A Parp Inhibitor (BMN 673) for Inoperable Advanced eNDometrial cAncer

Endometrial Cancer Clinical Trial

— PANDA  

Official title:

A Single Arm Phase II Trial of BMN 673 for Inoperable, Advanced Endometrial Cancer With Retrospective PTEN, MSI and MRE11 Analysis

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT02127151
• Other study ID #: UCL/13/0045
• Secondary ID: 2013-003469-32
• Status: Withdrawn
• Phase: Phase 2
• Start date: October 1, 2014
• Est. completion date: May 1, 2017

Study information

• Verified date: August 2021
• Source: University College, London
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A Single Arm Phase II Trial of BMN 673 for Inoperable, Advanced Endometrial Cancer With Retrospective PTEN, MSI and MRE11 Analysis

PTEN= Phosphatase and tensin homolog MSI= Microsatellite instability MRE11= Double-strand break repair protein MRE11A

This trial will investigate whether the drug BMN 673 has therapeutic benefit in the treatment of advanced endometrial cancer. Nearly 8,000 patients are diagnosed with endometrial cancer in the UK every year. A significant proportion are either diagnosed with advanced disease which may be inoperable and/or metastatic (i.e spread to other organs outside the endometrium), or curable disease which relapses following first line treatment. There is no established standard of care for these patients as both chemo and hormone therapy has limited effectiveness and survival benefit. Survival rates have not improved in the past 20 years. Furthermore there are no so called 'targeted' drugs licensed for its treatment i.e. drugs that block the growth and spread of cancer by interfering with specific molecules involved in tumor growth and progression. This leaves an unmet need for effective systemic treatments for advanced, inoperable and metastatic endometrial cancer.

BMN 673 has been shown to be potentially effective in treating cancers known to behave similarly to endometrial disease, both in the laboratory and in Phase I studies involving patients with advanced cancers. Similarly the drug appears to be relatively tolerable. A Phase II trial such as the one proposed by this application could demonstrate activity that might lead to a new effective treatment for patients with inoperable, advanced, recurrent or metastatic endometrial cancer, while the proposed substudy also presents the possibility of discovering a subset of patients more likely to derive benefit from BMN 673.

This trial is for adult women (18 and above) with advanced, inoperable or metastatic endometrial cancer. Patients will be recruited from approximately 15 National Health Service (NHS) Trusts based in the United Kingdom (UK). The study is expected to last approximately 18-24 months in terms of recruitment time, and a maximum of 100 eligible women will be registered. All patients will receive BMN 673 until their disease worsens or their doctor decides they should stop treatment.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: May 1, 2017
• Est. primary completion date: May 1, 2017
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Age = 18 years

• Histologically confirmed endometrial cancer. All histological subtypes except for carcinosarcoma are eligible

• Evidence of inoperable, advanced, recurrent or metastatic disease by imaging and/or histological criteria

• = 1 previous line of systemic cancer therapy for inoperable, advanced, recurrent or metastatic endometrial cancer. Chemotherapy in the adjuvant setting is not considered a prior line of therapy unless recurrence occurred during adjuvant treatment or = 6 months after the last treatment; first line treatment of advanced disease must include at least one cytotoxic agent to be considered as a line of therapy; prior hormonal treatment is not considered a line of therapy in any setting

• Written informed consent obtained prior to any screening procedures

• Patients must give consent for provision of archival histological tissue for the purposes of translational research. If archival tissue is not available or is of insufficient quantity and/or quality, the patient will have the option to consent to undergo biopsy where feasible. If biopsy is not feasible or the patient does not give consent for biopsy when archival tissue is not available, the patient will not be eligible for the trial. The quality and quantity of archival tissue will be assessed by a suitably qualified individual, usually a histopathologist, at site to ensure adequate tissue sample available for testing PTEN, MSI and MRE11

• Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0-2

• Life expectancy = 12 weeks

• Patient has at least one site of measurable disease on radiological imaging (i.e. target lesion) as per RECIST v1.1

• Evidence of non-childbearing status and must not be lactating OR must have postmenopausal status

