Interferon-α-2a with or without 13-cis retinoic acid in patients with progressive, measurable metastatic renal cell carcinoma -: Results of a randomized Phase II study (European Organization for Research and Treatment of Cancer Study 30951)

被引:22
作者
Fosså, SD [1 ]
Mickisch, GHJ
De Mulder, PHM
Horenblas, S
van Oosterom, AT
van Poppel, H
Fey, M
Croles, JJ
de Prijck, L
Van Glabbeke, M
机构
[1] Norwegian Radium Hosp, Dept Oncol, N-0310 Oslo, Norway
[2] Erasmus Univ, Med Ctr, Dept Urol, Rotterdam, Netherlands
[3] Univ Nijmegen, Med Ctr, Dept Internal Med, Nijmegen, Netherlands
[4] Antoni Van Leeuwenhoek Ziekenhuis, Netherlands Canc Inst, Amsterdam, Netherlands
[5] Univ Ziekenhuis Antwerpen, Dept Oncol, Edegem, Belgium
[6] UZ Gasthiusberg, Dept Urol, Louvain, Belgium
[7] Inselspital Bern, Dept Med Oncol, CH-3010 Bern, Switzerland
[8] Jeroen Bosch Ziekenhuis, Dept Urol, sHertogenbosch, Netherlands
[9] European Org Res Treatment Canc, Ctr Data, Brussels, Belgium
关键词
metastatic renal cell carcinoma; interferon-alpha; 13-cis retinoic acid; response evaluation;
D O I
10.1002/cncr.20307
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BACKGROUND. in patients with metastatic renal cell carcinoma (MRCC), interferon-alpha (IFN) monotherapy leads to response rates of 5-15%, dependent on the selection of patients. In 1995, preclinical and clinical data indicated an improvement of these results if IFN was combined with 13-cis retinoic acid (CRA). METHODS. in a randomized Phase II study, patients with measurable MRCC received either subcutaneous IFN (9 MU daily; Arm A) or the same daily subcutaneous dose of IFN plus oral CRA (1 mg/kg; Arm B). A central expert panel reviewed the X-ray documentation of objective responses. RESULTS. In the 50 eligible patients from Arm A, the objective, expert-reviewed response rate was 6% (95% confidence interval [95% CI], 1.3-16.6%; 2 complete responses [CRs] and 1 partial response [PR]). A 19% response rate (95% CI, 9.4-32.0%) was stated for 53 eligible patients from Arm B (2 CRs and 8 PRs). Only one of the four CRs claimed by the clinical investigator was confirmed by the central review committee. Conversely, the expert committee deemed that 3 of 12 investigator-stated PRs were CRs. Constitutional toxicity (flu-like symptoms) and/or side effects from skin, mucosa, or eyes led to discontinuation of treatment in 22% of nonprogressing patients, more often in Arm B than in Arm A. CONCLUSIONS. The results from this randomized Phase II study support expansion of the trial into a Phase III study to evaluate the effect of IFN-CRA combination therapy on the survival of patients who undergo nephrectomy prior to IFN-based immunotherapy. The considerable interobserver variability of response evaluation (individual investigator vs. expert panel) indicates the necessity of a central review of claimed responses in future Phase II studies involving patients with MRCC. (C) 2004 American Cancer Society.
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收藏
页码:533 / 540
页数:8
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