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Detailed Sub-study Analysis of the SECRAB Trial: Quality of Life, Cosmesis and Chemotherapy Dose Intensity.
Fernando, I N; Lax, S; Bowden, S J; Ahmed, I; Steven, J H; Churn, M; Brunt, A M; Agrawal, R K; Canney, P; Stevens, A; Rea, D W.
Affiliation
  • Fernando IN; Cancer Centre, Queen Elizabeth Hospital, Birmingham, UK. Electronic address: indrajit.fernando@uhb.nhs.uk.
  • Lax S; Cancer Research UK Clinical Trials Unit, University of Birmingham, Birmingham, UK.
  • Bowden SJ; Cancer Research UK Clinical Trials Unit, University of Birmingham, Birmingham, UK.
  • Ahmed I; Cancer Research UK Clinical Trials Unit, University of Birmingham, Birmingham, UK.
  • Steven JH; Cancer Centre, Queen Elizabeth Hospital, Birmingham, UK.
  • Churn M; Clinical Oncology, Worcestershire Royal Hospital, Worcester, UK.
  • Brunt AM; Cancer Centre, Royal Stoke University Hospital, Stoke on Trent, UK; Keele University, Keele, UK.
  • Agrawal RK; The Shrewsbury and Telford NHS Trust, Shrewsbury, UK.
  • Canney P; Beatson West of Scotland Cancer Centre, Glasgow, UK.
  • Stevens A; Cancer Centre, Queen Elizabeth Hospital, Birmingham, UK.
  • Rea DW; Cancer Centre, Queen Elizabeth Hospital, Birmingham, UK; Cancer Research UK Clinical Trials Unit, University of Birmingham, Birmingham, UK.
Clin Oncol (R Coll Radiol) ; 35(6): 397-407, 2023 06.
Article in En | MEDLINE | ID: mdl-37012180
ABSTRACT

AIMS:

SECRAB was a prospective, open-label, multicentre, randomised phase III trial comparing synchronous to sequential chemoradiotherapy (CRT). Conducted in 48 UK centres, it recruited 2297 patients (1150 synchronous and 1146 sequential) between 2 July 1998 and 25 March 2004. SECRAB reported a positive therapeutic benefit of using adjuvant synchronous CRT in the management of breast cancer; 10-year local recurrence rates reduced from 7.1% to 4.6% (P = 0.012). The greatest benefit was seen in patients treated with anthracycline-cyclophosphamide, methotrexate, 5-fluorouracil (CMF) rather than CMF. The aim of its sub-studies reported here was to assess whether quality of life (QoL), cosmesis or chemotherapy dose intensity differed between the two CRT regimens. MATERIALS AND

METHODS:

The QoL sub-study used EORTC QLQ-C30, EORTC QLQ-BR23 and the Women's Health Questionnaire. Cosmesis was assessed (i) by the treating clinician, (ii) by a validated independent consensus scoring method and (iii) from the patients' perspective by analysing four cosmesis-related QoL questions within the QLQ-BR23. Chemotherapy doses were captured from pharmacy records. The sub-studies were not formally powered; rather, the aim was that at least 300 patients (150 in each arm) were recruited and differences in QoL, cosmesis and dose intensity of chemotherapy assessed. The analysis, therefore, is exploratory in nature.

RESULTS:

No differences were observed in the change from baseline in QoL between the two arms assessed up to 2 years post-surgery (Global Health Status -0.05; 95% confidence interval -2.16, 2.06; P = 0.963). No differences in cosmesis were observed (via independent and patient assessment) up to 5 years post-surgery. The percentage of patients receiving the optimal course-delivered dose intensity (≥85%) was not significantly different between the arms (synchronous 88% versus sequential 90%; P = 0.503).

CONCLUSIONS:

Synchronous CRT is tolerable, deliverable and significantly more effective than sequential, with no serious disadvantages identified when assessing 2-year QoL or 5-year cosmetic differences.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Breast Neoplasms Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Female / Humans Language: En Journal: Clin Oncol (R Coll Radiol) Journal subject: NEOPLASIAS Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Breast Neoplasms Type of study: Clinical_trials / Observational_studies / Prognostic_studies / Risk_factors_studies Aspects: Patient_preference Limits: Female / Humans Language: En Journal: Clin Oncol (R Coll Radiol) Journal subject: NEOPLASIAS Year: 2023 Document type: Article