Amplifying Outcomes: Checkpoint Inhibitor Combinations in First-Line Non-Small Cell Lung Cancer

Author:

Melosky Barbara1,Juergens Rosalyn2,Hirsh Vera3,McLeod Deanna4,Leighl Natasha5,Tsao Ming-Sound5,Card Paul B.4,Chu Quincy6

Affiliation:

1. BC Cancer Agency Vancouver Centre, Vancouver, British Columbia, Canada

2. Division of Medical Oncology, McMaster University, Juravinski Cancer Centre, Hamilton, Ontario, Canada

3. Montreal General Hospital, Royal Victoria Hospital and Department of Oncology, McGill University, Montreal, Quebec, Canada

4. Kaleidoscope Strategic Inc. Toronto, Ontario, Canada

5. Princess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, Ontario, Canada

6. Cross Cancer Institute and Department of Oncology, University of Alberta, Edmonton, Alberta, Canada

Abstract

Abstract Purpose Lung cancer is one of the most common types of cancer, resulting in approximately 1.8 million deaths worldwide. Immunotherapy using checkpoint inhibitors has become standard of care in advanced non-small cell lung cancer (NSCLC), and there is increasing interest in further improving outcomes through combination with other therapeutics. This systematic review evaluates emerging phase III data on the efficacy and safety of checkpoint inhibitor combinations as first-line treatment for advanced NSCLC. Materials and Methods Published and presented literature was searched using the key search terms “non-small cell lung cancer” AND “checkpoint-inhibitors” (OR respective aliases) AND phase III trials. Seven randomized phase III clinical trials reporting outcomes on checkpoint inhibitor combinations in first-line advanced NSCLC were identified. Results Four first-line trials reported outcomes for checkpoint inhibitor combinations in nonsquamous NSCLC. Pembrolizumab-chemotherapy, atezolizumab-chemotherapy, and atezolizumab-bevacizumab-chemotherapy showed significantly improved overall survival compared with controls in patients with advanced nonsquamous epidermal growth factor receptor-negative (EGFR−)/ anaplastic lymphoma kinase gene (ALK)− NSCLC. Two trials reported outcomes for squamous NSCLC, with pembrolizumab-chemotherapy reporting significantly improved overall survival (OS) compared with chemotherapy. The combination of nivolumab-ipilimumab in all-comer histology failed to improve OS compared with histology appropriate chemotherapy in patients regardless of their tumor mutational burden status. Based on improved survival and safety, either pembrolizumab monotherapy or pembrolizumab-chemotherapy administered based on PD-L1 status and histology is a preferred treatment option. Outcomes for atezolizumab-bevacizumab-chemotherapy in EGFR+/ALK+ patients are promising and require further exploration. Conclusion First-line checkpoint inhibitors added to standard therapies improve overall survival for nonsquamous EGFR−/ALK− and squamous advanced NSCLC.

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

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