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AustraLian Ovarian Cancer Assortment Trial to perform comprehensive genetic screens on women diagnosed with ovarian cancer.

AustraLian Ovarian Cancer Assortment Trial (ALLOCATE) to perform comprehensive genetic screens on women diagnosed with ovarian cancer for potential therapeutic targets and drug response modifiers, and to facilitate the biological assortment and selection of suitable patients for clinical trials of approved and investigational-targeted therapies.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12615000576527
Acronym
ALLOCATE
Enrollment
60
Registered
2015-06-03
Start date
2013-12-10
Completion date
2016-12-01
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This study aims to identify changes in the genes and proteins within the ovarian cancer tissues. Who is it for? You may be eligible to join this study if you are a female aged 18 years or above presenting at Royal Women's Hospital or the Peter MacCallum Cancer Centre with recurrent epithelial ovarian cancer (including peritoneal and fallopian tube cancers), regardless of histological subtype. Study details: All participants in this study will be required to undergo a biopsy procedure on a single occasion to obtain a tumour tissue sample, or have archived formalin-fixed, paraffin-embedded tumour tissue retrieved from pathology laboratory archives. A blood sample will also be drawn. The samples will then be analysed using a next generation sequencing panel targeted to ovarian cancer. Initially, our work will focus on getting a better understanding of the specific types of changes in ovarian cancer. Over time we hope to use that information to design and implement better treatments for women with ovarian cancer. No treatments will be administered as part of this study. This study was designed to enable women with advanced ovarian cancer to be rapidly selected for clinical trials of targeted therapies.

Interventions

No intervention(s) will be made, but we will take tumour tissue sample from participants either by biopsy, or use archived formalin-fixed, paraffin-embedded tissue from previous surgery, in addition to a blood sample. A single sample of each blood and tumour will be taken at the time of consent. We will perform a comprehensive genetic screen with a next-generation sequencing panel to help us identify changes in the genes and proteins within the cancer. Initially, our work will focus on getting

No intervention(s) will be made, but we will take tumour tissue sample from participants either by biopsy, or use archived formalin-fixed, paraffin-embedded tissue from previous surgery, in addition to a blood sample. A single sample of each blood and tumour will be taken at the time of consent. We will perform a comprehensive genetic screen with a next-generation sequencing panel to help us identify changes in the genes and proteins within the cancer. Initially, our work will focus on getting a better understanding of the specific types of changes in ovarian cancer. Over time we hope to use that information to design and implement better treatments for women with ovarian cancer.

Sponsors

The University of Melbourne
Lead SponsorUniversity

Study design

Allocation
Non-randomised trial
Intervention model
Single group
Primary purpose
Diagnosis
Masking
Blinded (masking used) (Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Women presenting at Royal Women's Hospital or the Peter MacCallum Cancer Centre with recurrent epithelial ovarian cancer (including peritoneal and fallopian tube cancers), regardless of histological subtype

Exclusion criteria

Exclusion from collection of fresh biopsy tissue if not deemed safe. Archival FFPE (paraffinised tumour sample) from previous surgery will be used in this case.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026