1p36/19q13 – Oligodendroglioma pin


1p36/19q13 – Oligodendroglioma

Alternate Test Names:
Oligodendroglioma Panel test (1p36/1q25 and 19q13/19p13)

Methodology: FISH

Clinical Significance:
Gliomas are the most common primary neoplasm of the central nervous system and can have strikingly different clinical behaviors and responses to therapy. Distinguishing between different subtypes is often less than perfect with significant inter-observer variability. Although attempts have been made to define clinical and histologic features that correlate with a favorable prognosis, none have been sufficiently reliable at predicting response to adjuvant chemotherapy. However, recent studies have shown that loss of 1p36 and 19q13 are associated with an oligodendroglial phenotype, favorable response to chemotherapy and overall prolonged survival. Fluorescence in-situ hybridization (FISH) studies provide a direct method for identifying loss of 1p36 and 19q13 in formalin-fixed, paraffin-embedded tissue sections. Loss of 1p36 and 19q13 is detected by assessing the ratio of 1p36 and 19q13 to their corresponding reference genes, 1q25 and 19p13, respectively, and by assessing the number of nuclei showing clear 1p36 and 19q13 deletion, according to guidelines defined by the International Society of Pediatric Oncology (ISPO).

Probe type: Dual color enumeration (x2)

Organ: Brain/CNS

Disease State: Astrocytoma, Oligodendroglioma

CPT Code(s): 88374x2

Turnaround Time: Within 3-4 business days of receipt

Schedule: Monday, Tuesday, Wednesday, Friday

Specimen Requirements:
• Formalin-fixed, paraffin-embedded tissue block or cell block - OR -
• Minimum of 5 unstained slide cut at 4µm for each test requested