Immunotherapy in Non–Small Cell Lung Cancer: Facts and Hopes

Author:

Doroshow Deborah B.12,Sanmamed Miguel F.3456,Hastings Katherine2,Politi Katerina127,Rimm David L.127,Chen Lieping3,Melero Ignacio456,Schalper Kurt A.127,Herbst Roy S.12

Affiliation:

1. 1Department of Medicine (Section of Medical Oncology), Yale University School of Medicine, New Haven, Connecticut.

2. 2Yale Cancer Center, Yale University School of Medicine, New Haven, Connecticut.

3. 3Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut.

4. 4Clinica Universidad de Navarra and CIMA, Pamplona, Spain.

5. 5CIBERONC, Madrid, Spain.

6. 6Insitituto de Investigacion Sanitaria de Navarra (IDISNA), Pamplona, Spain.

7. 7Department of Pathology, Yale University School of Medicine, New Haven, Connecticut.

Abstract

AbstractImmune-checkpoint inhibitors (ICI), particularly inhibitors of the PD-1 axis, have altered the management of non–small cell lung cancer (NSCLC) over the last 10 years. First demonstrated to improve outcomes in second-line or later therapy of advanced disease, ICIs were shown to improve overall survival compared with chemotherapy in first-line therapy for patients whose tumors express PD-L1 on at least 50% of cells. More recently, combining ICIs with chemotherapy has been shown to improve survival in patients with both squamous and nonsquamous NSCLC, regardless of PD-L1 expression. However, PD-L1 and, more recently, tumor mutational burden have not proven to be straightforward indicative biomarkers. We describe the advances to date in utilizing these biomarkers, as well as novel markers of tumor inflammation, to ascertain which patients are most likely to benefit from ICIs. Ongoing translational work promises to improve the proportion of patients who benefit from these agents.

Funder

Yale SPORE in Lung Cancer

Miguel Servet

Publisher

American Association for Cancer Research (AACR)

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