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Poster Display session

149P - POSITION: Characterising risk factors and outcomes in patients (pts) with stage III unresectable non-small cell lung cancer (uNSCLC) who fail to complete concurrent chemoradiotherapy (cCRT) or progress during or shortly after cCRT

Date

22 Mar 2024

Session

Poster Display session

Topics

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Giannis Mountzios

Citation

Annals of Oncology (2024) 9 (suppl_3): 1-12. 10.1016/esmoop/esmoop102573

Authors

G. Mountzios1, J. Weng2, E. Zairi3, K. Hsieh4, P. Chander5, W.C.N. Dunlop6, Y. Qiao5, A. Wang5, A. Januszewski7

Author affiliations

  • 1 Henry Dunant Hospital Centre, Athens/GR
  • 2 MD Anderson Cancer Center, Houston/US
  • 3 St. Luke's Hospital, 564 29 - Thessaloniki/GR
  • 4 Icahn School of Medicine at Mount Sinai, New York/US
  • 5 AstraZeneca, Gaithersburg/US
  • 6 AstraZeneca, CB2 1RY - Cambridge/GB
  • 7 St. Bartholomew's Hospital - Barts Health NHS Trust, London/GB

Resources

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Abstract 149P

Background

PACIFIC established consolidation durvalumab as standard of care for pts with Stage III uNSCLC and no progression after complete cCRT. POSITION aims to identify factors associated with failure to complete cCRT and progression during or shortly after cCRT.

Methods

A retrospective cohort study was conducted using a US-based real-world dataset (Tempus). Eligible pts had Stage III uNSCLC diagnosed from 2010 to 2021 and received cCRT without durvalumab. Pts had incomplete cCRT (Group A), progressed during/within 42 days of complete cCRT (Group B) or completed cCRT without progression (Group C). Descriptive statistics were applied to pt characteristics/disposition. Median overall survival (mOS) was estimated by Kaplan-Meier analysis. Multivariable logistic regression was used to identify factors associated with incomplete cCRT and progression during or shortly after cCRT.

Results

Overall, 2076 pts comprised Groups A (n=477; 23.0%), B (n=264; 12.7%), and C (n=1335; 64.3%). Median age was 65 yrs (range, 34-86) and 55.2% were male. Higher proportions of Group A and B (vs Group C) had ECOG PS ≥2 (21.2%, 20.0%, vs 16.1%), Stage III B/C NSCLC at diagnosis (43.5%, 48.9%, vs 39.7%), and Charlson Comorbidity Index (CCI) ≥1 (40.0%, 32.6%, vs 31.8%). From CRT initiation, mOS (95% CI) was 21.6 mo (17.2, 28.0) for Group A, 10.1 mo (7.2, 12.5) for Group B, and 32.4 mo (29.8, 34.6) for Group C. Black race (odds ratio [OR]: 1.67 [95% CI: 1.22, 2.28]) and higher CCI (CCI=1 OR: 1.39 [95% CI: 1.05, 1.83]; CCI≥2 OR: 1.57 [95% CI: 1.11, 2.19]) were associated with higher risks of incomplete cCRT. Among pts who completed cCRT, Stage III B/C NSCLC at diagnosis (OR: 1.63 [95% CI: 1.20, 2.23]) and cerebrovascular (OR: 2.49 [95% CI: 1.06, 5.49]) or renal (OR: 3.50 [95% CI: 1.32, 8.81]) comorbidities were associated with progression during or shortly after cCRT.

Conclusions

Per these analyses, pts who do not complete and/or progress during or shortly after cCRT (Groups A and B) appear frailer (vs Group C), with poor PS and high comorbidity burden. Pts with incomplete cCRT (Group A) are also more likely to be Black. Clinical trials focusing on these pts are warranted.

Editorial acknowledgement

Medical writing support for the development and submission of this abstract, under the direction of the authors, was provided by Eric Exner, MD, PhD of Ashfield MedComms (Milwaukee, WI, USA), an Inizio company, and was funded by AstraZeneca.

Legal entity responsible for the study

AstraZeneca.

Funding

AstraZeneca.

Disclosure

G. Mountzios: Non-Financial Interests, Personal, Invited Speaker: ELCC, ESMO, WCLC, ASCO; Non-Financial Interests, Personal, Writing Engagements: ESMO, ASCO; Financial Interests, Personal, Speaker’s Bureau:MSD; Financial Interests, Personal, Advisory Board:MSD, BMS, AstraZeneca Roche, Novartis, Takeda Sanofi, Gilead, Amgen; Non-Financial Interests, Personal, Officer: ESMO; Financial Interests, Institutional, Funding: GSK, MSD; Non-Financial Interests, Personal, Project Lead: AstraZeneca; Financial Interests, Personal, Principal Investigator:MSD, BMS, AstraZeneca Roche, Novartis, Takeda Sanofi, Gilead, Amgen, Bioatlas, Syneos Health; Non-Financial Interests, Personal, Member: ESMO, ASCO, IASCL; Financial Interests, Personal, Advisory Role:MSD, BMS, AstraZeneca Roche, Novartis, Takeda Sanofi, Gilead, Amgen. J. Weng: Financial Interests, Institutional, Full or part-time Employment: MD Anderson Cancer Center; Non-Financial Interests, Personal, Advisory Role: AstraZeneca. E. Zairi: Financial Interests, Personal, Advisory Board: Amgen; Non-Financial Interests, Personal, Member: ESMO; Financial Interests, Personal, Advisory Role: Amgen. K. Hsieh: Other, Personal and Institutional, Research Grant: AstraZeneca. P. Chander: Financial Interests, Institutional, Full or part-time Employment: AstraZeneca; Financial Interests, Institutional, Stocks/Shares: AstraZeneca. W.C.N. Dunlop: Financial Interests, Personal and Institutional, Full or part-time Employment: AstraZeneca; Financial Interests, Personal and Institutional, Stocks/Shares: AstraZeneca. Y. Qiao: Financial Interests, Institutional, Full or part-time Employment: AstraZeneca; Financial Interests, Institutional, Stocks/Shares: AstraZeneca. A. Wang: Financial Interests, Personal, Full or part-time Employment: AstraZeneca. A. Januszewski: Non-Financial Interests, Personal, Invited Speaker: BTOG; Financial Interests, Personal, Advisory Board:MSD, Roche, AstraZeneca, BMS, Pfizer; Financial Interests, Institutional, Funding: Gilead, Pfizer; Other, Personal and Institutional, Project Lead: Gilead, MSD; Other, Institutional, Principal Investigator: AbbVie, MSD, Roche, AstraZeneca; Non-Financial Interests, Personal, Member: ESMO, ASCO, IASLC.

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