Comparison of high-dose therapy and autologous stem-cell transplantation with conventional therapy for Hodgkin's disease induction failure:: A case-control study

被引:124
作者
André, M
Henry-Amar, M
Pico, JL
Brice, P
Blaise, D
Kuentz, M
Coiffier, B
Colombat, P
Cahn, JY
Attal, M
Fleury, J
Milpied, N
Nedellec, G
Biron, P
Tilly, H
Jouet, JP
Gisselbrecht, C
机构
[1] Hop St Louis, Inst Hematol, F-75010 Paris, France
[2] Ctr Francois Baclesse, Clin Res Unit, F-14021 Caen, France
[3] Ctr Francois Baclesse, INSERM, CJF 9603, GRECAN, F-14021 Caen, France
[4] Inst Gustave Roussy, Bone Marrow Transplantat Unit, Villejuif, France
[5] Inst J Paoli I Calmettes, Bone Marrow Transplantat Unit, F-13009 Marseille, France
[6] Hop Henri Mondor, Bone Marrow Transplantat Unit, F-94010 Creteil, France
[7] Ctr Hosp Lyon Sud, Dept Hematol, F-69310 Pierre Benite, France
[8] Hop Bretonneau, Dept Hematol, Tours, France
[9] Hop Jean Minjoz, Dept Hematol, F-25030 Besancon, France
[10] Hop Purpan, Dept Hematol, Toulouse, France
[11] Ctr Jean Perrin, Bone Marrow Transplantat Unit, Clermont Ferrand, France
[12] CHU Hotel Dieu, Dept Hematol, Nantes, France
[13] Hop Percy, Dept Hematol, Clamart, France
[14] Ctr Henri Becquerel, Dept Hematol, F-76038 Rouen, France
[15] Hop Claude Huriez, Dept Hematol, Lille, France
[16] Ctr Leon Berard, Dept Hematol, F-69373 Lyon, France
关键词
D O I
10.1200/JCO.1999.17.1.222
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To determine the prognostic factors and outcome of first-line induction failure Hodgkin's disease patients who were treated with ct salvage regimen of high-dose chemotherapy and autologous stem-cell transplantation, and to compare them with matched, conventionally treated patients. Patients and Methods: We retrospectively analyzed data relating to 86 Hodgkin's disease patients who underwent autologous stem-cell transplantation after Failure of the first chemotherapy regimen, either because they did not enter a complete remission and experienced progression of disease less than 3 months after the end of their first-line treatment or because they showed evidence of disease progression during first-line therapy. Graft patients were matched with 258 conventionally treated patients (three controls per ease) for age, sex, clinical stage, B symptoms, and time at risk; patient data were obtained from international databases. Results: Among the 86 graft patients, the median age at diagnosis was 29 years (range, 14 to 57 years). Thirty-nine percent of patients had stage II disease, 23% had stage III disease, and 38% had stage IV disease. Seventy percent of the patients received chemotherapy and 30% received combined modality therapy; 60% of the patients received a seven- or eight-drug regimen. After this first-line treatment, 91% had disease progression and 9% had a brief partial response. Eighty patients received a second-line treatment pretransplantation status was as follows: 24% of patients had a complete remission, 38% had a partial remission (PR), 14% had stable disease, and disease progression occurred in 24%. With a median follow-up of 22 months (range, 4 to 105 months) from diagnosis, the 5-year event-free survival and overall survival rates from transplantation were 25% and 35% (95% confidence intervals, 15 to 36 and 23 to 49), respectively, In multivariate analysis, the pretransplantation disease status after salvage therapy was the only significant prognostic factor for survival (PR: relative risk = 2.8, P = .017; progressive disease: relative risk(RR) = 5.26, P < .001). From diagnosis, the 6-year overall survival rates of the graft patients and 258 matched conventionally treated patients were 38% and 29%, respectively (P = .058). Conclusion: Autologous stem-cell transplantation represents the best therapeutic option currently available for patients with primary induction failure and is associated with acceptable toxicity. Response to second-line treatment before high-dose chemotherapy is the only prognostic factor that can be correlated with survival. J Clin Oncol 17:222-229. (C) 1999 by American Society of Clinical Oncology.
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页码:222 / 229
页数:8
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