Jumbou O, N'Guyen J M, Tessier M H, Legoux B, Dréno B
Department of Dermatology, Hôtel-Dieu, Pl. A.Ricordeau, 44093 Nantes cedex 1, France.
Br J Dermatol. 1999 Mar;140(3):427-31. doi: 10.1046/j.1365-2133.1999.02704.x.
Although interferon-alfa (IFN-alpha) has proved effective in treating epidermotropic cutaneous T-cell lymphoma (ECTL), few studies have considered the follow-up of treated patients and whether complete remission was maintained. We studied 51 patients (one stage Ia, seven stage Ib, one stage IIa, 30 stage IIb, 11 stage III (Sézary syndrome) and one stage IV) who received low-dose IFN-alpha as monotherapy for ECTL (mean daily dose of IFN-alpha 2.7 x 106 units for 14.9 months), giving special consideration to the significance of My7 (CD13) antigen expression by epidermal basal cells in predicting the maintenance of complete remission. For a mean follow-up period of 43.4 months, the results showed 21 complete remissions, 13 partial remissions and 17 patients with stable or progressive disease. Twelve patients died during the follow-up (3-52 months). IFN-alpha led to an improved response in the early stages, with a greater number of complete remissions (P = 0.03) and partial remissions (P = 0.01). The mean time to complete remission was 4 months, regardless of clinical stage (P = 0.1). Of 21 patients in complete remission, 57% had a relapse within a mean period of 7.5 months. For patients maintained in complete remission, the mean period of response was 31 months. The length of complete remission was independent of clinical stage, and My7 antigen expression was not predictive of complete remission.
尽管干扰素-α(IFN-α)已被证明对治疗亲表皮性皮肤T细胞淋巴瘤(ECTL)有效,但很少有研究考虑对接受治疗的患者进行随访以及完全缓解是否得以维持。我们研究了51例患者(1例Ia期、7例Ib期、1例IIa期、30例IIb期、11例III期(塞扎里综合征)和1例IV期),这些患者接受低剂量IFN-α作为ECTL的单一疗法(IFN-α平均每日剂量为2.7×10⁶单位,持续14.9个月),特别考虑了表皮基底细胞My7(CD13)抗原表达在预测完全缓解维持方面的意义。平均随访期为43.4个月,结果显示21例完全缓解、13例部分缓解以及17例病情稳定或进展的患者。12例患者在随访期间死亡(3 - 52个月)。IFN-α在疾病早期导致更好的反应,完全缓解(P = 0.03)和部分缓解(P = 0.01)的患者数量更多。达到完全缓解的平均时间为4个月,与临床分期无关(P = 0.1)。在21例完全缓解的患者中,57%在平均7.5个月内复发。对于维持完全缓解的患者,平均缓解期为31个月。完全缓解的时长与临床分期无关,并且My7抗原表达不能预测完全缓解。