Phase I trial of capecitabine in combination with interferon alpha in patients with metastatic renal cancer: toxicity and pharmacokinetics

被引:16
|
作者
Chang, DZ
Olencki, T
Budd, GT
Peereboom, D
Ganapathi, R
Osterwalder, B
Bukowski, R
机构
[1] Cleveland Clin Fdn, Expt Therapeut Program, Taussig Canc Ctr, Cleveland, OH 44195 USA
[2] F Hoffmann La Roche & Co Ltd, CH-4002 Basel, Switzerland
关键词
capecitabine; interferon; renal cancer; pharmacokinetics;
D O I
10.1007/s002800100366
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The present study was designed to determine the toxicity and maximum tolerated doses of oral intermittent oral capecitabine and subcutaneous (s.c.) rHuIFNalpha2a in patients with metastatic renal cell carcinoma (RCC). The pharmacokinetics of capecitabine and its metabolites were also investigated. Methods: A total of 27 patients were treated at four dose levels of capecitabine (825 or 1000 mg/m(2) twice daily orally, days 1-14, 22-36) and rHuIFNalpha2a (1.5 or 3.0 MU/m(2) s.c. three tithes weekly). Unchanged capecitabine and its metabolites were analyzed in plasma using liquid chromatography/mass spectrometry in ten patients. Results: The toxicity of combined capecitabine and rHuIFNa2a was moderate. Patients experienced mild nausea/vomiting (70%) and diarrhea (63%). The hand-foot syndrome was seen in 67% of patients and was generally mild, as was hematologic toxicity. Dose-limiting toxicity included diarrhea, mucositis, neutropenia and the hand-foot syndrome. The dose level recommended for further trials included capecitabine 1000 mg/m(2) twice daily and rHuIFNa2a 3.0 MU/m(2) three times weekly. One patient had a partial response of a liver lesion (duration >200 days). Pharmacokinetic parameters of capecitabine and its metabolites (5'-deoxy-5-fluorouridine, 5-fluorouracil and alpha-fluoro-beta-alanine) were similar to those reported by other authors. There was rapid conversion to 5'-deoxyuridine. The peak plasma concentrations of capecitabine occurred between 0.5 and 3.0 h. Conclusions: The combination of capecitabine and rHuIFNa2a was well tolerated. The recommended dose levels for phase 11 trials are: rHuIFNalpha2a 3.0 MU/m2 s.c. three times weekly and oral capecitabine 1000 mg/m(2) twice daily for 2 weeks. No evidence of an effect of rHuIFNa2a on the pharmacokinetics of capecitabine or its metabolites was apparent. A phase II trial in untreated patients with metastatic RCC is planned.
引用
收藏
页码:493 / 498
页数:6
相关论文
共 50 条
  • [41] Phase I combination study of trabectedin and capecitabine in patients with advanced malignancies
    Lia Gore
    E. Rivera
    M. Basche
    S. L. Moulder-Thompson
    J. Li
    S. Eppers
    S. Grolnic
    C. O’Bryant
    D. Cleere
    Y. A. Elsayed
    S. G. Eckhardt
    Investigational New Drugs, 2012, 30 : 1942 - 1949
  • [42] A Phase II Trial of Gemcitabine, Capecitabine, and Bevacizumab in Metastatic Renal Carcinoma
    Chung, Elizabeth K.
    Posadas, Edwin M.
    Kasza, Kristen
    Karrison, Theodore
    Manchen, Elizabeth
    Hahn, Olwen M.
    Stadler, Walter M.
