Prakash Satwani

ORCID: 0000-0003-3867-9066
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About
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Research Areas
  • Hematopoietic Stem Cell Transplantation
  • Acute Lymphoblastic Leukemia research
  • Immune Cell Function and Interaction
  • Childhood Cancer Survivors' Quality of Life
  • CAR-T cell therapy research
  • Acute Myeloid Leukemia Research
  • Renal Transplantation Outcomes and Treatments
  • Cytomegalovirus and herpesvirus research
  • Neutropenia and Cancer Infections
  • Lymphoma Diagnosis and Treatment
  • Hemoglobinopathies and Related Disorders
  • Polyomavirus and related diseases
  • Immunotherapy and Immune Responses
  • T-cell and B-cell Immunology
  • Immunodeficiency and Autoimmune Disorders
  • Virus-based gene therapy research
  • Prenatal Screening and Diagnostics
  • Autoimmune and Inflammatory Disorders Research
  • Neonatal Respiratory Health Research
  • Transplantation: Methods and Outcomes
  • Pneumocystis jirovecii pneumonia detection and treatment
  • Mesenchymal stem cell research
  • Chronic Lymphocytic Leukemia Research
  • Hematological disorders and diagnostics
  • Neonatal Health and Biochemistry

Columbia University
2015-2025

Columbia University Irving Medical Center
2016-2025

New York Hospital Queens
2006-2024

NewYork–Presbyterian Hospital
2006-2024

Pediatrics and Genetics
2004-2021

Morgan Stanley Children's Hospital
2008-2021

Mahatma Gandhi Memorial Medical College
2020-2021

In-Q-Tel
2015

Presbyterian Hospital
2004-2013

Naval Medical Center Portsmouth
2013

Although transplant practices have changed over the last decades, no information is available on trends in incidence and outcome of chronic graft-versus-host disease (cGVHD) time. This study used central database Center for International Blood Marrow Transplant Research (CIBMTR) to describe time cGVHD incidence, nonrelapse mortality, risk factors cGVHD. The 12-year period was divided into 3 intervals, 1995 1999, 2000 2003, 2004 2007, included 26,563 patients with acute leukemia, myeloid...

10.1016/j.bbmt.2014.10.021 article EN cc-by-nc-nd Biology of Blood and Marrow Transplantation 2014-10-30

Tisagenlecleucel is a CD19-specific chimeric antigen receptor T-cell therapy, US Food and Drug Administration-approved for children, adolescents, young adults (CAYA) with relapsed and/or refractory (RR) B-cell acute lymphoblastic leukemia (B-ALL). The Administration registration tisagenlecleucel was based on complete response (CR) rate of 81%, 12-month overall survival (OS) 76%, event-free (EFS) 50%. We report clinical outcomes analyze covariates after commercial tisagenlecleucel.We...

10.1200/jco.20.03585 article EN Journal of Clinical Oncology 2021-12-09

Steroid-refractory acute graft-versus-host disease (SR-aGVHD) following hematopoietic cell transplantation (HSCT) is associated with poor clinical outcomes. Currently, there are no safe and effective therapies approved for use in the pediatric population under age of 12 years. Accordingly, an urgent need new treatments that safe, well tolerated, managing this debilitating potentially fatal complication HSCT. In early phase trials, mesenchymal stromal cells (MSCs) have demonstrated efficacy...

10.1016/j.bbmt.2020.01.018 article EN cc-by-nc-nd Biology of Blood and Marrow Transplantation 2020-02-01

Abstract Purpose Pediatric oncology patients undergoing active chemotherapy are suspected to be at a high risk for severe disease secondary acute respiratory syndrome coronavirus‐2 (SARS‐CoV‐2) infection; however, data support this lacking. We aim describe the characteristics of coronavirus 2019 (COVID‐19) in population and also its impact on pediatric cancer care New York region during peak pandemic. Patients Methods This multicenter, retrospective study included 13 institutions. Clinical...

10.1002/pbc.28843 article EN Pediatric Blood & Cancer 2020-12-18

Chimeric antigen receptor (CAR) T cells provide a therapeutic option in hematologic malignancies. However, treatment failure after initial response approaches 50%. In allogeneic hematopoietic cell transplantation, optimal fludarabine exposure improves immune reconstitution, resulting lower nonrelapse mortality and increased survival. We hypothesized that lymphodepleting chemotherapy before CAR T-cell therapy would improve outcomes. retrospective analysis of patients with relapsed/refractory...

10.1182/bloodadvances.2021006418 article EN cc-by-nc-nd Blood Advances 2021-11-17

Nonresponse and relapse after CD19-chimeric antigen receptor (CAR) T-cell therapy continue to challenge survival outcomes. Phase II landmark data from the ELIANA trial demonstrated nonresponse rates of 14.5% 28%, respectively, whereas use in real-world setting showed 15% 37%. Outcome analyses describing fate post-CAR remain limited. Here, we aim establish outcomes both CD19+ CD19- relapses explore treatment variables associated with inferior survival.

10.1200/jco.22.01076 article EN Journal of Clinical Oncology 2022-09-15

Infants with B-cell acute lymphoblastic leukemia (B-ALL) have poor outcomes because of chemotherapy resistance leading to high relapse rates. Tisagenlecleucel, a CD19-directed chimeric antigen receptor T-cell (CART) therapy, is US Food and Drug Administration approved for relapsed or refractory B-ALL in patients ≤25 years; however, the safety efficacy this therapy young largely unknown children <3 years age were excluded from licensing studies. We retrospectively evaluated data Pediatric...

