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2012 EDUCATIONAL BOOK - American Society of Clinical Oncology

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SAFETY OF DIPG BIOPSY IN CHILDREN<br />

Fig. 1. Plan neuroimaging that shows the trajectory<br />

from a trancerebellar approach. E � Entry; T � Target.<br />

(A) Three-dimensional neuroimaging plan. (B) Axial<br />

gadolinium-enhanced T1-weighted magnetic resonance<br />

image. (C) Sagittal gadolinium-enhanced T1-weighted<br />

magnetic resonance image. (D) Coronal gadoliniumenhanced<br />

T1-weighted magnetic resonance image.<br />

In addition, to increase direct application <strong>of</strong> chemotherapeutic<br />

agents to the DIPG, attempts have been pursued to<br />

circumvent the blood-brain barrier using the convectionenhanced<br />

delivery technique. Theoretically, the safety <strong>of</strong><br />

this procedure is similar to that <strong>of</strong> biopsy. Preclinical models<br />

and clinical trials have demonstrated the feasibility, efficacy,<br />

and safety <strong>of</strong> this technique. 24 Moreover, two children<br />

with brainstem lesions demonstrated no neurologic deficits<br />

after infusion. 25 Therapeutic protocols are currently under<br />

way, but the choice <strong>of</strong> the appropriate agent to deliver with<br />

this technique remains in question.<br />

Fig. 2. Plan neuroimaging showing the trajectory<br />

with a transfrontal approach. E � Entry; T � Target.<br />

(A) Three-dimensional neuroimaging plan. (B) Axial<br />

gadolinium-enhanced T1-weighted magnetic resonance<br />

image. (C) Sagittal gadolinium-enhanced T1-weighted<br />

magnetic resonance image. (D) Coronal Gadoliniumenhanced<br />

T1-weighted magnetic resonance image.<br />

Why Perform a Biopsy for Patients with Newly<br />

Diagnosed DIPG?<br />

The lack <strong>of</strong> samples from patients with newly diagnosed<br />

DIPG has limited our understanding <strong>of</strong> tumor biology, which<br />

hinders the development <strong>of</strong> newer therapies for patients<br />

with these devastating tumors. As targeted therapy development<br />

undoubtedly requires tissue, it could be argued that<br />

such advances will only be optimized with the knowledge<br />

that biopsies provide in terms <strong>of</strong> tumor biology and the<br />

identification <strong>of</strong> new targets. In recent papers, authors<br />

defend the idea that a biopsy <strong>of</strong> patients with newly diag-<br />

631

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