Table 1.
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.