Kees M, Dimou G, Sillaber C, Drach J, Ackermann J, Lechner K, Gisslinger H
Division of Haematology and Blood Coagulation, Department of Internal Medicine I, University of Vienna, Vienna, Austria.
Leuk Lymphoma. 2003 Nov;44(11):1943-6. doi: 10.1080/1042819031000123492.
Remarkable results of the treatment of refractory multiple myeloma with thalidomide have been reported. In most preceding studies, the given thalidomide dose was escalated to a maximum tolerated dose of up to 800 mg/d. The frequency of adverse effects correlates with dose intensity. Since a significant gain of therapeutic effects could not be observed as thalidomide dosage was escalated, the optimal dose of thalidomide remains to be determined. We report the results of a study with low dose thalidomide (median administered dose 100 mg/d, range 50-400 mg/d). Twenty-four relapsed (n = 19) or resistant (n = 5) multiple myeloma patients were included in the study. Twelve patients (50%) received thalidomide as monotherapy, 8 patients (33%) received a combination of thalidomide and dexamethasone (every 4 weeks 40 mg/day for 4 days) and 4 patients (17%) who were resistant to vincristine, doxorubicin, dexamethasone (VAD) received VAD combined with thalidomide. Overall, a response was observed in 12 patients (50%). Of the 12 patients treated with low dose thalidomide alone 5 (42%) responded, of the 8 patients who received a combination of thalidomide and dexamethasone 5 (63%) responded and of the 4 patients who had thalidomide in addition to VAD 2 patients (50%) responded. In 3 patients, thalidomide treatment had to be discontinued because of side effects and 1 patient died before response could be assessed. We conclude that low dose thalidomide is an effective and safe rescue therapy in relapsing or refractory multiple myeloma. Response to thalidomide might be dependent on prognostic parameters and tumor burden. To answer these questions larger prospective studies are necessary.
已有报告称沙利度胺治疗难治性多发性骨髓瘤取得了显著疗效。在大多数先前的研究中,所给予的沙利度胺剂量逐渐增加至最大耐受剂量,高达800毫克/天。不良反应的发生率与剂量强度相关。由于随着沙利度胺剂量的增加未观察到治疗效果的显著提升,沙利度胺的最佳剂量仍有待确定。我们报告了一项低剂量沙利度胺(中位给药剂量100毫克/天,范围50 - 400毫克/天)的研究结果。该研究纳入了24例复发(n = 19)或耐药(n = 5)的多发性骨髓瘤患者。12例患者(50%)接受沙利度胺单药治疗,8例患者(33%)接受沙利度胺与地塞米松联合治疗(每4周40毫克/天,连用4天),4例对长春新碱、阿霉素、地塞米松(VAD)耐药的患者接受VAD联合沙利度胺治疗。总体而言,12例患者(50%)出现缓解。在仅接受低剂量沙利度胺治疗的12例患者中,5例(42%)有反应,在接受沙利度胺与地塞米松联合治疗的8例患者中,5例(63%)有反应,在除VAD外还接受沙利度胺治疗的4例患者中,2例(50%)有反应。3例患者因副作用不得不停止沙利度胺治疗,1例患者在评估反应前死亡。我们得出结论,低剂量沙利度胺是复发或难治性多发性骨髓瘤的一种有效且安全的挽救治疗方法。对沙利度胺的反应可能取决于预后参数和肿瘤负荷。为回答这些问题,有必要进行更大规模的前瞻性研究。