Misset J L, Mathé G, Gastiaburu J, Goutner A, Dorval T, Gouveia J, Hayat M, Jasmin C, Schwarzenberg L, Machover D, Ribaud P, De Vassal F, Horoszewicz J S
Anticancer Res. 1982 Jan-Apr;2(1-2):63-6.
18 patients with malignant gammapathies (16 with myeloma and 2 with Waldenström's disease) were treated with human fibroblastic Interferon (beta IF). This was administered i.v. 6 X 10(6) units weekly (7 patients) or 3 X 10(6) units twice weekly (11 patients). during at least 3 months if tolerated. Treatment was discontinued because of side effects in three patients. Reduction of the M component, by at least 25% from the initial value, was obtained in 3 patients. In one case the disappearance of a urinary Bence Jones protein was observed. In 4 cases, there was a significant reduction of bone marrow infiltration by plasma cells. In 5 cases, major alleviation or disappearance of bone pain was observed. Duration of treatment seemed to be an important factor for activity. Immune monitoring with currently available tests, mainly natural cytoxicity, yielded no correlation with therapeutic effect in these patients. This preliminary study demonstrates the effect of fibroblastic Interferon in myeloma. However, further studies are necessary to determine the population of patients most likely to benefit from treatment, the best modalities, possible special indications, dose schedules and duration of treatment. As it is not myelosuppressive it could be indicated in the frequent situation of advanced myeloma with bone marrow failure, contra-indicating combination chemotherapy.
18例恶性γ球蛋白病患者(16例骨髓瘤患者和2例瓦尔登斯特伦病患者)接受了人成纤维细胞干扰素(β干扰素)治疗。治疗方式为静脉注射,7例患者每周注射6×10⁶单位,11例患者每周两次,每次注射3×10⁶单位,若能耐受则至少持续治疗3个月。3例患者因副作用而停药。3例患者的M成分从初始值降低了至少25%。1例患者尿本周氏蛋白消失。4例患者浆细胞对骨髓的浸润显著减少。5例患者骨痛明显缓解或消失。治疗持续时间似乎是影响疗效的一个重要因素。用目前可用的检测方法(主要是自然细胞毒性)进行免疫监测,结果显示这些患者的治疗效果与免疫监测结果无相关性。这项初步研究证明了成纤维细胞干扰素对骨髓瘤的疗效。然而,有必要进一步开展研究,以确定最可能从治疗中获益的患者群体、最佳治疗方式、可能的特殊适应证、给药方案以及治疗持续时间。由于它不具有骨髓抑制作用,对于晚期骨髓瘤伴骨髓衰竭而禁忌联合化疗的常见情况,它可能是一种治疗选择。