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Prasanna Ananth, MD, MPH

Associate Professor of Pediatrics (Hematology Oncology)

Contact Information

Prasanna Ananth, MD, MPH

Research Summary

Dr. Ananth's research focuses on investigating ways to optimize supportive and palliative care for children with advanced cancer. Prior work explored how children with chronic, life-threatening illness utilize hospital resources in the last year of life; pediatric palliative care mitigates hospital use; enrollment in early phase clinical trials influences end-of-life care; and how providers, patients, and families perceive medical marijuana in pediatric oncology practice. Her ongoing work seeks to define attributes of high quality care for children with advanced cancer.

Extensive Research Description

Dr. Ananth's primary research agenda is to investigate mechanisms of optimizing supportive and palliative care for children with advanced cancer. Among adults with cancer, intense end-of-life care is defined by metrics such as hospitalizations in the last weeks of life and delayed hospice referral. No comparable quality measures exist for children with advanced cancer. In a published multi-center study, Dr. Ananth and her colleagues previously identified that children with cancer spend a substantial proportion of their last year of life admitted to the hospital, receiving interventions such as surgeries or mechanical ventilation. In two subsequent studies, they found that pediatric palliative care consultation may have a measurable impact on reducing hospital resource use and that enrollment in early phase clinical trials may influence timing of palliative care engagement. This has yielded her current research, in which she is developing patient- and family-centered, provider-informed quality measures that can be used to assess end-of-life care and develop prospective interventions.

Coauthors

Research Interests

Medical Oncology; Palliative Care; Pediatrics; Outcome Assessment, Health Care; Clinical Trials, Phase I as Topic; Medical Marijuana

Selected Publications

Clinical Trials

ConditionsStudy Title
Brain and Nervous System; PediatricsA Phase 3 Randomized Study of Selumetinib Versus Carboplatin/Vincristine in Newly Diagnosed or Previously Untreated Neurofibromatosis Type 1 (NF1) Associated Low-Grade Glioma (LGG)
Lymphoid LeukemiaA Phase II Trial of Tisagenlecleucel in First-line High-risk (HR) Pediatric and Young Adult Patients With B-cell Acute Lymphoblastic Leukemia (B-ALL) Who Are Minimal Residual Disease (MRD) Positive at the End of Consolidation (EOC) Therapy
Brain and Nervous SystemA Phase 3 Randomized Non-Inferiority Study of Carboplatin and Vincristine Versus Selumetinib (NSC# 748727) in Newly Diagnosed or Previously Untreated Low-Grade Glioma (LGG) Not Associated With BRAFV600E Mutations or Systemic Neurofibromatosis Type 1 (NF1)
Unknown SitesPrOspective Non-interventional Study in Patients With Locally Advanced or Metastatic TRK Fusion Cancer Treated With Larotrectinib
Brain and Nervous System; PediatricsA Target Validation/Phase1 Study of BGB-290 in Combination With Temozolomide in Adolescent and Young Adult IDH1/2 Newly Diagnosed and Recurrent Mutant Gliomas
Leukemia, not otherwise specified; Leukemia, other; PediatricsA Phase 3 Randomized Trial of Inotuzumab Ozogamicin (NSC#: 772518) for Newly Diagnosed High-Risk B-ALL; Risk-Adapted Post-Induction Therapy for High-Risk B-ALL, Mixed Phenotype Acute Leukemia, and Disseminated B-LLy
Leukemia, other; PediatricsA Phase 3 Trial Investigating Blinatumomab ( NSC# 765986) in Combination With Chemotherapy in Patients With Newly Diagnosed Standard Risk or Down Syndrome B-Lymphoblastic Leukemia (B-ALL) and the Treatment of Patients With Localized B-Lymphoblastic Lymphoma (B-LLy)
Leukemia, not otherwise specified; Leukemia, otherA Phase IB/II Study of Venetoclax (ABT-199) in Combination With Liposomal Vincristine in Patients With Relapsed or Refractory T-Cell or B-Cell Acute Lymphoblastic Leukemia
Bones and Joints; Kidney; Pediatrics; Soft TissuePhase 3 Accelerated BEP: A Randomised Phase 3 Trial of Accelerated Versus Standard BEP Chemotherapy for Patients With Intermediate and Poor-risk Metastatic Germ Cell Tumors
Bones and Joints; Brain and Nervous System; Leukemia, not otherwise specified; Leukemia, other; Lymphoid LeukemiaNCI-COG Pediatric MATCH (Molecular Analysis for Therapy Choice) Screening Protocol
Soft TissueA Phase 2 Study of Anti-PD-L1 Antibody (Atezolizumab) in Alveolar Soft Part Sarcoma
Other Male Genital; OvaryActive Surveillance, Bleomycin, Carboplatin, Etoposide, or Cisplatin in Treating Pediatric and Adult Patients With Germ Cell Tumors
Bones and Joints; Brain and Nervous System; Eye and Orbit; Hodgkin's Lymphoma; Kidney; Leukemia, other; Liver; Lymphoid Leukemia; Myeloid and Monocytic Leukemia; Non-Hodgkin's Lymphoma; Other Digestive Organ; Other Endocrine System; Other Female Genital; Other Male Genital; Other Respiratory and Intrathoracic Organs; Other Skin; Other Urinary; Ovary; Pediatrics; Small Intestine; Soft TissueThe Project: Every Child Protocol: A Registry, Eligibility Screening, Biology and Outcome Study
Unknown SitesEffects of Dexrazoxane Hydrochloride on Biomarkers Associated With Cardiomyopathy and Heart Failure After Cancer Treatment (HEART)
Brain and Nervous SystemBiomarkers in Tumor Tissue Samples From Patients With Newly Diagnosed Neuroblastoma or Ganglioneuroblastoma
Unknown SitesNeuropsychological and Behavioral Testing in Younger Patients With Cancer
PediatricsA Randomized Phase 3 Trial of Vinorelbine, Dactinomycin, and Cyclophosphamide (VINO-AC) Plus Maintenance Chemotherapy With Vinorelbine and Oral Cyclophosphamide (VINO-CPO) vs Vincristine, Dactinomycin and Cyclophosphamide (VAC) Plus VINO-CPO Maintenance in Patients With High Risk Rhabdomyosarcoma (HR-RMS)
PediatricsA Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of Relatlimab Plus Nivolumab in Pediatric and Young Adults With Hodgkin and Non-Hodgkin Lymphoma (RELATIVITY-069)
PediatricsA Phase 3 Study of Selumetinib (NSC# 748727) or Selumetinib in Combination With Vinblastine for Non-NF1, Non-TSC Patients With Recurrent or Progressive Low-Grade Gliomas (LGGs) Lacking BRAFV600E or IDH1 Mutations