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Update on the treatment of multiple myeloma.

机译:多发性骨髓瘤的治疗更新。

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The patient with multiple myeloma should be carefully evaluated from the standpoint of symptoms, physical findings, and laboratory data. If there are no symptoms or evidence of early or impending complications, the patient should not be treated. He or she should be followed and treatment delayed until progression of the disease occurs. If the patient is younger than 70 years, autologous peripheral blood stem cell transplantation should be considered. Hematopoietic stem cells should be collected before the patient is exposed to alkylating agents. If the patient is older than 70 years, chemotherapy is indicated. The two major shortcomings of autologous stem cell transplantation are: A) failure to eradicate myeloma, and B) contamination of autologous peripheral blood stem cells. Most physicians initially treat the patient with vincristine, doxorubicin (Adriamycin), and dexamethasone (VAD) for three to four months and then collect the peripheral blood stem cells. One can then proceed with transplant or treat the patient with alkylating agents and delay the transplant until the patient progresses. In a prospective trial comparing autologous bone marrow transplantation with conventional chemotherapy, five-year overall survival favored the transplant group (52% versus 12%). In a randomized trial of 400 patients from France, there was no difference in event-free or overall survival between double and single autologous stem cell transplant when evaluated at two years. In a subsequent evaluation, patients with a low beta(2)-microglobulin value at diagnosis appeared to have better results with a double transplant. There is no evidence that combinations of chemotherapeutic agents are more effective than melphalan and prednisone. Allogeneic transplantation is associated with a high mortality. Depletion of T-cells or a mini-allogeneic transplant may be beneficial in an effort to reduce mortality. Thalidomide produces objective response in approximately 30% of refractory patients. The use of intravenous bisphosphonates is recommended for patients with skeletal lesions. Hypercalcemia and renal failure must be treated promptly.
机译:多发性骨髓瘤患者应从症状,体格检查和实验室数据的角度进行仔细评估。如果没有症状或早期或即将发生并发症的迹象,则不应对患者进行治疗。应该跟踪他或她,并延迟治疗直至疾病进展。如果患者未满70岁,则应考虑自体外周血干细胞移植。在患者暴露于烷基化剂之前,应收集造血干细胞。如果患者年龄超过70岁,则需要化疗。自体干细胞移植的两个主要缺点是:A)无法根除骨髓瘤,和B)自体外周血干细胞受到污染。大多数医生最初使用长春新碱,阿霉素(阿霉素)和地塞米松(VAD)治疗患者三至四个月,然后收集外周血干细胞。然后可以进行移植或用烷化剂治疗患者,并推迟移植直至患者进展。在一项将自体骨髓移植与传统化学疗法进行比较的前瞻性试验中,移植组的五年总生存期相对较高(52%对12%)。在一项来自法国的400名患者的随机试验中,两年后进行评估时,双重和单一自体干细胞移植的无事件生存期或总生存期无差异。在随后的评估中,诊断为低β(2)-微球蛋白值的患者似乎通过双重移植获得了更好的结果。没有证据表明化疗药物的组合比美法仑和泼尼松更有效。同种异体移植与高死亡率有关。 T细胞的耗竭或小型同种异体移植可能有助于降低死亡率。沙利度胺在大约30%的难治性患者中产生客观反应。建议骨骼损伤患者使用静脉注射双膦酸盐。高钙血症和肾衰竭必须及时治疗。

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