A baby who was born with a large tumour on his leg has been spared chemotherapy and surgery, after whole genome sequencing at Addenbrookeѻý revealed the lump was harmless.
WATCH: Sara and Michael Bell with 11 week old Oliver
Link: https://www.youtube.com/watch?v=cdOpVYU5aqE
It was like a miracle, a miracle test that told us he didn't have cancer and we could go back to our normal lives.
Michael, Oliver's father
Sara and Michael received concerning news about their baby Oliver just a few days before his birth. An ultrasound showed a large tumour on his right leg measuring approximately 6cm in length.
After his birth, blood tests were taken and within two days the family were referred to the paediatric oncology team at ѻý ѻý Foundation Trust (CUH).
Sara explained:
“It was really scary. At Addenbrookeѻý more blood tests were taken and we were preparing for the worst. Then a consultant offered us Whole Genome Sequencing.
“Dr Behjati explained that results from this test, which just needed another sample of Oliverѻý blood, would give us the most amount of detail possible on what we were dealing with.”
Dr Sam Behjati, consultant paediatric oncologist CUH
Link: https://youtu.be/R_O54-ZSANU
Oliverѻý tumour initially looked like a type of sarcoma called infantile fibrosarcoma which we typically treat with surgery, chemotherapy or other specific drugs
Dr Sam Behjati, consultant paediatric oncologist CUH
Dr Sam Behjati is consultant paediatric oncologist at CUH and group leader at the Wellcome Sanger Institute. He treated Oliver and said:
“Under the microscope, Oliverѻý tumour initially looked like a type of sarcoma called infantile fibrosarcoma which we typically treat with surgery, chemotherapy or other specific drugs.
“Although initially Oliverѻý seemed to be an infantile fibrosarcoma, standard molecular test did not confirm this diagnosis.
"Whole genome sequencing solved the mystery. It highlighted that Oliverѻý tumour had a particular mutation which completely changed the diagnosis of Oliverѻý tumour from cancer into a benign tumour type called myofibroma.
“With this revised diagnosis we were able to change our treatment plan, opting to simply observe the tumour in the first instance, which has since started to shrink without any treatment.”
Whole Genome Sequencing
Whole Genome Sequencing is the process of determining the entirety, or nearly the entirety, of the DNA sequence of a personѻý genome at a single time.
It captures both large and small variants that can be missed with other targeted approaches. In Oliverѻý case, the whole genome of the tumour was sequenced and compared to the sequenced DNA in his blood cells.
The test is available on the ѻý National Genomic Test Directory and is offered routinely for all children with cancer at CUH.
Patients are referred to CUH from hospitals across the East of England for this highly specialised treatment.
Scientists at East Genomic Laboratory Hub provide expert analysis and interpretation of the patients WGS reports to help inform the clinical teamѻý decisions on the best course of treatment.
I burst in to tears and my Dad obviously thought the worst and hugged me ... and I told him it's ok, it's good news.
Sara, Oliver's mother
Oliverѻý mother Sara said:
“For the first eight weeks of Oliver being born, we lived with the prospect of cancer dominating all our lives and chemotherapy being the next step. Two weeks after his whole genome test, everything changed. We found out his tumour is benign and itѻý getting smaller without any treatment. We couldn’t be more relieved.”
“The team at Addenbrookeѻý were incredible. They were honest with us at every step keeping us well informed of what we were dealing with.
“Oliver is now getting bigger and stronger every day. Itѻý fantastic.”
Oliverѻý father Michael added:
“Our lives were turned upside down when we thought Oliver would need surgery and chemotherapy. Receiving such clarity on the type of tumour we were dealing was so important.
“We know we are really lucky to have such an outcome and it enabled us to live our lives again.”
Professor Dame Sue Hill from the National Genomic Medicine Service commented:
“I've been able to see first-hand what this has meant for Oliver and his family, which is a powerful demonstration of the power of genomics to drive real benefits for patients and families.”
A video showing feedback from two families (including Sara and Michael) about their experience of whole genome sequencing and what the results meant to them,
Cambridge Children's Hospital
Baby Oliverѻý case is an example of how young people and their families from across the East of England, and beyond, will benefit from Cambridge Childrenѻý Hospital.
The new hospital will co-locate world-class scientists and doctors to deliver the latest in diagnostics and treatment.
By building this specialist new facility on the Cambridge Biomedical Campus we will be able to use whole genome sequencing to drive cutting edge treatment and therapies for more children and young people across the whole region and beyond.
