A Randomized Trial Comparing Concurrent versus Sequential Radiation and Endocrine Therapy in Early-Stage, Hormone-Responsive Breast Cancer

Author:

McGee Sharon F.12,Clemons Mark12ORCID,Pond Gregory3ORCID,Caudrelier Jean-Michel1,Liu Michelle2,Alzahrani Mashari Jemaan1ORCID,Ng Terry L.12ORCID,Awan Arif A.12,Sehdev Sandeep1ORCID,Hilton John12,Savard Marie-France12ORCID,Fallowfield Lesley4,Kumar Vikaash5,Freedman Orit6,Vandermeer Lisa2,Hutton Brian2ORCID,Bourque Jean-Marc17ORCID

Affiliation:

1. Department of Medicine, Division of Medical Oncology, The Ottawa Hospital, University of Ottawa, Ottawa, ON K1H 8L6, Canada

2. Cancer Therapeutics Program, Ottawa Hospital Research Institute, Ottawa, ON K1H 8L6, Canada

3. Department of Oncology, McMaster University, Hamilton, ON L8S 4L8, Canada

4. SHORE-C, Brighton & Sussex Medical School, University of Sussex, Brighton BN1 9RH, UK

5. Markham Stouffville Hospital, Markham, ON L3P 7P3, Canada

6. Lakeridge Health, Oshawa, ON L1G 8A2, Canada

7. Centre Hospitalier de l’Universite de Montréal (CHUM), Montreal, QC H2X 0A9, Canada

Abstract

Concerns exist regarding increased toxicities, including endocrine therapy toxicity, with concurrent radiation and endocrine therapy in early breast cancer (EBC). We present a pragmatic, randomized trial comparing concurrent versus sequential endocrine and radiotherapy in hormone-responsive EBC. In this multicenter trial, patients were randomized to receive adjuvant endocrine therapy concurrent with, or sequential to, radiotherapy. The primary outcome was change in endocrine therapy toxicity from baseline to 3 months post radiotherapy using the Functional Assessment of Cancer Therapy–Endocrine Symptom (FACT-ES) score. From September 2019 to January 2021, 133 patients were randomized to concurrent endocrine and radiotherapy, and 127 to sequential treatment. Most patients were post-menopausal (72.7%, 189/260) with stage 1 disease (65.8%, 171/260). Tamoxifen was the endocrine therapy of choice for 69.6% (181/260) of patients, and an aromatase inhibitor for the remainder. The median total radiation dose and fractions were 40.1 Gray (range 26–50) and 15 fractions (range 5–25), respectively. For the primary outcome of change in endocrine therapy toxicity per FACT-ES scores from baseline to 3 months post radiotherapy, no significant difference was found between the groups (median [range] = −4.9 (−82, 38.8) for concurrent and −5.1 (−42, 40) for sequential, p = 0.87). This is the first trial to investigate the impact of concurrent versus sequential adjuvant endocrine and radiotherapy on endocrine therapy-related toxicities. The findings provide further support to allow the optimal timing of radiation and endocrine therapy to be tailored for the individual patient.

Funder

Rethinking Clinical Trials Program

Ottawa Hospital Foundation and its generous donors

Canadian Cancer Clinical Trials Network

Publisher

MDPI AG

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