Outcomes of Patients With Metastatic Renal Cell Carcinoma and End-Stage Renal Disease Receiving Dialysis and Targeted Therapies: A Single Institution Experience

被引:32
作者
Shetty, Aditya V. [1 ]
Matrana, Marc R. [2 ]
Atkinson, Bradley J. [3 ]
Flaherty, Amber L. [4 ]
Jonasch, Eric [5 ]
Tannir, Nizar M. [5 ]
机构
[1] Univ Texas Houston, Sch Med, Internal Med Residency Program, Houston, TX USA
[2] Ochsner Med Ctr, Dept Hematol & Oncol, New Orleans, LA 70121 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Pharm, Clin Programs, Houston, TX 77030 USA
[4] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Hematol & Med Oncol Fellowship Program, Tampa, FL 33612 USA
[5] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Hemodialysis; Kidney cancer; Kidney disease; mTOR inhibitors; VEGF tyrosine kinase inhibitors; SUNITINIB; SURVIVAL; SORAFENIB; PAZOPANIB;
D O I
10.1016/j.clgc.2014.01.004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Data are limited regarding outcomes in patients with end-stage renal disease (ESRD) and metastatic renal cell carcinoma (mRCC) receiving targeted therapy. We retrospectively identified patients with mRCC and ESRD treated at the University of Texas M.D. Anderson Cancer Center from 2002 to 2012. Fourteen patients were identified with a median number of targeted therapies (TTs) per patient of 3 (range, 1-4). Outcomes in patients with mRCC and ESRD were similar to those reported in patients with normal kidney function. Introduction: Limited data are available regarding patients with renal cell carcinoma and ESRD treated with TTs. The objective of this study was to explore the tolerability and safety of TT in patients with mRCC and ESRD. Patients and Methods: We retrospectively identified patients with mRCC and ESRD treated at the University of Texas M. D. Anderson Cancer Center from 2002 to 2012. Patient characteristics including demographic, histology, treatment, and adverse events are reported. Duration of treatment (TOT) was determined from date of drug initiation to discontinuation. Overall survival (OS) was determined from initiation of TT to death. Statistics are descriptive. Results: Fourteen patients were identified. Ten patients had clear-cell histology and 4 had papillary histology. The median number of TTs per patient was 3 (range, 1-4) with median TOT of 28 months for all TTs. Eighty-eight percent of all toxicities were Grade 1 to 2; no Grade 4 toxicities were noted. Treatment discontinuations included 3 patients treated with sorafenib due to hand-foot syndrome, intolerable fatigue, and squamous cell skin cancer development; 2 patients treated with pazopanib due to intolerable fatigue and increased transaminase levels; and 1 patient treated with everolimus due to pneumonitis. Eight patients died from progressive disease. Median OS from initiation of TT was 28.5 months and 35 months from time of diagnosis. Conclusion: Toxicities were mild to moderate and consistent with those reported in previous studies. TTs appear to be safe, well tolerated and produce antitumor response in patients with mRCC and ESRD receiving dialysis. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:348 / 353
页数:6
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