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一项比较联合电子束放疗与化疗与局部治疗在蕈样肉芽肿初始治疗中的随机试验。

A randomized trial comparing combination electron-beam radiation and chemotherapy with topical therapy in the initial treatment of mycosis fungoides.

作者信息

Kaye F J, Bunn P A, Steinberg S M, Stocker J L, Ihde D C, Fischmann A B, Glatstein E J, Schechter G P, Phelps R M, Foss F M

机构信息

National Cancer Institute-Navy Medical Oncology Branch, Bethesda, Md 20814.

出版信息

N Engl J Med. 1989 Dec 28;321(26):1784-90. doi: 10.1056/NEJM198912283212603.

Abstract

Mycosis fungoides is a T-cell lymphoma that arises in the skin and progresses at highly variable rates. Nonradomized studies have suggested that early aggressive therapy may improve the prognosis in this usually fatal disease. We studied 103 patients with mycosis fungoides, who, after complete staging, were randomly assigned to receive either combination therapy, consisting of 3000 cGy of electron-beam radiation to the skin combined with parenteral chemotherapy with cyclophosphamide, doxorubicin, etoposide, and vincristine (n = 52) or sequential topical treatment (n = 51). The prognostic factors were well balanced in the two groups. Combined therapy produced considerable toxicity: 12 patients required hospitalization for fever and transient neutropenia, 5 had congestive heart failure, and 2 were later found to have acute nonlymphocytic leukemia. Patients receiving combined therapy had a significantly higher rate of complete response, documented by biopsy, than patients receiving conservative therapy (38 percent vs. 18 percent; P = 0.032). After a median follow-up of 75 months, however, there was no significant difference between the treatment groups in disease-free or overall survival. We conclude that early aggressive therapy with radiation and chemotherapy does not improve the prognosis for patients with mycosis fungoides as compared with conservative treatment beginning with sequential topical therapies.

摘要

蕈样肉芽肿是一种起源于皮肤且进展速度高度可变的T细胞淋巴瘤。非随机研究表明,早期积极治疗可能会改善这种通常致命疾病的预后。我们研究了103例蕈样肉芽肿患者,在完成全面分期后,他们被随机分配接受联合治疗,即对皮肤进行3000 cGy的电子束放疗并联合使用环磷酰胺、阿霉素、依托泊苷和长春新碱进行胃肠外化疗(n = 52)或序贯局部治疗(n = 51)。两组的预后因素平衡良好。联合治疗产生了相当大的毒性:12例患者因发热和短暂性中性粒细胞减少需要住院治疗,5例出现充血性心力衰竭,2例后来被发现患有急性非淋巴细胞白血病。接受联合治疗的患者经活检记录的完全缓解率显著高于接受保守治疗的患者(38%对18%;P = 0.032)。然而,在中位随访75个月后,治疗组在无病生存期或总生存期方面没有显著差异。我们得出结论,与从序贯局部治疗开始的保守治疗相比,早期采用放疗和化疗的积极治疗并不能改善蕈样肉芽肿患者的预后。

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