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Poster session 04

964P - PACIFIC on the West Coast: Exploring reasons for not receiving consolidative durvalumab in the treatment of locally advanced lung cancer

Date

10 Sep 2022

Session

Poster session 04

Topics

Clinical Research;  Immunotherapy

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Jamie Feng

Citation

Annals of Oncology (2022) 33 (suppl_7): S438-S447. 10.1016/annonc/annonc1063

Authors

J. Feng1, M. Denault1, S. Kuang1, A. Shokoohi1, B. Leung1, M. Liu2, E. Berthelet2, J. Laskin1, S. Sun1, T. Zhang2, C. Ho1, B. Melosky1

Author affiliations

  • 1 Medical Oncology, BC Cancer Agency - Vancouver, V5Z 4E6 - Vancouver/CA
  • 2 Radiation Oncology, BC Cancer Agency - Vancouver, V5Z 4E6 - Vancouver/CA

Resources

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Abstract 964P

Background

Standard treatment for locally advanced non-small cell lung cancers (NSCLC) is chemoradiotherapy (CRT) followed by a year of consolidative durvalumab (Antonia SJ, et al. NEJM, 2017). British Columbia started funding durvalumab for this indication in February 2020. Previous reports indicate close to half of eligible patients are not getting durvalumab (Denault MH, et al. JTO 2022). This study elaborates on reasons why patients did not get durvalumab in British Columbia, Canada from January 2020 to December 2021.

Methods

Patients treated with concurrent chemoradiation from Jan 1, 2020 – Dec 31, 2021 were reviewed. Data was collected on systemic therapy, radiation therapy, timing between CRT and oncologist followup, biomarkers and reasons for not starting durvalumab.

Results

371 patients underwent concurrent chemoradiation of which 171 patients did not get durvalumab. After chart review, 83 patients form the cohort of which 50 were stage 3A, 28 were stage 3B and 5 were stage 3C. 88 patients were excluded for the following reasons: durvalumab via access program (n=39), not completing curative dose radiation therapy (<50Gy; n=19), stage II or IV (n=22) and non-NSCLC pathology (n=8). 65 patients had PD-L1 testing: 24 were PD-L1 <1%, 23 were PD-L1 1-49% and 18 were PD-L1 >50%. In patients with biomarker testing, 12 were KRAS positive, 9 were EGFR positive and 3 were ALK positive. The top reason for not receiving durvalumab was progression (22; 26.5%). In 15 instances, durvalumab was either not discussed by the medical provider or declined by the patient. The next most common reasons were surgical resection (n=13), chemoradiation toxicity (n=11) and contraindications (n=10).

Conclusions

Our cohort highlights a multitude of reasons why patients did not get immunotherapy after CRT with the most common being progression. Although not included in PACIFIC, trimodality therapy remains an option for locally advanced lung cancers in carefully selected patients. Toxicity secondary to chemoradiation did lead to durvalumab omission in some patients. This study highlights an opportunity to improve outcomes in locally advanced lung cancer in British Columbia, Canada using continued education about the benefit of consolidative durvalumab to both patients and providers.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Has not received any funding.

Disclosure

J. Feng: Financial Interests, Personal, Other, Coverage of travelling expenses to present this abstract at the ESMO 2022 Conference: AstraZeneca. M. Denault: Financial Interests, Personal, Other, Coverage of travelling expenses to present this abstract at the ESMO 2022 Conference: AstraZeneca. J. Laskin: Financial Interests, Personal, Invited Speaker: Roche, Pfizer, Eli Lilly, Jazz; Financial Interests, Institutional, Research Grant: Roche. S. Sun: Financial Interests, Personal, Advisory Role: AstraZeneca, Bristol Myers Squibb, Merck, Novartis, Pfizer, Takeda. T. Zhang: Non-Financial Interests, Member: ASTRO, CARO, ASCO. C. Ho: Financial Interests, Personal, Advisory Board: AbbVie, Amgen, AstraZeneca, Bayer, BMS, Eisai, EMD Serono, Janssen, Merck, Novartis, Pfizer, Roche, Takeda; Financial Interests, Institutional, Research Grant: AstraZeneca, EMD Serono, Roche; Non-Financial Interests, Principal Investigator: Roche, AstraZeneca, EMD Serono. B. Melosky: Financial Interests, Personal, Advisory Board: Roche, AstraZeneca, Pfizer, Merck, BMS, Novartis, Janzen, Sanofi. All other authors have declared no conflicts of interest.

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