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血清β-2微球蛋白在低度淋巴瘤中的预后价值

Prognostic value of serum beta-2 microglobulin in low-grade lymphoma.

作者信息

Litam P, Swan F, Cabanillas F, Tucker S L, McLaughlin P, Hagemeister F B, Rodriguez M A, Velasquez W S

机构信息

University of Texas M.D. Anderson Cancer Center, Houston.

出版信息

Ann Intern Med. 1991 May 15;114(10):855-60. doi: 10.7326/0003-4819-114-10-855.

Abstract

OBJECTIVE

To evaluate serum beta-2 microglobulin (beta-2M) and other prognostic indicators in previously untreated low-grade lymphoma.

DESIGN

Cohort study of 80 patients with uniformly treated low-grade lymphoma, followed for a median of 21 months. These 80 patients, all of whom had serum beta-2M drawn within 2 weeks before starting therapy, were derived from a cohort of 119 previously untreated patients entered into one of three clinical trials.

SETTING

Tertiary referral cancer center.

PATIENTS

Eighty previously untreated stage I to IV patients (mean age, 55 years).

INTERVENTION

Treatment was given according to Ann Arbor stage: Patients in stage IV were treated with CHOP-bleomycin and maintained on interferon therapy; those in stage III received CHOP-bleomycin and radiotherapy; and those in stages I and II received COP-bleomycin and radiotherapy.

MEASUREMENTS

Outcome was determined by assessing complete remission rate and time to treatment failure. Univariate and multivariate analyses were used.

RESULTS

The complete remission rate for patients with a beta-2M level of 3.0 mg/L or greater was 36% compared with 71% for those with a level of less than 3.0 mg/L. Using multivariate analysis that tested beta-2M as a continuous variable, it was selected as the most significant factor for complete response. The adjusted odds ratio was 0.285 (95% CI, 0.101 to 0.809). The Ann Arbor stage had marginal significance (adjusted odds ratio, 0.435; CI, 0.150 to 1.263). For time to treatment failure, beta-2M was the only variable retained in the multivariate model. At 42 months, no patient with a beta-2M level of 3.0 mg/L or greater was projected to be in remission as compared with 85% of patients with a beta-2M level of less than 3.0 mg/L.

CONCLUSIONS

The serum beta-2M level is a good predictor of complete response and time to treatment failure. A larger number of patients should be studied to clarify the role of other potentially independent variables such as stage and age.

摘要

目的

评估血清β2微球蛋白(β2M)及其他预后指标在初治低度淋巴瘤中的情况。

设计

对80例接受统一治疗的低度淋巴瘤患者进行队列研究,中位随访时间为21个月。这80例患者均在开始治疗前2周内检测了血清β2M,他们来自119例初治患者组成的队列,这些患者参与了三项临床试验中的一项。

地点

三级转诊癌症中心。

患者

80例初治的Ⅰ至Ⅳ期患者(平均年龄55岁)。

干预措施

根据Ann Arbor分期进行治疗:Ⅳ期患者接受CHOP-博来霉素方案治疗并接受干扰素维持治疗;Ⅲ期患者接受CHOP-博来霉素方案治疗及放疗;Ⅰ期和Ⅱ期患者接受COP-博来霉素方案治疗及放疗。

测量指标

通过评估完全缓解率和治疗失败时间来确定结局。采用单因素和多因素分析。

结果

β2M水平≥3.0mg/L的患者完全缓解率为36%,而β2M水平<3.0mg/L的患者完全缓解率为71%。在将β2M作为连续变量进行检验的多因素分析中,它被选为完全缓解的最显著因素。调整后的优势比为0.285(95%可信区间,0.101至0.809)。Ann Arbor分期具有边缘显著性(调整后的优势比,0.435;可信区间,0.150至1.263)。对于治疗失败时间,β2M是多因素模型中唯一保留的变量。在42个月时,预计β2M水平≥3.0mg/L的患者无一人处于缓解状态,而β2M水平<3.0mg/L的患者中有85%处于缓解状态。

结论

血清β2M水平是完全缓解和治疗失败时间的良好预测指标。应研究更多患者以阐明其他潜在独立变量如分期和年龄的作用。

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