10.1182/bloodadvances.2021006393 article EN cc-by-nc-nd Blood Advances 2022-05-17

Allogeneic hematopoietic stem cell transplantation (allo-HSCT) with myeloablative conditioning is associated a 10%-40% risk of day +100 transplantation-related mortality (TRM). We evaluated the feasibility and safety reduced-toxicity allo-HSCT in 100 consecutive children adolescent recipients (mean age, 9.2 ± 6.8 years). The mean duration follow-up was 1278 1042 days. Fifty patients had malignant disease. median time to neutrophil recovery 18 days, platelet 43 Median donor chimerism...

10.1016/j.bbmt.2012.12.005 article EN cc-by-nc-nd Biology of Blood and Marrow Transplantation 2012-12-16

Sickle cell disease (SCD) is a hereditary hemoglobinopathy that affects over 100,000 people in the United States. Patients with SCD are known to experience suboptimal health-related quality of life (HRQoL). In addition physical manifestations SCD, psychological and social stress, along academic difficulties, secondary chronicity its complications often affect patients SCD. Although medical therapy has improved, allogeneic hematopoietic transplantation (allo-HCT) remains only curative...

10.1016/j.bbmt.2014.12.007 article EN cc-by-nc-nd Biology of Blood and Marrow Transplantation 2015-01-02

Clinical outcomes in children with steroid-refractory acute graft-versus-host disease (SR-aGVHD) are generally poor, a high mortality rate and limited therapeutic options. Here we report our updated investigational experience mesenchymal stromal cell (MSC) therapy remestemcel-L multicenter expanded access protocol (ClinicalTrials.gov identifier NCT00759018) 241 aGVHD who failed to respond steroids or without other secondary tertiary immunosuppressive therapies. A total of grade B-D SR-aGVHD...

10.1016/j.bbmt.2020.01.026 article EN cc-by-nc-nd Biology of Blood and Marrow Transplantation 2020-02-07

Chimeric antigen receptor (CAR) T cells have transformed the therapeutic options for relapsed/refractory (R/R) B-cell acute lymphoblastic leukemia. Data CAR therapy in extramedullary (EM) involvement are limited. Retrospective data were abstracted from Pediatric Real World Consortium (PRWCC) of 184 infused patients 15 US institutions. Response (complete response) rate, overall survival (OS), relapse-free (RFS), and duration aplasia (BCA) referred tisagenlecleucel with EM disease (both...

10.1182/bloodadvances.2021005564 article EN cc-by-nc-nd Blood Advances 2021-11-18

In humans receiving intestinal transplantation (ITx), long-term multilineage blood chimerism often develops. Donor T cell macrochimerism (≥4%) frequently occurs without graft-versus-host disease (GVHD) and is associated with reduced rejection. Here we demonstrate that patients had high (GvH) to host-versus-graft (HvG) clonal ratios in their allografts. These GvH clones entered the circulation, where peak levels were declines HvG early after transplant, suggesting reactions may contribute...

10.1172/jci141698 article EN Journal of Clinical Investigation 2021-02-25

Abstract Viral infections remain a major risk in immunocompromised pediatric patients, and virus-specific T cell (VST) therapy has been successful for treatment of refractory viral prior studies. We performed phase II multicenter study (NCT03475212) the patients with inborn errors immunity and/or post allogeneic hematopoietic stem transplant using partially-HLA matched VSTs targeting cytomegalovirus, Epstein-Barr virus, or adenovirus. Primary endpoints were feasibility, safety, clinical...

10.1038/s41467-024-47057-2 article EN cc-by Nature Communications 2024-04-18

BACKGROUND Autologous hematopoietic cell transplantation (auto‐HCT) is a standard therapy for relapsed classic Hodgkin lymphoma (cHL) and diffuse large B‐cell (DLBCL); however, long‐term outcomes are not well described. METHODS This study analyzed survival, nonrelapse mortality, late effects, subsequent malignant neoplasms (SMNs) in 1617 patients who survived progression‐free ≥2 years after auto‐HCT cHL or DLBCL between 1990 2008. The median age at was 40 years; the follow‐up 10.6 years....

10.1002/cncr.31114 article EN publisher-specific-oa Cancer 2017-11-10

Acute graft-versus-host disease (aGVHD) still remains a major limiting factor following allogeneic stem cell transplantation (AlloSCT) in pediatric recipients. Mycophenolate mofetil (MMF), an uncompetitive selective inhibitor of inosine monophosphate dehydrogenase, is new immunosuppressant agent without mucosal, hepatic, or renal toxicity compared to other prophylactic aGVHD drugs. Although there has been extensive pharmacokinetic (PK) experience with MMF administration solid organ children,...

10.1016/j.bbmt.2009.10.007 article EN cc-by-nc-nd Biology of Blood and Marrow Transplantation 2009-10-15

Summary Immune reconstitution appears to be delayed following myeloablative conditioning (MAC) and umbilical cord blood transplantation (UCBT) in paediatric recipients. Although reduced toxicity (RTC) versus MAC prior allogeneic stem cell is associated with decreased transplant‐related mortality, the effects of RTC UCBT on immune risk graft‐versus‐host disease (GVHD) are unknown. In 88 consecutive recipients UCBT, we assessed recovery immunoglobulin at days +100, 180 365 analysed factors...

10.1111/j.1365-2141.2011.08822.x article EN British Journal of Haematology 2011-08-16
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