Genomic sequencing of tumours from paediatric cancer patients experiencing a relapse enabled 107 patients to receive an appropriate matched therapy that is not the standard of care, according to data from the international clinical trial MAPPYACTS.

Paediatric cancers have a high rate of remission, with 85 percent of patients surviving five years or longer after diagnosis. However, if the cancer returns, treatment options are limited.

“The main purpose was to genetically profile the patients' tumours and use that to suggest a treatment,” said Birgit Geoerger, MD, PhD, a professor of paediatric clinical research at Gustave Roussy Cancer Center in France. “Are there molecular alterations that we can target with these newer drugs?”

In many cases, paediatric cancers are subjected to gene panel sequencing, in which common cancer driver genes are sequenced to look for mutations.

While this information can provide valuable insights about how the tumour operates, it is not often used to guide treatment decisions. “There are not a lot of trials testing targeted therapies in children,” Geoerger said.

Findings are published in Cancer Discovery, a journal of the American Association for Cancer Research.

Geoerger and colleagues initiated the MAPPYACTS clinical trial to prospectively recruit paediatric patients with relapsed cancers and perform comprehensive whole exome sequencing (WES) and/or RNA sequencing in order to recommend a therapy tailored to each patient.

They collected tissue samples from 774 patients, 632 of which were successfully sequenced. A clinical molecular tumour board then reviewed the sequencing data from each patient.

Mutations were considered “ready for routine use” if there was significant clinical evidence that a drug could effectively treat tumours harbouring the mutation.

Mutations were considered “potentially actionable” if any evidence existed that an approved or investigational drug (a drug being tested in clinical trials) could target the mutated protein or another member of the affected signalling pathway.

The clinical molecular tumour board identified 432 patients with potentially actionable alterations, 107 of whom were then treated with a matched targeted therapy, either alone (57 percent), in combination with chemotherapy (37 percent) or in combination with another targeted therapy (11 percent).

Notably, 42 percent of the “ready for routine use” alterations found in this study were previously unknown or had not been identified by previous diagnostics.

The majority of cancers with “ready for routine use” mutations were tumours of the central nervous system, such as gliomas and medulloblastomas, or anaplastic large cell lymphomas.

Geoerger said this lack of detection was not because tests for these alterations do not exist, but because they are not always used.

“It didn’t mean an alteration couldn’t be found, rather that nobody looked for it,” she said.

The overall response rate of patients who received a matched therapy was 17 percent, with a 41 percent disease control rate. Among patients with alterations ready for routine use, all of whom received their treatments as a monotherapy, the objective response rate was 38 percent.

Patients with potentially actionable mutations that were not ready for routine use had an overall response rate of 14 percent.

The researchers also investigated the possibility of using circulating tumour DNA (ctDNA) (fragments of tumour cell DNA that circulate in the blood) to identify targetable mutations.

Though the researchers did not make treatment decisions based on this arm of the study, they successfully performed WES on ctDNA from 128 patients with matched tumour WES and found 94 potentially actionable mutations, 35 of which had not been detected by tumour WES.

Sequencing of ctDNA also successfully identified 76 percent of potentially actionable alterations that were found in tumour tissue.

In addition to accounting for tumour heterogeneity that traditional biopsies may miss, Geoerger hopes that liquid biopsies can spare some children from invasive procedures and allow also for the profiling of tumours that are difficult to biopsy or resect, such as those found in the central nervous system.

Overall, Geoerger feels that this study provides evidence for widespread genetic sequencing of paediatric cancers and the matching of patients’ tumour genetic profiles with targeted therapies and their combinations, research that she and her colleagues are continuing in the concurrent AcSé-ESMART trial and the upcoming MAPPYACTS 2 trial.

“Our recommendation would be to have a sequencing panel for the ‘ready for routine use’ mutations and fusions,” Geoerger said.

“Nearly everybody should have that as part of their diagnostic setup.”

Source: American Association for Cancer Research