Beiteke U, Ruppert P, Garbe C, Oxenfarth R, Kastl I, Türker T, Tronnier H, Frosch P J
Hautklinik der Städtischen Kliniken Dortmund.
Hautarzt. 1993 Jun;44(6):365-71.
In the dermatological department of Dortmund's Municipal Medical Centre, between May 1986 and April 1991 a total of 105 patients with primary malignant melanoma (stage I) underwent adjuvant treatment with 5 million IU natural interferon beta as a 30-min i.v. infusion three times weekly for 6 months. During follow-up the patients were examined at short intervals and all recurrences and disease-related cases of death were documented up to September 1992. We evaluated the outcome of patients treated with interferon beta (n = 96 with valid notes of tumour thickness) compared with untreated historical controls (n = 288) matched for tumour thickness, localization, and sex, taken from the Central Malignant Melanoma Registry (CMMR) of the German Dermatological Society. Therefore, the main prognostic factors were identical between cases and controls. A computerized randomization was used to fit three control patients to each treated patient. Survival rate and recurrence-free survival were estimated in both groups for a period of 5 years. During the follow-up 3 patients died in the interferon beta group and the 5-year survival rate was 95%, as against 89% in the control group (P < 0.05 for difference between survival curves). Recurrence-free survival curves were also more favourable for interferon-treated patients than for the control group (P = 0.06). A detailed analysis of high-risk patients with tumour thickness of over 1.5 mm also demonstrated obviously better survival (5 years: 95% vs 77%; P = 0.012) and recurrence-free survival rates (5 years: 75% vs 53%; P < 0.05).(ABSTRACT TRUNCATED AT 250 WORDS)
1986年5月至1991年4月期间,多特蒙德市立医疗中心皮肤科共有105例原发性恶性黑色素瘤(I期)患者接受了辅助治疗,使用500万国际单位的天然β干扰素,通过静脉输注30分钟,每周3次,共6个月。在随访期间,对患者进行了短期检查,并记录了截至1992年9月的所有复发情况和与疾病相关的死亡病例。我们评估了接受β干扰素治疗的患者(n = 96,有肿瘤厚度的有效记录)的结果,并与未治疗的历史对照组(n = 288)进行了比较,对照组在肿瘤厚度、位置和性别方面与治疗组匹配,数据来自德国皮肤病学会的中央恶性黑色素瘤登记处(CMMR)。因此,病例组和对照组的主要预后因素相同。使用计算机随机化方法,为每名接受治疗的患者匹配3名对照患者。估计两组患者5年的生存率和无复发生存率。在随访期间,β干扰素组有3例患者死亡,5年生存率为95%,而对照组为89%(生存曲线差异P < 0.05)。接受干扰素治疗患者的无复发生存曲线也比对照组更有利(P = 0.06)。对肿瘤厚度超过1.5 mm的高危患者进行的详细分析也显示,其生存率(5年:95%对77%;P = 0.012)和无复发生存率(5年:75%对53%;P < 0.05)明显更好。(摘要截断于250字)