Takayoshi Kotoe, Sagara Kosuke, Uchino Keita, Kusaba Hitoshi, Sakamoto Naotaka, Iguchi Atsushi, Baba Eishi
Department of Medical Oncology, Clinical Research Institute, National Hospital Organization Kyushu Medical Center, 1-8-1 Jigyouhama, Chuo-ku, Fukuoka, 810-8563, Japan.
Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.
BMC Cancer. 2015 May 22;15:426. doi: 10.1186/s12885-015-1443-2.
Metastatic renal cell carcinoma (mRCC) had been a chemo-refractory disease, but recent advances in multiple kinase inhibitors such as sunitinib have dramatically changed the clinical course of mRCC. Sunitinib is used for mRCC chemotherapy based on the favorable results of a recent clinical trial, but specific biomarkers predicting efficacy and safety are not yet available. Locally advanced bile duct carcinoma (BDC) has generally been treated with single agent gemcitabine or as doublet therapy with cisplatin. Concomitant occurrence of mRCC and BDC is extremely rare, and a standard therapeutic strategy has not been established.
A 65-year-old woman was diagnosed as having multiple mRCC and intercurrent, locally advanced BDC. A single course of combination therapy with sunitinib (25 mg/day, day2-15) and gemcitabine (750 mg/m(2), days 1, 8) was administered, and this showed obvious effects, with partial response for mRCC and stable disease for BDC. However, the patient also experienced severe adverse events, including hematological and various non-hematological toxicities; the combination therapy was then terminated on day 13 after its initiation. She recovered on day 28 and is alive 3.5 years after the diagnosis. The plasma trough levels of sunitinib and its active metabolite SU12662 on day 13 were 91.5 ng/mL and 19.2 ng/mL, respectively, which were relatively higher than in previous reports. Analysis of her single nucleotide polymorphisms (SNPs) detected TC in ABCB1 3435C/T, TC in 1236C/T and TT in 2677G/T, suggesting a possible TTT haplotype.
A rare case of double cancer of mRCC and BDC was treated by combination chemotherapy. Although unknown synergistic mechanisms of these agents may be involved, severe toxicities might be possibly associated with high sunitinib exposure. Further exploration of combination therapy with sunitinib and gemcitabine is required.
转移性肾细胞癌(mRCC)曾是一种化疗难治性疾病,但近年来舒尼替尼等多种激酶抑制剂的进展显著改变了mRCC的临床进程。基于近期一项临床试验的良好结果,舒尼替尼被用于mRCC化疗,但尚未有预测疗效和安全性的特异性生物标志物。局部晚期胆管癌(BDC)一般采用吉西他滨单药治疗或与顺铂联合的双药治疗。mRCC和BDC同时发生极为罕见,尚未确立标准治疗策略。
一名65岁女性被诊断为患有多发mRCC及并发的局部晚期BDC。给予一个疗程的舒尼替尼(25mg/天,第2 - 15天)与吉西他滨(750mg/m²,第1、8天)联合治疗,显示出明显效果,mRCC部分缓解,BDC病情稳定。然而,患者也出现了严重不良事件,包括血液学及各种非血液学毒性;联合治疗在开始后第13天终止。她在第28天康复,诊断后3.5年仍存活。第13天舒尼替尼及其活性代谢物SU12662的血浆谷浓度分别为91.5ng/mL和19.2ng/mL,相对高于既往报道。对其单核苷酸多态性(SNP)分析检测到ABCB1 3435C/T为TC、1236C/T为TC以及2677G/T为TT,提示可能存在TTT单倍型。
采用联合化疗治疗了一例罕见的mRCC和BDC双癌病例。尽管可能涉及这些药物未知的协同机制,但严重毒性可能与舒尼替尼高暴露有关。需要进一步探索舒尼替尼与吉西他滨的联合治疗。