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| [ ...Back to search results ] | [ Print-friendly version ] |
| Endocrine +/- Surgical Therapy for Elderly women with Mammary cancer |
| Source of record | UK Clinical Trials Gateway |
| ISRCTN | ISRCTN36767778 |
| Date ISRCTN assigned | 30/04/2007 |
| Local reference number(s) | UI06/7672 and 112984 |
| Public title | Endocrine +/- Surgical Therapy for Elderly women with Mammary cancer |
| Scientific title | |
| Acronym | ESTEeM |
| Disease/condition/study domain | Breast cancer |
| Study hypothesis | That Primary Endocrine Therapy (PET) with Arimidex is non-inferior to surgery plus adjuvant Arimidex therapy in terms of overall survival. |
| Design/methodology | A randomised, multi-centre, controlled, open label, prospective, parallel group, two-armed, non-inferiority clinical trial, with equal randomisation, to receive either PET with Arimidex (Arimidex alone arm) or surgery plus adjuvant Arimidex therapy (Surgery plus Arimidex arm). |
| Research ethics review | Ethics approval has been received from the Central Manchester Research Ethics Committee on the 12th Decemeber 2006 (ref: 06/Q1407/250). |
| Countries of trial | United Kingdom |
| Participants - inclusion criteria | 1. Female patients equal to or over 75 years of age* 2. Primary operable (TNM categories: T1, T2, T3, N0, N1, M0) invasive breast cancer (core biopsy or diagnostic incision biopsy proven) 3. Suitable for surgery. This may include local or general anaesthesia, and must remove all clinically palpable disease with clear pathological margins. Axillary staging for the clinically un-involved axilla will depend on local protocols and patient tolerance 4. Moderate or strongly oEstrogen Receptor (ER) positive, i.e. H score greater than or equal to 100 or Allred score greater than or equal to five 5. Ability to give informed consent 6. Written informed consent 7. Willing to complete the questionnaires for the additional trial evaluations 8. Able to start trial treatment within four weeks of randomisation * The inclusion criteria do not restrict for health status as we wish to leave flexibility for surgeons around the country to offer trial participation to those women for whom they feel PET is a reasonable option. This will give Surgeons discretion to select patients according to their own current practice and also give us a breadth of patient fitness levels, which will enable discrimination of those who are and are not suitable for PET on analysis. |
| Participants - exclusion criteria | 1. Disease unsuitable for surgery, e.g., locally advanced or metastatic disease, extreme physical frailty precluding adequate surgery under either local or general anaesthesia 2. Multifocal or bilateral invasive breast cancer 3. Previous invasive breast cancer 4. Previous or concurrent anti-oestrogen therapy for breast cancer 5. Previous solid cancers other than breast in the last ten years (except in the case of completely excised basal cell carcinoma/nonmelanomatous skin malignancy) 6. Inability to comply with study procedures 7. History of severe renal impairment (creatinine clearance less than 20 ml/min) 8. History of moderate or severe hepatic disease (transaminases greater than 3 x Upper Limit of Normal [ULN] or bilirubin greater than 1.5 x ULN) 9. Known hypersensitivity to anastrozole or to any of the following excipients: Lactose Monohydrate, Povidone, Sodium Starch Glycollate, Magnesium Stearate, Hypromellose, Macrogol 300, or Titanium Dioxide 10. Concurrent Hormone Replacement Therapy (HRT) or therapy with any other oestrogen containing preparation 11. Hereditary problems of galactose intolerance, the Lapp lactase deficiency or glucose-galactose malabsorption The presence of osteoporosis at baseline is NOT an exclusion criteria. |
| Patient information material | |
| Anticipated start date | 30/04/2007 |
| Anticipated end date | 29/04/2010 |
| Status of trial | Ongoing |
| Target number of participants | 1200 |
| Interventions | Arimidex alone arm: The standard therapeutic dose of Arimidex (1 mg orally, once daily) will be given until five years post-randomisation and whilst the disease remains responsive (i.e., absence of metastatic disease and absence of new primary breast cancer), there is continued clinically beneficial response of the primary tumour, and the patient tolerates therapy. Surgery plus Arimidex arm: Women will be offered a choice of surgery appropriate to their preferences, the extent of their disease and their fitness for anaesthesia. In all cases ALL palpable disease MUST be excised with a clear margin. Failure to achieve a clear margin will necessitate further surgery to re-excise the involved margins unless the patient has become unfit or refuses. The standard therapeutic dose of Arimidex (1 mg orally, once daily) will be given until five years post-randomisation or until local/regional disease recurrence, new primary breast cancer, metastatic disease or drug intolerance develops. Arimidex therapy is to start within four weeks of the final date of surgery. Contact information for second sponsor: The University of Leeds (UK) c/o Jonathan Gower Faculty of Medicine and Health Room 7.11, Level 7 Worsley Building University of Leeds Clarendon Way Leeds LS2 9NL United Kingdom |
