Harvard Medical School Aug 2018 - Jul 2019
Faculty Member
Unum Therapeutics Aug 2018 - Jul 2019
Senior Medical Director
Beth Israel Deaconess Medical Center Apr 2018 - Jun 2019
Director of Phase I Clinical Research
Spring Bank Pharmaceuticals, Inc. May 2019 - Jun 2019
Consultant
Beth Israel Deaconess Medical Center Aug 2018 - Jun 2019
Associate Member, Cancer Research Institute
Education:
Arizona State University - W. P. Carey School of Business 2012 - 2013
Master of Business Administration, Masters, Finance
Rutgers University
Bachelors, Bachelor of Arts, Biology
Sackler School of Medicine
Doctor of Medicine, Doctorates, Medicine
Skills:
Oncology Clinical Trials Clinical Research Translational Research Molecular Biology Cancer Research Cancer Medicine Drug Development Biotechnology Genomics Biomarkers Pharmacology Immunology Laboratory Translational Medicine Drug Discovery Genetics Clinical Development Mirna Medical Research Immunohistochemistry Assay Development Lung Cancer Medical Writing Personalized Medicine Molecular Diagnostics Molecular Genetics
Cancer Treatment Centers of America 14200 W Celebrate Life Way, Goodyear, AZ 85338 6232073000 (Phone)
Procedures:
Biological Therapy Chemotherapeutic Agents Chemotherapy Medical Oncology
Conditions:
Cancer Cancer Treatment (Oncology) Complications Hematologic Malignancies Lung Cancer Skin Cancer Thoracic Cancers
Languages:
English
Hospitals:
Cancer Treatment Centers of America 14200 W Celebrate Life Way, Goodyear, AZ 85338
Cancer Treatment Centers of America at Western Regional Medical Center 14200 West Fillmore Street, Goodyear, AZ 85338
Philosophy:
I deliver novel, targeted and investigational therapies to advanced cancer patients," says Dr. Glen Weiss on his role at Cancer Treatment Centers of America. "Using new tools in genomics and proteomics, I help design personalized therapies for advanced cancer patients based on the unique biology of their tumor. I design and collaborate on clinical trials, and specialize in thoracic cancer, skin cancers and rare uncommon cancers.
Education:
Medical School Tel Aviv University / Sackler Faculty Of Medicine Medical School SUNY Downstate Medical Center Medical School University Of Colorado Health Sciences Center
Dr. Weiss graduated from the Columbia University College of Physicians and Surgeons in 1992. He works in Garnerville, NY and 1 other location and specializes in Ophthalmology. Dr. Weiss is affiliated with Good Samaritan Regional Medical Center and Nyack Hospital.
Cancer Treatment Center Of America 14200 W Celebrate Life Way, Goodyear, AZ 85338 6232073307 (phone), 6232073921 (fax)
Education:
Medical School Tel Aviv Univ, Sackler Sch of Med, Tel Aviv Yafo, Israel Graduated: 2001
Procedures:
Chemotherapy
Conditions:
Cervical Cancer Non-Hodgkin's Lymphoma Rectal, Abdomen, Small Intestines, or Colon Cancer Uterine Cancer
Languages:
English
Description:
Dr. Weiss graduated from the Tel Aviv Univ, Sackler Sch of Med, Tel Aviv Yafo, Israel in 2001. He works in Goodyear, AZ and specializes in Hematology/Oncology. Dr. Weiss is affiliated with Cancer Treatment Centers Of America At Western Regional Medical Center.
Disclosed herein are methods used in the identification of cancer patients likely or unlikely to respond to systemic chemotherapy, methods of treating cancer patients based upon the identification, and kits that facilitate the identification. The methods and kits involve detecting the expression of specific microRNA.
Provided herein are methods for identifying a cancer patient responsive to treatment with an EGFR tyrosine kinase inhibitor. One method comprises obtaining a biopsy from the patient and measuring the number of copies of miR-128in DNA extracted from the biopsy. A patient responsive to EGFR tyrosine kinase inhibitor treatment has a cancer with less than two copies of miR-128DNA. Another method comprises measuring miR-128or miR-128level in a biopsy obtained from the patient and comparing that level to miR-128or miR-128level in a normal tissue sample. A patient responsive to treatment with an EGFR tyrosine kinase inhibitor has a cancer expressing a lower level of miR-128or miR-128relative to normal tissue. Further provided herein are methods for treating cancer in a patient in need thereof. One method comprises measuring the level of miR-128or miR-128in a biopsy obtained from the patient and administering to the patient an EGFR tyrosine kinase inhibitor. Another method comprises measuring the number of copies of miR-128in DNA extracted from a biopsy obtained from the patient and administering to the patient an EGFR tyrosine kinase inhibitor. A further method comprises administering to a cancer patient an EGFR tyrosine kinase inhibitor and an miR-128inhibitor, administering an miR-128a mimic, or administering an miR-128mimic. Also provided herein are compositions used to treat cancer in a patient. The compositions comprise an EGFR tyrosine kinase inhibitor and an miR-128inhibitor (or an miR-128inhibitor), and the cancer is characterized as having 2 or more copies of miR-128DNA at the cellular level.
Methods And Kits To Predict Therapeutic Outcome Of Tyrosine Kinase Inhibitors
Methods of using specific microRNA to identify subjects with non-small cell lung cancer likely or unlikely to respond to treatment with tyrosine kinase inhibitors such as erlotinib, sunitinib, or vandetanib; methods of treating subjects based on identification of said subjects as likely to respond to treatment with tyrosine kinase inhibitors; and kits that facilitate the performance of the methods are disclosed.
Methods Of Predicting The Risk Of Recurrence Of Cancer
This disclosure provides a biomarker profile, which is linked to cancer cell chemo-resistance. The disclosure further provides methods of diagnosis and theranosis, and screening of new therapeutic agents using these biomarkers in the profile, and kits for employing these methods and compositions.
Systems And Methods Of Cancer Staging And Treatment
Methods of assessing the sensitivity of a cancer cell to a tyrosine kinase inhibitor are disclosed. Such methods include assessing the expression of miR-497 and correlating reduced expression with sensitivity to the tyrosine kinase inhibitor. Also disclosed are methods of assessing the sensitivity of a cell to a tyrosine kinase inhibitor that includes assessing the expression of FGF1, HOXC10, and/or LHFP. Additionally disclosed are methods of treating patients with tyrosine kinase inhibitors such as sunitinib based on results obtained from the disclosed methods and kits that facilitate the methods.
Mot Cells As A Therapeutic Screening Tool For Regulatory T-Cell Activity
- SCOTTSDALE AZ, US - Rochester MN, US Glen J. WEISS - Phoenix AZ, US
International Classification:
G01N 33/50
Abstract:
The present invention includes a method for screening one or more agents that modulate Regulatory T cell (Treg) activity, the method comprising the steps of: incubating a population CD4+ cells isolated from human blood peripheral mononuclear cells the CD4+ cells in contact with MoT cells in the presence of the one or more agents suspected of modulating Treg activity; detecting activation of the CD4+ cells without or with the agent; and comparing the activation of the CD4+ cells without or with the agent, wherein a change in activation following incubation with the agent relative to the activation of the PBMCs following incubation without the agent indicates that the agent is a modulator of Treg activity.
cell cancers, preventing development, growth and survival of certain cancer cells. Results showed a durable clinical benefit tumor shrinkage visible on X-ray or other physical exam or improvement in symptoms without tumor growth," said Glen Weiss, MD, director of Thoracic Oncology at Virginia G. P