New data from the largest clinical trial in newly diagnosed patients with a life-threatening form of leukemia showed that long-term use of imatinib mesylate (Gleevec) can halt progression to advanced disease stages in the 6th year of treatment.
Results of the International Randomized Interferon versus STI571 (IRIS) study reveal that after 2 years of treatment the rate of disease progression continued to decline and fell to 0% in the study's 6th year. In addition, the estimated overall 6-year survival rate for patients treated with imatinib was 88%.
Lead investigators presented findings from this landmark study involving more than 1,100 newly diagnosed patients with Philadelphia chromosome–positive (Ph+) chronic myeloid leukemia (CML) at the 49th Annual Meeting of the American Society of Hematology (ASH).
Patients in the initial (chronic) phase of CML who received continuous treatment with imatinib did not progress to advanced stages of the disease. Without treatment, CML typically progresses over 3 to 5 years from the initial phase through a transition (accelerated) phase to a rapidly fatal form called blast crisis.
"If this survival trend continues, many patients with CML may approach normal life expectancy with continued Gleevec treatment," said Brian Druker, MD, director of the Oregon Health & Science University Cancer Institute Center.
Most CML patients are in the chronic phase when the disease is diagnosed. Before imatinib was available, about 50% of patients with Ph+ CML progressed from the initial phase to more advanced stages after only 3 to 5 years. Once patients reached the final blast crisis phase, survival was generally three to 6 months. With a unique 6-year record of safety and efficacy, imatinib remains the first-line drug therapy for all patients with Ph+ CML.
Imatinib has continued to be generally well tolerated as initial drug therapy for Ph+ CML in chronic phase. At the 6-year follow-up, the type and frequency of adverse events were similar to previously reported profiles. Newly occurring or worsening grade 3 or 4 hematologic or biochemical adverse events were infrequent.