中国肿瘤临床
中國腫瘤臨床
중국종류림상
CHINESE JOURNAL OF CLINICAL ONCOLOGY
2014年
8期
503-507
,共5页
马芹%张会来%王华庆%陈青青%刘霞%侯芸
馬芹%張會來%王華慶%陳青青%劉霞%侯蕓
마근%장회래%왕화경%진청청%류하%후예
淋巴细胞绝对数%弥漫大B细胞淋巴瘤%预后%非霍奇金淋巴瘤
淋巴細胞絕對數%瀰漫大B細胞淋巴瘤%預後%非霍奇金淋巴瘤
림파세포절대수%미만대B세포림파류%예후%비곽기금림파류
absolute lymphocyte count%diffuse large B-cell lymphoma (DLBCL)%prognosis%non-Hodgkin lymphoma (NHL)
目的:探讨弥漫大B细胞淋巴瘤患者在首次诊断时外周血淋巴细胞绝对数(absolute lymphocyte count,ALC)与其临床特征及预后之间的关系。方法:回顾性的分析天津医科大学肿瘤医院2002年2月至2008年4月收治143例初治弥漫大B细胞淋巴瘤患者的临床特征及预后,分析不同ALC水平与患者各临床特征之间的关系。结果:将143例弥漫大B细胞淋巴瘤患者分为高ALC(ALC≥1.0×109/L)组和低ALC(ALC<1.0×109/L)组,低ALC组患者常伴随B症状、高IPI评分、Ann Arbor分期较晚以及乳酸脱氢酶水平、β2-微球蛋白水平升高(P<0.05)。而且高ALC组患者的缓解率比低ALC组高(P=0.003)。多因素分析显示Ann ArborⅢ/Ⅳ期、ALC<1.0×109/L是弥漫大B细胞淋巴瘤患者预后较差的独立因素。ALC降低组常伴有Ann Arbor分期的升高。结论:ALC是弥漫大B细胞淋巴瘤患者新的独立预后因素。
目的:探討瀰漫大B細胞淋巴瘤患者在首次診斷時外週血淋巴細胞絕對數(absolute lymphocyte count,ALC)與其臨床特徵及預後之間的關繫。方法:迴顧性的分析天津醫科大學腫瘤醫院2002年2月至2008年4月收治143例初治瀰漫大B細胞淋巴瘤患者的臨床特徵及預後,分析不同ALC水平與患者各臨床特徵之間的關繫。結果:將143例瀰漫大B細胞淋巴瘤患者分為高ALC(ALC≥1.0×109/L)組和低ALC(ALC<1.0×109/L)組,低ALC組患者常伴隨B癥狀、高IPI評分、Ann Arbor分期較晚以及乳痠脫氫酶水平、β2-微毬蛋白水平升高(P<0.05)。而且高ALC組患者的緩解率比低ALC組高(P=0.003)。多因素分析顯示Ann ArborⅢ/Ⅳ期、ALC<1.0×109/L是瀰漫大B細胞淋巴瘤患者預後較差的獨立因素。ALC降低組常伴有Ann Arbor分期的升高。結論:ALC是瀰漫大B細胞淋巴瘤患者新的獨立預後因素。
목적:탐토미만대B세포림파류환자재수차진단시외주혈림파세포절대수(absolute lymphocyte count,ALC)여기림상특정급예후지간적관계。방법:회고성적분석천진의과대학종류의원2002년2월지2008년4월수치143례초치미만대B세포림파류환자적림상특정급예후,분석불동ALC수평여환자각림상특정지간적관계。결과:장143례미만대B세포림파류환자분위고ALC(ALC≥1.0×109/L)조화저ALC(ALC<1.0×109/L)조,저ALC조환자상반수B증상、고IPI평분、Ann Arbor분기교만이급유산탈경매수평、β2-미구단백수평승고(P<0.05)。이차고ALC조환자적완해솔비저ALC조고(P=0.003)。다인소분석현시Ann ArborⅢ/Ⅳ기、ALC<1.0×109/L시미만대B세포림파류환자예후교차적독립인소。ALC강저조상반유Ann Arbor분기적승고。결론:ALC시미만대B세포림파류환자신적독립예후인소。
Objective: We investigated the clinical significance and prognostic value of peripheral blood absolute lymphocyte count (ALC) in the diagnosis of diffuse large B-cell lymphoma. Methods:The medical records of 143 patients with diffuse large B-cell lymphoma were reviewed. These patients were diagnosed and underwent surgery in Tianjin Medical University Cancer Institute and Hospital, China, between February 2002 and April 2008. The correlation between different ALC levels and clinical features was statisti-cally analyzed. Results:Patients with low ALC (<1.0×109/L) at diagnosis showed B symptoms, an international prognostic index score of ≥2, advanced clinical stage (Ann Arbor III/IV), high lactate dehydrogenase level, and high β2-microglobulin level (P<0.05). Pa-tients with high ALC (≥1.0 × 109/L) responded well to treatment (P=0.003). In multivariate analysis, Ann Arbor stage and ALC level were independent prognostic factors of patients with diffuse large B-cell lymphoma. Patients with low ALC often exhibited advanced clinical stage (Ann ArborⅢ/Ⅳ). Conclusions:ALC level obtained at diagnosis is a novel, powerful prognostic factor of diffuse large B-cell lymphoma.