Anagnostopoulos Athanasios, Galani Eleni, Gika Dimitra, Sotou Danai, Evangelopoulou Aikaterini, Dimopoulos Meletios Athanasios
Department of Clinical Therapeutics, University of Athens School of Medicine, 227 Kifissias Avenue, Kifissia, 145 61, Athens, Greece.
Ann Hematol. 2004 Oct;83(10):658-60. doi: 10.1007/s00277-004-0896-1. Epub 2004 Jul 23.
The aim of this study was to assess the effect of systemic chemotherapy on the monoclonal protein levels of patients with solid tumors who also have a monoclonal gammopathy of undetermined significance (MGUS). All patients with solid tumors who were referred to our department for consideration of systemic chemotherapy were evaluated with serum protein electrophoresis (SPEP) for the presence of MGUS. When MGUS was confirmed with immunofixation, serial SPEP was performed during and after completion of chemotherapy. Over a 6-year period, 21 patients with solid tumors and MGUS were prospectively identified and assessed. At least 50% reduction of serum monoclonal protein was noted in 4 of 11 patients treated with paclitaxel or docetaxel with a platinum analogue and in 5 of 7 patients who received an irinotecan-containing regimen. Our data indicate that in MGUS patients treated with irinotecan-containing chemotherapy regimens, a high incidence of reduction in their monoclonal protein levels is observed. Since topotecan, another topoisomerase I inhibitor, has some activity in multiple myeloma, further evaluation of irinotecan may be warranted. Evaluation of larger numbers of MGUS patients treated with chemotherapy for their underlying malignancy may help identify "in vivo" potentially active agents and regimens for patients with overt myeloma.
本研究的目的是评估全身化疗对同时患有意义未明的单克隆丙种球蛋白病(MGUS)的实体瘤患者单克隆蛋白水平的影响。所有因考虑全身化疗而转诊至我科的实体瘤患者均接受血清蛋白电泳(SPEP)检查,以确定是否存在MGUS。当免疫固定法确诊为MGUS后,在化疗期间及化疗结束后进行系列SPEP检查。在6年期间,前瞻性地确定并评估了21例患有实体瘤和MGUS的患者。在11例接受紫杉醇或多西他赛联合铂类类似物治疗的患者中,有4例血清单克隆蛋白水平至少降低了50%;在7例接受含伊立替康方案治疗的患者中,有5例出现这种情况。我们的数据表明,在接受含伊立替康化疗方案治疗的MGUS患者中,观察到其单克隆蛋白水平降低的发生率很高。由于另一种拓扑异构酶I抑制剂托泊替康在多发性骨髓瘤中有一定活性,因此可能有必要对伊立替康进行进一步评估。对更多因潜在恶性肿瘤接受化疗的MGUS患者进行评估,可能有助于识别对明显骨髓瘤患者“体内”有潜在活性的药物和方案。