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Dr. Kobos is on Doximity

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  • Office

    1275 York Ave
    # Memorial
    New York, NY 10065
    Phone+1 212-639-5966

Education & Training

  • New York Presbyterian Hospital (Cornell Campus)
    New York Presbyterian Hospital (Cornell Campus)Fellowship, Pediatric Hematology/Oncology, 2005 - 2008
  • New York Presbyterian Hospital (Cornell Campus)
    New York Presbyterian Hospital (Cornell Campus)Residency, Pediatrics, 2002 - 2005
  • New York Medical College
    New York Medical CollegeClass of 2002

Certifications & Licensure

  • NY State Medical License
    NY State Medical License 2004 - 2026
  • American Board of Pediatrics Pediatrics
  • American Board of Pediatrics Pediatric Hematology-Oncology

Clinical Trials

Publications & Presentations

PubMed

Abstracts/Posters

  • Four-Year Follow-up of the Phase 3 Pollux Study of Daratumumab Plus Lenalidomide and Dexamethasone (D-Rd) Versus Lenalidomide and Dexamethasone (Rd) Alone in Relapsed ...
    Rachel Kobos, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/7/2019
  • Efficacy and Safety of Daratumumab, Bortezomib, and Dexamethasone (D-Vd) Versus Bortezomib and Dexamethasone (Vd) in First Relapse Patients (pts) with Multiple Myeloma...
    Rachel Kobos, 61st Annual American Society of Hematology Meeting, Orlando, FL, 12/8/2019
  • Effectiveness of Daratumumab in Combination with Lenalidomide and Dexamethasone (DRd) Vs. Common Standard-of-Care Regimens in Patients with Non-Transplant Newly Diagno...
    Rachel Kobos, 61st Annual American Society of Hematology Meeting, 61st Annual American Society of Hematology Meeting - Orlando, FL, 12/7/2019

Lectures

  • One-Year Update of a Phase 3 Randomized Study of Daratumumab Plus Bortezomib, Melphalan, and Prednisone (D-VMP) Versus Bortezomib, Melphalan, and Prednisone (VMP) in P... 
    2018 ASH Annual Meeting - San Diego, CA - 12/1/2018
  • Clofarabine with Topotecan, Vinorelbine, and Thiotepa (TVTC) in Children and Young Adults with Relapsed or Refractory Acute Myeloid Leukemia 
    2018 ASH Annual Meeting - San Diego, CA - 12/1/2018

Press Mentions

  • Janssen Presents Longer-Term Data for TECVAYLI® (Teclistamab-Cqyv) Showing a Duration of Response of 22 Months in Patients with Relapsed or Refractory Multiple Myeloma
    Janssen Presents Longer-Term Data for TECVAYLI® (Teclistamab-Cqyv) Showing a Duration of Response of 22 Months in Patients with Relapsed or Refractory Multiple MyelomaJune 10th, 2023
  • FDA Approves Biweekly Teclistamab Dosing Regimen for Patients with Multiple Myeloma
    FDA Approves Biweekly Teclistamab Dosing Regimen for Patients with Multiple MyelomaFebruary 22nd, 2024
  • FDA Approves Tecvayli at Reduced Dosing Frequency for Relapsed/Refractory Multiple Myeloma
    FDA Approves Tecvayli at Reduced Dosing Frequency for Relapsed/Refractory Multiple MyelomaFebruary 24th, 2024
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