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Open AccessJournal ArticleDOI

Prognostic impact of elevated pretransplantation serum ferritin in patients undergoing myeloablative stem cell transplantation

TLDR
The results argue that iron overload plays an important role in transplantation outcome for patients with acute leukemia or MDS, as it does in thalassemia and suggest future prospective trials to examine the potential benefit of chelation therapy in this setting.
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This article is published in Blood.The article was published on 2007-05-15 and is currently open access. It has received 384 citations till now. The article focuses on the topics: Transplantation & Myelodysplastic syndromes.

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Journal ArticleDOI

Ferritin for the Clinician

TL;DR: Ferritin is directly implicated in less common but potentially devastating human diseases including sideroblastic anemias, neurodegenerative disorders, and hemophagocytic syndrome and recent research describes novel functions of ferritin independent of iron storage.
Journal ArticleDOI

Towards a unifying, systems biology understanding of large-scale cellular death and destruction caused by poorly liganded iron: Parkinson’s, Huntington’s, Alzheimer’s, prions, bactericides, chemical toxicology and others as examples

TL;DR: This work highlights specifically the role of iron metabolism, and the detailed speciation of iron, in chemical and other toxicology, and has significant implications for the use of iron chelating substances as nutritional or therapeutic agents in inhibiting both the progression of these mainly degenerative diseases and the sequelae of both chronic and acute toxin exposure.
References
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Journal ArticleDOI

A Proportional Hazards Model for the Subdistribution of a Competing Risk

TL;DR: This article proposes methods for combining estimates of the cause-specific hazard functions under the proportional hazards formulation, but these methods do not allow the analyst to directly assess the effect of a covariate on the marginal probability function.
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Survival in medically treated patients with homozygous beta-thalassemia.

TL;DR: Univariate analysis demonstrated that factors affecting cardiac disease-free survival were age at the start of chelation therapy and life-table analysis to estimate freedom from cardiac disease over time.
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Bone Marrow Transplantation in Patients with Thalassemia

TL;DR: It is concluded that for patients under 16 years of age, transplantation of bone marrow from an HLA-identical donor offers a high probability of complication-free survival, particularly if they do not have hepatomegaly or portal fibrosis.
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Marrow Transplantation in Patients with Thalassemia Responsive to Iron Chelation Therapy

TL;DR: The high probability of cure with little early or late morbidity and mortality suggests that patients with class 1 thalassemia who have HLA-identical donors available should be treated by bone marrow transplantation.
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