Researchers report that the outcome of patients with a rare type of astrocytoma, a neuron tumour, is worse than expected

31 Mar 2023
Researchers report that the outcome of patients with a rare type of astrocytoma, a neuron tumour, is worse than expected

A team of researchers from the Nagoya University Graduate School of Medicine has reported that patients with a rare form of brain and spinal cord cancer, localised isocitrate dehydrogenase wild-type (IDHwt) histologically diffuse astrocytoma, have a poor prognosis similar to the most malignant types of brain and spinal cord tumours.

Their findings, published in the journal Scientific Reports, point to the need for strong postoperative care for patients with this type of tumour. 

Gliomas are a tumour that originate in the glial cells that surround neurons in the brain.

Under the microscope, gliomas can be divided into several types based on the type of cells they invade.

These include astrocytomas, which, as their name suggests, infect astrocytes, an important type of neuron.  

In 2016, to improve prognosis and patient management, the WHO classification of central nervous system tumours included a new classification of ‘diffuse gliomas’, based on the presence or absence of specific mutations.

Two rare types of diffuse astrocytomas are infiltrative and localised isocitrate dehydrogenase wild-type (IDHwt) diffuse astrocytomas.

Since they are so rare, there is a lack of information on whether the infiltrative or localised characteristics affect their prognosis and what this means for the patient. 

The Nagoya University research team, led by Yuji Kibe and Kazuya Motomura of the Department of Neurosurgery, analysed localised IDHwt astrocytomas and found that all resulted in malignant recurrence and a poor clinical prognosis similar to that of glioblastomas.

Glioblastomas are among the most malignant tumours, with an average survival time of 8 months and less than 7% of patients survive for five years. 

Motomura believes that the findings of the group are important for doctors and patients.

“All tumours that we investigated had a dismal prognosis despite multidisciplinary treatment,” he said.  “For patients with gliomas, our research results should lead patients to receive the proper clinical diagnosis and treatment. For physicians, IDHwt astrocytomas must be followed with great caution, even after total removal. Strong postoperative therapy should be considered. As almost all patients with diffuse astrocytomas present with radiographic imaging findings suggesting a localised tumour mass, physicians may misdiagnose the patient with a low-grade tumour instead of a malignant tumour; therefore, our findings suggest physicians should consider the possibility of such tumours.” 

Article: Imaging features of localised IDH wild-type histologically diffuse astrocytomas: a single-institution case series

Source: Nagoya University