Abstract 1390P
Background
HER2 mutations (HER2m) are a potential therapeutic target in 2–3% of patients with non-squamous NSCLC; however, real-world evidence on demographics and outcomes is limited. We assessed patient characteristics and treatment patterns for advanced HER2m NSCLC at a French and a German academic centre.
Methods
Adults with advanced HER2m non-squamous NSCLC were identified at Institut Curie, France (study: 1 Jan 2011–22 Apr 2022) and Thoraxklinik Heidelberg, Germany (1 Jan 2014–5 May 2022). Lines of therapy (L) and treatment pathways were characterised. Demographic/clinical characteristics were analysed by descriptive statistics; survival was assessed by Kaplan–Meier analysis. Real-world progression-free survival (rwPFS) was time between L start and earliest progression event (Germany), discontinuation due to progression (France), next L start or death.
Results
Of 55 patients with advanced HER2m NSCLC (n=17, France; n=38, Germany), the median age at diagnosis was 66 years, 63.6% were female and 74.6% had ECOG scores of 0 or 1. 48 patients (87.3%) received at least 1L, 29 (52.7%) received at least 2L and 19 (34.5%) received at least 3L. The most common regimens were carboplatin + pemetrexed (13/48, 27.1%) and carboplatin + pemetrexed + pembrolizumab (9/48, 18.8%) in 1L and pembrolizumab (6/29, 21.0%), carboplatin + pembrolizumab + pemetrexed (3/29, 10.3%) and pemetrexed (3/29, 10.3%) in 2L. The most common treatment pathway began with non-platinum-based chemotherapy or platinum-based chemotherapy in 1L (26/48, 54.2%) and immunotherapy in 2L (7/26, 26.9%) (Table). Median real-world overall survival from the start of 1L was 16.5 months (95% CI: 12.3–29.8). Median rwPFS in the 1L was 5.1 months (95% CI: 3.5–8.5).
Conclusions
Chemotherapy was the mainstay in 1L; diverse regimens were used in 2L. Poor survival suggests a need for novel therapeutic options for advanced HER2m NSCLC. Table: 1390P
Regimen | 1L (n=48) | 2L (n=29) | 3L (n=19) | |||
n | % | n | % | n | % | |
HER2 targeteda | 1 | 2.1 | 1 | 3.4 | 4 | 21.1 |
HER2 targeteda + IMT | 0 | 0 | 0 | 0 | 1 | 5.3 |
HER2 targeteda + non-plat | 0 | 0 | 4 | 13.8 | 0 | 0 |
IMT | 3 | 6.3 | 8 | 27.6 | 1 | 5.3 |
IMT + non-HER2 targetedb + non-plat + plat | 1 | 2.1 | 0 | 0 | 0 | 0 |
IMT + non-plat + plat | 11 | 22.9 | 3 | 10.3 | 1 | 5.3 |
Non-HER2 targetedb | 1 | 2.1 | 1 | 3.4 | 0 | 0 |
Non-HER2 targetedb + non-plat | 0 | 0 | 2 | 6.9 | 2 | 10.5 |
Non-HER2 targetedb + non-plat + plat | 4 | 8.3 | 0 | 0 | 0 | 0 |
Non-plat | 1 | 2.1 | 6 | 20.7 | 7 | 36.8 |
Non-plat + plat | 26 | 54.2 | 4 | 13.8 | 3 | 15.8 |
aNeratinib, afatinib, poziotinib, trastuzumab, or trastuzumab emtansine. bAlectinib, bevacizumab, ceritinib, or ramucirumab. IMT, immunotherapy; non-plat, non-platinum-based chemotherapy; plat, platinum-based chemotherapy.
Clinical trial identification
Editorial acknowledgement
Medical writing and editorial assistance were provided by Julia C. Jones (PharmD, PhD), Erica Cave (PhD), and Daria Renshaw from IQVIA, funded by the study sponsors.
Legal entity responsible for the study
AstraZeneca, Daiichi Sankyo.
Funding
AstraZeneca, Daiichi Sankyo.
