Safety profile and clinical outcome of adjuvant radiation therapy and intermediate-dose interferon in comparison with intermediate-dose interferon alone in patients with melanoma metastases in regional lymph nodes and unfavorable prognostic factors.

M Kukushkina, S Korovin, S Diedkov, V Ostafiichuk, A Diedkov
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Abstract

Aim: To assess the safety profile and efficacy of adjuvant radiation therapy and intermediate-dose interferon in comparison with intermediate-dose interferon alone in patients with synchronous and metachronous skin melanoma metastases in regional lymph nodes with unfavorable prognostic factors.

Materials and methods: 96 patients with synchronous and metachronous skin melanoma metastases in regional lymph nodes (stage III according to American Joint Committee on Cancer) and unfavorable prognostic factors were randomized in 2 groups: one of them (n = 45) received regional radiation therapy 50-55 Gy and intermediate dose of α2b-interferon (RT + IFN) in adjuvant setting and another one (n = 51) intermediate dose of α2b-interferon alone (IFN).

Results: The most common adverse events in both groups were pyrexia and fatigue but grades 3-4 were observed more frequently in the RT + IFN group than in the IFN group (24.4 and 42.2% vs 11.8 and 27.5% respectively). 3-year recurrence-free survival was 78.5% in the RT + IFN group and 73.8% in the IFN group (p = 0.72), 3-year progression-free survival was 63.2% in the RT + IFN group comparing with 57.2% in the IFN group (p = 0.59) and 3-year overall survival was 77.1% and 66.7%, respectively (p = 0.29). Median of recurrence-free, progression-free and overall survival was not reached in any group.

Conclusions: Radiation therapy and intermediate-dose interferon in adjuvant setting tends to improve recurrence-free, progression-free and overall survival comparing with intermediate-dose interferon alone in patients with synchronous and metachronous skin melanoma metastases in regional lymph nodes and unfavorable prognostic factors but it needs further investigation in larger groups of patients.

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辅助放射治疗和中剂量干扰素与单独中剂量干扰素在黑色素瘤区域淋巴结转移和不良预后因素患者中的安全性和临床结果比较
目的:评价辅助放疗联合中剂量干扰素治疗伴有不良预后因素的皮肤黑色素瘤区域淋巴结同步和异时转移患者的安全性和有效性,并与单独应用中剂量干扰素进行比较。材料与方法:96例伴有同步和异时性皮肤黑色素瘤局部淋巴结转移(美国癌症联合委员会III期)且预后因素不利的患者随机分为两组:一组(n = 45)接受50-55 Gy局部放疗和辅助治疗中剂量α2b-干扰素(RT + IFN),另一组(n = 51)单独接受中剂量α2b-干扰素(IFN)。结果:两组最常见的不良事件为发热和疲劳,但RT + IFN组3-4级的不良事件发生率高于IFN组(分别为24.4%和42.2% vs 11.8%和27.5%)。RT + IFN组3年无复发生存率为78.5%,IFN组为73.8% (p = 0.72), RT + IFN组3年无进展生存率为63.2%,IFN组为57.2% (p = 0.59), 3年总生存率分别为77.1%和66.7% (p = 0.29)。无复发、无进展和总生存期的中位数在任何组中均未达到。结论:与单独使用中剂量干扰素相比,在伴有同步和异时性皮肤黑色素瘤区域淋巴结转移及预后不利因素的患者中,放疗和中剂量干扰素辅助治疗更倾向于改善无复发、无进展和总生存率,但需要在更大的患者群体中进一步研究。
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来源期刊
Experimental oncology
Experimental oncology Medicine-Oncology
CiteScore
1.40
自引率
0.00%
发文量
49
期刊介绍: The Experimental Oncology is an English-language journal that publishes review articles, original contributions, short communications, case reports and technical advances presenting new data in the field of experimental and fundamental oncology. Manuscripts should be written in English, contain original work, which has not been published or submitted for publication elsewhere. It also implies the transfer of the Copyright from the author to “Experimental Oncology”. No part of journal publications may be reproduced, stored in a retrieval system or transmitted in any form or by any means without the prior permission of the publisher.
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