Prognostic Impact of Dihydropyrimidine Dehydrogenase Germline Variants in Unresectable Non-Small Cell Lung Cancer Patients Treated with Platin-Based Chemotherapy

Author:

Guijarro-Eguinoa Javier1,Arjona-Hernandez Sara2,Stewart Stefan1ORCID,Pernia Olga34,Arias Pedro5,Losantos-García Itsaso6ORCID,Rubio Tania34,Burdiel Miranda34,Rodriguez-Antolin Carlos34ORCID,Cruz-Castellanos Patricia47,Higuera Oliver7ORCID,Borobia Alberto M.1,Rodriguez-Novoa Sonia8ORCID,de Castro-Carpeño Javier47ORCID,Ibanez de Caceres Inmaculada34ORCID,Rosas-Alonso Rocio45ORCID

Affiliation:

1. Clinical Pharmacology Department, La Paz University Hospital, 28046 Madrid, Spain

2. Laboratory Medicine Department, Puerta Del Mar University Hospital, 11009 Cadiz, Spain

3. Cancer Epigenetics Laboratory, Genetics Department, La Paz University Hospital, 28046 Madrid, Spain

4. Experimental Therapies and Novel Biomarkers in Cancer, Hospital La Paz Institute for Health Research—IdiPAZ, 28029 Madrid, Spain

5. Pharmacogenetics Laboratory, Genetics Department, La Paz University Hospital, 28046 Madrid, Spain

6. Biostatistics Department, Hospital La Paz Institute for Health Research—IdiPAZ, 28029 Madrid, Spain

7. Oncology Department, La Paz University Hospital, 28046 Madrid, Spain

8. Genetics of Metabolic Diseases Laboratory, Genetics Department, La Paz University Hospital, 28046 Madrid, Spain

Abstract

Platin-based chemotherapy is the standard treatment for patients with non-small cell lung cancer (NSCLC). However, resistance to this therapy is a major obstacle in successful treatment. In this study, we aimed to investigate the impact of several pharmacogenetic variants in patients with unresectable NSCLC treated with platin-based chemotherapy. Our results showed that DPYD variant carriers had significantly shorter progression-free survival and overall survival compared to DPYD wild-type patients, whereas DPD deficiency was not associated with a higher incidence of high-grade toxicity. For the first time, our study provides evidence that DPYD gene variants are associated with resistance to platin-based chemotherapy in NSCLC patients. Although further studies are needed to confirm these findings and explore the underlying mechanisms of this association, our results suggest that genetic testing of DPYD variants may be useful for identifying patients at a higher risk of platin-based chemotherapy resistance and might be helpful in guiding future personalized treatment strategies in NSCLC patients.

Funder

Instituto de Salud Carlos III

Publisher

MDPI AG

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Computer Science Applications,Spectroscopy,Molecular Biology,General Medicine,Catalysis

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