Disclosure
P. Christopoulos: Financial Interests, Personal, Advisory Board: AstraZeneca, Boehringer Ingelheim, Chugai, Pfizer, Novartis, MSD, Takeda, Roche, Daiichi Sankyo; Financial Interests, Personal, Writing Engagement: Gilead; Financial Interests, Personal, Invited Speaker: Thermo Fisher; Financial Interests, Institutional, Funding: AstraZeneca, Boehringer Ingelheim, Amgen, Novartis, Roche; Financial Interests, Personal, Funding: Takeda. N. Girard: Financial Interests, Personal, Invited Speaker: AstraZeneca, BMS, MSD, Roche, Pfizer, Mirati, Amgen, Novartis, Sanofi, Gilead; Financial Interests, Personal, Advisory Board: AstraZeneca, BMS, MSD, Roche, Pfizer, Janssen, Boehringer, Novartis, Sanofi, AbbVie, Amgen, Lilly, Grunenthal, Takeda, Owkin, Leo Pharma, Daiichi Sankyo, Ipsen; Financial Interests, Institutional, Research Grant, Local: Roche, Sivan, Janssen; Financial Interests, Institutional, Funding: BMS, Leo Pharma; Financial Interests, Institutional, Research Grant: MSD; Non-Financial Interests, Officer, International Thymic malignancy interest group, president: ITMIG; Other, Family member is an employee: AstraZeneca. L. Zhang: Financial Interests, Personal, Full or part-time Employment: Daiichi Sankyo; Financial Interests, Institutional, Funding, Funding for study and publication: Daiichi Sankyo, AstraZeneca. Z. Mbanya: Financial Interests, Personal, Full or part-time Employment: AstraZeneca. K. Dunton: Financial Interests, Personal, Full or part-time Employment: Daiichi Sankyo. A. Ali: Financial Interests, Personal, Full or part-time Employment: Daiichi Sankyo; Financial Interests, Personal, Full or part-time Employment, Prior employer: AstraZeneca. M. Berktas: Financial Interests, Personal, Other, I receive regular consultancy fee for my scientific services, I am the project lead for the project from which 2 abstracts were created and submitted to ESMO 2023 congress: AstraZeneca. L. Delmastro: Financial Interests, Personal, Full or part-time Employment: AstraZeneca; Financial Interests, Institutional, Funding, Funding for study & publication: AstraZeneca, Daiichi Sankyo. A. Struebing: Financial Interests, Personal, Full or part-time Employment: Daiichi Sankyo. Y. Xiong: Financial Interests, Personal, Full or part-time Employment: Daiichi Sankyo; Financial Interests, Personal, Full or part-time Employment, Prior employer: Becton Dickinson. S. Lay-Flurrie: Financial Interests, Personal, Full or part-time Employment: IQVIA; Financial Interests, Personal, Full or part-time Employment, Previous employer: University of Oxford; Financial Interests, Institutional, Funding, Funding for study & publication: AstraZeneca, Daiichi Sankyo. P. Hindocha: Financial Interests, Institutional, Funding, Funding for study & publication: AstraZeneca, Daiichi Sankyo; Financial Interests, Personal, Full or part-time Employment: IQVIA. T. Mehdikhanova: Financial Interests, Institutional, Funding, Funding for study and publication: AstraZeneca, Daiichi Sankyo; Financial Interests, Personal, Full or part-time Employment: IQVIA.
Resources from the same session
1368P - LUMINATE 102: A real-world study on biomarker testing rates among patients with non-small cell lung cancer (NSCLC) across lines of therapy
Presenter: Charu Aggarwal
Session: Poster session 20
1369P - BrigAlec study: Focus on alectinib efficacy after brigatinib exposure in BrigALK2 study (GFPC 02-2019)
Presenter: Renaud Descourt
Session: Poster session 20
1370P - Efficacy and safety of ensartinib in ALK-positive non-small cell lung cancer patients with brain metastases: A multicenter, open-label, single-arm, phase II study
Presenter: Jianhua Chang
Session: Poster session 20
1371P - First-line alectinib vs. brigatinib in advanced metastatic NSCLC with ALK rearrangement: Real-world data
Presenter: Young Kyung Jeon
Session: Poster session 20
1372P - Repotrectinib in patients (pts) with NTRK fusion-positive (NTRK+) advanced solid tumors, including NSCLC: Update from the phase I/II TRIDENT-1 trial
Presenter: Ben Solomon
Session: Poster session 20
1373P - Efficacy and safety of taletrectinib in patients (Pts) with ROS1+ non-small cell lung cancer (NSCLC): Interim analysis of global TRUST-II study
Presenter: Maurice Pérol
Session: Poster session 20
1374P - Survival and therapy analysis of small-scale ROS1-mutant non-small cell lung cancer (NSCLC) patients
Presenter: Moritz Glaser
Session: Poster session 20
1375P - Beamion Lung 1, an ongoing phase Ia/Ib trial of the HER2 TKI, BI 1810631 in patients (pts) with advanced solid tumors with HER2 aberrations: Latest data
Presenter: Frans Opdam
Session: Poster session 20
1377P - Differential impact of EGFR exon 20 insertion location on tyrosine kinase inhibitor sensitivity
Presenter: Xiuning Le
Session: Poster session 20
1378P - Efficacy and safety of tunlametinib (HL-085) combined with vemurafenib in patients with advanced BRAF V600-mutated solid tumors: A multicenter, phase I study
Presenter: Yuan-Kai Shi
Session: Poster session 20