Site-Specific Response and Resistance Patterns in Patients with Advanced Non-Small-Cell Lung Cancer Treated with First-Line Systemic Therapy

Author:

Brown Lauren Julia1234ORCID,Ahn Julie25,Gao Bo123ORCID,Gee Harriet3456,Nagrial Adnan123,Hau Eric2345,Silva Inês Pires da1237

Affiliation:

1. Department of Medical Oncology, Westmead Hospital, Sydney, NSW 2145, Australia

2. Blacktown Cancer and Haematology Centre, Blacktown Hospital, Sydney, NSW 2148, Australia

3. Faculty of Medicine and Health, University of Sydney, Camperdown, NSW 2050, Australia

4. Westmead Institute for Medical Research, Westmead, NSW 2145, Australia

5. Sydney West Radiation Oncology Network (SWRON), Sydney, NSW 2145, Australia

6. Children’s Medical Research Institute, Westmead, NSW 2145, Australia

7. Melanoma Institute Australia, Wollstonecraft, NSW 2065, Australia

Abstract

Patients with advanced NSCLC have heterogenous responses to immune checkpoint inhibitors (ICIs) with or without chemotherapy. In NSCLC, the impact of the distribution of metastatic sites and the response to systemic therapy combinations remain poorly understood. In a retrospective cohort study of patients with unresectable stage III/IV NSCLC who received first-line systemic therapy, we sought to assess the association between the site of metastases with patterns of response and progression. Data regarding demographics, tumour characteristics (including site, size, and volume of metastases), treatment, and outcomes were examined at two cancer care centres. The endpoints included organ site-specific response rate, objective response rate (ORR), progression-free survival (PFS), and overall survival (OS). Two-hundred and eighty-five patients were included in the analysis. In a multivariate analysis, patients with bone metastases had a reduced ORR, PFS, and OS. Primary resistance was also more likely in patients with bone metastases. Patients with bone or liver metastases had a shorter OS when receiving ICIs with or without chemotherapy, but not with chemotherapy alone, suggesting an immunological basis for therapeutic resistance. A directed assessment of the tumour microenvironment in these locations and a deeper understanding of the drivers of organ-specific resistance to immunotherapy are critical to optimise novel combination therapies and sequencing in these patients.

Funder

Western Sydney Local Health District 2023 Research and Education Network Grant

Jerry Koutt’s ICPMR Postgraduate Scholarship

University of Sydney Postgraduate Award

Publisher

MDPI AG

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