A PREDICTIVE MODEL FOR AGGRESSIVE NON-HODGKINS-LYMPHOMA

被引:4442
|
作者
SHIPP, MA
HARRINGTON, DP
ANDERSON, JR
ARMITAGE, JO
BONADONNA, G
BRITTINGER, G
CABANILLAS, F
CANELLOS, GP
COIFFIER, B
CONNORS, JM
COWAN, RA
CROWTHER, D
DAHLBERG, S
ENGELHARD, M
FISHER, RI
GISSELBRECHT, C
HORNING, SJ
LEPAGE, E
LISTER, TA
MEERWALDT, JH
MONTSERRAT, E
NISSEN, NI
OKEN, MM
PETERSON, BA
TONDINI, C
VELASQUEZ, WA
YEAP, BY
机构
[1] HARVARD UNIV, SCH MED, BOSTON, MA 02115 USA
[2] EASTERN COOPERAT ONCOL GRP, DENVER, CO USA
[3] NEBRASKA LYMPHOMA STUDY GRP, OMAHA, NE USA
[4] CANC & LEUKEMIA GRP B, LEBANON, NH USA
[5] BUNDESMINIST FORSCH & TECHNOL STUDY, ESSEN, GERMANY
[6] MD ANDERSON CANC CTR, HOUSTON, DC USA
[7] HARVARD UNIV, SCH MED, BOSTON, MA 02115 USA
[8] GRP ETUD LYMPHOMES ADULTE, PARIS, FRANCE
[9] BRITISH COLUMBIA CANC AGCY, VANCOUVER, BC, CANADA
[10] MANCHESTER LYMPHOMA GRP, MANCHESTER, ENGLAND
[11] SW ONCOL GRP, SAN ANTONIO, TX USA
[12] STANFORD UNIV, STANFORD, CA 94305 USA
[13] ST BARTHOLOMEWS HOSP, LONDON EC1A 7BE, ENGLAND
[14] EUROPEAN ORG RES TREATMENT CANC, LYMPHOMA COOPERAT GRP, BRUSSELS, BELGIUM
[15] HOSP CLIN BARCELONA, BARCELONA 36, SPAIN
[16] FINSEN INST, DK-2100 COPENHAGEN, DENMARK
[17] IST NAZL TUMORI, I-20133 MILAN, ITALY
来源
NEW ENGLAND JOURNAL OF MEDICINE | 1993年 / 329卷 / 14期
关键词
D O I
10.1056/nejm199309303291402
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Although many patients with intermediate-grade or high-grade (aggressive) non-Hodgkin's lymphoma are cured by combination chemotherapy, the remainder are not cured and ultimately die of their disease. The Ann Arbor classification, used to determine the stage of this disease, does not consistently distinguish between patients with different long-term prognoses. This project was undertaken to develop a model for predicting outcome in patients with aggressive non-Hodgkin's lymphoma on the basis of the patients' clinical characteristics before treatment. Methods. Adults with aggressive non-Hodgkin's lymphoma from 16 institutions and cooperative groups in the United States, Europe, and Canada who were treated between 1982 and 1987 with combination-chemotherapy regimens containing doxorubicin were evaluated for clinical features predictive of overall survival and relapse-free survival. Features that remained independently significant in step-down regression analyses of survival were incorporated into models that identified groups of patients of all ages and groups of patients no more than 60 years old with different risks of death. Results. In 2031 patients of all ages, our model, based on age, tumor stage, serum lactate dehydrogenase concentration, performance status, and number of extranodal disease sites, identified four risk groups with predicted five-year survival rates of 73 percent, 51 percent, 43 percent, and 26 percent. In 1274 patients 60 or younger, an age-adjusted model based on tumor stage, lactate dehydrogenase level, and performance status identified four risk groups with predicted five-year survival rates of 83 percent, 69 percent, 46 percent, and 32 percent. In both models, the increased risk of death was due to both a lower rate of complete responses and a higher rate of relapse from complete response. These two indexes, called the international index and the age-adjusted international index, were significantly more accurate than the Ann Arbor classification in predicting long-term survival. Conclusions. The international index and the age-adjusted international index should be used in the design of future therapeutic trials in patients with aggressive non-Hodgkin's lymphoma and in the selection of appropriate therapeutic approaches for individual patients.
引用
收藏
页码:987 / 994
页数:8
相关论文
共 50 条
  • [1] A PREDICTIVE MODEL FOR NON-HODGKINS-LYMPHOMA
    ATKINS, CD
    NEW ENGLAND JOURNAL OF MEDICINE, 1994, 330 (08): : 574 - 574
  • [2] TREATMENT OF AGGRESSIVE NON-HODGKINS-LYMPHOMA IN THE ELDERLY
    NOVITZKY, N
    KING, HS
    JOHNSON, C
    JACOBS, P
    AMERICAN JOURNAL OF HEMATOLOGY, 1995, 49 (02) : 103 - 108
  • [3] STAGING SYSTEMS FOR AGGRESSIVE NON-HODGKINS-LYMPHOMA
    ARMITAGE, JO
    ANNALS OF ONCOLOGY, 1992, 3 (09) : 675 - 676
  • [4] NOPE FOR RELAPSED AGGRESSIVE DIFFUSE NON-HODGKINS-LYMPHOMA
    BEZWODA, WR
    BEZWODA, MA
    SEYMOUR, L
    DANSEY, R
    ARIAD, S
    LEUKEMIA & LYMPHOMA, 1993, 10 (4-5) : 329 - 333
  • [5] CHEMOTHERAPY FOR HODGKINS-DISEASE AND AGGRESSIVE NON-HODGKINS-LYMPHOMA - MORE IS BETTER, OR IS IT
    DODWELL, DJ
    DECAMPOS, ES
    RADFORD, JA
    DRUGS, 1992, 44 (01) : 1 - 8
  • [6] NON-HODGKINS-LYMPHOMA
    TUBIANA, M
    CARDE, P
    BURGERS, JMV
    COSSET, JM
    VANGLABBEKE, M
    SOMERS, R
    CANCER SURVEYS, 1985, 4 (02) : 377 - 398
  • [7] NON-HODGKINS-LYMPHOMA
    GREINER, TC
    MEDEIROS, LJ
    JAFFE, ES
    CANCER, 1995, 75 (01) : 370 - 380
  • [8] NON-HODGKINS-LYMPHOMA
    MORENO, AJ
    SANDERS, LR
    BATTAFARANO, NJ
    DORAN, TM
    TURNBULL, GL
    CLINICAL NUCLEAR MEDICINE, 1986, 11 (11) : 801 - 802
  • [9] THE PRESENT STATUS OF THERAPY FOR PATIENTS WITH AGGRESSIVE NON-HODGKINS-LYMPHOMA
    VOSE, JM
    ARMITAGE, JO
    ANNALS OF ONCOLOGY, 1991, 2 : 171 - 176
  • [10] NON-HODGKINS-LYMPHOMA
    HOLDERMAN, RD
    TEREZHALMY, GT
    DELBALSO, AM
    ORAL SURGERY ORAL MEDICINE ORAL PATHOLOGY ORAL RADIOLOGY AND ENDODONTICS, 1987, 63 (03): : 386 - 389