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Prognostic factors in Waldenstrom's macroglobulinemia: description of the complications during the evolution-preliminary results on 101 patients.

作者信息

Stalnikiewicz Laure, Carrotte-Lefebvre Isabelle, Detourmignies Laurence, Rose Christian, Cazin Bruno, Leblond Véronique, Morel Pierre

机构信息

Service Hematologie Clinique, Centre Hospitalier Schaffner, Lens, France.

出版信息

Semin Oncol. 2003 Apr;30(2):216-9. doi: 10.1053/sonc.2003.50076.

DOI:10.1053/sonc.2003.50076
PMID:12720139
Abstract

Data on clinical features observed in patients with Waldenstrom's macroglobulinemia (WM) during follow-up remain limited. Therefore, we evaluated 860 follow-up procedures in 101 patients. Median age was 66 years and 5-year overall survival 72%, with a median follow-up of 36 months in surviving patients. Sixteen patients presented at diagnosis with two or three cytopenias lasting for at least 3 months (multiple cytopenias [MC]), and MC improved after treatment in eight patients, 4 to 18 months later. MC was observed during at least 6 consecutive months in 23 other patients, 2 to 73 months (median, 24) after diagnosis. MC occurred off-therapy in 12 patients, and on-therapy in 11. Regression occurred in three of the former patients, and in seven of the latter (6 to 24 months after completion of treatment; median, 7). Finally, the 4-year estimated cause-specific cumulative incidence was 40% in the 101 patients. A second malignancy was observed in 11 patients, histological transformation in three, and rapid rise of M-component in only six patients. In conclusion, the present analysis pointed out a high incidence of long lasting MC during the evolution of WM, and a low frequency of rapid rise of M component.

摘要

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Prognostic factors in Waldenstrom's macroglobulinemia: description of the complications during the evolution-preliminary results on 101 patients.
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Immunoglobulin M monoclonal gammopathies of undetermined significance and indolent Waldenstrom's macroglobulinemia recognize the same determinants of evolution into symptomatic lymphoid disorders: proposal for a common prognostic scoring system.意义未明的免疫球蛋白M单克隆丙种球蛋白病和惰性华氏巨球蛋白血症识别向有症状淋巴样疾病演变的相同决定因素:关于通用预后评分系统的提议
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