Fulvestrant +/- Akt Inhibition in Advanced Aromatase Inhibitor Resistant Breast Cancer

NCT ID: NCT01992952

Last Updated: 2025-11-26

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 149 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2014-05-07
• Study Completion Date: 2025-12-31

Brief Summary

This is a two stage study, with an initial dose escalation phase I study and subsequent double blind randomised phase II controlled trial. Eligible patients are post-menopausal women with metastatic ER+ breast cancer not suitable for surgical resection. Patients should be suitable for endocrine treatment, but have received no more than 3 previous lines of endocrine treatment and up to 1 line of chemotherapy for metastatic disease. They will also have had progressive disease during treatment with an aromatase inhibitor. Following the dose-escalation in stage 1, patients will be randomised to receive fulvestrant plus either placebo or 480mg (or maximum tolerated dose) of AZD5363 oral capsules or tablets taken once daily.

Patients will receive fulvestrant in combination with either placebo or AZD5363 until disease progression. Patients may continue to receive fulvestrant and AZD5363/placebo treatment even after the last trial visit.

Detailed Description

Phase 1 (n=9-12)

As fulvestrant and AZD5363 have not previously been administered to this population, we have incorporated an initial phase I dose escalation:

• 3 patients will receive fulvestrant 500mg on day 1 and 400mg AZD5363 oral capsules or tablets bd 4 days on and 3 days off. They will be assessed for dose limiting toxicity (DLT) on day 1, 15 and 28 of cycle 1. The safety review committee (SRC) will meet to review DLT reports when the third patient finishes cycle 1.
• If 400mg is tolerable (0/3-6 or 1-6 has a DLT) then the dose of AZD5363 will be escalated to 480mg.
• If 480mg is tolerable in a cohort of 6 patients then 480mg will be the Maximum tolerated dose (MTD).
• If 480mg is not tolerable (2/6 patients have a DLT), then the 400mg dose will be the MTD.
• If 400mg is not tolerable (2 or more patients have a DLT) then the dose will be reduced to 320mg for the next cohort of 6 patients.
• if 320mg is tolerable in a cohort of 6 patients, then 320mg will be the MTD.
• if 320mg is not tolerable, then the trial will not proceed. If patients are withdrawn for reasons other than toxicity during Stage 1 before DLT assessments then they will be replaced.

Phase 2 (n=136)

Recruitment in to Phase 2 will commence after all 6 patients in Stage 1 have completed at least 1 cycle of therapy and the SRC have given the go-ahead. Patients will be randomised to one of two arms:

Arm A (control arm): Fulvestrant + placebo The control arm will consist continuous 28 day cycles of fulvestrant 500mg on day 1, plus placebo capsule or tablet bd 4 days on and 3 days off.

Arm B (experimental arm): Fulvestrant + AZD5363 The experimental arm will consist continuous 28 day cycles of fulvestrant 500mg on day 1, plus AZD5363 capsule or tablet bd 4 days on and 3 days off.

A further safety assessment will be made after 20 patients have been randomised to receive AZD5363 or placebo and have at least 1 cycle of protocol treatment in stage 2.

Phase 2 will have 3 stages, this is because we want to investigate whether tumours with certain characteristics are more likely to respond to the AZD5363. As mentioned above, we will test the tumour tissue for the presence of a PIK3CA mutation (a gene encoding catalytic subunit of class 1 PI3K) and for low levels of phosphatase and tensin homolog (PTEN). Laboratory research has shown that tumours with these characteristics may respond better to the AZD5363. Tumours which do not have these characteristics are called wild-type, and we want to make sure we don't recruit too many of these patients if they might not benefit from the treatment.

We will start off by recruiting all eligible patients. However, when we know that we have 40 patients with wild-type tumours, and they have been on trial treatment for eight weeks, we will stop recruiting patients with wild-type tumours. This means that we will do a blood test to confirm the tumour has the PIK3CA mutation before a patient can be entered onto the study.

We will perform a review of the tumour measurements in this wild-type group to determine whether the tumours of the patients receiving AZD5363 have shrunk more than patients receiving placebo. If there is no evidence that the tumour has shrunk in the AZD5363 group compared to placebo, we will not recruit any more patients with wild-type tumours. If there is evidence that that the tumours have shrunk in the AZD5363 group, we will start recruiting patients with wild-type tumours again.

Conditions

Estrogen Receptor Positive Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: QUADRUPLE

Study Groups

AZD5363 plus fulvestrant

Fulvestrant 500mg and AZD5363 4 days on 3 days off at dose determined in safety run in (maximum 480mg and minimum 320mg bd)

Group Type: EXPERIMENTAL

AZD5363

Intervention Type: DRUG

Up to 480mg oral tablets twice a day, taken four days on, 3 days off treatment.

Fulvestrant

Intervention Type: DRUG

2 x 250mg injections, received on Days 1 and 15 of cycle 1, and on day 1 of each subsequent 28 day cycle.

Placebo plus fulvestrant

Fulvestrant 500mg D1, D15 (cycle 1) and D1 of a 28 cycle thereafter. AZD5363 placebo 4 days on 3 days off

Group Type: ACTIVE_COMPARATOR

Placebo

Intervention Type: DRUG

Placebo tablets taken twice a day, 4 days on treatment, 3 days off treatment

Fulvestrant

Intervention Type: DRUG

2 x 250mg injections, received on Days 1 and 15 of cycle 1, and on day 1 of each subsequent 28 day cycle.

Interventions

AZD5363

Up to 480mg oral tablets twice a day, taken four days on, 3 days off treatment.

