Semin Respir Crit Care Med 2016; 37(05): 771-782
DOI: 10.1055/s-0036-1592298
Review Article
Thieme Medical Publishers 333 Seventh Avenue, New York, NY 10001, USA.

Immunotherapy for Lung Cancer: No Longer an Abstract Concept

Kristen A. Marrone
1   Division of Upper Aerodigestive, Department of Oncology, Sidney Kimmel Cancer Center at Johns Hopkins University, Baltimore, Maryland
,
Jarushka Naidoo
1   Division of Upper Aerodigestive, Department of Oncology, Sidney Kimmel Cancer Center at Johns Hopkins University, Baltimore, Maryland
,
Julie R. Brahmer
1   Division of Upper Aerodigestive, Department of Oncology, Sidney Kimmel Cancer Center at Johns Hopkins University, Baltimore, Maryland
› Author Affiliations
Further Information

Publication History

Publication Date:
12 October 2016 (online)

Abstract

The treatment paradigm for lung cancer has been transformed in recent years by the use of immunotherapy, specifically, immune checkpoint antibodies (mAb), which are agents designed to reinvigorate an immune-mediated anticancer response by releasing the effects of tumor-mediated immunosuppression. Late-phase clinical trials of these agents in patients with advanced lung cancers have translated into improved clinical outcomes compared with standard-of-care chemotherapy for the treatment of metastatic non-small cell lung cancer, and have resulted in FDA approvals for two immune checkpoint mAbs in the second-line setting. In addition, promising results have been seen in early-phase clinical studies in small cell lung cancer (SCLC) and for immune checkpoint combinations in NSCLC thus far. While the efficacy of these agents is exciting, they have also been associated with a unique profile of immune-mediated toxicity that is distinct from classic cytotoxic therapies. As these agents move into the lung cancer clinic, we must seek to maximize the therapeutic potential of this class of agents through optimization of patient selection, improved response assessments, and exploring rational combinations of immune checkpoint mAbs with other potentially synergistic therapies, to improve response rates and extend the “tail on the curve.”

 
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