Your browser doesn't support javascript.
loading
Neoadjuvant pembrolizumab+chemotherapy/adjuvant pembrolizumab for Early-Stage Triple-Negative breast cancer: Quality-of-Life results from randomized KEYNOTE-522 study.
Dent, Rebecca; Cortés, Javier; Pusztai, Lajos; McArthur, Heather; Kümmel, Sherko; Bergh, Jonas; Denkert, Carsten; Park, Yeon Hee; Hui, Rina; Harbeck, Nadia; Takahashi, Masato; Untch, Michael; Fasching, Peter A; Cardoso, Fatima; Haiderali, Amin; Jia, Liyi; Nguyen, Allison Martin; Pan, Wilbur; O'Shaughnessy, Joyce; Schmid, Peter.
Afiliación
  • Dent R; National Cancer Center Singapore and Duke-NUS Medical School, Division of Medical Oncology, Singapore.
  • Cortés J; International Breast Cancer Center (IBCC), Pangaea Oncology, Quironsalud Group, Barcelona, Spain; Medical Scientia Innovation Research (MedSIR), Barcelona, Spain; Faculty of Biomedical and Health Sciences, Department of Medicine, Universidad Europea de Madrid, Madrid, Spain.
  • Pusztai L; Yale Cancer Center, Yale University School of Medicine, New Haven, CT, USA.
  • McArthur H; UT Southwestern Medical Center, Dallas, TX, USA.
  • Kümmel S; Breast Unit, Kliniken Essen-Mitte Evang, Huyssens-Stiftung, Essen, Germany; Charité - Universitätsmedizin Berlin, Department of Gynecology with Breast Center, Berlin, Germany.
  • Bergh J; Department of Oncology-Pathology, Karolinska Institutet and Breast Cancer Centre, Cancer theme, Karolinska Comprehensive Cancer & University Hospital, Karolinska CCC and Cancer Core Europe, Solna, Sweden.
  • Denkert C; Institute of Pathology, Philipps University Marburg, Marburg, Germany.
  • Park YH; Hematology-Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
  • Hui R; Westmead Breast Cancer Institute, Westmead Hospital and the University of Sydney, Sydney, NSW, Australia; Centre of Cancer Medicine, School of Clinical Medicine, University of Hong Kong.
  • Harbeck N; Breast Center, Dept. OB&GYN and CCC Munich, LMU University Hospital, Germany, Munich.
  • Takahashi M; Department of Breast Surgery, Hokkaido University Hospital, Sapporo, Japan.
  • Untch M; Breast Cancer Center, Helios Klinikum Berlin-Buch, Berlin, Germany.
  • Fasching PA; University Hospital Erlangen, Comprehensive Cancer Center Erlangen-EMN, Erlangen, Germany.
  • Cardoso F; Breast Unit, Champalimaud Clinical Center/Champalimaud Foundation, Lisbon, Portugal.
  • Haiderali A; Center for Observational and Real-World Evidence, Merck & Co., Inc, Rahway, NJ, USA.
  • Jia L; Biostatistics and Research Division Sciences, Merck & Co., Inc, Rahway, NJ, USA.
  • Nguyen AM; Biostatistics and Research Decision Sciences-Epidemiology, Patient-Centered Endpoints & Strategy, Merck & Co., Inc, Rahway, NJ, USA.
  • Pan W; Global Clinical Development, Merck & Co., Inc, Rahway, NJ, USA.
  • O'Shaughnessy J; Baylor University Medical Center, Texas Oncology, US Oncology, Dallas, 214-370-1000, TX, USA.
  • Schmid P; Centre for Experimental Cancer Medicine, Barts Cancer Institute, Queen Mary University of London, London, UK.
J Natl Cancer Inst ; 2024 Jun 24.
Article en En | MEDLINE | ID: mdl-38913881
ABSTRACT

BACKGROUND:

In KEYNOTE-522 (NCT03036488), neoadjuvant pembrolizumab+chemotherapy then adjuvant pembrolizumab significantly improved pathological complete response and event-free survival vs neoadjuvant chemotherapy in early-stage triple-negative breast cancer (TNBC). We report patient-reported outcomes (PROs) from KEYNOTE-522.

METHODS:

Patients were randomized 21 to neoadjuvant pembrolizumab 200 mg or placebo every 3 weeks, plus 4 cycles of paclitaxel+carboplatin then 4 cycles of doxorubicin (or epirubicin)+cyclophosphamide. After surgery, patients received adjuvant pembrolizumab or placebo for up to 9 cycles. EORTC QLQ-30 and QLQ-BR23 were prespecified secondary objectives. Between-group differences in least squares (LS) mean change from baseline (day 1/cycle 1 in both neoadjuvant and adjuvant phases) to the prespecified latest time point with ≥60%/80% completion/compliance were assessed using a longitudinal model (no alpha error assigned).

RESULTS:

Week 21 (neoadjuvant phase) and week 24 (adjuvant phase) were the latest time points at which completion/compliance rates were ≥60%/80%. In the neoadjuvant phase, between-group differences (pembrolizumab+chemotherapy [N = 762] vs placebo+chemotherapy [N = 383]) in LS mean change from baseline to week 21 in QLQ-C30 GHS/QoL, emotional functioning, and physical functioning were -1.04 (95% CI, -3.46 to 1.38), -0.69 (95% CI, -3.13 to 1.75), and -2.85 (95% CI, -5.11 to - 0.60), respectively. In the adjuvant phase, between-group differences (pembrolizumab [N = 539] vs placebo [N = 308]) in LS mean change from baseline to week 24 were -0.41 (95% CI, -2.60 to 1.77), -0.60 (95% CI, -2.99 to 1.79), and -1.57 (95% CI, -3.36 to 0.21).

CONCLUSIONS:

No substantial differences in PRO assessments were observed between neoadjuvant pembrolizumab+chemotherapy followed by adjuvant pembrolizumab vs neoadjuvant placebo+chemotherapy in early-stage TNBC. TRIAL REGISTRATION ClinicalTrials.gov, NCT03036488.
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Natl Cancer Inst Año: 2024 Tipo del documento: Article País de afiliación: Singapur

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Natl Cancer Inst Año: 2024 Tipo del documento: Article País de afiliación: Singapur