Mark N. Stein, MD, Medical Oncology ...

Dr. Mark N. Stein

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Columbia University Irving Medical Center

Expert in Prostate Cancer
Studies Cancer
18 reported clinical trials
33 drugs studied

Area of expertise

1

Prostate Cancer

Global Leader

Mark N. Stein has run 12 trials for Prostate Cancer. Some of their research focus areas include:

Stage IV
MET positive
KIT positive
2

Cancer

Mark N. Stein has run 6 trials for Cancer. Some of their research focus areas include:

Stage IV

Affiliated Hospitals

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Columbia University Irving Medical Center

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Columbia University Medical Center

Clinical Trials Mark N. Stein is currently running

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Surgery + Immunotherapy + Targeted Therapy

for Kidney Cancer

The purpose of this study is to determine if the use of immunotherapy nivolumab and the targeted therapy cabozantinib prior to removal of the kidney, will increase the number subjects who are without any visible kidney cancer in their body at some point during the course of treatment.

Recruiting

1 award

Phase 2

10 criteria

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Registry

for Advanced Prostate Cancer

Our intent is to establish the International Registry to Improve Outcomes in Men with Advanced Prostate Cancer (IRONMAN) as a prospective, international cohort of minimum 5,000 men with advanced cancer, including men with mHSPC and M0/M1 CRPC. The goal is to establish a population-based registry and recruit patients across academic and community practices from Australia, Barbados, Brazil, Canada, Ireland, Jamaica, Kenya, Nigeria, Norway, Spain, South Africa, Sweden, Switzerland, the United Kingdom (UK), and the United States (US). Target accrual number and number of participating sites are subject to change based on accrual, funding, and interest in participation by other international sites. This cohort study will facilitate a better understanding of the variation in care and treatment of advanced prostate cancer across countries and across academia and community based practices. Detailed data will be collected from patients at study enrollment and then during follow-up, for a minimum of five years. Patients will be followed prospectively for overall survival, clinically significant adverse events, comorbidities, changes in cancer treatments, and PROMs. PROMs questionnaires will be collected at enrollment and every three months thereafter. Physician Questionnaires will be collected from all participating sites at patient enrollment, time of first change in treatment and/or one year follow-up, at each subsequent change of treatment, and discontinuation of treatment. As such, this registry will help identify the treatment sequences or combinations that optimize overall survival and PROMs for men with mHSPC and M0/M1 CRPC. By collecting blood at enrollment, time of first change in treatment and/or one year follow-up (plasma, cell free DNA, buffy coat / RNA), this registry will further identify and validate molecular phenotypes of disease that predict response and resistance to specific therapeutics. Additionally, every effort will be made to collect blood specimen at each subsequent change in treatment due to progression of disease. When feasible, existing tumor tissue may be collected for correlation with described blood based studies. All samples will be used for future research. This cohort study will provide the research community with a unique biorepository to identify biomarkers of treatment response and resistance.

Recruiting

1 award

N/A

5 criteria

More about Mark N. Stein

Clinical Trial Related

3 years of experience running clinical trials · Led 18 trials as a Principal Investigator · 4 Active Clinical Trials

Treatments Mark N. Stein has experience with

  • Nivolumab
  • Cabozantinib
  • Degarelix
  • Docetaxel
  • Leuprolide Acetate
  • REGN2810

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