatment outcome of stage iv nonsquamous nonsmall cell lung cancer patients presenting to tertiary care hospital in North India
Background: Better planning of limited resources in oncology is possible with more real-world data of lung cancer, one of the most common causes of cancer related mortality in India and Globe. Aim: This study aimed to evaluate the clinical profile and treatment outcomes in patients with Stage IV adenocarcinoma of lung at our center. Materials and Methods: One hundred and eighty-two patients with Stage IV adenocarcinoma of lung were prospectively screened and analyzed, of which 107 patients who met the inclusion criteria were included in the final analysis. Patients with epidermal growth factor receptor (EGFR) and echinodermal microtubule-associated protein-like 4-anaplastic lymphoma kinase (EML4-ALK) genomic alterations were treated with tyrosine kinase inhibitors and others were treated as per standard chemotherapy regimens. Response rates (RRs), progression-free survival (PFS), and overall survival (OS) were measured. Results: Median age of patients was 55.6 years (range, 26–82) with a male-to-female ratio of 1.23:1. Analyses for EGFR and EML4-ALK alterations were possible for 104 (96.3%) patients and were detected in 31.7% and 8.7% patients, respectively. The overall RR for the entire cohort was 51.4%, while median PFS and median OS were 6.9 and 13.7 months, respectively. Median PFS for the EGFR-mutated and ALK-rearranged group was 9.6 and 10.2 months, respectively, which was higher than non-EGFR non-ALK patients. Median OS for the whole cohort was 13.7 months, while median OS was not reached for EGFR and ALK altered groups. Conclusions: As patients with driver mutations like EGFR and ALK have better prognosis than those who do not, every patient diagnosed with advanced nonsmall cell lung cancer should be offered mutational analysis.
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