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A lead researcher in a lab with his team looking at a lab bench.

Genetic and Cellular Analysis

No two cancers are the same. Even with the same diagnosis, each child’s cancer can have a unique genetic fingerprint. By studying these differences through advanced testing, researchers and clinicians can design new, personalised treatments that target each child’s cancer more precisely, while sparing healthy cells. By successfully doing this, we can unlock treatments with fewer side effects and improve quality of life. 

While this approach has been very successful for certain low grade tumours, fast growing aggressive cancers remain challenging to treat. Our researchers are pushing the boundaries of analysis to find smarter, targeted therapies that only attack cancer cells. 

Research focus areas

Novel technology

Our team is developing state-of-the-art technologies to help establish improved genetic and cellular investigations that can be performed to inform diagnosis and guide prognosis and treatment for children with cancer in WA.

Precision genetics

Every cancer is different. By analysing each child’s cancer at the genetic and cellular level, we aim to understand the genetic changes that can drive cancer, and design treatments that target them. 

Personalised therapies

Personalised medicine helps us understand what is different in each child’s cancer and then identify treatments tailored specifically for each child. Genetic and cellular analysis is vital to help clinicians personalise treatments for each patient. This includes treatments that target cancer cells and spare healthy cells.

Immunotherapies

Our team is studying how a child’s rapidly developing immune system interacts with cancer cells and exploring how we can harness the body’s own defences to better fight the cancer. We aim to design new immunotherapies that work hand-in-hand with personalised treatments to benefit children with hard-to-treat cancers.

Impact on treatment & diagnosis

Analysing the unique genetic features of a child’s cancer could help clinicians and researchers to:

  • Provide a faster and more accurate diagnosis, so treatment can start sooner
  • Identify treatments that are more likely to work for the specific cancer type and child
  • Avoid unnecessary treatments, thereby minimising side effects

Thanks to national collaborations like AIM-BRAIN and ZERO Childhood Cancer, rapid DNA analysis is already transforming how we diagnose and treat childhood cancers. Clinicians can identify the exact cancer subtype sooner and choose treatments that are more likely to work for each child. 

Rishi headshot

Professor Rishi Kotecha

Theme Lead, Genetic and Cellular Analysis

Professor Kotecha is a highly qualified clinician-scientist. He has been working as a Consultant in Child and Adolescent Haematology/Oncology in Perth, Western Australia since 2012, is Co-Head of The Kids Research Institute Australia Leukaemia Translational Research team and is a Clinical Professor at The University of Western Australia. He currently holds a NHMRC Investigator Grant (2025-2029) and was named the 2024 Cancer Council of Western Australia Cancer Researcher of the year.

Nationally, Professor Kotecha chairs the ANZCHOG Leukaemia–Lymphoma Group and serves as Clinical Lead for paediatric blood cancer in WA, driving strategic planning and equitable access to medicines for children with haematological malignancy. Internationally, he is an active member of the Children's Oncology Group acute lymphoblastic leukaemia committee and the INTERFANT committee, contributing to the design of global clinical trials for children and infants with leukaemia. His goal is to translate preclinical discoveries into frontline clinical trials to improve outcomes for children with blood cancer.