Personalized dosing breakthrough tested for adult leukemia treatment

NCT ID NCT00136435

Summary

This study tested whether adjusting the dose of a key chemotherapy drug (L-asparaginase) based on individual patient measurements could help adults with acute lymphoblastic leukemia complete their full treatment course. It involved 100 adults aged 18-50 who received multi-phase chemotherapy over about two years. The main goal was to see if this personalized approach made it easier for patients to finish all planned doses while monitoring survival outcomes and side effects.

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Contacts and locations

Locations

  • Dana-Farber Cancer Institute

    Boston, Massachusetts, 02115, United States

  • Hospital Maisonneuve-Rosemont

    Montreal, Quebec, Canada

  • London Health Sciences Centre

    London, Ontario, Canada

  • Manitoba Blood & Marrow Transplant Program CancerCare Manitoba

    Winnipeg, Manitoba, Canada

  • Massachusetts General Hospital

    Boston, Massachusetts, 02115, United States

  • McMaster University Medical Center

    Hamilton, Ontario, Canada

  • Queen Elizabeth II

    Halifax, Canada

  • Queen's University

    Kingston, Ontario, Canada

  • Royal Victoria Hospital

    Montreal, Quebec, Canada

  • Saskatoon Cancer Centre

    Saskatoon, Saskatchewan, Canada

  • Sunnybrook Health Sciences Centre

    Toronto, Ontario, Canada

  • University Of Columbia Medical Center

    New York, New York, United States

Conditions

Explore the condition pages connected to this study.