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Neoadjuvant pembrolizumab plus chemotherapy/adjuvant pembrolizumab for early-stage triple-negative breast cancer: quality-of-life results from the 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.
Affiliation
  • Dent R; National Cancer Center Singapore and Duke-National University of Singapore (NUS) Medical School, Division of Medical Oncology, Singapore, Singapore.
  • Cortés J; Medica Scientia Innovation Research (MEDSIR), Barcelona, Spain.
  • Pusztai L; International Breast Cancer Center (IBCC), Pangaea Oncology, Quiron Group, Barcelona, Spain.
  • McArthur H; Universidad Europea de Madrid, Faculty of Biomedical and Health Sciences, Department of Medicine, Madrid, Spain.
  • Kümmel S; IOB Madrid, Institute of Oncology, Hospital Beata Maria Ana, Madrid, Spain.
  • Bergh J; Yale Cancer Center, Yale University School of Medicine, New Haven, CT, USA.
  • Denkert C; UT Southwestern Medical Center, Dallas, TX, USA.
  • Park YH; Breast Unit, Kliniken Essen-Mitte Evang, Huyssens-Stiftung, Essen, Germany.
  • Hui R; Department of Gynecology with Breast Center, Charité - Universitätsmedizin Berlin, Berlin, Germany.
  • Harbeck N; 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.
  • Takahashi M; Institute of Pathology, Philipps University Marburg, Marburg, Germany.
  • Untch M; Hematology-Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
  • Fasching PA; Westmead Breast Cancer Institute, Westmead Hospital and the University of Sydney, Sydney, NSW, Australia.
  • Cardoso F; Centre of Cancer Medicine, School of Clinical Medicine, University of Hong Kong, Hong Kong.
  • Haiderali A; Breast Center, Department of OB&GYN and CCC Munich, LMU University Hospital, Munich, Germany.
  • Jia L; Department of Breast Surgery, Hokkaido University Hospital, Sapporo, Japan.
  • Nguyen AM; Breast Cancer Center, Helios Klinikum Berlin-Buch, Berlin, Germany.
  • Pan W; University Hospital Erlangen, Comprehensive Cancer Center Erlangen-EMN, Erlangen, Germany.
  • O'Shaughnessy J; Breast Unit, Champalimaud Clinical Center/Champalimaud Foundation, Lisbon, Portugal.
  • Schmid P; Center for Observational and Real-World Evidence, Merck & Co., Inc., Rahway, NJ, USA.
J Natl Cancer Inst ; 116(10): 1654-1663, 2024 Oct 01.
Article in En | MEDLINE | ID: mdl-38913881
ABSTRACT

BACKGROUND:

In KEYNOTE-522 (NCT03036488), neoadjuvant pembrolizumab plus chemotherapy and 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 plus carboplatin and then 4 cycles of doxorubicin (or epirubicin) plus cyclophosphamide. After surgery, patients received adjuvant pembrolizumab or placebo for up to 9 cycles. European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC QLQ-C30) and EORTC Breast Cancer-Specific Quality of Life Questionnaire (EORTC QLQ-BR23) were prespecified secondary objectives. Between-group differences in least squares (LS) mean change from baseline (day 1 of cycle 1 in both neoadjuvant and adjuvant phases) to the prespecified latest time point with at least 60% completion and at least 80% 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 plus chemotherapy [n = 762] vs placebo plus chemotherapy [n = 383]) in LS mean change from baseline to week 21 in QLQ-C30 global health status/quality of life (GHS/QoL), emotional functioning, and physical functioning were -1.04 (95% confidence interval = -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 plus chemotherapy followed by adjuvant pembrolizumab vs neoadjuvant placebo plus chemotherapy in early-stage TNBC. TRIAL REGISTRATION ClinicalTrials.gov, NCT03036488.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Antineoplastic Combined Chemotherapy Protocols / Neoadjuvant Therapy / Antibodies, Monoclonal, Humanized / Triple Negative Breast Neoplasms Limits: Adult / Aged / Female / Humans / Middle aged Language: En Journal: J Natl Cancer Inst Year: 2024 Type: Article Affiliation country: Singapore

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Antineoplastic Combined Chemotherapy Protocols / Neoadjuvant Therapy / Antibodies, Monoclonal, Humanized / Triple Negative Breast Neoplasms Limits: Adult / Aged / Female / Humans / Middle aged Language: En Journal: J Natl Cancer Inst Year: 2024 Type: Article Affiliation country: Singapore