• Adequate bone marrow and organ function

Exclusion Criteria:

• Prior treatment with a poly adenosine diphosphate ribose polymerase (PARP) inhibitor

• Progressive disease = 3 months after platinum-based chemotherapy

• Active uncontrolled infection including known Hepatitis B, Hepatitis C or HIV

• Obstruction of the gastrointestinal tract or other reason preventing effective oral administration of medication

• Serious concomitant non-malignant disease, uncontrolled organ dysfunction or medical disorder considered by the Investigator to make the subject unsuitable for trial participation including any psychiatric disorder that prevents informed consent

• Significant active cardiovascular disease

• Symptomatic brain metastases

• Immunosuppressant therapy or considered to be otherwise immunocompromised

• Myelodysplastic syndrome/acute myeloid leukaemia

• Major surgery = 28 days prior to registration, or ongoing clinically significant post-surgical complications

• Chemotherapy, radiotherapy (a single fraction of palliative radiotherapy is allowed provided that the site being treated is not subsequently used as a target lesion as per RECIST v1.1 for the purpose of assessing tumour response on trial), immunotherapy or other investigational therapy for cancer = 21 days prior to registration (42 days for nitrosoureas, mitomycin-C)

• Unresolved clinically significant toxicities from prior systemic therapy

• Known hypersensitivity to any of the agents or excipients to be administered

• Unwillingness or inability to comply with the trial protocol

• Patients with a history of other malignancy = 3 years prior to registration with the exceptions of a) cone-biopsied in situ carcinoma of the cervix uteri; b) basal or squamous cell carcinoma of the skin.

Related Conditions & MeSH terms

• Endometrial Cancer
• Endometrial Neoplasms

Intervention

Drug:
• BMN 673
Starting oral dose of 1.0 mg once daily to be taken until progression, death, unacceptable toxicity, withdrawal consent or any other criterion felt by the Investigator to preclude continuation of treatment.

Locations

Country	Name	City	State
United Kingdom	The Clatterbridge Cancer Centre	Bebington	Wirral
United Kingdom	Royal Sussex County Hospital	Brighton	East Sussex
United Kingdom	Bristol Haematology and Oncology Centre	Bristol
United Kingdom	Velindre Cancer Centre	Cardiff	South Glamorgan
United Kingdom	Western General Hospital	Edinburgh	Lothian
United Kingdom	The Beatson West of Scotland Cancer Centre	Glasgow	Greater Glasgow
United Kingdom	East Kent Hospitals University NHS Foundation Trust	Kent
United Kingdom	St James's University Hospital	Leeds	South Yorkshire
United Kingdom	Guy's Hospital	London
United Kingdom	St Bartholomew's Hospital	London	Greater London
United Kingdom	University College Hospital	London	Greater London
United Kingdom	The Royal Marsden Hospital (London and Surrey)	London And Surrey
United Kingdom	The Christie Hospital	Manchester	Greater Manchester
United Kingdom	Northern Centre for Cancer Care	Newcastle
United Kingdom	The Churchill Hospital	Oxford	Oxfordshire
United Kingdom	Royal Marsden Hospital (Sutton)	Sutton	Surrey

Sponsors (2)

Lead Sponsor	Collaborator
University College, London	Medivation, Inc.

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Progression free survival (PFS) rate	Measured from date of first BMN 673 dose to first progression (defined using Response Evaluation Criteria in Solid Tumours (RECIST) v1.1) or death, whichever is the sooner.	6 months
Secondary	Best Response	Measured from the date of first BMN 673 dose.	Up to 30 months
Secondary	Overall survival (OS)		Up to 30 months
Secondary	Response at each radiological assessment		Up to 30 months
Secondary	Duration of Response (DoR)		Up to 30 months
Secondary	Median PFS		Up to 30 months
Secondary	Safety and toxicity	Common Terminology Criteria for Adverse Events (CTCAE) v4.03 grade 3-4 toxicity; dose reductions, omissions, delays; exposure; compliance.	Up to 30 months

External Links

•   Trial page on the University College London (UCL) Cancer Trials Centre website