Summary: Researchers have developed a novel blood test that allows for the minimally invasive detection and monitoring of IDH1 mutant gliomas, offering an alternative to traditional biopsy methods.

Takeaways:

  1. Minimally Invasive Detection: The mt-IDHIdx blood test detects IDH1 mutations in gliomas using just 2ml of blood, reducing the need for invasive tissue biopsies.
  2. High Accuracy: Validation of the test across a study population demonstrated a sensitivity of 75.0% and specificity of 88.7%, providing reliable diagnostic accuracy compared to the traditional tissue-based gold standard.
  3. Clinical Impact: With the recent FDA approval of vorasidenib for IDH1 mutant gliomas, this test could soon be used for patient stratification and ongoing disease monitoring, enhancing treatment outcomes.

Glioma represents the most common central nervous system cancer in adults. The current classification scheme uses molecular alterations, particularly IDH1.R132H, to stratify lesions into distinct prognostic groups.

Currently, neuroimaging followed by tissue biopsy testing (surgical biopsy and/or resection) is the gold standard for diagnosing IDHI mutant gliomas. However, this process poses procedural risks and may not fully reflect the diverse and evolving tumor landscape. Also, preoperative knowledge of the IDH mutation status can influence operative procedural planning.

Now researchers from Massachusetts General Hospital detailed a new blood-based test, mt-IDHIdx, that allows for the minimally invasive detection of tumor-derived extracellular RNA using only 2ml of blood.

The researchers performed validation testing across the study population (n=133), which included 80 patients with IDH1.R132H glioma, 44 patients with IDH1 wild-type gliomas and nine healthy controls.

Study Results

Results from our plasma testing demonstrate an overall sensitivity of 75.0% (95% CI: 64.1%–84.0%), specificity 88.7% (95% CI: 77.0%–95.7%), positive predictive value 90.9%, and negative predictive value 70.1% compared to the tissue gold standard.

In addition to fundamental diagnostic applications, the study also highlights the utility of the platform for blood-based monitoring and surveillance.

Finally, the optimized workflow enables rapid and efficient completion of both tumor tissue and plasma testing in under four hours from the time of sampling.

What are the Next Steps?

Detection of the IDH1 mutation in blood means that these tumors can be diagnosed without a biopsy, and can be monitored overtime to track disease progression, response to treatment or recurrence using a simple blood sample.

Importantly, the FDA recently approved a drug (vorasidenib) for this mutation in glioma—this means that the test, once approved, can be used to stratify these patients for this treatment and can monitor disease course.