Challenges faced when identifying patients for combination immunotherapy

Author:

Ernstoff Marc S1,Gandhi Shipra1,Pandey Manu2,Puzanov Igor1,Grivas Petros3,Montero Alberto3,Velcheti Vamsidhar3,Turk Mary Jo4,Diaz-Montero Claudia Marcela4,Lewis Lionel D5,Morrison Carl67

Affiliation:

1. Department of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA

2. Department of Medicine University of Buffalo Jacobs School of Medicine & Biomedical Sciences, Buffalo, NY, USA

3. Departments of Hematology-Oncology, Cleveland Clinic Foundation, Cleveland, OH, USA

4. Department of Immunology & Microbiology, Geisel School of Medicine, Lebanon, NH, USA

5. Department of Medicine, Geisel School of Medicine, Lebanon, NH, USA

6. Department of Pathology, Roswell Park Cancer Institute, Buffalo, NY, USA

7. OmniSeq, Buffalo, NY, USA

Abstract

In 1996, Jim Allison demonstrated that blocking the immune regulatory molecule CTLA-4 with anit-CTLA4 antibody led to enhance tumor responses in mice. It would take an additional 15 years for human studies to confirm the potency and clinical efficacy of anti-CTLA4, ultimately leading to US FDA approval of the first checkpoint inhibitor, ipilimumab. Now with a plethora of immune-modulating agents demonstrating single agent safety and benefit across many tumor types, investigation on the optimal combination of immune-based therapies has begun in earnest. While there are many challenges, a central one is how to select which combination for which patient is the best. Here we review the current approaches that a practitioner can use to achieve this therapeutic goal.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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