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多发性骨髓瘤治疗的最新进展。

Update on the treatment of multiple myeloma.

作者信息

Kyle R A

机构信息

Division of Hematology and Internal Medicine, Mayo Clinic and Foundation, 200 First Street SW, Rochester, MN 55905, USA.

出版信息

Oncologist. 2001;6(2):119-24. doi: 10.1634/theoncologist.6-2-119.

Abstract

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.

摘要

应从症状、体格检查结果和实验室数据等方面对多发性骨髓瘤患者进行仔细评估。如果没有症状或早期或即将出现并发症的证据,则不应治疗该患者。应密切随访患者,推迟治疗直至疾病进展。如果患者年龄小于70岁,应考虑进行自体外周血干细胞移植。造血干细胞应在患者接触烷化剂之前采集。如果患者年龄大于70岁,则应进行化疗。自体干细胞移植的两个主要缺点是:A)未能根除骨髓瘤;B)自体外周血干细胞受到污染。大多数医生最初用长春新碱、多柔比星(阿霉素)和地塞米松(VAD)治疗患者三到四个月,然后采集外周血干细胞。然后可以进行移植,或者用烷化剂治疗患者并推迟移植直至患者病情进展。在一项比较自体骨髓移植与传统化疗的前瞻性试验中,五年总生存率移植组更优(52%对12%)。在法国一项400例患者的随机试验中,两年评估时双次和单次自体干细胞移植的无事件生存率或总生存率无差异。在随后的评估中,诊断时β2微球蛋白值低的患者进行双次移植似乎效果更好。没有证据表明化疗药物联合使用比美法仑和泼尼松更有效。异基因移植的死亡率很高。T细胞清除或小型异基因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缓解。对于有骨骼病变的患者,建议使用静脉双膦酸盐。高钙血症和肾衰竭必须及时治疗。

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