Literature DB >> 33184452

Allogeneic hematopoietic stem cell transplant in rare hematologic disorders: a single center experience from Pakistan.

Maryam Khan1, Raheel Iftikhar2, Tariq Ghafoor1, Fayyaz Hussain1, Qamar Un Nisa Chaudhry1, Syed Kamran Mahmood1, Nighat Shahbaz1, Mehreen Ali Khan1, Tariq Azam Khattak1, Ghassan Umair Shamshad1, Jahanzeb Rehman1, Sundas Ali3, Zunaira Shah4, Abdul Rafae5, Muhammad Farhan1, Faiz Anwer6, Parvez Ahmed7.   

Abstract

Management of rare hematological disorders pose unique diagnostic and therapeutic challenges due to unusual occurrence and limited treatment options. We retrospectively identified 45 patients receiving matched related donor transplant for rare hematological disorders from 2006 to 2019. Patients were divided into two groups (1) malignant and (2) non malignant. The malignant disorder group included four patients while the nonmalignant group included 41 patients divided into immune dysregulation (n = 23), bone marrow failure (n = 10), metabolic (n = 5), and bleeding diathesis (n = 3). Twenty-six (57.8%) patients received myeloablative conditioning (MAC) and 16 (35.6%) received reduced intensity conditioning (RIC), while 3 (6.6%) patients with severe combined immunodeficiency received stem cell infusion alone without conditioning. The cumulative incidence (CI) of grade II-IV acute GVHD (aGVHD) was 39.1% (n = 18) and chronic GVHD (cGVHD) 15.2% (n = 7). There was no primary graft failure while CI of secondary graft failure was 9%. Overall survival (OS) and disease-free survival (DFS) was 82.2% and 77.8% respectively. Group wise OS was 75% in the malignant group, 82.6% in the immune dysregulation group, 80% in patients with metabolic disorders and bone marrow failure, while 100% in patients with bleeding diathesis. This retrospective analysis shows that hematopoietic stem cell transplant can be a feasible treatment option for rare hematological disorders.

Entities:  

Year:  2020        PMID: 33184452     DOI: 10.1038/s41409-020-01126-4

Source DB:  PubMed          Journal:  Bone Marrow Transplant        ISSN: 0268-3369            Impact factor:   5.483


  31 in total

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Review 2.  Chronic granulomatous disease: lessons from a rare disorder.

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Journal:  Biol Blood Marrow Transplant       Date:  2011-01       Impact factor: 5.742

3.  HLH-2004: Diagnostic and therapeutic guidelines for hemophagocytic lymphohistiocytosis.

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Journal:  Pediatr Blood Cancer       Date:  2007-02       Impact factor: 3.167

4.  Indications for Hematopoietic Cell Transplantation and Immune Effector Cell Therapy: Guidelines from the American Society for Transplantation and Cellular Therapy.

Authors:  Abraham S Kanate; Navneet S Majhail; Bipin N Savani; Christopher Bredeson; Richard E Champlin; Stephen Crawford; Sergio A Giralt; Charles F LeMaistre; David I Marks; James L Omel; Paul J Orchard; Jeanne Palmer; Wael Saber; Paul A Veys; Paul A Carpenter; Mehdi Hamadani
Journal:  Biol Blood Marrow Transplant       Date:  2020-03-09       Impact factor: 5.742

5.  Practice parameter for the diagnosis and management of primary immunodeficiency.

Authors:  Francisco A Bonilla; David A Khan; Zuhair K Ballas; Javier Chinen; Michael M Frank; Joyce T Hsu; Michael Keller; Lisa J Kobrynski; Hirsh D Komarow; Bruce Mazer; Robert P Nelson; Jordan S Orange; John M Routes; William T Shearer; Ricardo U Sorensen; James W Verbsky; David I Bernstein; Joann Blessing-Moore; David Lang; Richard A Nicklas; John Oppenheimer; Jay M Portnoy; Christopher R Randolph; Diane Schuller; Sheldon L Spector; Stephen Tilles; Dana Wallace
Journal:  J Allergy Clin Immunol       Date:  2015-09-12       Impact factor: 10.793

6.  Care for patients with ultra-rare disorders.

Authors:  Raoul C M Hennekam
Journal:  Eur J Med Genet       Date:  2010-12-10       Impact factor: 2.708

7.  Establishing diagnostic criteria for severe combined immunodeficiency disease (SCID), leaky SCID, and Omenn syndrome: the Primary Immune Deficiency Treatment Consortium experience.

Authors:  William T Shearer; Elizabeth Dunn; Luigi D Notarangelo; Christopher C Dvorak; Jennifer M Puck; Brent R Logan; Linda M Griffith; Donald B Kohn; Richard J O'Reilly; Thomas A Fleisher; Sung-Yun Pai; Caridad A Martinez; Rebecca H Buckley; Morton J Cowan
Journal:  J Allergy Clin Immunol       Date:  2013-11-28       Impact factor: 10.793

Review 8.  Congenital dyserythropoietic anemia type II: epidemiology, clinical appearance, and prognosis based on long-term observation.

Authors:  Hermann Heimpel; Volker Anselstetter; Ladislav Chrobak; Jonas Denecke; Beate Einsiedler; Kerstin Gallmeier; Antje Griesshammer; Thorsten Marquardt; Gritta Janka-Schaub; Martina Kron; Elisabeth Kohne
Journal:  Blood       Date:  2003-08-21       Impact factor: 22.113

Review 9.  Rare Disease Terminology and Definitions-A Systematic Global Review: Report of the ISPOR Rare Disease Special Interest Group.

Authors:  Trevor Richter; Sandra Nestler-Parr; Robert Babela; Zeba M Khan; Theresa Tesoro; Elizabeth Molsen; Dyfrig A Hughes
Journal:  Value Health       Date:  2015-08-18       Impact factor: 5.725

10.  Silvery hair syndrome in two cousins: Chediak-Higashi syndrome vs Griscelli syndrome, with rare associations.

Authors:  R Raghunatha Reddy; Balaji M Babu; B Venkateshwaramma; Ch Hymavathi
Journal:  Int J Trichology       Date:  2011-07
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