Referring clinicians

Personalise

The Precision Care Initiative collaborates with oncologists in the Australian public healthcare system to provide expert molecular insights for cancer care. Our multidisciplinary team offers specialised consultation services to support both oncologists and their patients.

��Through our collaborative approach, we:

Review complex molecular findings with referring oncologists
Explore targeted therapy options based on genomic results
Assess the clinical significance of identified variants (both somatic and germline)
Welcome oncologist participation in case discussions about their patients

Our service enhances your oncology practice by providing detailed molecular insights to support treatment planning.

1.�� Service Overview

This is a quaternary genomic interpretation service, which assists with the primary clinician’s management plan.
The case will be reviewed by core multidisciplinary expertise, including oncology, genetics, molecular pathology.
This clinic is currently supported by MRFF funding and there are no costs to access the service.

2.�� When to Refer

This service is suitable for patients who have received tumour molecular results and would benefit from further review or interpretation within the current clinical context.
The clinic is designed to support local clinicians and is not a treatment or a second opinion service.

3.�� Quick Process Guide

To submit a referral, use the referral form link.
Once a referral form has been submitted, you will hear back from the clinic staff within 5 days.

4.�� Clinic Contact Information

P:��02 9382 5111
F:��02 9382 5180
E: seslhd-nccc-referrals@health.nsw.gov.au

Patient flow

FAQ

Based on the provided reports, we offer integrated somatic and germline analysis, personalised recommendations, and access to a network of specialists in medical oncology, cancer genetics, pathology, and bioinformatics.
Refer patients with complex molecular profiles, rare cancers, or those who may benefit from targeted therapies or clinical trials based on genomic alterations.
Please provide:��

A brief clinical history, including the latest clinical letter, for additional context.

Relevant pathology reports

Existing molecular testing results corresponding to the pathology report of the tested tissue,

Relevant radiology reports.

Our ��guides you through the required information.
Yes, our multidisciplinary team can help interpret complex molecular findings and provide clinically relevant summaries to support your decision-making process.
Yes, our clinic can help in interpreting molecular testing reports from various platforms, not just CaSP profiling. This includes reports from LifeStrands and other genomic testing services. Our team is experienced in analysing and providing recommendations based on a wide range of molecular testing methodologies. Whether you have questions about therapy suggestions in these reports or need help interpreting complex findings, we are here to support you in making informed decisions for your patients.
Our clinic can provide advice on additional appropriate molecular testing options based on each patient's specific case. This may include recommendations for NGS panels, RNA sequencing, or other relevant tests. As part of our advisory role, we can discuss the potential benefits and limitations of these tests, including any associated out-of-pocket expenses for non-Medicare funded investigations. However, the final decision to proceed with any recommended tests remains with you and your patient.
Yes, we can help to identify suitable clinical trials within Australia based on a patient's molecular profile and assist with the referral process.
We provide a prioritised list of treatment options and can assist in exploring compassionate access programs or alternative funding routes where appropriate.
We provide recommendations to support your ongoing management of the patient. Our service includes an initial MDT discussion and recommendation. If desired, we can arrange a one-time follow-up consultation for patients who wish to discuss the findings further.
Our recommendations are designed to complement your treatment plan. We provide evidence-based suggestions to support your decision-making process, recognising that you have the most comprehensive understanding of your patient's overall care.
You will receive recommendations typically within 7-10 working days after the MDT discussion. New referrals received before 5pm on the Thursday prior, will be discussed at the next scheduled MDT meeting.��Those received after will be discussed at the MDT meeting the following fortnight.
Yes, we encourage referring oncologists to join our fortnightly MDT meetings. Details for participation are provided via email following review and triage of the referral.
There are currently no costs for referring clinicians or patients.
Our clinic maintains current expertise through multiple channels:

Omico Framework: We are integrated into the Omico network, giving us access to a broad base of expertise in genomic cancer medicine.

Ongoing Research: Our team actively participates in precision oncology research projects.

Literature Monitoring: We regularly review the latest publications and developments in precision oncology.

Conference Participation: Team members attend key oncology conferences to stay abreast of emerging trends and findings.
The clinic aims to support clinicians integrating molecular results into routine care. To understand if the clinic has been of any benefit to your provision of precision oncology, we will invite you to participate in a 5-minute online survey following receipt of the MDT recommendations. Participation is voluntary.