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Pilot for a Randomised Comparison of Anastrozole Commenced Before and Continued During Adjuvant Radiotherapy for Breast Cancer Versus Anastrozole and Subsequent Ant-Oestrogen Therapy Delayed Until After Radiotherapy


Phase 4
18 Years
N/A
Open (Enrolling)
Both
Breast Cancer

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Trial Information

Pilot for a Randomised Comparison of Anastrozole Commenced Before and Continued During Adjuvant Radiotherapy for Breast Cancer Versus Anastrozole and Subsequent Ant-Oestrogen Therapy Delayed Until After Radiotherapy


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.


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.

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Local failure within irradiation volume

Principal Investigator

Ass. Prof. Peter H Graham, MBBS FRANZCR

Investigator Role:

Principal Investigator

Investigator Affiliation:

Cancer Care Centre, St George Hospital, Sydney

Authority:

Australia: Department of Health and Ageing Therapeutic Goods Administration

Study ID:

STARS-Pilot (05/55 Graham)

NCT ID:

NCT00126360

Start Date:

August 2005

Completion Date:

May 2016

Related Keywords:

  • Breast Cancer
  • Breast Cancer
  • Timing of Radiotherapy
  • Local Control
  • Breast Neoplasms

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