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Prognostic significance of tumor burden in the blood of patients with erythrodermic primary cutaneous T-cell lymphoma

机译:红皮病性原发性皮肤T细胞淋巴瘤患者血液中肿瘤负荷的预后意义

摘要

Erythrodermic cutaneous T-cell lymphoma (CTCL) includes patients with erythrodermic mycosis fungoides who may or may not exhibit blood involvement and Sezary syndrome and in whom hematological involvement is, by definition, present at diagnosis. These patients were stratified into 5 hematologic stages (H0-H4) by measuring blood tumor burden, and these data were correlated with survival. The study identified 57 patients: 3 had no evidence of hematologic involvement (H0), 8 had a peripheral blood T-cell clone detected by polymerase chain reaction (PCR) analysis of the T-cell receptor gene and less than 5% Searzy cells on peripheral blood smear (H1), and 14 had either a T-cell clone detected by Southern blot analysis or PCR positivity with more than 5% circulating Sezary cells (H2), Twenty-four patients had absolute Sezary counts of more than 1 x 10(9) cells per liter (H3), and 8 patients had counts in excess of 10 x 10(9) cells per liter (H4), The disease-specific death rate was higher with increasing hematologic stage, after correcting for age at diagnosis. A univariate analysis of 30 patients with defined lymph node stage found hematologic stage (P = .045) and lymph node stage (P = .013) but not age (P = .136) to be poor prognostic indicators of survival. Multivariate analysis identified only lymph node stage to be prognostically important, although likelihood ratio tests indicated that hematologic stage provides additional information (P = .035), Increasing tumor burden in blood and lymph nodes of patients with erythrodermic CTCL was associated with a worse prognosis,The data imply that a hematologic staging system could complement existing tumor-node metastasis staging criteria in erythrodermic CTCL, (C) 2001 by The American Society of Hematology.
机译:红皮病性皮肤T细胞淋巴瘤(CTCL)包括患有红皮病性真菌病真菌病的患者,他们可能会或可能不会出现血液受累和Sezary综合征,并且从定义上说,血液学受累存在于诊断中。通过测量血液肿瘤负荷将这些患者分为5个血液学阶段(H0-H4),这些数据与生存率相关。这项研究确定了57例患者:3例没有血液学受累(H0)的证据,8例通过T细胞受体基因的聚合酶链反应(PCR)分析检测到外周血T细胞克隆,并且在肝细胞上的Searzy细胞少于5%外周血涂片(H1),其中14例通过Southern印迹分析检测到T细胞克隆或PCR阳性,循环Sezary细胞(H2)超过5%,二十四名患者的Sezary绝对计数超过1 x 10 (9)每升(H3)细胞,并且8位患者的计数超过每升(H4)10 x 10(9)个细胞,在校正诊断年龄后,随着血液学阶段的增加,疾病特异性死亡率更高。对30例定义为淋巴结分期的患者进行单因素分析,发现血液学分期(P = .045)和淋巴结分期(P = .013)但年龄没有差异(P = .136)是不良的生存预后指标。多因素分析表明,只有淋巴结分期对预后具有重要意义,尽管似然比测试表明血液分期提供了更多信息(P = .035),红皮CTCL患者血液和淋巴结中肿瘤负荷增加与预后较差有关,数据暗示血液学分期系统可以补充美国血液学协会(C)2001年红皮病CTCL中现有的肿瘤淋巴结转移分期标准。

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