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[多发性骨髓瘤的治疗]

[The treatment of multiple myeloma].

作者信息

Ludwig H, Kührer I

机构信息

Medizinische Abteilung mit Onkologie, Wilhelminespital der Stadt Wien.

出版信息

Wien Klin Wochenschr. 1994;106(14):448-54.

PMID:7941591
Abstract

Median survival in patients with multiple myeloma, which amounted to 6-12 months during the pre-chemotherapy era, was improved to 28-43 months following the introduction of chemotherapy. Usually patients with stage II or III myeloma require treatment. Conventional chemotherapy with melphalan-prednisone is undertaken if their prognosis is good; in case of poor prognosis and good general condition, a more aggressive polychemotherapy is given. High-dose melphalan therapy alone induces high remission rates, but fails to prolong remission duration or survival. Resistance to cytostatic drugs due to the p-glycoprotein coded by the MDR-gene is treated by a combination of cyclosporin-A or verapamil and VAD. For the treatment of relapses or of primarily resistant patients several second-line regimens are available. As remission maintenance therapy, interferon has so far yielded the best results. Trials of other cytokines such as interleukin-2 and interleukin-4 are still inconclusive. For autologous bone marrow transplantation, primary reduction of the tumour mass by conventional polychemotherapy is recommended. Subsequently, high-dose melphalan or cyclophosphamide-busulfan--with or without total body irradiation--is used for conditioning and followed by the transplantation of either autologous bone marrow or peripheral blood stem cells. Significantly higher remission rates and longer survival of the patients may be expected. Allogenous bone marrow transplantation is burdened with a high early mortality rate, but it also promises longer disease-free survival times. Bone marrow transplantation should be performed as early as possible in the course of the disease. More controlled studies are required before a definite evaluation of its efficacy is possible.

摘要

多发性骨髓瘤患者的中位生存期,在化疗前时代为6至12个月,化疗引入后提高到了28至43个月。通常II期或III期骨髓瘤患者需要治疗。如果预后良好,采用美法仑-泼尼松进行常规化疗;如果预后不良但一般状况良好,则给予更积极的多药化疗。单独的大剂量美法仑治疗可诱导较高的缓解率,但无法延长缓解持续时间或生存期。由MDR基因编码的p-糖蛋白导致的对细胞毒性药物的耐药性,通过环孢素A或维拉帕米与VAD联合治疗。对于复发或原发性耐药患者的治疗,有几种二线方案可供选择。作为缓解维持治疗,干扰素迄今为止产生了最佳效果。其他细胞因子如白细胞介素-2和白细胞介素-4的试验仍无定论。对于自体骨髓移植,建议通过常规多药化疗初步缩小肿瘤体积。随后,使用大剂量美法仑或环磷酰胺-白消安(有或无全身照射)进行预处理,然后移植自体骨髓或外周血干细胞。预计患者的缓解率会显著提高,生存期会延长。异体骨髓移植的早期死亡率很高,但也有望实现更长的无病生存期。骨髓移植应在疾病过程中尽早进行。在对其疗效进行明确评估之前,需要更多的对照研究。

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[The treatment of multiple myeloma].[多发性骨髓瘤的治疗]
Wien Klin Wochenschr. 1994;106(14):448-54.
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[Diagnosis and therapy of multiple myeloma: current aspects].[多发性骨髓瘤的诊断与治疗:当前进展]
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Evolution of multiple myeloma treatment from melphalan monotherapy to bone marrow transplantation.多发性骨髓瘤治疗从美法仑单一疗法到骨髓移植的演变。
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High-dose therapy and autologous peripheral blood stem cells transplantation followed by a very low reduced intensity regimen with fludarabine + cyclophosphamide and allograft improve complete remission rate in de novo multiple myeloma patients.大剂量疗法及自体外周血干细胞移植,随后采用氟达拉滨+环磷酰胺的极低强度预处理方案及同种异体移植,可提高初诊多发性骨髓瘤患者的完全缓解率。
Am J Hematol. 2006 Dec;81(12):973-8. doi: 10.1002/ajh.20677.