A prognostic model for prolonged event-free survival after autologous or allogeneic blood or marrow transplantation for relapsed and refractory Hodgkin's disease
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作者:
Hahn, T
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Hahn, T
Benekli, M
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Benekli, M
Wong, C
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Wong, C
Moysich, KB
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Moysich, KB
Hyland, A
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Hyland, A
Michalek, AM
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Michalek, AM
Alam, A
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Alam, A
Baer, MR
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Baer, MR
Bambach, B
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Bambach, B
Czuczman, MS
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Czuczman, MS
Wetzler, M
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Wetzler, M
Becker, JL
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
Becker, JL
McCarthy, PL
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机构:Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
McCarthy, PL
机构:
[1] Roswell Pk Canc Inst, Dept Med, Buffalo, NY 14263 USA
[2] Roswell Pk Canc Inst, Dept Educ, Buffalo, NY 14263 USA
[3] Roswell Pk Canc Inst, Dept Epidemiol, Buffalo, NY 14263 USA
[4] Roswell Pk Canc Inst, Dept Pediat, Buffalo, NY 14263 USA
[5] Roswell Pk Canc Inst, Lab Med, Buffalo, NY 14263 USA
There are several prognostic models for Hodgkin's disease (HD) patients, but none evaluating patient characteristics at time of blood and marrow transplantation (BMT). We developed a prognostic model for event-free survival (EFS) post-BMT based on HD patient characteristics measured at the time of autologous ( auto) or allogeneic ( allo) BMT. Between 1/1991 and 12/2001, 64 relapsed or refractory HD patients received an auto ( n = 46) or allo ( n = 18) BMT. A multivariate prognostic model was developed measuring time to relapse, progression or death. Median follow-up was 51.7 months; median EFS for auto and allo BMT was 36 and 3 months, respectively ( P = 0.001). Significant multivariate predictors of shorter EFS were chemotherapy-resistant disease, KPS <90 and >= 3 chemotherapy regimens pre-BMT. Patients with two to three adverse factors had significantly shorter EFS at 2 years ( 58 vs 11% in auto; 38 vs 0% in allo BMT patients). Despite a selection bias favoring auto BMT, the model was valid in both auto and allo BMT groups. We were able to differentiate patients at high vs low risk for adverse outcomes post-BMT. This prognostic model may prove useful in predicting patient outcomes and identifying high-risk patients for novel treatment strategies. Validation of this model in a larger cohort of patients is warranted.