五线疗法治疗 ALK 阳性肺癌脑转移灶和脑膜转移灶患者的十年生存率:病例报告

Wanda Liguigli, Roberto Barbieri, R. Cengarle, Anita Rimanti, Giovanna Catania, Francesca Turina, Camilla Pesoni, Maurizio Cantore
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摘要

4%-5%的肺腺癌患者会出现无性淋巴瘤激酶(ALK)易位。2012年10月,我们诊断出一名42岁女性患有ALK易位肺腺癌,并伴有胸膜和骨转移。化疗16个月后,由于腹腔淋巴结进展,患者开始接受克唑替尼治疗。28 个月后,脑部磁共振成像显示脑部疾病进展,CT 扫描显示肺部疾病进展。患者接受了全脑放疗,并开始服用色瑞替尼,但六个月后因3级胃肠道毒性而停药。2017年6月,记录到脑膜疾病进展,患者开始服用布加替尼。41个月后,脑部CT扫描显示多处病变,于是开始使用乐拉替尼。患者目前仍在继续接受治疗,同时保持良好的生活质量。ALK抑制剂的出现改变了这些患者的预后,即使是脑和脑膜转移性疾病患者。
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Ten Years Survival in a Patient with Brain and Meningeal Metastases from ALK-Positive Lung Cancer Treated with Five Lines of Therapy: A Case Report
Anaplastic lymphoma kinase (ALK) translocation is observed in 4–5% of lung adenocarcinoma patients. In October 2012, we diagnosed a translocated ALK lung adenocarcinoma with pleural and bone metastases in a 42-year-old woman. After 16 months of chemotherapy, due to progression of the abdominal lymph nodes, the patient started Crizotinib. After 28 months, brain MRI documented progression of brain disease and a CT scan showed lung progression. The patient underwent whole-brain radiotherapy and Ceritinib was started but discontinued after six months due to grade 3 gastrointestinal toxicity. In June 2017, progression of meningeal disease was documented and the patient started Brigatinib. After 41 months the brain CT scan showed multiple lesions and Lorlatinib was started. The patient is still continuing this therapy while maintaining a good quality of life. The advent of ALK inhibitors has changed the prognosis of these patients even in cases of cerebral and meningeal metastatic disease.
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