Genitourinary Service, Division of Medical Oncology and the Department of Medical Imaging, Memorial Sloan-Kettering Cancer Center, New York, NY, USA.
Med Oncol. 2011 Dec;28(4):1527-9. doi: 10.1007/s12032-010-9640-y. Epub 2010 Aug 10.
A 70-year-old man with metastatic renal cell carcinoma developed progressive liver metastases after 8 weeks of treatment with the multitargeted tyrosine kinase inhibitor (TKI) sunitinib. He then participated in the phase III placebo-controlled clinical trial of the oral mammalian target of rapamycin (mTOR) inhibitor everolimus, initially randomized to placebo (but had disease progression after 3 months) and crossed over to everolimus at time of unblinding. The patient had stable disease after 8 weeks (two cycles) of everolimus that was maintained until 28 months of therapy, at which time the patient had achieved a partial response. This case illustrates the potential for patients with metastatic renal cell carcinoma, a malignancy with historically poor prognosis, to derive long-term benefit from everolimus when used in a manner consistent with its approved indication (after TKI therapy with sunitinib or sorafenib).
一位 70 岁男性,转移性肾细胞癌患者,在接受多靶点酪氨酸激酶抑制剂(TKI)舒尼替尼治疗 8 周后出现进行性肝转移。随后,他参加了口服哺乳动物雷帕霉素靶蛋白(mTOR)抑制剂依维莫司的 III 期安慰剂对照临床试验,最初随机分配至安慰剂组(但在 3 个月时疾病进展),并在揭盲时交叉至依维莫司组。该患者在接受依维莫司治疗 8 周(两个周期)后疾病稳定,一直持续到 28 个月的治疗,此时患者达到部分缓解。该病例说明了对于转移性肾细胞癌(一种预后历来较差的恶性肿瘤)患者,当依维莫司按照其批准的适应证(在舒尼替尼或索拉非尼的 TKI 治疗之后)使用时,患者可能会从中获得长期获益。