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.

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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64Cu-LLP2A Imaging

for Blood Cancers

This phase of the protocol (protocol part B), seeks to evaluate the new formulation in healthy normal volunteers to confirm the new formulation provides comparable human dosimetry to which was seen and published in protocol part A. Additionally, the new formulation will be studied utilizing an expanded patient population to include patients with confirmed diagnosis of multiple myeloma (MM), low-grade lymphoma, or MM and lymphoma patients who are status post bone marrow transplant (BMT) with negative imaging and suspected recurrence.

Recruiting

1 award

Phase < 1

4 criteria

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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

More about Amanda Cashen, MD

Clinical Trial Related

9 years of experience running clinical trials · Led 22 trials as a Principal Investigator · 5 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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