PROGNOSTIC VALUE OF SERUM BETA-2 MICROGLOBULIN IN LOW-GRADE LYMPHOMA

被引:86
作者
LITAM, P [1 ]
SWAN, F [1 ]
CABANILLAS, F [1 ]
TUCKER, SL [1 ]
MCLAUGHLIN, P [1 ]
HAGEMEISTER, FB [1 ]
RODRIGUEZ, MA [1 ]
VELASQUEZ, WS [1 ]
机构
[1] UNIV TEXAS, MD ANDERSON CANCER CTR, 1515 HOLCOMBE BLVD, BOX 68, HOUSTON, TX 77030 USA
关键词
D O I
10.7326/0003-4819-114-10-855
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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: Eight 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-blemycin and maintained on interferon therapy; those in stage III received CHOP-bleomycin and radiotherapy; and those in stage 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 large number of patients should be studied to clarify the role of other potentially independent variables such as stage and age.
引用
收藏
页码:855 / 860
页数:6
相关论文
共 44 条
[1]   BETA-2 MICROGLOBULIN IN MULTIPLE-MYELOMA [J].
ALEXANIAN, R ;
BARLOGIE, B ;
FRITSCHE, H .
AMERICAN JOURNAL OF HEMATOLOGY, 1985, 20 (04) :345-351
[2]   SERUM BETA-2-MICROGLOBULIN AND ITS PROGNOSTIC VALUE IN LYMPHOMAS [J].
AMLOT, PL ;
ADINOLFI, M .
EUROPEAN JOURNAL OF CANCER, 1979, 15 (05) :791-796
[3]   GENETIC-CONTROL OF HLA-A AND B-ANTIGENS IN SOMATIC-CELL HYBRIDS - REQUIREMENT FOR BETA-2 MICROGLOBULIN [J].
ARCEGOMEZ, B ;
JONES, EA ;
BARNSTABLE, CJ ;
SOLOMON, E ;
BODMER, WF .
TISSUE ANTIGENS, 1978, 11 (02) :96-112
[4]   MAJOR HISTOCOMPATIBILITY COMPLEX - GENETICS AND BIOLOGY .2. [J].
BACH, FH ;
VANROOD, JJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (16) :872-878
[5]   MAJOR HISTOCOMPATIBILITY COMPLEX - GENETICS AND BIOLOGY .3. [J].
BACH, FH ;
VANROOD, JJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1976, 295 (17) :927-936
[6]   SERUM BETA-2-MICROGLOBULIN AND SURVIVAL DURATION IN MULTIPLE-MYELOMA - A SIMPLE RELIABLE MARKER FOR STAGING [J].
BATAILLE, R ;
DURIE, BGM ;
GRENIER, J .
BRITISH JOURNAL OF HAEMATOLOGY, 1983, 55 (03) :439-447
[7]  
BERGGARD I, 1968, J BIOL CHEM, V243, P4095
[8]  
BODMER WF, 1981, TISSUE ANTIGENS, V17, P9
[9]  
CARBONE PP, 1971, CANCER RES, V31, P1860
[10]  
CHILD JA, 1980, CANCER-AM CANCER SOC, V45, P318, DOI 10.1002/1097-0142(19800115)45:2<318::AID-CNCR2820450220>3.0.CO