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. 2021 Apr;7(2):a006023. doi: 10.1101/mcs.a006023

Table 1.

Interpretation of MRI findings related to type and time of treatment

MRI date (months postdiagnosis) Vinblastinea status Dabrafenib/trametinib statusb Tumor mass dimensions (cm) Radiologist interpretation/notes Reason for MRI
SI TRV AP
A
Initial diagnosis Prior Prior 1.7 1.5 1.5 No significant contrast enhancement associated with this lesion, and no abnormal contrast enhancement appreciated in the remainder of the brain Sudden onset nystagmus and loss of vision in left eye
46 mo Prior Prior 2.0 2.5 2.6 T2 prolongation mass lesion centered within the midbrain; increased in size since the previous study Preoperative evaluation prior to initial biopsy and tumor resection
47 mo Prior Prior 2.1 2.9 2.8 Mass lesion minimally increased in size compared to previous imaging; central portion of the lesion shows increased T2 signal compared to the peripheral portion and enhances diffusely with contrast Routine surveillance
50 mo Prior Prior 2.1 2.6 2.7 Mass unchanged to slightly decreased in size when compared to previous imaging Evaluation prior to commencing chemotherapy
52 mo Prior Prior 1.8 2.5 2.8 Expansile, T2 prolongation mass lesion with slight decrease in size; central area of the mass shows increased T2 signal and contrast enhancement Routine surveillance
B
57 mo Active (3 mo) Prior 1.7 2.6 2.7 Complex appearing mass within the midbrain, with measurements comparable to prior imaging Disease assessment/postchemotherapy commencement
60 mo Active (6 mo) Prior 2.0 2.8 2.6 Increased size of mass compared to most recent imaging. Routine surveillance
63 mo Active (9 mo) Prior 2.6 3.2 2.8 Increased size of both the solid and cystic components of the midbrain mass compared to previous MRI Routine surveillance
64 mo Stopped Prior 2.9 3.5 2.8 Slight further increase in size of the cystic portion of the mixed solid and cystic mass; enhancing solid component appears unchanged Routine surveillance
65 mo Stopped Prior NA NA NA Almost complete resection of the enhancing tissue in the central lesion; residual crescent of T2 signal abnormality is still concerning for nonenhancing tumor Intraoperative during tumor resection
68 mo Stopped Prior 1.7 2.3 2.4 New avidly enhancing nodules along the anterior aspect of the mass, suggestive of tumor progression. Routine surveillance
C
71 mo Stopped Active (2 mo) 1.6 2.2 2.3 Similar in size with decreased enhancement Routine surveillance
74 mo Stopped Active (5 mo) 1.5 2.2 2.2 Stable appearance of residual tumor Routine surveillance
78 mo Stopped Active (9 mo) 1.4 2.0 2.2 No evidence of tumor progression Routine surveillance
81 mo Stopped Active (12 mo) 1.4 2.0 2.2 Essentially unchanged in imaging appearance and tumor dimensions Routine surveillance
84 mo Stopped Active (15 mo) 1.4 2.0 2.0 Stable nonenhancing, lobulated midbrain mass; unchanged mild to moderate enlargement of the lateral and third ventricles Routine surveillance

“Prior” refers to the time period before therapy initiation. (MRI) Magnetic resonance imaging, (SI) superior to inferior, (TRV) transverse, (AP) anteroposterior.

aVinblastine dosage, 6 mg/m2/dose intravenously every 2 wk.

bDabrafenib dosage, 150 mg twice a day; trametinib dosage, 1.5 mg twice a day.