ArticleFrontiers in immunology2026
The conditional benefit of being alive and disease free at 2 years after transplant: a long term survival evaluation among 456 patients affected by acute myeloid leukemia.
Article in Frontiers in immunology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
21 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Risk factors for relapse and non-relapse mortality (NRM) in the first years after allogeneic hematopoietic stem cells transplant (allo-HSCT) for acute myeloid leukemia (AML) are well known, but their correlation with long-term survivorship is unclear. This study aims to evaluate factors that impact on long-term survival after allo-HSCT in AML. We retrospectively analyzed data of 456 consecutive patients who received a first allo-HSCT in our center, regardless of conditioning intensity, GvHD prophylaxis, donor matching and HSC source. At transplant, two hundred and four patients (44%) were in CR1, 62 patients (14%) in CR>1, 27 (6%) in CR MRD+ and 163 patients (36%) in active disease (AD). Two-hundred and thirty-nine patients (52%) were alive 2 years after allo-HSCT. Median follow-up was 6.1 years. The 5 years OS was 63% for CR1, 38% for CR>1 and 25% for AD. However, in patients alive and disease free 2 years after allo-HSCT the probability of being alive for 3 more years was 86% for CR1, 72% for CR>1 and 79% for AD, with no statistically significant differences between CR>1 and AD. Other variables associated with better outcomes included younger age, more recent transplantation, and having a female donor for a male recipient. Relapse remained the main cause of death, even among long-term survivors. In conclusion, the negative impact of advanced disease at the time of allo-HSCT appears to progressively reduce after transplantation, highlighting the excellent long-term outcomes of patients who remain disease-free at 2 years after allo-HSCT, regardless of pre-transplantation disease status.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.