STARS Breast Trial (Study of Anastrozole and Radiotherapy Sequencing Pilot)

St George Hospital

Status and phase

Unknown

Phase 4

Conditions

Breast Cancer

Treatments

Drug: Timing of Anastrozole in respect to radiotherapy

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00126360

STARS-Pilot (05/55 Graham)

Details and patient eligibility

About

This is a randomized study comparing the use of Anastrozole before and continuing during radiotherapy for breast cancer compared to the use of anastrozole after irradiation.

Full description

Adjuvant radiotherapy is well established as the primary modality to enhance local control in breast cancer. The use of adjuvant hormone therapy such as tamoxifen has shown to improve local control to a relatively minor amount on its own and does enhance local control of adjuvant radiotherapy. There is however, conflicting in vitro and clinical data regarding the effects of different sequences on tamoxifen and radiotherapy in terms of both local control and enhancement of radiotherapy toxicities.

Aromatase inhibitors such as anastrazole are establishing themselves as a class of drug superior to tamoxifen for the control of estrogen dependent breast cancers and overall are better tolerated with the exception of greater bone loss.

As the key question is whether the sequencing of the aromatase inhibitor anastrozole alters local control by acting as an enhancer of the radiation breast cancer cell kill, it is therefore the aim of this study to compare 3 months of anastrozole prior to radiotherapy versus 3 months of anastrozole after radiotherapy with a specific objective of reducing the baseline ratio of in- field radiotherapy failure from 6% to 3%.This pilot study is preliminary to a planned long term study to investigate local failure.

For the pilot a period of 6 months with all contributing centres open will provide a good test of recruitment matching estimates. 100 patients will provide a good sample to compare to the 270 tamoxifen treated women in the breast boost study for quality of life. It will also provide a 95% CI on the proportion of complying women in the order of ± 5% if 85 to 90 % of women comply.

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Age 18 or more years. No upper limit.
Post total mastectomy or lumpectomy. All planned surgery complete.
Margins clear (no tumour contacting the inked margin)
Tumour oestrogen or progesterone receptor positive
Planned dose to irradiated volumes at least the biological equivalent of 45 Gy in 25 fractions or more.
ECOG 0-2
Patients post menopausal using same criteria as ATAC study.
Written informed consent

Exclusion criteria

Previous radiotherapy to the area to be treated.
Previous invasive malignancy within 5 years of current breast cancer diagnosis with the exception of cervix in-situ or skin cancer other than melanoma.
Patients with clinical evidence of metastatic disease.
Previous hormonal breast therapy.
Ongoing hormone replacement therapy.