Disease relapse post remission is a major predictor of poor outcome for patients with AML. The relapse rates range from 40% for patients with favorable cytogenetic abnormalities at diagnosis to 90% for patients with adverse cytogenetics. 1 Patients who relapse respond heterogeneously to salvage treatment. Long-term disease control may be achieved by allogenic hematopoietic cell transplantation (HCT) for patients achieving CR2. 2 Predictors for outcome following HCT in CR2 are described in limited case series. [3][4][5] We recently reported 6 in a single-center retrospective study on the outcomes of 94 adult patients with AML transplanted in CR2, and identified three categories of patients stratified for overall survival (OS): a favorable risk group of patients with duration of CR1 ⩾ 6 months, age o55 years and HCT-specific comorbidity index (HCT-CI) 7 0-3; an intermediate risk group with duration of CR1 ⩾ 6 months, age o55 years and HCT-CI 4-5; and a high-risk group with duration of CR1 o6 months or age ⩾ 55 years, with respective 5-year survival rates of 53, 31 and 6%. Survival was not influenced by cytogenetic risk, donor type and conditioning intensity. We concluded that the stratification model for patients transplanted with AML in CR2 may be used to determine which patients can derive the most benefit from allogeneic HCT. As a next step, we investigated the impact of the same parameters comprising the risk model in an independent multicenter cohort. Retrospectively collected data from a second cohort of 267 patients were contributed by Canadian and international transplant centers.The study included 267 patients aged 18-70 years with AML transplanted in CR2, from related (n = 102) or unrelated (n = 165