| Primary outcome measure(s) | To compare surgery plus Arimidex with Arimidex alone (PET) in older women with ER positive breast cancer in terms of overall survival in order to determine whether Arimidex alone provides anti-cancer efficacy which is not inferior to surgery plus adjuvant Arimidex therapy. Overall survival will be measured from the time of randomisation to the date of death from any cause. |
| Secondary outcome measure(s) | To compare surgery plus Arimidex with Arimidex alone (PET) in older women with ER positive breast cancer in terms of: 1. Quality of Life (QoL), in order to determine whether Arimidex alone is superior to surgery plus Arimidex in terms of QoL: quality of life data will be recorded at baseline, at an early post-randomisation visit (six weeks post randomisation on the Arimidex alone arm and two weeks post-surgery on the Surgery plus Arimidex arm) and at four monthly time points up to 24 months and then annually to five years post randomisation: a. Functional Assessment of Cancer Therapy for Breast cancer and Endocrine Sub-scale (FACT-B+ES) will be completed at all of the above time points and at progression or recurrence/new breast primary/metastatic disease b. A Mini Mental State Examination (MMSE) and an Instrumental Activities of Daily Living (IADL) questionnaire will be completed at baseline c. An Activities of Daily Living (ADL) questionnaire will be completed at baseline, at the early post-randomisation visit and at the four month visit d. A Geriatric Depression Score questionnaire will be completed at all visits up to 24 months e. A Patient Perceptions Questionnaire will be given at baseline, 12 months and at progression or local/regional recurrence 2. Breast cancer specific survival: breast cancer specific survival will be measured from the time of randomisation to the date of death related to breast cancer 3. Failure-free survival: failure-free survival is measured from the time of randomisation to the date of first investigation of either local or regional disease recurrence (for patients in the Surgery plus Arimidex arm), disease progression (for patients in the Arimidex alone arm), metastatic disease, or death from any cause, whichever date is the earliest 4. Local disease control, as secondary outcome measures to assess non-inferior anti-cancer efficacy of Arimidex alone: treatment response for patients randomised to Arimidex alone will be categorised as either ¿clinically beneficial¿ (which will include complete response, partial response, or static disease) or Progressive Disease (PD), according to Response Evaluation Criteria in Solid Tumours (RECIST) criteria. Progressive disease will be classed as failure of local disease control. Duration of local disease control is defined as the time from randomisation to PD/local recurrence/regional recurrence in the axilla 5. Health economic assessment: the health economics assessment using the EuroQoL (EQ-5D) instrument will be completed at the early post-randomisation visit, 4, 8, 12, 16, 20 and 24 months post-randomisation, and yearly thereafter until five years post-randomisation and at progression or recurrence/new breast primary/metastatic disease Contralateral breast cancer rates, treatment related adverse events and skeletal related events will also be summarised. |
| Sources of funding | 1. Cancer Research UK (UK) (ref: C20169/A7251) 2. Astra Zeneca (UK) (ref: D5392L00021) |
| Sponsor name | The University of Sheffield (UK) |
| Sponsor details | c/o Richard Hudson 231 Glossop Road Sheffield United Kingdom S10 2GW |
| Sponsor website | http://www.shef.ac.uk/ |
| Contact name | Miss Lynda Wyld |
| Contact details | Academic Surgical Oncology Unit Room K133, Floor K Royal Hallamshire Hospital Glossop Road Sheffield United Kingdom S10 2JF |
| More information | For more up-to-date information please go to the ISRCTN link below. |
| Link to record in ISRCTN Register | ISRCTN36767778 |
| Date last extracted from ISRCTN register | 17/04/2008 |
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