Clinical features affecting efficacy of immune checkpoint inhibitors in pretreated patients with advanced NSCLC: a Danish nationwide real-world study

Authors

  • Mette T. Mouritzen Department of Oncology, Aalborg University Hospital, Aalborg, Denmark; Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark
  • Karen F. Junker Department of Oncology, Copenhagen E, Denmark
  • Andreas Carus Department of Oncology, Aalborg University Hospital, Aalborg, Denmark; Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark
  • Morten Ladekarl Department of Oncology, Aalborg University Hospital, Aalborg, Denmark; Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark
  • Peter Meldgaard Department of Oncology, Aarhus University Hospital, Aarhus N, Denmark
  • Anders W. M. Nielsen Department of Oncology, Aarhus University Hospital, Aarhus N, Denmark
  • Anna Livbjerg Department of Oncology, Aarhus University Hospital, Aarhus N, Denmark
  • Jacob W. Larsen Department of Oncology, Region Hospital West Jutland, Herning, Denmark
  • Halla Skuladottir Department of Oncology, Region Hospital West Jutland, Herning, Denmark
  • Charlotte Kristiansen Department of Oncology, Vejle Hospital, University Hospital of Southern Denmark, Vejle, Denmark
  • Kim Wedervang Department of Oncology, Hospital Sønderjylland, Sønderborg, Denmark
  • Tine Schytte Department of Oncology, Odense University Hospital, Odense, Denmark; Department of Clinical Research, University of Southern Denmark, Odense, Denmark; Odense Patient data Explorative Network (OPEN), Odense, Denmark
  • Karin H. Hansen Department of Oncology, Odense University Hospital, Odense, Denmark; Department of Clinical Research, University of Southern Denmark, Odense, Denmark; Odense Patient data Explorative Network (OPEN), Odense, Denmark
  • Anne-Cathrine Østby Department of Clinical Oncology and Palliative Care, Zealand University Hospital, Roskilde, Denmark
  • Malene S. Frank Department of Clinical Oncology and Palliative Care, Zealand University Hospital, Roskilde, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen N, Denmark
  • Jakob Lauritsen Department of Clinical Oncology and Palliative Care, Zealand University Hospital, Roskilde, Denmark
  • Jens B. Sørensen Department of Oncology, Copenhagen E, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen N, Denmark
  • Seppo W. Langer Department of Oncology, Copenhagen E, Denmark; Department of Clinical Medicine, University of Copenhagen, Copenhagen N, Denmark
  • Gitte F. Persson Department of Clinical Medicine, University of Copenhagen, Copenhagen N, Denmark; Department of Oncology, Copenhagen University Hospital, Herlev, Denmark
  • Jon L. Andersen Department of Oncology, Copenhagen University Hospital, Herlev, Denmark
  • Pernille H. Homann Department of Oncology, North Zealand Hospital, Hillerød, Denmark
  • Emilie B. Kristensen Department of Oncology, North Zealand Hospital, Hillerød, Denmark
  • Lars B. Drivsholm Department of Oncology, North Zealand Hospital, Hillerød, Denmark
  • Martin Bøgsted Department of Hematology, Aalborg University Hospital, Aalborg, Denmark; Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark
  • Heidi S. Christensen Department of Hematology, Aalborg University Hospital, Aalborg, Denmark; Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark; Department of Clinical Medicine, Aalborg University, Aalborg, Denmark
  • Mette Pøhl Department of Oncology, Copenhagen E, Denmark
  • Birgitte Bjørnhart Department of Oncology, Odense University Hospital, Odense, Denmark; Department of Clinical Research, University of Southern Denmark, Odense, Denmark; Odense Patient data Explorative Network (OPEN), Odense, Denmark

DOI:

https://doi.org/10.1080/0284186X.2021.2023213

Keywords:

Cancer immunotherapy, clinical prognostic factors, immune-checkpoint inhibitors, non-small cell lung cancer, real-world evidence

Abstract

Background

Immune checkpoint inhibitors (ICIs) are implemented as standard treatment for patients with advanced non-small cell lung cancer (NSCLC) in first-line and subsequent-line treatment. However, certain subgroups such as patients with older age, poor performance status (PS), and severe comorbidity are underrepresented in the randomized controlled trials (RCTs). This study aimed to assess overall survival (OS), treatment data, and clinical features affecting second- or subsequent-line ICI efficacy in an unselected, Danish, nationwide NSCLC population.

Methods

Patients with advanced NSCLC who started nivolumab or pembrolizumab as second-line or subsequent-line treatment between 1 September 2015, and 1 October 2018, were identified from institutional records of all Danish oncology departments. Clinical and treatment data were retrospectively collected. Descriptive statistics and survival analyses were performed.

Results

Data were available for 840 patients; 49% females. The median age was 68 years (19% were ≥75 years), 19% had PS ≥2, and 36% had moderate to severe comorbidity. The median OS (mOS) was 12.2 months; 15.1 months and 10.0 months in females and males, respectively. The median time-to-treatment discontinuation (mTTD) and median progression-free survival (mPFS) was 3.2 and 5.2 months, respectively. Patients with PS ≥2 had a mOS of 4.5 months, mTTD of 1.1 month, and mPFS of 2.0 months. In multivariable Cox regression analysis, male sex (HR = 1.35, 95% CI 1.11–1.62), PS >0 (PS 1, HR = 1.88, 95% CI 1.52–2.33; PS ≥2, HR = 4.15, 95% CI 3.13–5.5), liver metastases (HR = 1.72, 95% CI 1.34–2.22), and bone metastases (HR = 1.27, 95% CI 1.03–1.58) were significant poor prognostic OS factors.

Conclusions

Danish real-world patients with advanced NSCLC treated with second- or subsequent-line ICI had an OS comparable to results from RCTs. Women, frail and older patients constituted a higher proportion than in previous RCTs. Clinical features associated with poor OS were male sex, PS ≥1 (in particular PS ≥2), bone-, and liver metastases.

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Published

2022-04-03

How to Cite

Mouritzen, M. T., Junker, K. F., Carus, A., Ladekarl, M., Meldgaard, P., Nielsen, A. W. M., … Bjørnhart, B. (2022). Clinical features affecting efficacy of immune checkpoint inhibitors in pretreated patients with advanced NSCLC: a Danish nationwide real-world study. Acta Oncologica, 61(4), 409–416. https://doi.org/10.1080/0284186X.2021.2023213