Nationwide survey on the use of horse antithymocyte globulins (ATGAM) in patients with acquired aplastic anemia: A report on behalf of the French Reference Center for Aplastic Anemia. Issue 5 (14th February 2018)
- Record Type:
- Journal Article
- Title:
- Nationwide survey on the use of horse antithymocyte globulins (ATGAM) in patients with acquired aplastic anemia: A report on behalf of the French Reference Center for Aplastic Anemia. Issue 5 (14th February 2018)
- Main Title:
- Nationwide survey on the use of horse antithymocyte globulins (ATGAM) in patients with acquired aplastic anemia: A report on behalf of the French Reference Center for Aplastic Anemia
- Authors:
- Peffault de Latour, Régis
Tabrizi, Reza
Marcais, Ambroise
Leblanc, Thierry
Lamy, Thierry
Mohty, Mohamad
Tavitian, Suzanne
Jubert, Charlotte
Pasquet, Marlène
Galambrun, Claire
Nguyen, Stéphanie
Cahn, Jean Yves
Braun, Thorsten
Deconinck, Eric
Bay, Jacques Olivier
Sicre de Fontbrune, Flore
Barraco, Fiorenza
Socié, Gérard - Abstract:
- Abstract: Antithymocyte globulins (ATG) plus cyclosporine (CSA) is the gold standard immunosuppressive treatment (IST) for patients with aplastic anemia. A prospective randomized trial showed in 2011 that hATG was superior to rabbit ATG for first‐line treatment of severe AA. The French Health Agency (ANSM) permitted a patient‐named authorization for temporary use (ATU) program of hATG (ATGAM, Pfizer) in patients with AA in 2011 since commercial access to hATG is not approved. We took advantage of this program to analyze the outcomes of 465 patients who received antithymocyte globulins (ATGAM) plus CSA as first line treatment ( n = 379; 81.5%), or for refractory ( n = 26) or relapsed disease ( n = 33), from September 2011 to March 2017. In the entire cohort one year, 72% of the patients had partial and 13% had complete response, with worse response for patients with severe AA and a longer interval between diagnosis and IST (more than 6 months). Severe adverse events were mainly linked to infections (24%), hemorrhages (6%), and elevated liver function tests (5%). Overall at 12 months, 9.7% of patients required second line IST and 15.6% received transplantation. Fifty‐five patients died during the study mainly because of infections (53%). Factors predicting independently worse survival were age over 40 years, neutrophils less than 0.5 × 10 9 /L, male gender and longer delay between diagnosis and hATG (>6 months period). This study does illustrate the results of ATGAM withAbstract: Antithymocyte globulins (ATG) plus cyclosporine (CSA) is the gold standard immunosuppressive treatment (IST) for patients with aplastic anemia. A prospective randomized trial showed in 2011 that hATG was superior to rabbit ATG for first‐line treatment of severe AA. The French Health Agency (ANSM) permitted a patient‐named authorization for temporary use (ATU) program of hATG (ATGAM, Pfizer) in patients with AA in 2011 since commercial access to hATG is not approved. We took advantage of this program to analyze the outcomes of 465 patients who received antithymocyte globulins (ATGAM) plus CSA as first line treatment ( n = 379; 81.5%), or for refractory ( n = 26) or relapsed disease ( n = 33), from September 2011 to March 2017. In the entire cohort one year, 72% of the patients had partial and 13% had complete response, with worse response for patients with severe AA and a longer interval between diagnosis and IST (more than 6 months). Severe adverse events were mainly linked to infections (24%), hemorrhages (6%), and elevated liver function tests (5%). Overall at 12 months, 9.7% of patients required second line IST and 15.6% received transplantation. Fifty‐five patients died during the study mainly because of infections (53%). Factors predicting independently worse survival were age over 40 years, neutrophils less than 0.5 × 10 9 /L, male gender and longer delay between diagnosis and hATG (>6 months period). This study does illustrate the results of ATGAM with CSA in a true‐life perspective and confirms ATGAM as standard of care IST to treat patients with AA not eligible for HSCT. … (more)
- Is Part Of:
- American journal of hematology. Volume 93:Issue 5(2018:May)
- Journal:
- American journal of hematology
- Issue:
- Volume 93:Issue 5(2018:May)
- Issue Display:
- Volume 93, Issue 5 (2018)
- Year:
- 2018
- Volume:
- 93
- Issue:
- 5
- Issue Sort Value:
- 2018-0093-0005-0000
- Page Start:
- 635
- Page End:
- 642
- Publication Date:
- 2018-02-14
- Subjects:
- Hematology -- Periodicals
616.15 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1096-8652 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ajh.25050 ↗
- Languages:
- English
- ISSNs:
- 0361-8609
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0824.800000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 14164.xml