Durable Red Blood Cell Transfusion Independence in a Patient with an MDS/MPN Overlap Syndrome Following Discontinuation of Iron Chelation Therapy
Background. Hematologic improvement (HI) occurs in some patients with acquired anemias and transfusional iron overload receiving iron chelation therapy (ICT) but there is little information on transfusion status after stopping chelation. Case Report. A patient with low IPSS risk RARS-T evolved to my...
Saved in:
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2015-01-01
|
Series: | Case Reports in Hematology |
Online Access: | http://dx.doi.org/10.1155/2015/253294 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
_version_ | 1832550205414703104 |
---|---|
author | Harpreet Kochhar Chantal S. Leger Heather A. Leitch |
author_facet | Harpreet Kochhar Chantal S. Leger Heather A. Leitch |
author_sort | Harpreet Kochhar |
collection | DOAJ |
description | Background. Hematologic improvement (HI) occurs in some patients with acquired anemias and transfusional iron overload receiving iron chelation therapy (ICT) but there is little information on transfusion status after stopping chelation. Case Report. A patient with low IPSS risk RARS-T evolved to myelofibrosis developed a regular red blood cell (RBC) transfusion requirement. There was no response to a six-month course of study medication or to erythropoietin for three months. At 27 months of transfusion dependence, she started deferasirox and within 6 weeks became RBC transfusion independent, with the hemoglobin normalizing by 10 weeks of chelation. After 12 months of chelation, deferasirox was stopped; she remains RBC transfusion independent with a normal hemoglobin 17 months later. We report the patient’s course in detail and review the literature on HI with chelation. Discussion. There are reports of transfusion independence with ICT, but that transfusion independence may be sustained long term after stopping chelation deserves emphasis. This observation suggests that reduction of iron overload may have a lasting favorable effect on bone marrow failure in at least some patients with acquired anemias. |
format | Article |
id | doaj-art-3b64bad0d5ef4093b9a651be6ad5b016 |
institution | Kabale University |
issn | 2090-6560 2090-6579 |
language | English |
publishDate | 2015-01-01 |
publisher | Wiley |
record_format | Article |
series | Case Reports in Hematology |
spelling | doaj-art-3b64bad0d5ef4093b9a651be6ad5b0162025-02-03T06:07:28ZengWileyCase Reports in Hematology2090-65602090-65792015-01-01201510.1155/2015/253294253294Durable Red Blood Cell Transfusion Independence in a Patient with an MDS/MPN Overlap Syndrome Following Discontinuation of Iron Chelation TherapyHarpreet Kochhar0Chantal S. Leger1Heather A. Leitch2Department of Medicine, University of St. Eustatius, Tucker, GA 30084, USADivision of Hematology, St. Paul’s Hospital, University of British Columbia, Vancouver, BC, V6Z 2A5, CanadaDivision of Hematology, St. Paul’s Hospital, University of British Columbia, Vancouver, BC, V6Z 2A5, CanadaBackground. Hematologic improvement (HI) occurs in some patients with acquired anemias and transfusional iron overload receiving iron chelation therapy (ICT) but there is little information on transfusion status after stopping chelation. Case Report. A patient with low IPSS risk RARS-T evolved to myelofibrosis developed a regular red blood cell (RBC) transfusion requirement. There was no response to a six-month course of study medication or to erythropoietin for three months. At 27 months of transfusion dependence, she started deferasirox and within 6 weeks became RBC transfusion independent, with the hemoglobin normalizing by 10 weeks of chelation. After 12 months of chelation, deferasirox was stopped; she remains RBC transfusion independent with a normal hemoglobin 17 months later. We report the patient’s course in detail and review the literature on HI with chelation. Discussion. There are reports of transfusion independence with ICT, but that transfusion independence may be sustained long term after stopping chelation deserves emphasis. This observation suggests that reduction of iron overload may have a lasting favorable effect on bone marrow failure in at least some patients with acquired anemias.http://dx.doi.org/10.1155/2015/253294 |
spellingShingle | Harpreet Kochhar Chantal S. Leger Heather A. Leitch Durable Red Blood Cell Transfusion Independence in a Patient with an MDS/MPN Overlap Syndrome Following Discontinuation of Iron Chelation Therapy Case Reports in Hematology |
title | Durable Red Blood Cell Transfusion Independence in a Patient with an MDS/MPN Overlap Syndrome Following Discontinuation of Iron Chelation Therapy |
title_full | Durable Red Blood Cell Transfusion Independence in a Patient with an MDS/MPN Overlap Syndrome Following Discontinuation of Iron Chelation Therapy |
title_fullStr | Durable Red Blood Cell Transfusion Independence in a Patient with an MDS/MPN Overlap Syndrome Following Discontinuation of Iron Chelation Therapy |
title_full_unstemmed | Durable Red Blood Cell Transfusion Independence in a Patient with an MDS/MPN Overlap Syndrome Following Discontinuation of Iron Chelation Therapy |
title_short | Durable Red Blood Cell Transfusion Independence in a Patient with an MDS/MPN Overlap Syndrome Following Discontinuation of Iron Chelation Therapy |
title_sort | durable red blood cell transfusion independence in a patient with an mds mpn overlap syndrome following discontinuation of iron chelation therapy |
url | http://dx.doi.org/10.1155/2015/253294 |
work_keys_str_mv | AT harpreetkochhar durableredbloodcelltransfusionindependenceinapatientwithanmdsmpnoverlapsyndromefollowingdiscontinuationofironchelationtherapy AT chantalsleger durableredbloodcelltransfusionindependenceinapatientwithanmdsmpnoverlapsyndromefollowingdiscontinuationofironchelationtherapy AT heatheraleitch durableredbloodcelltransfusionindependenceinapatientwithanmdsmpnoverlapsyndromefollowingdiscontinuationofironchelationtherapy |