Aoki Yuka, Hayashi Toshiaki, Ikeda Hiroshi, Ishida Tadao
Department of Internal Medicine, Sapporo Jikeikai Hospital.
Department of Hematology, Teine Keijinkai Hospital.
Rinsho Ketsueki. 2018;59(3):275-280. doi: 10.11406/rinketsu.59.275.
A 77-year-old man suffering from back and arm pain was referred for anemia to the hospital by an orthopedic clinic. Serum examination of the patient revealed monoclonal IgA, and he consulted the Sapporo Medical University Hospital, where he was diagnosed with multiple myeloma complicated with AL amyloidosis. He was then enrolled for a randomized double-blind study aimed to compare between melphalan-prednisone (MP) and thalidomide-melphalan-prednisone (MPT) treatments, which revealed the patient to be in the MP arm. This treatment induced a temporary partial response. After progression, he was treated with three variable combinations: 1) bortezomib and MP, 2) lenalidomide and dexamethasone, and 3) pomalidomide and dexamethasone. However, none of these treatments provided a stable response. Further, thalidomide in combination with bortezomib and dexamethasone was provided as the fifth-line treatment. After four cycles of this treatment, he achieved VGPR that lasted for 11 months. Our case report suggests that because there is a lack of a standard strategy for MM that is refractory to several agents, treatment should be selected on the basis of previous treatments and general condition of patients.
一名77岁患有背部和手臂疼痛的男性因贫血被骨科诊所转诊至医院。对该患者进行血清检查发现单克隆IgA,随后他前往札幌医科大学医院就诊,被诊断为多发性骨髓瘤合并AL淀粉样变性。他随后参加了一项随机双盲研究,旨在比较美法仑-泼尼松(MP)与沙利度胺-美法仑-泼尼松(MPT)治疗方案,结果显示该患者被分入MP组。这种治疗诱导了暂时的部分缓解。病情进展后,他接受了三种不同的联合治疗方案:1)硼替佐米与MP,2)来那度胺与地塞米松,3)泊马度胺与地塞米松。然而,这些治疗均未产生稳定的缓解。此外,沙利度胺联合硼替佐米和地塞米松作为五线治疗方案给予。经过四个周期的该治疗后,他达到了持续11个月的VGPR(非常好的部分缓解)。我们的病例报告表明,由于对于多种药物难治的多发性骨髓瘤缺乏标准治疗策略,应根据患者既往治疗情况和一般状况来选择治疗方案。