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Description and prognostic significance of the kinetics of minimal residual disease status in adults with acute lymphoblastic leukemia treated with HyperCVAD.
Cassaday, Ryan D; Stevenson, Philip A; Wood, Brent L; Becker, Pamela S; Hendrie, Paul C; Sandmaier, Brenda M; Radich, Jerald L; Shustov, Andrei R.
Afiliación
  • Cassaday RD; Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
  • Stevenson PA; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Wood BL; Clinical Statistics Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Becker PS; Department of Laboratory Medicine, University of Washington School of Medicine, Seattle, Washington.
  • Hendrie PC; Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
  • Sandmaier BM; Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington.
  • Radich JL; Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
  • Shustov AR; Department of Medicine, University of Washington School of Medicine, Seattle, Washington.
Am J Hematol ; 93(4): 546-552, 2018 08.
Article en En | MEDLINE | ID: mdl-29318644
ABSTRACT
HyperCVAD is a commonly-used regimen for adults with newly-diagnosed acute lymphoblastic leukemia (ALL). However, relatively little is known about the application of minimal residual disease (MRD) detection with this treatment. To address this, we studied 142 adults with ALL treated with hyperCVAD over a 10-year period who had MRD assessed by either multi-parameter flow cytometry or (for patients with Philadelphia chromosome positive ALL) reverse transcriptase polymerase chain reaction for the BCR-ABL1 translocation. In a multivariate analysis, patients who achieved MRD negativity (MRDNeg ) at any point had significantly better overall survival (OS; hazard ratio [HR] 0.43; P = .01) and event-free survival (EFS; HR 0.27; P < .01). Of 121 patients with MRD assessed at various points within 90 days of starting hyperCVAD, 50% (n = 61) had achieved MRDNeg . Among those that became MRDNeg , the median time to MRDNeg was 68 days. Time to MRDNeg was significantly associated with EFS (P = .009), but not OS (P = .19), implying increasingly better EFS the earlier MRDNeg is achieved. These data add to our understanding of MRD assessment during treatment with hyperCVAD, aide clinicians with predicting relapse risk, and provide additional historical data on which future clinical trials can be designed.
Asunto(s)

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Hematol Año: 2018 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Leucemia-Linfoma Linfoblástico de Células Precursoras Tipo de estudio: Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Am J Hematol Año: 2018 Tipo del documento: Article