Gemcitabine in Newly-Diagnosed Diffuse Intrinsic Pontine Glioma

This is an interventional basic science trial for Diffuse Intrinsic Pontine Glioma Read More

Inclusion Criteria:

1. Age greater than or equal to 3 years and less than 18 years at the time of enrollment

2. Patients must meet both of the following:

   • Clinical findings consistent with a presumed new diagnosis of DIPG
   • Brain MRI findings consistent with a new diagnosis of DIPG in the opinion of the treating pediatric neuro-oncologist and neurosurgeon

3. Organ Function Requirements

   Adequate bone marrow function defined as:

   • Platelet count ≥100,000/µl (no platelet transfusion for more than 3 days)
   • Hemoglobin >8 g/dl and absolute neutrophil count (ANC) ≥1,000/µl

   Adequate coagulation defined as:

   • Prothrombin time (PT) and activated partial thromboplastin time (aPTT) ≤ upper limit of normal (ULN) for age.

   Adequate renal function defined as:

   • Creatinine clearane or radioisotope GFR > 70 ml/min/1.73 m2 or

   • Maximum serum creatinine (mg/dL) based on age/gender as follows:

     • Male 3 to <6 yrs: 0.8 mg/dL
     • Female 3 to <6 yrs: 0.8 mg/dL
     • Male 6 to <10 yrs: 1.0 mg/dL
     • Female 6 to <10 yrs: 1.0 mg/dL
     • Male 10 to <13 yrs : 1.2 mg/dL
     • Female 10 to <13 yrs: 1.2 mg/dL
     • Male 13 to <16 yrs: 1.5 mg/dL
     • Female 13 to <16 yrs: 1.4 mg/dL
     • Male 16 to <18 yrs : 1.7 mg/dL
     • Female 16 to <18 yrs: 1.4 mg/dL

   The threshold creatinine values in this Table were derived from the Schwartz formula for estimating GFR (Schwartz et al. J. Peds, 106:522, 1985) utilizing child length and stature data published by the CDC.

   Adequate liver function defined as:

   • Total bilirubin <3x ULN for age and SGOT (AST) and SGPT (ALT) <2.5x ULN for age

4. Patients must meet one of the following performance scores:

   • ECOG performance status scores of 0, 1, or 2;
   • Karnofsky score of ≥ 60 for patients > 16 years of age; or
   • Lansky score of ≥ 60 for patients ≤ 16 years of age
5. Pontine tumor biopsy is planned for the clinical care of the patient independent of study participation by the treating pediatric neurosurgeon and neuro-oncologist.
6. Informed consent and assent obtained as appropriate.

Exclusion Criteria:

1. Pregnant or breastfeeding patients due to teratogenic effects seen in animal/human studies.
2. Patients who have received any tumor-directed therapy prior to biopsy. Concurrent treatment with corticosteroids is allowed.
3. Patients with intratumoral hemorrhage larger than 0.5 cm on preoperative imaging.
4. Patients with personal or family history of bleeding disorders.
5. Patients with uncontrolled intercurrent illness including, but not limited to ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements.