TY - JOUR
T1 - Systemic and Intracranial Efficacy and Safety of Trastuzumab Deruxtecan in Patients with HER2-Mutant Non-Small Cell Lung Cancer across Treatment Lines
T2 - Evidence from the TRACER/HERTras Real-World Cohort
AU - Illini, Oliver
AU - Hund, Anna-Carina
AU - Kopp, Hans-Georg
AU - Moskovitz, Mor
AU - Mountzios, Giannis
AU - Brueckl, Wolfgang M
AU - Früh, Martin
AU - Leßmann, Marie-Elisabeth
AU - Christopoulos, Petros
AU - Stenzinger, Albrecht
AU - Thomas, Michael
AU - Gillis, Roni
AU - Peled, Nir
AU - Acker, Fabian
AU - Addeo, Alfredo
AU - Charpidou, Andriani
AU - Grohé, Christian
AU - Mauti, Laetitia
AU - Rothschild, Sacha I
AU - Schmid, Sabine
AU - Schumann, Christian
AU - Urban, Damien
AU - Wurm, Robert
AU - Ekman, Simon
AU - Skribek, Marcus
AU - Glanemann, Franziska
AU - Wiesweg, Marcel
AU - Ackermann, Christoph Jakob
AU - Agelaki, Sofia
AU - Hoffknecht, Petra
AU - Jakopović, Marko
AU - Kern, Jens
AU - König, David
AU - Kostenzer, Katharina
AU - Kropf-Sanchen, Cornelia
AU - Laack, Eckart
AU - Lang, David
AU - Nagl, Laurenz
AU - Pall, Georg
AU - Reck, Martin
AU - Kian, Waleed
AU - Allemann, Anna T
AU - Alt, Jürgen
AU - Araújo, David
AU - Bokas, Alexandros
AU - Hannah, Fabikan
AU - Julie, Krainer-Jacobs
AU - Weinlinger, Christoph
AU - de Langen, Adrianus Johannes
AU - Fergadis, Evangelos Georgios
AU - Fountzilas, Elena
AU - Froesch, Patrizia
AU - Frost, Nikolaj
AU - Griesinger, Frank
AU - Jordan, Franziska
AU - Karanikiotis, Charisios
AU - Kiesewetter, Barbara
AU - Korantzis, Ippokratis
AU - Machado, Andrea Lopes
AU - Economopoulou, Panagiota
AU - Pilz, Arnold
AU - Reimann, Patrick
AU - Rittmeyer, Achim
AU - Saad, Akram
AU - Samitas, Konstantinos
AU - Schulmann, Karsten
AU - Shah, Riyaz
AU - Stratmann, Jan Alexander
AU - Taghizadeh, Hossein
AU - Tammoscheit, Kai
AU - Tufman, Amanda
AU - Weber, Jan-Phillip
AU - Wöll, Ewald
AU - Valipour, Arschang
AU - Overbeck, Tobias R
AU - Hochmair, Maximilian J
N1 - Copyright © 2026. Published by Elsevier Inc.
PY - 2026/2/24
Y1 - 2026/2/24
N2 - INTRODUCTION: HER2 mutations define a distinct, therapeutically actionable subset of non-small cell lung cancer (NSCLC). Trastuzumab deruxtecan (T-DXd) has demonstrated strong activity in clinical trials, but real-world data are limited.METHODS: We conducted a retrospective, multinational cohort study of patients with advanced HER2-mutant NSCLC treated with T-DXd outside clinical trials between August 2021 and January 2025 across 68 centers in Europe and Israel. The primary endpoint was objective response rate (ORR). Secondary endpoints included progression-free survival (PFS), overall survival (OS), intracranial efficacy, and safety.RESULTS: Among 168 patients (median age 62 years; 59% female; 56% never-smokers), the ORR was 54.8% (95%CI, 46.9-62.4) and disease control rate 88.7% (95%CI, 82.9-93.1). Median PFS was 7.2 months (95%CI, 6.2-9.7) and OS 18.3 months (95%CI, 13.3-24.8). Treatment-naïve patients (n=18) achieved an ORR of 72.2% (95%CI, 46.5-90.3) and median OS of 22.1 months (95%CI, 10.0-NE). Patients with measurable brain metastases (n=27) had an intracranial ORR of 74.1% (95%CI, 53.7-88.9), including 25.9% complete responses. Grade ≥3 treatment-related adverse events occurred in 32% of patients. Interstitial lung disease (ILD)/pneumonitis occurred in 14% (four fatal cases) of patients, without consistent predictors.CONCLUSIONS: In the largest real-world cohort reported to date, T-DXd demonstrated robust systemic and intracranial activity in HER2-mutant NSCLC, including treatment-naïve patients and those with active brain metastases who were largely excluded from prior studies. Toxicity was consistent with previous reports, with ILD remaining the main safety concern. These findings support integration of HER2-targeted therapies into evolving treatment algorithms.
AB - INTRODUCTION: HER2 mutations define a distinct, therapeutically actionable subset of non-small cell lung cancer (NSCLC). Trastuzumab deruxtecan (T-DXd) has demonstrated strong activity in clinical trials, but real-world data are limited.METHODS: We conducted a retrospective, multinational cohort study of patients with advanced HER2-mutant NSCLC treated with T-DXd outside clinical trials between August 2021 and January 2025 across 68 centers in Europe and Israel. The primary endpoint was objective response rate (ORR). Secondary endpoints included progression-free survival (PFS), overall survival (OS), intracranial efficacy, and safety.RESULTS: Among 168 patients (median age 62 years; 59% female; 56% never-smokers), the ORR was 54.8% (95%CI, 46.9-62.4) and disease control rate 88.7% (95%CI, 82.9-93.1). Median PFS was 7.2 months (95%CI, 6.2-9.7) and OS 18.3 months (95%CI, 13.3-24.8). Treatment-naïve patients (n=18) achieved an ORR of 72.2% (95%CI, 46.5-90.3) and median OS of 22.1 months (95%CI, 10.0-NE). Patients with measurable brain metastases (n=27) had an intracranial ORR of 74.1% (95%CI, 53.7-88.9), including 25.9% complete responses. Grade ≥3 treatment-related adverse events occurred in 32% of patients. Interstitial lung disease (ILD)/pneumonitis occurred in 14% (four fatal cases) of patients, without consistent predictors.CONCLUSIONS: In the largest real-world cohort reported to date, T-DXd demonstrated robust systemic and intracranial activity in HER2-mutant NSCLC, including treatment-naïve patients and those with active brain metastases who were largely excluded from prior studies. Toxicity was consistent with previous reports, with ILD remaining the main safety concern. These findings support integration of HER2-targeted therapies into evolving treatment algorithms.
U2 - 10.1016/j.jtho.2026.103651
DO - 10.1016/j.jtho.2026.103651
M3 - Journal article
C2 - 41747890
SN - 1556-0864
SP - 103651
JO - Journal of Thoracic Oncology
JF - Journal of Thoracic Oncology
ER -