Victor Lewis | UCalgary Profiles ...

Dr. Victor Lewis, MD

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Alberta Children's Hospital

Studies Cancer
Studies Acute Lymphoblastic Leukemia
28 reported clinical trials
81 drugs studied

About Victor Lewis, MD

Education:

  • Completed medical training in Pakistan.

Experience:

  • Served as an internist before specializing further.
  • Retrained in Pediatrics, Pediatric Hematology/Oncology, and Transplantation at the University of Minnesota, USA.
  • Has been with the University of Calgary and Alberta Children's Hospital since 2002, focusing on pediatric leukemia, lymphoma, and transplantation.
  • Currently the Director of the Oncology and Blood and Marrow Transplant sections at Alberta Children's Hospital.
  • Co-leads both the Phase I/II program and the developmental therapeutics program at the institution.

Area of expertise

1

Cancer

Victor Lewis, MD has run 6 trials for Cancer. Some of their research focus areas include:

Stage I
Stage IV
Stage II
2

Acute Lymphoblastic Leukemia

Victor Lewis, MD has run 5 trials for Acute Lymphoblastic Leukemia. Some of their research focus areas include:

BCR-ABL1 fusion positive
ABL-class fusion positive
Philadelphia chromosome positive

Affiliated Hospitals

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Alberta Children's Hospital

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Alberta Children's Hospital (Adults And Pediatrics)

Clinical Trials Victor Lewis, MD is currently running

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Inotuzumab Ozogamicin

for Acute Lymphoblastic Leukemia

This phase III trial studies whether inotuzumab ozogamicin added to post-induction chemotherapy and immunotherapy (chemo-immunotherapy) for patients with High-Risk B-cell Acute Lymphoblastic Leukemia (B-ALL) improves outcomes. Inotuzumab ozogamicin is a monoclonal antibody, which is a type of protein that can bind to certain targets on the surface of cells. Inotuzumab ozogamicin is a monoclonal antibody that is linked to a type of chemotherapy called calicheamicin. Inotuzumab attaches to cancer cells by binding to the CD22 protein on the surface of the cancer cell and delivering calicheamicin inside the cells to kill them. Other drugs used in the chemotherapy regimen, such as cyclophosphamide, cytarabine, dexamethasone, doxorubicin, daunorubicin, methotrexate, leucovorin, mercaptopurine, prednisone, thioguanine, vincristine, and pegaspargase or calaspargase pegol work in different ways to stop the growth of cancer cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Blinatumomab is a specialized type of monoclonal antibody known as a bispecific T-cell engager (BiTE). It works by simultaneously binding to CD19 on cancer cells and CD3 on normal immune cells, bringing them together to destroy leukemia cells. Blinatumomab is a standard part of chemo-immunotherapy treatment for B-ALL. This trial also studies the outcomes of patients with mixed phenotype acute leukemia (MPAL), and B-lymphoblastic lymphoma (B-LLy) when treated with ALL therapy without inotuzumab ozogamicin or blinatumomab. The overall goal of this study is to understand if adding inotuzumab ozogamicin to standard of care chemo-immunotherapy maintains or improves outcomes in High Risk B-cell Acute Lymphoblastic Leukemia (HR B-ALL). The first part of the study includes the first phase of therapy: Induction. This part will collect information on the leukemia, as well as the effects of the initial treatment, to classify patients into post-induction treatment groups. On the second part of this study, patients with HR B-ALL will receive the remainder of the chemotherapy cycles (consolidation, blinatumomab block 1, interim maintenance 1, blinatumomab block 2, delayed intensification, interim maintenance 2, maintenance), with some patients randomized to receive inotuzumab. The patients that receive inotuzumab will not receive part of consolidation or part of delayed intensification. Other aims of this study include evaluating 1) side effects of treatment using patient-reported outcomes and health-related quality of life, 2) the best ways to help patients adhere to oral chemotherapy regimens, 3) the relationship between levels of inotuzumab ozogamicin in the blood and side effects, 4) the impact of chemo-immunotherapy on the immune system and risk of infection, and 5) the impact of social determinants of health on outcomes. Finally, this study will be the first to track the outcomes of subjects with disseminated B-cell Lymphoblastic Leukemia (B-LLy) or Mixed Phenotype Acute Leukemia (MPAL) when treated with B-ALL chemotherapy.

Recruiting

2 awards

Phase 3

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Tabelecleucel

for Post-Transplant Cancer

The purpose of this study is to determine the clinical benefit and characterize the safety profile of tabelecleucel for the treatment of Epstein-Barr virus-associated post-transplant lymphoproliferative disease (EBV+ PTLD) in the setting of (1) solid organ transplant (SOT) after failure of rituximab (SOT-R) and rituximab plus chemotherapy (SOT-R+C) or (2) allogeneic hematopoietic cell transplant (HCT) after failure of rituximab.

Recruiting

2 awards

Phase 3

12 criteria

More about Victor Lewis, MD

Clinical Trial Related

6 years of experience running clinical trials · Led 28 trials as a Principal Investigator · 14 Active Clinical Trials

Treatments Victor Lewis, MD has experience with

  • Cyclophosphamide
  • Etoposide
  • Radiation Therapy
  • Vincristine Sulfate
  • Carboplatin
  • Dexamethasone

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