Optimal timing of allogeneic hematopoietic stem cell transplantation in patients with myelodysplastic syndrome. Issue 7 (30th May 2013)
- Record Type:
- Journal Article
- Title:
- Optimal timing of allogeneic hematopoietic stem cell transplantation in patients with myelodysplastic syndrome. Issue 7 (30th May 2013)
- Main Title:
- Optimal timing of allogeneic hematopoietic stem cell transplantation in patients with myelodysplastic syndrome
- Authors:
- Alessandrino, Emilio Paolo
Porta, Matteo G. Della
Malcovati, Luca
Jackson, Christopher H
Pascutto, Cristiana
Bacigalupo, Andrea
Teresa van Lint, Maria
Falda, Michele
Bernardi, Massimo
Onida, Francesco
Guidi, Stefano
Iori, Anna Paola
Cerretti, Raffaella
Marenco, Paola
Pioltelli, Pietro
Angelucci, Emanuele
Oneto, Rosi
Ripamonti, Francesco
Rambaldi, Alessandro
Bosi, Alberto
Cazzola, Mario - Abstract:
- <abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Allogeneic hematopoietic stem cell transplantation (HSCT) represents the only curative treatment for patients with myelodysplastic syndrome (MDS), but involves non‐negligible morbidity and mortality. Registry studies have shown that advanced disease stage at transplantation is associated with inferior overall survival. To define the optimal timing of allogeneic HSCT, we carried out a decision analysis by studying 660 patients who received best supportive care and 449 subjects who underwent transplantation. Risk assessment was based on both the International Prognostic Scoring System (IPSS) and the World Health Organization classification‐based Prognostic Scoring System (WPSS). We used a continuous‐time multistate Markov model to describe the natural history of disease and evaluate the effect of allogeneic HSCT on survival. This model estimated life expectancy from diagnosis according to treatment policy at different risk stages. Relative to supportive care, estimated life expectancy increased when transplantation was delayed from the initial stages until progression to intermediate‐1 IPSS‐risk or to intermediate WPSS‐risk stage, and then decreased for higher risks. Modeling decision analysis on WPSS versus IPSS allowed better estimation of the optimal timing of transplantation. These observations indicate that allogeneic HSCT offers optimal survival benefits when the procedure is<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Allogeneic hematopoietic stem cell transplantation (HSCT) represents the only curative treatment for patients with myelodysplastic syndrome (MDS), but involves non‐negligible morbidity and mortality. Registry studies have shown that advanced disease stage at transplantation is associated with inferior overall survival. To define the optimal timing of allogeneic HSCT, we carried out a decision analysis by studying 660 patients who received best supportive care and 449 subjects who underwent transplantation. Risk assessment was based on both the International Prognostic Scoring System (IPSS) and the World Health Organization classification‐based Prognostic Scoring System (WPSS). We used a continuous‐time multistate Markov model to describe the natural history of disease and evaluate the effect of allogeneic HSCT on survival. This model estimated life expectancy from diagnosis according to treatment policy at different risk stages. Relative to supportive care, estimated life expectancy increased when transplantation was delayed from the initial stages until progression to intermediate‐1 IPSS‐risk or to intermediate WPSS‐risk stage, and then decreased for higher risks. Modeling decision analysis on WPSS versus IPSS allowed better estimation of the optimal timing of transplantation. These observations indicate that allogeneic HSCT offers optimal survival benefits when the procedure is performed before MDS patients progress to advanced disease stages. Am. J. Hematol. 88:581–588, 2013. © 2013 Wiley Periodicals, Inc.</p> </abstract> … (more)
- Is Part Of:
- American journal of hematology. Volume 88:Issue 7(2013:Jul.)
- Journal:
- American journal of hematology
- Issue:
- Volume 88:Issue 7(2013:Jul.)
- Issue Display:
- Volume 88, Issue 7 (2013)
- Year:
- 2013
- Volume:
- 88
- Issue:
- 7
- Issue Sort Value:
- 2013-0088-0007-0000
- Page Start:
- 581
- Page End:
- 588
- Publication Date:
- 2013-05-30
- 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.23458 ↗
- 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:
- 3304.xml