Moderate hypofractionation remains the standard of care for whole-breast radiotherapy in breast cancer. Considerations regarding FAST and FAST-Forward
Creators
- 1. Department of Radiation Oncology, University Hospital Schleswig-Holstein, Kiel (Germany)
- 2. Department of Radiation Oncology, St. Marien-Krankenhaus, Siegen (Germany)
- 3. Partner Site Munich, Deutsches Konsortium für Translationale Krebsforschung (dktk), Munich (Germany)
- 4. Department of Radiation Medicine (IRM), Helmholtz Zentrum München (HMGU), Neuherberg (Germany)
- 5. Department of Radiation Oncology, Technische Universität München (TUM), Munich (Germany)
Description
Moderate hypofractionation is the standard of care for adjuvant whole-breast radiotherapy after breast-conserving surgery for breast cancer. Recently, 10-year results from the FAST and 5‑year results from the FAST-Forward trial evaluating adjuvant whole-breast radiotherapy in 5 fractions over 5 weeks or 1 week have been published. This article summarizes recent data for moderate hypofractionation and results from the FAST and FAST-Forward trial on ultra-hypofractionation. While the FAST trial was not powered for comparison of local recurrence rates, FAST-Forward demonstrated non-inferiority for two ultra-hypofractionated regimens in terms of local control. In both trials, the higher-dose experimental arms resulted in elevated rates of late toxicity. For the lower dose experimental arms of 28.5 Gy over 5 weeks and 26 Gy over 1 week, moderate or marked late effects were similar in the majority of documented items compared to the respective standard arms, but significantly worse in some subdomains. The difference between the standard arm and the 26 Gy of the FAST-Forward trial concerning moderate or marked late effects increased with longer follow-up in disadvantage of the experimental arm for most items. For now, moderate hypofractionation with 40–42.5 Gy over 15–16 fractions remains the standard of care for the majority of patients with breast cancer who undergo whole-breast radiotherapy without regional nodal irradiation after breast-conserving surgery.
Availability note (English)
Available from: http://dx.doi.org/10.1007/s00066-020-01744-3Additional details
Identifiers
Publishing Information
- Journal Title
- Strahlentherapie und Onkologie
- Journal Volume
- 197
- Journal Issue
- 4
- Journal Page Range
- p. 269-280
- ISSN
- 0179-7158
- CODEN
- STONE4
INIS
- Country of Publication
- Germany
- Country of Input or Organization
- Germany
- INIS RN
- 52046576
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- CARCINOMAS; CLINICAL TRIALS; DECISION MAKING; DELAYED RADIATION EFFECTS; EARLY RADIATION EFFECTS; EDEMA; ELDERLY PEOPLE; EXTERNAL BEAM RADIATION THERAPY; FRACTIONATED IRRADIATION; GY RANGE 10-100; MAMMARY GLANDS; RADIATION DOSES; RADIODERMATITIS; SHRINKAGE; SURGERY; TOXICITY
- Descriptors DEC
- ABSORBED DOSE RANGE; ADULTS; AGE GROUPS; AGED ADULTS; ANIMALS; BIOLOGICAL EFFECTS; BIOLOGICAL RADIATION EFFECTS; BODY; DERMATITIS; DISEASES; DOSES; GLANDS; GY RANGE; HUMAN POPULATIONS; INJURIES; IRRADIATION; LOCAL RADIATION EFFECTS; MAMMALS; MAN; MEDICINE; MINORITY GROUPS; NEOPLASMS; NUCLEAR MEDICINE; ORGANS; PATHOLOGICAL CHANGES; POPULATIONS; PRIMATES; RADIATION DOSE RANGES; RADIATION EFFECTS; RADIATION INJURIES; RADIOLOGY; RADIOTHERAPY; SKIN DISEASES; SYMPTOMS; TESTING; THERAPY; VERTEBRATES