Inspired by a patient. See: https://childnervoussystem.blogspot.com/2015/05/venriculomegaly-in-nf1.html
Kondyli M, Larouche V, Saint-Martin C, Ellezam B, Pouliot L,
Sinnett D, Legault G, Crevier L, Weil A, Farmer JP, Jabado N, Perreault
S. Trametinib for progressive pediatric low-grade gliomas. J Neurooncol. 2018
Nov;140(2):435-444.
Abstract
INTRODUCTION:
Pediatric pilocytic astrocytomas (PAs) are low grade gliomas
and the most common brain tumors in children. They often represent a
therapeutic challenge when incompletely resected as they can recur and progress
despite the use of several lines of chemotherapeutic agents or even radiation
therapy. Genetic alterations leading to activation of the
mitogen-activated-protein-kinase pathway are a hallmark of this disease and
offer an interesting therapeutic alternative through the use of targeted
inhibitors.
METHODS:
Here, we describe six children with sporadic PA who were
treated with trametinib, a MEK inhibitor, following progression under
conventional therapies. Retrospective chart review was performed.
RESULTS:
The median age at diagnosis was 2.3 years (y) old [range 11
months (m)-8.5 y old]. KIAA1549-BRAF fusion was identified in five cases, and
hotspot FGFR1/NF1/PTPN11 mutations in one. All patients received at least one
previous line of chemotherapy (range 1-4). The median time on treatment was 11
m (range 4-20). Overall, we observed two partial responses and three minor
responses as best response; three of these patients are still on therapy.
Treatment was discontinued in the patient with progressive disease. The most
frequent toxicities were minor to moderately severe skin rash and
gastro-intestinal symptoms. Two patients had dose reduction due to skin
toxicity. Quality of life was excellent with decreased hospital visits and a
close to normal life.
CONCLUSION:
Trametinib appears to be a suitable option for refractory
pediatric low-grade glioma and warrants further investigations in case of
progression.
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