Patil Vijay, Noronha Vanita, Vallathol Dilip Harindran, Menon Nandini, Mahajan Abhishek, Janu Amit, Purandare Nilendu, Prabhash Kumar
Department of Medical Oncology, Tata Memorial Centre, HBNI, Mumbai 400012, India.
Both contributed equally.
Ecancermedicalscience. 2022 Jun 16;16:1414. doi: 10.3332/ecancer.2022.1414. eCollection 2022.
Leptomeningeal metastasis (LMM) from non-small cell lung cancer (NSCLC) is often an underdiagnosed entity, has a dismal prognosis and has very limited data from low- and middle-income countries.
A single-centre study, which included 1148 adult patients diagnosed as NSCLC, with Eastern Oncology Cooperative Group 0-2, as identified from data of four prospective randomised controlled trials. Two trials included patients who had epidermal growth factor sensitive mutations (CTRI/2015/08/006113 and CTRI/2016/08/007149) and the other two included squamous cell carcinoma (CTRI/2013/02/003422) and adenocarcinoma patients (CTRI/2014/08/00484). The key objectives were to estimate the incidence, risk factors, time to development and outcomes for LMM.
Out of 1148 patients, 36 patients (0.031%; 95%CI: 0.022-0.043) developed leptomeningeal metastasis. In these patients, median time to development of LM was 14.92 months (interquartile range: 7.7-21.84). Among the tested factors, the presence of brain metastasis was the only statistically significant risk factor associated with the development of LMM (-value = 0.035). The median overall survival (OS) after the development of LM was 61 days (95%CI: 38.95-83.05). The median OS in driver mutated patients was 66 days (95% CI: 14.74-117.26) versus 51 days (95% CI: 14.5-87.5) (-value = 0.201) in non-driver mutated patients. Only 6 (19.4%) out of 31 epidermal growth factor receptor-mutated patients received osimertinib. Patients treated with osimertinib had a median OS of 245 days (95% CI: 215.48-274.52) versus 52 days (95% CI: 22.62-81.38) for those without (-value = 0.327).
The incidence of LMM is low in the Indian population. In our study, there was no single factor which impacted survival in patients who developed LMM. This suggests that the overall prognosis is poor in patients with LMM where access to newer therapeutic modalities is limited.
非小细胞肺癌(NSCLC)的软脑膜转移(LMM)常常是一种诊断不足的疾病,预后很差,且来自低收入和中等收入国家的数据非常有限。
一项单中心研究,纳入了1148例被诊断为NSCLC的成年患者,这些患者来自四项前瞻性随机对照试验的数据,东部肿瘤协作组评分为0 - 2分。两项试验纳入了具有表皮生长因子敏感突变的患者(CTRI/2015/08/006113和CTRI/2016/08/007149),另外两项试验纳入了鳞状细胞癌患者(CTRI/2013/02/003422)和腺癌患者(CTRI/2014/08/00484)。主要目标是估计LMM的发病率、危险因素、发生时间和结局。
在1148例患者中,36例(0.031%;95%置信区间:0.022 - 0.043)发生了软脑膜转移。在这些患者中,发生软脑膜转移的中位时间为14.92个月(四分位间距:7.7 - 21.84)。在检测的因素中,脑转移的存在是与LMM发生相关的唯一具有统计学意义的危险因素(P值 = 0.035)。软脑膜转移发生后的中位总生存期(OS)为61天(95%置信区间:38.95 - 83.05)。驱动基因突变患者的中位OS为66天(95%置信区间:14.74 - 117.26),而非驱动基因突变患者为51天(95%置信区间:14.5 - 87.5)(P值 = 0.201)。31例表皮生长因子受体突变患者中只有6例(19.4%)接受了奥希替尼治疗。接受奥希替尼治疗的患者中位OS为245天(95%置信区间:215.48 - 274.52),未接受治疗的患者为52天(95%置信区间:22.62 - 81.38)(P值 = 0.327)。
印度人群中LMM的发病率较低。在我们的研究中,没有单一因素影响发生LMM患者的生存。这表明在获得更新治疗方式有限的LMM患者中,总体预后较差。