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首页> 外文期刊>BioMed research international >Clinical Factors Associated with Response or Survival after Chemotherapy in Patients with Waldenström Macroglobulinemia in Korea
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Clinical Factors Associated with Response or Survival after Chemotherapy in Patients with Waldenström Macroglobulinemia in Korea

机译:韩国Waldenström巨球蛋白血症患者化疗后反应或生存相关的临床因素

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摘要

Waldenström’s macroglobulinemia (WM) is a B-cell proliferative malignancy characterized by immunoglobulin M monoclonal gammopathy and bone marrow infiltration by lymphoplasmacytic cells. Clinical features and cytogenetics of WM in Asia including Republic of Korea remain unclear. Moreover, no study has reported treatment outcomes in patients with WM treated with novel agent combined with conventional chemotherapy. This study investigated clinical features and assessed treatment outcomes with novel agent and conventional chemotherapy in Republic of Korea. Data from all (n=71) patients with newly diagnosed WM at 17 hospitals who received chemotherapy between January 2005 and December 2012 were collected retrospectively. The median age of patients was 66 years (range: 37–92 years) and male to female ratio was 5 : 1. Patients treated with novel agent combined chemotherapy displayed higher overall response rate (ORR) compared to conventional chemotherapy alone (92.9% versus 52.6%,P=0.006). The 5-year overall survival rate was 62.6% (95% confidence interval: 34.73–111.07). Use of novel agents produced higher ORR but survival benefit was not apparent due to the small number of patients and short follow-up duration. Further studies are needed to confirm the efficacy of novel agents in patients with WM.
机译:Waldenström的巨球蛋白血症(WM)是一种B细胞增殖性恶性肿瘤,其特征是免疫球蛋白M单克隆丙种球蛋白病和淋巴浆细胞的骨髓浸润。在包括大韩民国在内的亚洲,WM的临床特征和细胞遗传学仍不清楚。此外,尚无研究报道用新药联合常规化疗治疗WM患者的治疗结果。这项研究调查了大韩民国的临床特征,并评估了使用新型药物和常规化疗的治疗效果。回顾性收集2005年1月至2012年12月间在17所医院接受化疗的所有(n = 71)初诊WM患者的数据。患者的中位年龄为66岁(范围:37-92岁),男女之比为5:1.与单独使用常规化疗相比,接受新型药物联合化疗的患者的总缓解率(ORR)更高(92.9% 52.6%,P = 0.006)。 5年总生存率为62.6%(95%置信区间:34.73–111.07)。使用新型药物可产生更高的ORR,但由于患者人数少且随访时间短,生存获益并不明显。需要进一步的研究来确认新型药物对WM患者的疗效。

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