Fan WuQiang, Sloane Jason, Nachtigall Lisa B
Neuroendocrine and Pituitary Tumor Clinical Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
Diabetes Center, Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts.
J Endocr Soc. 2019 Aug 7;3(10):1887-1891. doi: 10.1210/js.2019-00217. eCollection 2019 Oct 1.
Non-small cell lung cancer with pituitary metastasis (NSCLC-PM) is a devastating disease; however, treatment is being revolutionized by a novel therapy targeting highly specific tumor signals, such as the mutation of epidermal growth factor receptors (EGFRs). Long-term management of hormonal defects in this population has become a unique neuroendocrine clinical challenge. We report the case of a 73-year-old female nonsmoker who was diagnosed with stage IV non-small cell lung cancer. The initial staging evaluation revealed a 7 × 11 × 21-mm sellar lesion abutting the optic chiasm and causing clinical hypopituitarism. The patient received three cycles of chemotherapy with carboplatin and pemetrexed, which was discontinued because of major cumulative side effects of myelosuppression and kidney disease. Eight months later, scans demonstrated evidence of disease progression. A repeated lung nodule biopsy revealed an exon 19 deletion mutation. EGFR-targeted therapy with osimertinib 80 mg daily was initiated. A complete resolution of the pituitary lesion was evident on a follow-up pituitary MRI 5 weeks later and was sustained 1 year after. However, the panhypopituitarism persisted. This is an illustrative case of NSCLC-PM with exon 19 deletion mutation, wherein osimertinib, a third-generation EGFR‒tyrosine kinase inhibitor, eradicated the sellar metastasis and prevented the need for radiotherapy. However, the neuroendocrine deficits persisted despite anatomic improvement.
伴有垂体转移的非小细胞肺癌(NSCLC-PM)是一种严重的疾病;然而,一种针对高度特异性肿瘤信号(如表皮生长因子受体(EGFR)突变)的新型疗法正在彻底改变其治疗方式。对这一人群激素缺陷的长期管理已成为神经内分泌领域一项独特的临床挑战。我们报告了一例73岁不吸烟女性患者,她被诊断为IV期非小细胞肺癌。初始分期评估发现一个7×11×21毫米的鞍区病变,紧邻视交叉并导致临床垂体功能减退。患者接受了三个周期的卡铂和培美曲塞化疗,但由于骨髓抑制和肾病的严重累积副作用而停药。八个月后,扫描显示疾病进展的迹象。再次进行的肺结节活检显示存在19号外显子缺失突变。开始使用奥希替尼每日80毫克进行EGFR靶向治疗。5周后的垂体MRI随访显示垂体病变完全消退,并在1年后持续缓解。然而,全垂体功能减退仍然存在。这是一例具有19号外显子缺失突变的NSCLC-PM病例,其中第三代EGFR酪氨酸激酶抑制剂奥希替尼消除了鞍区转移并避免了放疗的需要。然而,尽管解剖结构有所改善,但神经内分泌缺陷仍然存在。