Amanda F. Cashen, MD - Washington ...

Dr. Amanda Cashen, MD

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Washington University School of Medicine

Studies Acute Myeloid Leukemia
Studies Non-Hodgkin's Lymphoma
22 reported clinical trials
38 drugs studied

About Amanda Cashen, MD

Education:

  • MD from Washington University School of Medicine, 2015.

Experience:

  • Completed Residency in Internal Medicine at Barnes-Jewish Hospital/Washington University School of Medicine, 2018.
  • Finished Fellowship in Hematology and Oncology at Washington University School of Medicine, 2021.
  • Serving as an Assistant Professor of Medicine at Washington University School of Medicine since 2023.

Area of expertise

1

Acute Myeloid Leukemia

Amanda Cashen, MD has run 8 trials for Acute Myeloid Leukemia. Some of their research focus areas include:

Stage IV
2

Non-Hodgkin's Lymphoma

Amanda Cashen, MD has run 5 trials for Non-Hodgkin's Lymphoma. Some of their research focus areas include:

CD20 positive
Stage I
Stage II

Affiliated Hospitals

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Washington University School Of Medicine

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Siteman Cancer Center At West County Hospital

Clinical Trials Amanda Cashen, MD is currently running

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Thiotepa + Stem Cell Transplant

for Lymphoma

A serious consequence of systemic diffuse large B-cell lymphoma (DLBCL) is secondary central nervous system (CNS) relapse, which occurs in approximately 5% of all patients. Many CNS relapses occur within the first year after completion of frontline treatment and are associated with significantly increased mortality; thus, it is important to tailor frontline treatment to provide prophylaxis against CNS relapse in those patients who are determined to be high-risk. Autologous stem cell transplantation (ASCT) is standard of care for patients with DLBCL who relapse one year or more after first remission, and it has been shown to improve progression-free survival for patients with primary CNS lymphoma. The four-drug BEAM regimen (carmustine, etoposide, cytarabine, and melphalan) is the preferred conditioning regimen for DLBCL patients undergoing ASCT; however, patients with primary CNS lymphoma receive thiotepa plus carmustine as their conditioning regimen due to its better CNS penetration. This study tests the hypothesis that consolidation thiotepa/carmustine ASCT in first complete remission will reduce the risk of CNS relapse in transplant-eligible patients with DLBCL with no prior CNS disease at high risk of secondary CNS recurrence.

Recruiting

1 award

Phase 2

3 criteria

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Memory-like NK Cells after Haploidentical Transplant

for AML

This trial represents a single institution phase I/II pilot study with the primary objective of establishing the safety and feasibility of generating and infusing ML NK cells after TCRαβ haplo-HCT.

Recruiting

1 award

Phase 1 & 2

12 criteria

More about Amanda Cashen, MD

Clinical Trial Related

9 years of experience running clinical trials · Led 22 trials as a Principal Investigator · 4 Active Clinical Trials

Treatments Amanda Cashen, MD has experience with

  • Cytokine Induced Memory-like NK Cell Adoptive Therapy
  • Nivolumab
  • Rituximab
  • Fludarabine
  • Mosunetuzumab
  • Autologous Hematopoietic Stem Cell Transplantation

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