Maleddu Alessandra, Pantaleo Maria A, Castellucci Paolo, Astorino Maria, Nanni Cristina, Nannini Margherita, Busato Fiorenza, Di Battista Monica, Farsad Mohsen, Lodi Filippo, Boschi Stefano, Fanti Stefano, Biasco Guido
Institute of Hematology and Medical Oncology "L. & A. Seragnoli", Sant'Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy.
Tumori. 2009 May-Jun;95(3):382-4. doi: 10.1177/030089160909500320.
Sunitinib is an oral multitargeted tyrosine kinase inhibitor with antiangiogenic properties used for treatment of renal cell carcinoma and gastrointestinal stromal tumors at a dose of 50 mg/day consecutively for 4 weeks followed by 2 weeks off per cycle. At present, no data are available on the early prediction of sunitinib response in renal cell carcinoma. We report a clinical case of a patient with metastatic renal cell carcinoma diagnosed with 11C-acetate PET and conventional CT and treated with sunitinib. Partial and complete remission documented by CT was preceded by early functional tumor inhibition shown by 11C-acetate-PET after only 14 days of therapy. This case report highlights some interesting points related to the potential role of a novel non-FDG PET tracer, 11C-acetate, in the early prediction of the response to targeted therapies in metastatic renal cell carcinoma.
舒尼替尼是一种具有抗血管生成特性的口服多靶点酪氨酸激酶抑制剂,用于治疗肾细胞癌和胃肠道间质瘤,剂量为50毫克/天,连续服用4周,然后每个周期停药2周。目前,尚无关于肾细胞癌中舒尼替尼反应早期预测的数据。我们报告了一例转移性肾细胞癌患者的临床病例,该患者通过11C-乙酸盐PET和传统CT诊断,并接受了舒尼替尼治疗。在治疗仅14天后,11C-乙酸盐PET显示早期功能性肿瘤抑制,随后CT记录到部分和完全缓解。本病例报告突出了一些与新型非FDG PET示踪剂11C-乙酸盐在转移性肾细胞癌靶向治疗反应早期预测中的潜在作用相关的有趣观点。