AI Article Synopsis

  • Busulfan is the preferred drug for palliative therapy during the chronic phase of Chronic Myeloid Leukemia (CML), but hydroxyurea and interferon-alpha are being studied for their potential to extend this phase.
  • A multicenter study is assessing whether hydroxyurea or interferon-alpha can outperform busulfan regarding survival duration in CML patients, while also looking at disease evolution and prognostic criteria.
  • As of December 31, 1987, 326 patients have been randomized for the study with no significant survival differences found yet, although hydroxyurea showed fewer side effects.

Article Abstract

For palliative therapy during the chronic phase of CML busulfan has proved to be the drug of choice. During the past years hydroxyurea and also interferon-alpha have gained increasing significance since they might prolong the duration of the chronic phase. In a multicenter study it is being determined, whether the use of hydroxyurea or of interferon-alpha instead of busulfan prolongs the duration of the chronic phase of Philadelphia positive CML. Additional goals are the examination of whether the types of disease evolution and the terminal phases differ between the treatment groups, and the prospective recognition of prognostic criteria for the duration of the chronic phase of CML. By December 31, 1987, 326 CML-patients had been randomized, 150 for busulfan, 150 for hydroxyurea and 26 for interferon-alpha. The average age is 50 years. 59 patients reached the end of the chronic phase, 55 died. The mean observation time of all patients is 1.34 years. At present no significant difference in survival is recognizable between the busulfan and hydroxyurea groups. Fewer adverse effects have been observed in the hydroxyurea group. Philadelphia chromosome negative patients show a higher average age and tend to have lower white blood cell and platelet counts. The number of patients having received interferon-alpha is still too small to allow evaluation. This report intends to document organization and progress of this study which to our knowledge is, at present, the largest ongoing prospective multicenter study on the therapy of CML.

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Source
http://dx.doi.org/10.1007/BF00633471DOI Listing

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