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Poster session 15

1101P - Use of genomic sequencing for the determination of genomic alterations and new therapeutic opportunities in Spanish lung cancer (LC) patients (pts)

Date

10 Sep 2022

Session

Poster session 15

Topics

Genetic and Genomic Testing

Tumour Site

Small Cell Lung Cancer;  Non-Small Cell Lung Cancer

Presenters

Maria Rosario Garcia Campelo

Citation

Annals of Oncology (2022) 33 (suppl_7): S448-S554. 10.1016/annonc/annonc1064

Authors

M.R. Garcia Campelo1, E. Arriola2, D. Isla3, R. Bernabe Caro4, D. Perez Parente5, B. Moll5, J. Lavara Sanz5, S. Olson5, J. García González6

Author affiliations

  • 1 Dept. Medical Oncology, Instituto de Investigación Biomédica de A Coruña (INIBIC), 15006 - A Coruña/ES
  • 2 Medical Oncology Dept., Hospital del Mar - Parc de Salut Mar, 8003 - Barcelona/ES
  • 3 Medical Oncology Department, Hospital Clinico Universitario Lozano Blesa, 50009 - Zaragoza/ES
  • 4 Medical Oncology Department, Hospital Universitario Virgen del Rocio, 41013 - Seville/ES
  • 5 Medical Affairs Department, Roche Farma Spain, 28016 - Madrid/ES
  • 6 Medical Oncology Department, CHUS - Complejo Hospitalario Universitario de Santiago de Compostela SERGAS, 15706 - Santiago de Compostela/ES

Resources

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Abstract 1101P

Background

LC is the leading cause of cancer death worldwide. The accurate determination of genomic alterations can provide valuable information to find the best therapeutic approach for each pts. Thus, Foundation Medicine services were used to determine the genomic profile of Spanish LC pts with no previously identified mutations by immunohistochemistry in clinical practice.

Methods

Genomic profiling of LC pts who are likely to be refractory to previous treatments was carried out with FoundationOne® CDx (F1CDx) assay on DNA from tumour tissue or by FoundationOne®Liquid (F1Liquid) assay on circulating tumour DNA (ctDNA) from blood. Based on the results obtained, new therapeutic approaches and clinical trials were recommended.

Results

A total of 508 samples were analysed; 209 (41%) with F1CDx and 299 (59%) with F1Liquid. Overall, the most prevalent histologic diagnosis was adenocarcinoma (61%). The most common genomic alterations found in tumour tissue were tumour high mutational burden (TMB, 27%), EGFR (12%), ERBB2 (6%) and NF1 (6%), while in ctDNA were high TMB (13%), EGFR (18%), ERBB2 (3%) and MET (3%) (Table). Actionable alterations with at least one sensitizing therapy recommendation were detected in 57% of the solid samples and 42% of the ctDNA samples (Table). Actionable alterations with at least one clinical trial recommendation were detected in 89% and 68% of the tumour and ctDNA samples, respectively. Immunotherapies were recommended in 36.4% of pts, and targeted therapies in 62.6%. Table: 1101P

Genomic alterations and therapy recommendations in solid and liquid samples

Solid samples (n=209) Liquid samples (n=299)
Genomic alterations Therapy recommendations Genomic alterations Therapy recommendations
TMB 27% 47% 13% 30%
EGFR 12% 25% 18% 57%
ERBB2 6% 4% 3% 3%
NF1 6% 2% 2% 2%
MET 4% 1% 3% 1%
BRAF 4% 2% 2% 1%
ALK 4% 10% 1% 5%
RET 3% 2% 2% 1%
NTRK1 2% 1% - 1%
MAP2K1 1% 1% - -
ROS1 1% 3% - -
CD274 1% 1% - -
NRAS 1% - 1% -
HRAS 1% - - -
NF2 1% - - -
STK11 1% - - -

Conclusions

To date, this is the largest study characterizing the genomic profile of Spanish LC pts in this setting. Our results show that pts without previously identified mutations in clinical practice and scarce therapeutic alternatives could benefit from a more sensitive diagnostic tool and tailored therapeutic strategy recommendations.

Clinical trial identification

Editorial acknowledgement

The authors would like to thank Dr. Víctor Latorre, at Medical Statistics Consulting, for medical writing services.

Legal entity responsible for the study

Roche Farma, S.A.

Funding

Roche Farma S.A.

Disclosure

M.R. Garcia Campelo: Financial Interests, Advisory Board: Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer, PharmaMar, Bayer, AbbVie, GSK, Boehringer; Financial Interests, Invited Speaker: Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer, PharmaMar, Bayer, AbbVie, GSK, Boehringer; Financial Interests, Other, Travel/Accommodation/Expenses: Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer, Boehringer. E. Arriola: Financial Interests, Other, Honoraria (self): Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer, Boehringer, Takeda; Financial Interests, Advisory Board: Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer, Boehringer, Takeda; Financial Interests, Invited Speaker: Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer, Boehringer, Takeda; Financial Interests, Research Grant: Roche, BMS, Pfizer, Boehringer; Financial Interests, Other, Travel/Accommodation/Expenses: Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer; Financial Interests, Invited Speaker, Travel/Accommodation/Expenses: Boehringer. D. Isla: Financial Interests, Advisory Board: Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer, Bayer, AbbVie, Amgen, Boehringer, Takeda; Financial Interests, Invited Speaker: Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer, Bayer, Amgen, Boehringer, Sanofi; Financial Interests, Research Grant: Roche, BMS, AstraZeneca, Lilly; Financial Interests, Other, Travel/Accommodation/Expenses: Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer, Amgen, Boehringer. R. Bernabe Caro: Financial Interests, Advisory Board: Roche, BMS, AstraZeneca; Financial Interests, Invited Speaker: Roche, BMS, Amgen. D. Perez Parente: Financial Interests, Institutional, Full or part-time Employment: Roche. B. Moll, J. Lavara Sanz, S. Olson: Financial Interests, Full or part-time Employment: Roche. J. García González: Financial Interests, Advisory Board: Roche, Merck, BMS, AstraZeneca, Lilly, Pfizer, Boehringer; Financial Interests, Invited Speaker: Roche; Financial Interests, Other, Travel/Accommodation/Expenses: Roche, Merck, BMS, Boehringer.

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