Qiu B, Chen M
Dermatopathologic Research Laboratory, Hua Shan Hospital, Shanghai.
Chin Med J (Engl). 1996 May;109(5):404-6.
To evaluate the optimal dose and route of interferon-alpha-2b (INF-alpha-2b) given to the Chinese patients with cutaneous T-cell lymphomas (CTCL).
Sixteen Chinese patients with CTCL treated with INF-alpha-2b were evaluated. They were divided into groups according to the TNM Classification: I B (8 patients), II A (2), II B (5) and IV B (1). During induction INF-alpha-2b was given intramuscularly every other day or two times a week, beginning with a dose of 1-3 x 10(6) IU. Depending on tolerance, the dosage could be increased weekly to a maximum tolerated dose of 18 x 10(6) IU (mean, 6 x 10(6) IU/week) with administration two or three times a week. Patients with clinical response were given maintenance dosage from the start. Thereafter the dosage was gradually decreased after disappearance of skin lesions. Three patients were treated by combining intramuscular and intralesional injection of INF.
Six patients (I B, 2 patients: II A, 2, II B, 2) achieved complete response (CR). Seven patients (I B, 5 patients) showed partial response. The overall response rate in this group was 81.25%. The prominent initial clinical response in three patients was manifested early at one week after intramuscular treatment with INF and then the skin lesions were resistant to the therapy but disappeared rapidly by combining intralesional injection of INF. The conditions of those patients obtaining CR within 3 to 6 weeks were stable for 1-36 weeks.
This study had demonstrated that the overall response rate in treatment of patients with CTCL was 81.25% and higher (85.7%-87.5%) in the subgroups at early stages I and II of the disease. The dosage (mean dose of 6 x 10(6) IU/week) adopted by us is optimal for the Chinese patients with CTCL. Intralesional injection of INF could be recommended.
评估给予中国皮肤T细胞淋巴瘤(CTCL)患者的α-2b干扰素(INF-α-2b)的最佳剂量和给药途径。
对16例接受INF-α-2b治疗的中国CTCL患者进行评估。根据TNM分类将他们分组:I B期(8例患者)、II A期(2例)、II B期(5例)和IV B期(1例)。诱导治疗期间,INF-α-2b每隔一天或每周两次肌肉注射,起始剂量为1 - 3×10⁶IU。根据耐受性,剂量可每周增加至最大耐受剂量18×10⁶IU(平均6×10⁶IU/周),每周给药两到三次。有临床反应的患者从一开始就给予维持剂量。此后,皮肤病变消失后剂量逐渐减少。3例患者采用肌肉注射和病灶内注射INF联合治疗。
6例患者(I B期2例、II A期2例、II B期2例)达到完全缓解(CR)。7例患者(I B期5例)显示部分缓解。该组的总缓解率为81.25%。3例患者显著的初始临床反应在肌肉注射INF治疗1周后早期出现,随后皮肤病变对治疗产生抵抗,但通过联合病灶内注射INF迅速消失。在3至6周内获得CR的患者病情稳定1至36周。
本研究表明,CTCL患者的总缓解率为81.25%,在疾病的I期和II期早期亚组中更高(85.7% - 87.5%)。我们采用的剂量(平均剂量6×10⁶IU/周)对中国CTCL患者是最佳的。可推荐病灶内注射INF。