Intervention Type: DRUG

Placebo

Placebo tablets taken twice a day, 4 days on treatment, 3 days off treatment

Intervention Type: DRUG

Fulvestrant

2 x 250mg injections, received on Days 1 and 15 of cycle 1, and on day 1 of each subsequent 28 day cycle.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Post-menopausal Women
• Life expectancy 3 months
• Histological confirmation of ER+ breast cancer
• Clinical or histological confirmation of metastatic or locally advanced disease not amenable to surgical resection
• Measurable or non-measurable disease
• Adequate bone marrow, renal and hepatic function
• Eastern Cooperative Oncology Group (ECOG) performance status < or equal to 2
• Progressive disease whilst receiving an aromatase inhibitor (AI) for metastatic breast cancer (MBC)
• Relapsed with metastatic disease whilst receiving an AI in adjuvant setting
• Up to 3 prior lines of endocrine therapy for Advanced Breast Cancer
• Up to 1 line of chemotherapy for Advanced Breast Cancer
• Patient willing to donate archival tumour sample
• Patient willing to donate baseline blood sample
• Suitable for further endocrine therapy

Exclusion Criteria

• Previous treatment with fulvestrant or PI3K/mTOR(mammalian target of rapamycin )/Akt inhibitor therapy
• Treatment with chemotherapy, immunotherapy or targeted, biologic or tumour embolisation within 21 days of study drug administration
• Palliative radiotherapy within 7 days of study drug
• Clinically significant abnormalities in glucose metabolism
• Rapidly progressive visceral disease not suitable for further endocrine therapy
• Known brain or leptomeningeal metastases
• Any co-existing medical condition precluding trial entry including significant cardiac disease (to be defined in the protocol)
• Concomitant medication unsuitable for combination with trial medication

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Velindre NHS Trust

OTHER_GOV

Sponsor Role: lead

AstraZeneca

INDUSTRY

Sponsor Role: collaborator

Cenduit LLC

INDUSTRY

Sponsor Role: collaborator

Covance

INDUSTRY

Sponsor Role: collaborator

Cardiff and Vale University Health Board

OTHER_GOV

Sponsor Role: collaborator

Responsible Party

Dr Margherita Carucci

Clinical Trial Manager

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Sacha Howell, FRCP PhD

Role: STUDY_CHAIR

The University of Manchester and The Christie NHS Foundation Trust

Robert Jones, MRCP PhD

Role: STUDY_CHAIR

Cardiff University and Velindre Cancer Centre

Locations

Velindre NHS Trust

Cardiff, Cardiff, United Kingdom

Christie Hospital

Manchester, Greater Manchester, United Kingdom

Ysbyty Gwynedd

Bangor, , United Kingdom

Clatterbridge Cancer Centre

Bebington, , United Kingdom

Royal Blackburn Hospital

Blackburn, , United Kingdom

Blackpool Victoria Hospital

Blackpool, , United Kingdom

University Hospital of North Durham

Durham, , United Kingdom

Great Western General Hospital

Edinburgh, , United Kingdom

Calderdale and Huddersfield NHS Foundation Trust

Huddersfield, , United Kingdom

The Ipswich Hospital NHS Trust

Ipswich, , United Kingdom

University Hospitals Morecambe Bay

Lancaster, , United Kingdom

St James's University Hospital

Leeds, , United Kingdom

Mount Vernon Cancer Centre

London, , United Kingdom

Royal Free Hospital

London, , United Kingdom

Derriford Hospital

Plymouth, , United Kingdom

Royal Preston Hospital

Preston, , United Kingdom

Glan Clwyd Hospital

Rhyl, , United Kingdom

Queen's Hospital

Romford, , United Kingdom

Southampton General Hospital

Southampton, , United Kingdom

Royal Stoke University Hospital

Stoke-on-Trent, , United Kingdom

Royal Albert and Edward Infirmary -Wrightington

Wigan, , United Kingdom

Countries

United Kingdom

References

Howell SJ, Casbard A, Carucci M, Ingarfield K, Butler R, Morgan S, Meissner M, Bale C, Bezecny P, Moon S, Twelves C, Venkitaraman R, Waters S, de Bruin EC, Schiavon G, Foxley A, Jones RH. Fulvestrant plus capivasertib versus placebo after relapse or progression on an aromatase inhibitor in metastatic, oestrogen receptor-positive, HER2-negative breast cancer (FAKTION): overall survival, updated progression-free survival, and expanded biomarker analysis from a randomised, phase 2 trial. Lancet Oncol. 2022 Jul;23(7):851-864. doi: 10.1016/S1470-2045(22)00284-4. Epub 2022 Jun 4.

Reference Type: DERIVED

PMID: 35671774 (View on PubMed)

Jones RH, Casbard A, Carucci M, Cox C, Butler R, Alchami F, Madden TA, Bale C, Bezecny P, Joffe J, Moon S, Twelves C, Venkitaraman R, Waters S, Foxley A, Howell SJ. Fulvestrant plus capivasertib versus placebo after relapse or progression on an aromatase inhibitor in metastatic, oestrogen receptor-positive breast cancer (FAKTION): a multicentre, randomised, controlled, phase 2 trial. Lancet Oncol. 2020 Mar;21(3):345-357. doi: 10.1016/S1470-2045(19)30817-4. Epub 2020 Feb 5.

Reference Type: DERIVED

PMID: 32035020 (View on PubMed)

Related Links

https://doi.org/10.1016/S1470-2045(19)30817-4

Primary analysis results

https://doi.org/10.1016/S1470-2045(22)00284-4

Updated and expanded biomarker results

Other Identifiers

FAKTION

Identifier Type: -

Identifier Source: org_study_id