Vinod Prasad

Overview:

1. Expanding the role of umbilical cord blood transplants for inherited metabolic disorders.
2. Impact of histocompatibility and other determinants of alloreactivity on clinical outcomes of unrelated cord blood transplants.
3. Studies to analyse the impact of Killer Immunoglobulin receptors on the outcomes of hematopoietic stem cell transplantation utilizing haploidentical, CD34 selected, familial grafts.
4. Propective longitudinal study of serial monitoring of adenovirus in allogenic transpants(SMAART)patients.
5. Use of mesenchymal stem cells for the treatment of GVHD

Positions:

Professor of Pediatrics

Pediatrics, Transplant and Cellular Therapy
School of Medicine

Member of the Duke Cancer Institute

Duke Cancer Institute
School of Medicine

Education:

M.B.B.S. 1981

Maulana Azad Medical College (India)

Rotating Internship, Pediatrics & Orthopedics

Maulana Azad Medical College (India)

Junior Resident, Pediatrics & Orthopedics

Maulana Azad Medical College (India)

Junior Resident, Pediatrics

Lady Hardinge Medical College (India)

Senior Resident, Pediatrics

Lady Hardinge Medical College (India)

Senior House Officer, Pediatrics

Hospital for Sick Children (United Kingdom)

Fellow, Pediatric Hematology-Oncology, Pediatrics

Memorial Sloan-Kettering Cancer Center

Resident, Pediatrics

Cornell University

Grants:

Identifying Predictors of Poor Health-Related Quality of Life among Pediatric Hematopoietic Stem Cell Donors

Administered By
Pediatrics, Transplant and Cellular Therapy
Awarded By
National Marrow Donor Program
Role
Principal Investigator
Start Date
End Date

Open-label, Randomized, Multi-center, Parallel Group, Two-arm Study to Assess the Safety, Overall Tolerability, and Antiviral Activity of Brincidofovir vs Standard of Care for Trtmt of Adenovirus Infections in High-risk Pediatric Allo HCT Recipients

Administered By
Pediatrics, Transplant and Cellular Therapy
Awarded By
Chimerix, Inc.
Role
Principal Investigator
Start Date
End Date

A Phase 2, Single-arm, Open-label, Study to Evaluate the Safety and Efficacy of MGTA-456 in Patients with Inherited Metabolic Disorders (IMD) Undergoing Hematopoietic Stem Cell (HSC) Transplantation (HSCT)

Administered By
Pediatrics, Transplant and Cellular Therapy
Awarded By
Magenta Therapeutics
Role
Principal Investigator
Start Date
End Date

A Prospective Observational Study for the Long-Term Follow-Up of Subjects Previously Enrolled in Selected Clinical Studies of CMX001

Administered By
Pediatrics, Transplant and Cellular Therapy
Awarded By
Chimerix, Inc.
Role
Principal Investigator
Start Date
End Date

Magenta MGTA-456 (IMD-001) Stem Cell Laboratory (STCL) MTA

Administered By
Pediatrics, Transplant and Cellular Therapy
Awarded By
Magenta Therapeutics
Role
Principal Investigator
Start Date
End Date

Publications:

Variables affecting outcomes after allogeneic hematopoietic stem cell transplant for cerebral adrenoleukodystrophy.

