Mu Xiaoli, Li Yan
The Department of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Lung Cancer Center, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
Front Pharmacol. 2024 Dec 10;15:1413897. doi: 10.3389/fphar.2024.1413897. eCollection 2024.
Driver mutations in tyrosine kinases, such as the anaplastic lymphoma kinase (ALK) mutation, are known to play a critical role in the pathogenesis of non-small cell lung cancer (NSCLC) but are rarely observed in large cell neuroendocrine carcinoma (LCNEC). Multiple primary malignancies (MPMs) refer to the occurrence of two or more distinct primary malignancies within the same or different organs and tissues in a single patient, either simultaneously or sequentially.
We reported a case of advanced LCNEC as a heterochronous double primary malignancy, following a prior breast cancer diagnosis in a 55-year-old woman. Ten years after achieving remission from breast cancer, the patient was diagnosed with LCNEC, presenting with multiple brain metastases (BMs) after undergoing surgery and adjuvant radiochemotherapy. She tested positive for the ALK fusion gene and received lorlatinib as an initial treatment. After 6 weeks, there was a significant reduction in the tumor, and the treatment impact was evaluated as a partial response. The treatment has been continued for over 25 months since the initiation of ALK Tyrosine kinase inhibitor (ALK-TKI) therapy.
This case suggested that ALK-positive advanced LCNEC patients might benefit from first-line intervention with lorlatinib, particularly for managing brain metastases.
已知酪氨酸激酶中的驱动突变,如间变性淋巴瘤激酶(ALK)突变,在非小细胞肺癌(NSCLC)的发病机制中起关键作用,但在大细胞神经内分泌癌(LCNEC)中很少见。多原发性恶性肿瘤(MPMs)是指在同一患者的同一或不同器官和组织中同时或先后发生的两种或更多种不同的原发性恶性肿瘤。
我们报告了一例晚期LCNEC作为异时性双原发性恶性肿瘤的病例,该患者为一名55岁女性,之前被诊断患有乳腺癌。在乳腺癌缓解10年后,患者被诊断为LCNEC,在接受手术和辅助放化疗后出现多处脑转移(BMs)。她的ALK融合基因检测呈阳性,并接受洛拉替尼作为初始治疗。6周后,肿瘤明显缩小,治疗效果评估为部分缓解。自开始使用ALK酪氨酸激酶抑制剂(ALK-TKI)治疗以来,该治疗已持续超过25个月。
该病例表明,ALK阳性的晚期LCNEC患者可能从洛拉替尼的一线干预中获益,特别是在治疗脑转移方面。