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2011, 34 (02): : 150 - 154
  • [43] Phase I trial of capecitabine plus everolimus (RAD001) in patients with previously treated metastatic gastric cancer
    Taekyu Lim
    Jeeyun Lee
    Duk Joo Lee
    Ha Yeon Lee
    Boram Han
    Kyung Kee Baek
    Hee Kyung Ahn
    Su Jin Lee
    Se Hoon Park
    Joon Oh Park
    Young Suk Park
    Ho Yeong Lim
    Kyoung-Mee Kim
    Won Ki Kang
    Cancer Chemotherapy and Pharmacology, 2011, 68 : 255 - 262
  • [44] Phase I trial of capecitabine plus everolimus (RAD001) in patients with previously treated metastatic gastric cancer
    Lim, Taekyu
    Lee, Jeeyun
    Lee, Duk Joo
    Lee, Ha Yeon
    Han, Boram
    Baek, Kyung Kee
    Ahn, Hee Kyung
    Lee, Su Jin
    Park, Se Hoon
    Park, Joon Oh
    Park, Young Suk
    Lim, Ho Yeong
    Kim, Kyoung-Mee
    Kang, Won Ki
    CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2011, 68 (01) : 255 - 262
  • [45] Capecitabine and vinorelbine in elderly patients (≥65 years) with metastatic breast cancer:: a phase I trial (SAKK 25/99)
    Hess, D
    Thürlimann, B
    Pagani, O
    Aebi, S
    Rauch, D
    Ballabeni, P
    Rufener, B
    Castiglione-Gertsch, M
    Goldhirsch, A
    ANNALS OF ONCOLOGY, 2004, 15 (12) : 1760 - 1765
  • [46] A Phase I Trial of the PI3K Inhibitor Buparlisib Combined With Capecitabine in Patients With Metastatic Breast Cancer
    McRee, Autumn J.
    Marcom, Paul K.
    Moore, Dominic T.
    Zamboni, William C.
    Kornblum, Zachary A.
    Hu, Zhiyuan
    Phipps, Rachel
    Anders, Carey K.
    Reeder-Hayes, Katherine
    Carey, Lisa A.
    Weck, Karen E.
    Perou, Charles M.
    Dees, E. Claire
    CLINICAL BREAST CANCER, 2018, 18 (04) : 289 - 297
  • [47] A phase II trial of capecitabine in previously untreated patients with advanced and/or metastatic gastric cancer
    Hong, YS
    Song, SY
    Lee, SI
    Chung, HC
    Choi, SH
    Noh, SH
    Park, JN
    Han, JY
    Kang, JH
    Lee, KS
    Cho, JY
    ANNALS OF ONCOLOGY, 2004, 15 (09) : 1344 - 1347
  • [48] Weekly docetaxel in combination with capecitabine in patients with metastatic gastric cancer
    Chun, JH
    Kim, HK
    Lee, JS
    Choi, JY
    Hwangbo, B
    Lee, HG
    Park, SR
    Choi, IJ
    Kim, CG
    Ryu, KW
    Kim, YW
    Lee, JS
    Bae, JM
    AMERICAN JOURNAL OF CLINICAL ONCOLOGY-CANCER CLINICAL TRIALS, 2005, 28 (02): : 188 - 194
  • [49] Phase I Study of Axitinib in Combination with Cisplatin and Capecitabine in Patients with Previously Untreated Advanced Gastric Cancer
    Oh, Do-Youn
    Doi, Toshihiko
    Shirao, Kuniaki
    Lee, Keun-Wook
    Park, Sook Ryun
    Chen, Ying
    Yang, Liqiang
    Valota, Olga
    Bang, Yung-Jue
    CANCER RESEARCH AND TREATMENT, 2015, 47 (04): : 687 - 696
  • [50] Preoperative chemoradiation with capecitabine for rectal cancer in elderly patients: a phase I trial
    Yu Tang
    Wen-Yang Liu
    Jing Jin
    Hai-Zeng Zhang
    Lin Yang
    Hua Ren
    Hui Fang
    Wei-Hu Wang
    Yong-Wen Song
    Yue-Ping Liu
    Shu-Lian Wang
    Ye-Xiong Li
    International Journal of Colorectal Disease, 2016, 31 : 1547 - 1549