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) in early cerebral adrenoleukodystrophy can stabilize neurologic function and improve survival but has associated risks including transplant-related mortality (TRM), graft failure, and graft-versus-host disease (GVHD). An observational study of 59 patients with median age at allo-HSCT of 8 years addressed impact of donor source, donor match, conditioning regimen, and cerebral disease stage on first allo-HSCT outcomes. Efficacy analyses included 53 patients stratified by disease category: advanced disease (AD; n = 16) with Loes score >9 or neurological function score (NFS) >1 and 2 early disease (ED) cohorts (ED1 [Loes ≤4 and NFS ≤1; n = 24] and ED2 [Loes >4-9 and NFS ≤1; n = 13]). Survival free of major functional disabilities and without second allo-HSCT at 4 years was significantly higher in the ED (66%) vs AD (41%) cohort (P = .015) and comparable between ED1 and ED2 cohorts (P = .991). The stabilization of neurologic function posttransplant was greater in the ED vs AD cohort, with a median change from baseline at 24 months after allo-HSCT in NFS and Loes score, respectively, of 0 and 0.5 in ED1 (n = 13), 0.5 and 0 in ED2 (n = 6), and 2.5 and 3.0 (n = 4) in AD cohort. TRM was lower in the ED (7%) compared with the AD (22%) cohort; however, the difference was not significant (P = .094). Transplant-related safety outcomes were also affected by transplant-related characteristics: graft failure incidence was significantly higher with unrelated umbilical cord grafts vs matched related donors (P = .039), and acute GVHD and graft failure incidences varied by conditioning regimen. This study was registered at www://clinicaltrials.gov as #NCT02204904.
Authors
Chiesa, R; Boelens, JJ; Duncan, CN; Kühl, J-S; Sevin, C; Kapoor, N; Prasad, VK; Lindemans, CA; Jones, SA; Amartino, HM; Algeri, M; Bunin, N; Diaz-de-Heredia, C; Loes, DJ; Shamir, E; Timm, A; McNeil, E; Dietz, AC; Orchard, PJ
MLA Citation
Chiesa, Robert, et al. “Variables affecting outcomes after allogeneic hematopoietic stem cell transplant for cerebral adrenoleukodystrophy.Blood Adv, vol. 6, no. 5, Mar. 2022, pp. 1512–24. Pubmed, doi:10.1182/bloodadvances.2021005294.
URI
https://scholars.duke.edu/individual/pub1501830
PMID
34781360
Source
pubmed
Published In
Blood Adv
Volume
6
Published Date
Start Page
1512
End Page
1524
DOI
10.1182/bloodadvances.2021005294

Expanded Access Protocol of Umbilical Cord Blood Infusion for Children with Neurological Conditions: An Update.

Authors
McLaughlin, C; West, T; Hollowell, R; Skergan, N; Giguere, P; Vinesett, R; Arbuckle, E; Cash, J; Hoyle, K; Crane, S; Moore, L; Waters-Pick, B; Hawkins, T; Prasad, V; Sun, J; Kurtzberg, J
MLA Citation
McLaughlin, Colleen, et al. “Expanded Access Protocol of Umbilical Cord Blood Infusion for Children with Neurological Conditions: An Update.Stem Cells Transl Med, vol. 10, no. S1, Sept. 2021, pp. S7–8. Pubmed, doi:10.1002/sct3.13016.
URI
https://scholars.duke.edu/individual/pub1521970
PMID
35599372
Source
pubmed
Published In
Stem Cells Transl Med
Volume
10
Published Date
Start Page
S7
End Page
S8
DOI
10.1002/sct3.13016

Augmentation of Allogenic Cord Blood (CB) Transplantation for Inherited Metabolic Diseases with CB-Derived Intrathecal Cellular Therapy, Duoc-01

MLA Citation
Sun, Jessica, et al. “Augmentation of Allogenic Cord Blood (CB) Transplantation for Inherited Metabolic Diseases with CB-Derived Intrathecal Cellular Therapy, Duoc-01.” Biology of Blood and Marrow Transplantation, vol. 23, no. 3, 2017, pp. S100–01.
URI
https://scholars.duke.edu/individual/pub1452430
Source
wos-lite
Published In
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
Volume
23
Published Date
Start Page
S100
End Page
S101

Treatment of Adenovirus (AdV) Infection in Allogeneic Hematopoietic Cell Transplant (allo HCT) Patients (pts) with Brincidofovir: Final 36 Week Results from the Advise Trial

Authors
Prasad, VK; Papanicolaou, GA; Maron, GM; Vainorius, E; Brundage, TM; Chittick, G; Nichols, G; Grimley, MS
MLA Citation
URI
https://scholars.duke.edu/individual/pub1452561
Source
wos-lite
Published In
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
Volume
23
Published Date
Start Page
S52
End Page
S53

Outcomes of Umbilical Cord Blood Transplantation in Children with Batten Disease

Authors
Brondon, JE; Page, K; Polishchuk, V; Driscoll, TA; Parikh, S; Martin, PL; Kurtzberg, J; Prasad, VK
MLA Citation
Brondon, Jennifer E., et al. “Outcomes of Umbilical Cord Blood Transplantation in Children with Batten Disease.” Biology of Blood and Marrow Transplantation, vol. 25, no. 3, 2019.
URI
https://scholars.duke.edu/individual/pub1468384
Source
wos-lite
Published In
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
Volume
25
Published Date