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Temozolomide in combination with interferon-alfa versus temozolomide alone in patients with advanced metastatic melanoma: A randomized, phase III, multicenter study from the Dermatologic Cooperative Oncology Group
被引:82
|作者:
Kaufmann, R
Spieth, K
[1
]
Leiter, U
Mauch, C
von den Driesch, P
Vogt, T
Linse, R
Tilgen, W
Schadendorf, D
Becker, JC
Sebastian, G
Krengel, S
Kretschmer, L
Garbe, C
Dummer, R
机构:
[1] JW Goethe Univ, Dept Dermatol, Frankfurt, Germany
[2] Univ Tubingen, D-72074 Tubingen, Germany
[3] Univ Cologne, Cologne, Germany
[4] Univ Erlangen Nurnberg, D-8520 Erlangen, Germany
[5] Univ Regensburg, D-8400 Regensburg, Germany
[6] Helios Clin, Erfurt, Germany
[7] Univ Saarland, Homburg, Germany
[8] German Canc Res Ctr, Skin Canc Unit, Mannheim, Germany
[9] Univ Wurzburg, Wurzburg, Germany
[10] Univ Dresden, Dresden, Germany
[11] Univ Schleswig Holstein, Lubeck, Germany
[12] Univ Gottingen, Gottingen, Germany
[13] Univ Zurich, Zurich, Switzerland
关键词:
D O I:
10.1200/JCO.2005.01.1551
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Purpose Temozolomide (TMZ) has shown efficacy in metastatic melanoma equal to that of dacarbazine (DTIC), the standard chemotherapeutic agent for melanoma. As the combination with interferon-alfa (IFN-alpha) appears superior to single-agent DTIC regarding response rates, the purpose of this study was to compare TMZ alone and TMZ plus IFN-alpha in terms of objective response (OR), overall survival, and safety in a prospective, randomized, multicenter trial. Patients and Methods Two hundred ninety-four patients with untreated stage IV metastatic melanoma (American Joint Committee on Cancer staging system) were randomly assigned to receive either oral TMZ alone (200 mg/m(2)/day; days 1 through 5 every 28 days) or in combination with subcutaneous IFN-a (5 MU/m(2); days 1, 3, and 5 every week). Results Two hundred eighty-two patients were eligible for an intent-to-treat analysis, 271 patients were treated per protocol. In the TMZ + IFN-alpha arm, 33 (24.1 %) of 137 patients responded to therapy (partial or complete remission) whereas in the monotherapy arm, in 18 (13.4%) of 134 patients, a response was evident. Thus, the response rate was significantly higher in the combination arm (P = .036). Median survival time was 8.4 months for patients treated with TMZ (95% CI, 7.07 to 9.27) and 9.7 months for those treated with the combination (95% CI, 8.26 to 11.18; P = .16). Dose modifications and interval prolongations due to hematologic toxicity were significantly more frequent in the TMZ + IFN-alpha arm (P < .001). Conclusion In metastatic melanoma treatment with TMZ + IFN-alpha leads to a significantly superior OR rate compared to treatment with TMZ alone, which did not translate into prolonged survival in our study population.
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页码:9001 / 9007
页数:7
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