Oops, you're using an old version of your browser so some of the features on this page may not be displaying properly.

MINIMAL Requirements: Google Chrome 24+Mozilla Firefox 20+Internet Explorer 11Opera 15–18Apple Safari 7SeaMonkey 2.15-2.23

Poster session 16

1182P - US real-world (RW) patient characteristics with METex14 skipping advanced non-small cell lung cancer (aNSCLC)

Date

10 Sep 2022

Session

Poster session 16

Topics

Cancer Epidemiology

Tumour Site

Non-Small Cell Lung Cancer

Presenters

Ronan Kelly

Citation

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

Authors

R.J. Kelly1, X. Le2, K. Luttropp3, M. Yang4, F. Liu4, S. Huse5, M.L. Ganz5, B. Pfeiffer6, P.K. Paik7

Author affiliations

  • 1 Charles A. Sammons Cancer Center, Baylor University Medical Center, 75246 - Dallas/US
  • 2 Department Of Thoracic Head And Neck Medical Oncology, The University of Texas MD Anderson Cancer Center, 77030 - Houston/US
  • 3 Real World Evidence, Evidera, Stockholm/SE
  • 4 Emd Serono, Inc., an affiliate of Merck KGaA, located in Rockland/US
  • 5 Real World Evidence, Evidera, Waltham/US
  • 6 Global Evidence And Value Development, Merck Healthcare KGaA, Darmstadt/DE
  • 7 Department Of Medicine, Thoracic Oncology Service, Memorial Sloan-Kettering Cancer Center, New York, NY, USA; Department of Medicine, Weill Cornell Medical College, 10021 - New York/US

Resources

Login to get immediate access to this content.

If you do not have an ESMO account, please create one for free.

Abstract 1182P

Background

We evaluated the characteristics of adult patients (pts) with METex14 skipping aNSCLC using RW data predating the FDA approval of the two MET tyrosine kinase inhibitors (TKIs), tepotinib and capmatinib.

Methods

This retrospective cohort study used the electronic health record-derived de-identified Flatiron Health database to identify US pts with METex14 skipping aNSCLC who initiated first-line (1L) treatment from Jan 1, 2011 to Sep 30, 2019 with ≥3 months’ follow-up. The index date was the start of 1L therapy. Descriptive analyses assessed the distribution of sample demographics and clinical characteristics. Pt characteristics were categorized by line of therapy, with second line (2L) as a subset of 1L, and the presence of brain metastases (BM) at index.

Results

Of 108 pts with METex14 skipping aNSCLC who initiated 1L treatment, median age at index was 75 (range 46–85) yrs, 54.6% were female, and 52.8% (n=57) had 2L treatment (table). 63.0% pts had a history of smoking and most were Stage IIIB–IV at initial diagnosis (73.1%); 7.4% had squamous cell carcinoma. 75.9% had an index date of 2016–2019. Of 89/108 pts with genomic testing prior to 1L, no pts were reported to have KRAS, ROS-1 or BRAF mutations. Of 31 pts with available PD-L1 expression data, 13 (41.9%) had high PD-L1. Tumor mutation burden (TMB), assessed in 61 pts, was low (mean [SD], 6.6 [4.7]). Of 23 pts with BM at index (21.3%), median age was 72 (48–85) yrs, 56.5% were female, 73.9% had a history of smoking, and 91.3% had Stage IIIB–IV at initial diagnosis. Table: 1182P

Characteristics 1L (N=108) 2L (n=57) BM (n=23)
Age, years
Median (range) 75 (46–85) 73 (46–85) 72 (48–85)
Sex, n (%)
Female 59 (54.6) 34 (59.6) 13 (56.5)
Race, n (%)
White 77 (71.3) 39 (68.4) 14 (60.9)
BMI
Mean (SD) 26.8 (5.2) 26.5 (5.2) 28.6 (6.4)
Smoking history, n (%)
Yes 68 (63.0) 34 (59.6) 17 (73.9)
NSCLC diagnosis to treatment, days
Mean (SD) 241.7 (576.6) 366.1 (359.2) 207.7 (698.4)
Histology, n (%)
Non-squamous 94 (87.0) 47 (82.5) 22 (95.7)
Squamous 8 (7.4) 8 (14.0) 0
Sites of metastases, n (%)
Bone 44 (40.7) 27 (47.4) 12 (52.2)
Brain 23 (21.3) 12 (21.1) 23 (100)
Liver 15 (13.9) 7 (12.3) 5 (21.7)
ECOG PS, n (%)
0 21 (19.4) 9 (15.8) 3 (13.0)
1 37 (34.3) 20 (35.1) 8 (34.8)
2 13 (12.0) 11 (19.3) 3 (13.0)

Conclusions

Real-world pt demographics and clinical characteristics of the Flatiron cohort confirm pts with METex14 skipping as a distinct population of aNSCLC; older, with/without smoking history, with squamous/non-squamous histology, exclusive of KRAS, ROS-1 or BRAF mutations, and with high PD-L1 but low TMB. Analyses indicate a need for routine testing practices to identify pts prior to systemic therapy, since targeted MET TKI therapies are now available for use.

Clinical trial identification

Editorial acknowledgement

Editorial assistance (funded by Merck Healthcare KGaA, Darmstadt, Germany) was provided by Syneos Health, London, UK.

Legal entity responsible for the study

Merck Healthcare KGaA, Darmstadt, Germany.

Funding

Merck Healthcare KGaA, Darmstadt, Germany (CrossRef Funder ID: 10.13039/100009945).

Disclosure

R.J. Kelly: Financial Interests, Personal, Advisory Role: BMS; Merck Healthcare KGaA, Darmstadt, Germany; Eli Lilly; AstraZeneca; Daiichi Sankyo; EMD Serono, an affiliate of Merck KGaA; Novartis; Takeda; Eisai; Astellas; Ipsen; Novocure; Financial Interests, Institutional, Research Grant: BMS; Eli Lilly. X. Le: Financial Interests, Personal, Advisory Role: AstraZeneca; Eli Lilly; EMD Serono, an affiliate of Merck KGaA; Novartis; Daiichi Sankyo; Hengrui Therapeutics; Financial Interests, Personal, Research Grant: Eli Lilly; Boehringer Ingelheim. K. Luttropp, S. Huse, M.L. Ganz: Financial Interests, Personal, Full or part-time Employment: Evidera Ltd. M. Yang, F. Liu: Financial Interests, Personal, Full or part-time Employment: EMD Serono, Inc., Rockland, MA, USA, an affiliate of Merck KGaA. B. Pfeiffer: Financial Interests, Personal, Full or part-time Employment: Merck Healthcare KGaA, Darmstadt, Germany. P.K. Paik: Financial Interests, Personal, Advisory Role: AstraZeneca; Calithera; Lilly; Takeda; EMD Serono, an affiliate of Merck KGaA; Bicara; Boehringer Ingelheim; Xencor; CrownBio; Financial Interests, Institutional, Research Grant: EMD Serono, an affiliate Merck KGaA; Boehringer Ingelheim; Bicara.

This site uses cookies. Some of these cookies are essential, while others help us improve your experience by providing insights into how the site is being used.

For more detailed information on the cookies we use, please check our Privacy Policy.

Customise settings
  • Necessary cookies enable core functionality. The website cannot function properly without these cookies, and you can only disable them by changing your browser preferences.