Abstract

PurposeTo prospectively compare HRQoL effects of two modern adjuvant chemotherapy breast cancer treatment regimens at six time-points up to 16 months after random assignment.MethodsThe open-label, randomized, Phase 3 “Panther trial” was conducted between February 2007 and September 2011. 760 women, aged 65 years and younger, after surgery for non-metastatic node-positive or high-risk node-negative breast cancer were randomized 1:1 to the experimental group (four cycles of tailored and dose-dense adjuvant epirubicin and cyclophosphamide/2 weeks followed by four cycles of tailored dose-dense docetaxel/2 weeks) or standard group (three cycles of fluorouracil and epirubicin-cyclophosphamide/3 weeks followed by three cycles of docetaxel/3 weeks). HRQoL was assessed at all Swedish centres using EORTC QLQ-C30 and EORTC QLQ-BR23 at six points during 16 months before randomization.ResultsResponse rates to questionnaires were highest at baseline 728/780 (93%) and lowest 16 months after randomization, 557/750 (74%). HRQoL declined during treatment in both groups. At the end of treatment, the experimental group reported statistically significantly lower HRQoL (P < 0.001) than the standard group on global health status, physical functioning, role functioning, social functioning, fatigue, sexual functioning, and systemic therapy effects. No differences were found for emotional functioning, body image, and arm and breast symptoms. There were no statistically significant differences between the groups at the first follow-up and at subsequent assessments. HRQoL levels at the 16-month follow-up were similar to baseline values.ConclusionsNegative HRQoL impact of the dose-dense and tailored strategy appears to be prominent during treatment, but HRQoL recover once treatment ends.Trial Registration clinicaltrials.gov Identifier: NCT00798070; isrctn.org Identifier:ISRCTN39017665.

Highlights

  • Adjuvant chemotherapy increases survival in early breast cancer [1, 2]

  • The aim of the trial was to determine whether tailored dosedense adjuvant chemotherapy improves the outcomes of early breast cancer, compared with a conventional threeweekly chemotherapy schedule

  • health-related quality of life (HRQoL) in a tailored and dose-dense schedule was compared with a standard three-weekly schedule of adjuvant chemotherapy in breast cancer patients

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Summary

Introduction

Adjuvant chemotherapy increases survival in early breast cancer [1, 2]. After a median follow-up of 5.3 years there were 151 relapses or deaths due to breast cancer in the standard group and 118 in the experimental group (HR 0.79; 95% CI 0.61–1.01; log-rank P = 0.06). Increasing the dose density of adjuvant chemotherapy by more frequent administration is safe and results in fewer disease recurrences and fewer deaths from breast cancer as shown in a recent meta-analysis including 15,212 women in 15 randomized trials [4]. Based on these results dose-dense administration of chemotherapy will be further used

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