Success of Immunosuppressive Treatments in Patients with Chronic Graft-versus-Host Disease
•After stopping therapy for chronic GVHD, half restarted after a median of 3.4 months.•After 5.6 years, one-third each were still on IST, alive off IST, or dead/relapsed. Moderate to severe chronic graft-versus-host disease (GVHD) is treated with potent immunosuppressive therapy (IST) to modulate th...
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Published in | Biology of blood and marrow transplantation Vol. 24; no. 3; pp. 555 - 562 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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United States
Elsevier Inc
01.03.2018
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Abstract | •After stopping therapy for chronic GVHD, half restarted after a median of 3.4 months.•After 5.6 years, one-third each were still on IST, alive off IST, or dead/relapsed.
Moderate to severe chronic graft-versus-host disease (GVHD) is treated with potent immunosuppressive therapy (IST) to modulate the allo-immune response, control symptoms, and prevent further organ damage. We sought to understand the types of treatments used in clinical practice and the likelihood of successful treatment associated with each. A chart review was performed for 250 adult patients at Fred Hutchinson Cancer Research Center enrolled in a prospective observational study. After a median follow-up of 5.6 years for survivors, approximately one-third were still on IST (of whom half were on fourth or greater line of therapy), one-third were alive and off IST, and one-third had relapsed or died. Approximately half of survivors stopped all IST at least once, although half of these restarted IST after a median of 3.4 months (interquartile range, 2.3 to 8.0) off therapy. Successful discontinuation of IST for at least 9 months was associated with myeloablative conditioning (P = .04), more years since transplant (P = .009), and lack of oral (P < .001) and skin (P = .049) involvement compared with those who had to restart IST. We conclude that patients with chronic GVHD usually receive multiple lines and years of IST, with only a third off IST, alive, and free of malignancy at 5 years after chronic GVHD diagnosis. Patients stopping IST should be cautioned to self-monitor and continue close medical follow-up, especially for 3 to 6 months after stopping IST. |
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AbstractList | Moderate to severe chronic graft-versus-host disease (GVHD) is treated with potent immunosuppressive therapy (IST) to modulate the allo-immune response, control symptoms, and prevent further organ damage. We sought to understand the types of treatments used in clinical practice and the likelihood of successful treatment associated with each. A chart review was performed for 250 adult patients at Fred Hutchinson Cancer Research Center enrolled in a prospective observational study. After a median follow-up of 5.6 years for survivors, approximately one-third were still on IST (of whom half were on fourth or greater line of therapy), one-third were alive and off IST, and one-third had relapsed or died. Approximately half of survivors stopped all IST at least once, although half of these restarted IST after a median of 3.4 months (interquartile range, 2.3 to 8.0) off therapy. Successful discontinuation of IST for at least 9 months was associated with myeloablative conditioning (P = .04), more years since transplant (P = .009), and lack of oral (P < .001) and skin (P = .049) involvement compared with those who had to restart IST. We conclude that patients with chronic GVHD usually receive multiple lines and years of IST, with only a third off IST, alive, and free of malignancy at 5 years after chronic GVHD diagnosis. Patients stopping IST should be cautioned to self-monitor and continue close medical follow-up, especially for 3 to 6 months after stopping IST. Moderate to severe chronic graft-versus-host disease (GVHD) is treated with potent immunosuppressive therapy (IST) to modulate the allo-immune response, control symptoms, and prevent further organ damage. We sought to understand the types of treatments used in clinical practice and the likelihood of successful treatment associated with each. A chart review was performed for 250 adult patients at Fred Hutchinson Cancer Research Center enrolled in a prospective observational study. After a median follow-up of 5.6 years for survivors, approximately one-third were still on IST (of whom half were on fourth or greater line of therapy), one-third were alive and off IST, and one-third had relapsed or died. Approximately half of survivors stopped all IST at least once, although half of these restarted IST after a median of 3.4 months (interquartile range, 2.3 to 8.0) off therapy. Successful discontinuation of IST for at least 9 months was associated with myeloablative conditioning (P = .04), more years since transplant (P = .009), and lack of oral (P < .001) and skin (P = .049) involvement compared with those who had to restart IST. We conclude that patients with chronic GVHD usually receive multiple lines and years of IST, with only a third off IST, alive, and free of malignancy at 5 years after chronic GVHD diagnosis. Patients stopping IST should be cautioned to self-monitor and continue close medical follow-up, especially for 3 to 6 months after stopping IST. •After stopping therapy for chronic GVHD, half restarted after a median of 3.4 months.