Leukocyte nadir as a predictive factor for efficacy of adjuvant chemotherapy in breast cancer. Results from the prospective trial SBG 2000–1

Authors

  • Paula Poikonen-Saksela Comprehensive Cancer Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland
  • Henrik Lindman Department of Immunology, Genetics and Pathology University Hospital, Uppsala, Sweden
  • Asgerdur Sverrisdottir Department of Oncology, Södersjukhuset, Stocholm, Sweden
  • Per Edlund Department of Oncology, Gävle Hospital, Sweden
  • Kenneth Villman Department of Oncology, Örebro University Hospital, Örebro, Sweden
  • Lena Tennvall Nittby NittbyDepartment of Oncology, Skåne University Hospital, Malmö, Sweden
  • Søren Cold Department of Oncology, Odense University Hospital, Odense, Denmark
  • Troels Bechmann Department of Oncology, Hospital of South West Jutland, Esbjerg, Denmark
  • Lars Stenbygaard Department of Oncology, Aalborg University Hospital, Aalborg, Denmark
  • Bent Ejlertsen Department of Oncology, Rigshospitalet, Copenhagen, Denmark
  • Michael Andersson Department of Oncology, Rigshospitalet, Copenhagen, Denmark
  • Carl Blomqvist Comprehensive Cancer Center, Helsinki University Hospital and University of Helsinki, Helsinki, Finland; Department of Oncology, Örebro University Hospital, Örebro, Sweden
  • Jonas Bergh Department of Oncology-Pathology, Karolinska Institutet, Breast, Endocrine and Sarcoma Section, Cancer Theme, Karolinska University Hospital, Stockholm, Sweden
  • Johan Ahlgren Department of Oncology, Gävle Hospital, Sweden

DOI:

https://doi.org/10.1080/0284186X.2020.1757149

Abstract

Background: Retrospective studies have suggested that chemotherapy-induced leukopenia is associated with improved recurrence-free or overall survival. The SBG 2000–1 trial was designed to verify the favorable prognosis associated with chemotherapy-induced leukopenia in early breast cancer. Patients not experiencing chemotherapy-induced leukopenia were randomized into standard dosed or individually escalated chemotherapy doses based on the grade of leukopenia after a first standard dose.

Patients and methods: 1452 women in Sweden and Denmark with operable node-positive or high-risk node-negative breast cancer aged 18–60 years were recruited to participate in this trial. Participants received a first FEC cycle at standard doses (600/60/600 mg/m2). Patients (n = 1052) with nadir leukopenia grade 0–2 after the first cycle were randomized between either 6 standard FEC or 6 tailored FEC courses with doses of epirubicin and cyclophosphamide escalated during courses 2 and 3 and thereafter aimed at achieving grade 3 leukopenia. Patients with nadir leukopenia grade 3–4 after the first course continued treatment with standard FEC. Results of the randomized comparison has been published previously. The present study focuses on chemotherapy-induced leukopenia as a covariable with outcome in randomized and non-randomized patients. The prognostic value of leukopenia after course 3, was studied in a Cox model adjusted for cumulative doses of epirubicin and cyclophosphamide. The association of chemotherapy-induced leukopenia with prognosis was a preplanned secondary endpoint for this trial.

Results: The eight-year distant disease-free survival was 73%, 77%, 78% and 83% for patients with leucocyte nadir grade 0, 1, 2 and 3–4, respectively. Higher degree of leukopenia was highly significantly associated to improved distant disease-free survival (HR 0.84, 95% CI 0.74–0.96, p = .008) and overall survival (HR 0.87 (0.76–0.99, p = .032).

Conclusion: This prospective study confirms that chemotherapy-induced leukopenia is a covariable with outcome in primary breast cancer, even after adjustment for chemotherapy doses.

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Published

2020-07-02

How to Cite

Poikonen-Saksela, P., Lindman, H., Sverrisdottir, A., Edlund, P., Villman, K., Tennvall Nittby, L., … Ahlgren, J. (2020). Leukocyte nadir as a predictive factor for efficacy of adjuvant chemotherapy in breast cancer. Results from the prospective trial SBG 2000–1. Acta Oncologica, 59(7), 825–832. https://doi.org/10.1080/0284186X.2020.1757149