Health-related quality of life in the Swedish PREDIX HER2 trial, evaluating docetaxel, trastuzumab, pertuzumab versus trastuzumab emtansine as neoadjuvant treatment of HER2-positive breast cancer.

Authors

null

Yvonne Brandberg

Karolinska Institutet, Department of Oncology-Pathology (OnkPat), Karolinska University Hospital, Stockholm, Sweden

Yvonne Brandberg , Anne Andersson , Judith Bjohle , Ana Bosch , Lena Carlsson , Ann Charlotte Dreifaldt , Zakaria Einbeigi , Hanna Fredholm , Erika Isaksson-Friman , Theodoros Foukakis , Ellinor Elinder , Mats Hellstrom , Hemming Johansson , Tobias Lekberg , Henrik Lindman , Jonas C. S. Bergh , Thomas Hatschek

Organizations

Karolinska Institutet, Department of Oncology-Pathology (OnkPat), Karolinska University Hospital, Stockholm, Sweden, Umea University, Umea, Sweden, Karolinska University Hospital, Stockholm, Sweden, Lund University Cancer Center, Lund, Sweden, County Hospital, Sundsvall, Sweden, Orebro University Hospital, Orebro, Sweden, Sahlgrenska University Hospital, Gothenburg, Sweden, Capio St Göran, Stockholm, Sweden, Karolinska Institutet and University Hospital, Stockholm, Sweden, Sodersjukhuset, Stockholm, Sweden, Karolinska University Hospital, Clinical Trial Unit Oncology, Stockholm, Sweden, Department of Oncology, Karolinska Institutet and University Hospital, Stockholm, Sweden, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden, Uppsala University Hospital, Uppsala, Sweden

Research Funding

Other Foundation

Background: Neoadjuvant therapy combining docetaxel, trastuzumab and pertuzumab (DTP) was compared to trastuzumab emtansine (T-DM1) in the randomized phase 2 PREDIX HER2 trial. Patients, ≥18 years with HER2 positive breast cancer, ≥20mm or with verified lymph node metastases, were randomized to six courses of DTP (Standard arm) or T-DM1 (Experimental arm). Primary endpoint was pathological objective response to primary medical therapy at post-treatment surgery. Health related quality of life (HRQoL) was a secondary outcome, and is of specific interest as there was no difference between the randomization groups regarding the main endpoint (results presented in a separate abstract sent to ASCO 2019, Bergh et al.). Methods: Of 202 randomized patients, 190 are available for evaluation at this point. HRQoL was measured, using EORTC QLQ-C30 + EORTC QLQ-BR23, at baseline before randomization and after six courses. Results: No differences between the randomization arms were found at baseline. Results after six courses, based on 163 patients (86%) and adjusted to baseline values, revealed statistical significant differences (p≤0.01), favoring the experimental T-DM1 arm on 7 out of 15 of the EORTC QLQ-C30 variables (Physical functioning, Role functioning, Social functioning, Global quality of Life, Fatigue, Dyspnea, and Diarrhea). For the breast cancer specific questionnaire (EORTC-BR23), the experimental arm scored statistically significantly better on 5 out of 7 subscales (Body image, Sexual functioning, Sexual enjoyment, Systemic therapy side effects and Upset by hair loss). All of the statistical significant differences were of moderate or large clinical significance (≥10 scale scores). No differences between the randomization arms were found for the remaining HRQoL variables. Conclusions: The experimental arm reported better HRQoL than the control arm after six courses. Trastuzumab emtansine may be a useful treatment alternative due to better HRQoL and lower toxicity. Clinical trial information: NCT02568839

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Abstract Details

Meeting

2019 ASCO Annual Meeting

Session Type

Poster Session

Session Title

Breast Cancer—Local/Regional/Adjuvant

Track

Breast Cancer

Sub Track

Neoadjuvant Therapy

Clinical Trial Registration Number

NCT02568839

Citation

J Clin Oncol 37, 2019 (suppl; abstr 583)

DOI

10.1200/JCO.2019.37.15_suppl.583

Abstract #

583

Poster Bd #

75

Abstract Disclosures