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Published on: October 31, 2012
Evaluation of NIH consensus criteria for classification of late acute and chronic GVHD
Afonso C Vigorito1, Paulo V Campregher, Barry E Storer
1Bone Marrow Transplant Program at the State University of Campinas, Sao Paulo, Brazil.
Insights
The National Institutes of Health (NIH) criteria for chronic graft-versus-host disease (GVHD) did not significantly impact survival or treatment duration in patients post-hematopoietic cell transplantation (HCT). Late acute GVHD, however, increased mortality risks.
Area of Science:
- Hematology
- Immunology
- Oncology
Background:
- Historically, chronic graft-versus-host disease (GVHD) was defined by time post-hematopoietic cell transplantation (HCT).
- The 2005 National Institutes of Health (NIH) consensus proposed classifying GVHD based on clinical manifestations, not solely time.
Purpose of the Study:
- To evaluate the association between the presence of NIH criteria for chronic GVHD and patient outcomes.
- To determine if the NIH criteria accurately distinguish outcomes compared to historical definitions.
Main Methods:
- Retrospective analysis of 740 patients diagnosed with historically defined chronic GVHD after allogeneic HCT (1994-2000).
- Comparison of outcomes (survival, nonrelapse mortality, malignancy recurrence, treatment duration) based on NIH criteria for chronic GVHD.
Main Results:
- No significant association found between NIH criteria for chronic GVHD and survival, nonrelapse mortality, or treatment duration.
- Antecedent late acute GVHD was linked to increased nonrelapse mortality and prolonged treatment in patients with NIH chronic GVHD.
Conclusions:
- The NIH criteria for chronic GVHD did not significantly alter major outcomes in this cohort.
- Clinical trials can potentially include patients with late acute GVHD alongside NIH-defined chronic GVHD with appropriate stratification.
Abstract:
Historically, graft-versus-host disease (GVHD) beyond 100 days after hematopoietic cell transplantation (HCT) was called chronic GVHD, even if the clinical manifestations were indistinguishable from acute GVHD. In 2005, the National Institutes of Health (NIH) sponsored a consensus conference that proposed new criteria for diagnosis and classification of chronic GVHD for clinical trials. According to the consensus criteria, clinical manifestations rather than time after transplantation should be used in clinical trials to distinguish chronic GVHD from late acute GVHD, which includes persistent, recurrent, or late-onset acute GVHD. We evaluated major outcomes according to the presence or absence of NIH criteria for chronic GVHD in a retrospective study of 740 patients diagnosed with historically defined chronic GVHD after allogeneic HCT between 1994 and 2000. The presence or absence of NIH criteria for chronic GVHD showed no statistically significant association with survival, risks of nonrelapse mortality or recurrent malignancy, or duration of systemic treatment. Antecedent late acute GVHD was associated with an increased risk of nonrelapse mortality and prolonged treatment among patients with NIH chronic GVHD. Our results support the consensus recommendation that, with appropriate stratification, clinical trials can include patients with late acute GVHD as well as those with NIH chronic GVHD.
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