PET/CT-guided management of immune checkpoint blockade and multi-modal profiling following treatment in long-term responders with metastatic lung cancer in the National Network Genomic Medicine Lung Cancer Germany (nNGM)

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Contributors

  • National Network Genomic Medicine Lung Cancer (nNGM) - (Author)
  • Department of Internal Medicine I
  • Institute of Pathology
  • Charité – Universitätsmedizin Berlin
  • Max Delbrück Center for Molecular Medicine (MDC)
  • University of Potsdam
  • University Hospital Essen
  • National Center for Tumor Diseases (NCT) West
  • University Hospital Aachen
  • Bavarian Center for Cancer Research (BZKF)
  • University Hospital of Würzburg
  • Helios Hospital Emil von Behring
  • Institute for Lung Research GmbH
  • Asklepios Clincs München-Gauting
  • Evangelical Lung Clinic Berlin
  • Pius-Hospital Oldenburg
  • Immenhausen Lung Clinic
  • University Hospital Frankfurt
  • Frankfurt Cancer Institute
  • University Hospital Carl Gustav Carus Dresden
  • Asklepios Hospital Harburg
  • University Hospital Heidelberg
  • German Center for Lung Research (DZL)
  • Comprehensive Pneumology Center Munich (CPC-M) - Partner site Munich
  • Sana Hospital Offenbach
  • University Hospital Münster
  • Universitätsmedizin Mannheim
  • German Cancer Research Center (DKFZ)
  • University Hospital Regensburg
  • University Medical Center Göttingen
  • University of Göttingen
  • Translational Lung Research Center Heidelberg (TLRC) - DZL Heidelberg
  • Ulm University Medical Center
  • German Cancer Consortium (DKTK) partner site Berlin
  • Airway Research Center North (ARCN) - DZL Borstel

Abstract

BACKGROUND: The optimal duration of immune checkpoint blockade (ICB) in lung cancer remains undefined. Indefinite treatment in long-term responders increases healthcare burden, exposes patients to avoidable toxicities, and is not supported by any clinical and biological rationale or translational data. Prospective strategies to determine the optimal duration of immunotherapy in lung cancer are urgently needed.

PATIENTS AND METHODS: In this retrospective cohort study, 455 patients from 21 nNGM centers with ≥2 years of disease control on first-line ICB-based therapy were grouped into PET/CT-guided discontinuation (cohort A, n=126) or continued ICB without PET/CT (cohort B, n=329), and assessed for overall survival (OS). Matched pre- and post-ICB tumor samples from cohort A patients with persistent or progressive disease were analyzed by comprehensive genomic profiling, histological TIL quantification, and spatial transcriptomics to explore mechanisms of late resistance.

RESULTS: After a median follow-up of 55 months, cohort A showed significantly longer OS (median not reached vs. 82 months; HR 0.35 [0.18-0.67], p = 0.002), despite substantially shorter treatment duration (27 vs. 45 months; p < 0.001). Discontinuation was either PET-driven (A) or resulted from immune-related toxicity, progression, or patients' choice (B). Systematic re-biopsies in cohort A revealed a high incidence of second primary lung cancers (SPLC, 28%). All progression events were managed exclusively with local (ablative) treatments in 53% (A) vs. 17% (B). Post-treatment tumors exhibited features of acquired resistance, whereas SPLC displayed characteristics of primary resistance, including low PD-L1 expression, low TMB, and immunologically cold tumor microenvironments.

CONCLUSIONS: A structured discontinuation strategy appears to provide a safe approach for long-term ICB responders, enabling earlier detection of resistance before generalized progression. A confirmatory prospective non-inferiority randomized trial within the nNGM is underway.

Details

Original languageEnglish
Pages (from-to)686-700
Number of pages15
JournalAnnals of Oncology
Volume37
Issue number5
Early online date30 Dec 2025
Publication statusPublished - May 2026
Peer-reviewedYes

External IDs

Scopus 105030262553

Keywords

Sustainable Development Goals

Keywords

  • lung cancer, discontinuation, second primary lung cancer, resistance mechanisms, immune checkpoint blockade, long-term response