•After 5.6 years, one-third each were still on IST, alive off IST, or dead/relapsed. Moderate to severe chronic graft-versus-host disease (GVHD) is treated with potent immunosuppressive therapy (IST) to modulate the allo-immune response, control symptoms, and prevent further organ damage. We sought to understand the types of treatments used in clinical practice and the likelihood of successful treatment associated with each. A chart review was performed for 250 adult patients at Fred Hutchinson Cancer Research Center enrolled in a prospective observational study. After a median follow-up of 5.6 years for survivors, approximately one-third were still on IST (of whom half were on fourth or greater line of therapy), one-third were alive and off IST, and one-third had relapsed or died. Approximately half of survivors stopped all IST at least once, although half of these restarted IST after a median of 3.4 months (interquartile range, 2.3 to 8.0) off therapy. Successful discontinuation of IST for at least 9 months was associated with myeloablative conditioning (P = .04), more years since transplant (P = .009), and lack of oral (P < .001) and skin (P = .049) involvement compared with those who had to restart IST. We conclude that patients with chronic GVHD usually receive multiple lines and years of IST, with only a third off IST, alive, and free of malignancy at 5 years after chronic GVHD diagnosis. Patients stopping IST should be cautioned to self-monitor and continue close medical follow-up, especially for 3 to 6 months after stopping IST. Moderate to severe chronic graft-versus-host disease (GVHD) is treated with potent immunosuppressive therapy (IST) to modulate the allo-immune response, control symptoms and prevent further organ damage. We sought to understand the types of treatments used in clinical practice and the likelihood of successful treatment associated with each. A chart review was performed for 250 adult patients at Fred Hutchinson Cancer Research Center enrolled in a prospective observational study. After a median follow-up of 5.6 years for survivors, approximately one third were still on IST (of whom half were on 4 th or greater line of therapy), one third were alive and off IST, and one third had relapsed or died. Approximately half of survivors stopped all IST at least once, although half of these restarted IST after a median of 3.4 months off therapy (IQR 2.3-8.0 months). Successful discontinuation of IST for at least 9 months was associated with myeloblative conditioning (p=0.04), more years since transplant (p=0.009) and lack of oral (p<0.001) and skin (p=0.049) involvement compared to people who had to restart IST. We conclude that patients with chronic GVHD usually receive multiple lines and years of IST, with only a third off IST, alive and free of malignancy at 5 years after chronic GVHD diagnosis. Patients stopping IST should be cautioned to self-monitor and continue close medical follow up especially for 3-6 months after stopping IST. |
Author | Onstad, Lynn Storer, Barry E. Martin, Paul J. Krakow, Elizabeth F. Nguyen, Tam D. Rodrigues, Morgani Hall, A. Marcie Bar, Merav Carpenter, Paul A. Salit, Rachel B. Flowers, Mary E. Lee, Stephanie J. |
AuthorAffiliation | 2 Department of Medical Oncology, University of Washington, Seattle WA, USA 1 Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA 3 University of North Carolina, School of Medicine, Chapel Hill, NC, USA; Center for Oncology, Hematology and Bone Marrow Transplantation, Hospital Israelita Albert Einstein, Brazil |
AuthorAffiliation_xml | – name: 3 University of North Carolina, School of Medicine, Chapel Hill, NC, USA; Center for Oncology, Hematology and Bone Marrow Transplantation, Hospital Israelita Albert Einstein, Brazil – name: 1 Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA – name: 2 Department of Medical Oncology, University of Washington, Seattle WA, USA |
Author_xml | – sequence: 1 givenname: Stephanie J. orcidid: 0000-0003-2600-6390 surname: Lee fullname: Lee, Stephanie J. email: sjlee@fhcrc.org organization: Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 2 givenname: Tam D. surname: Nguyen fullname: Nguyen, Tam D. organization: School of Medicine, University of North Carolina, Chapel Hill, North Carolina – sequence: 3 givenname: Lynn surname: Onstad fullname: Onstad, Lynn organization: Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 4 givenname: Merav surname: Bar fullname: Bar, Merav organization: Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 5 givenname: Elizabeth F. surname: Krakow fullname: Krakow, Elizabeth F. organization: Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 6 givenname: Rachel B. surname: Salit fullname: Salit, Rachel B. organization: Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 7 givenname: Paul A. surname: Carpenter fullname: Carpenter, Paul A. organization: Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 8 givenname: Morgani surname: Rodrigues fullname: Rodrigues, Morgani organization: Center for Oncology, Hematology and Bone Marrow Transplantation, Hospital Israelita Albert Einstein, São Paulo, Brazil – sequence: 9 givenname: A. Marcie surname: Hall fullname: Hall, A. Marcie organization: Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 10 givenname: Barry E. surname: Storer fullname: Storer, Barry E. organization: Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 11 givenname: Paul J. surname: Martin fullname: Martin, Paul J. organization: Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington – sequence: 12 givenname: Mary E. surname: Flowers fullname: Flowers, Mary E. organization: Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, Washington |
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Copyright | 2017 The American Society for Blood and Marrow Transplantation Copyright © 2017 The American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved. |
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Keywords | Chronic graft-versus-host disease Allogeneic hematopoietic cell transplantation Immunosuppressive treatment |
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Snippet | •After stopping therapy for chronic GVHD, half restarted after a median of 3.4 months.•After 5.6 years, one-third each were still on IST, alive off IST, or... Moderate to severe chronic graft-versus-host disease (GVHD) is treated with potent immunosuppressive therapy (IST) to modulate the allo-immune response,... |
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SubjectTerms | Allogeneic hematopoietic cell transplantation Chronic graft-versus-host disease Immunosuppressive treatment |
Title | Success of Immunosuppressive Treatments in Patients with Chronic Graft-versus-Host Disease |
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