Poly ICLC for the Treatment of Progressive or Recurrent Low-Grade Gliomas in Children and Young Adults with Neurofibromatosis Type 1

Inclusion Criteria

• Patients must be less than 22 years at the time of enrollment; there is no lower age limit
• All participants must have an identified pathogenetic constitutional NF1 mutation OR the clinical diagnosis of NF1 using the National Institutes of Health (NIH) Consensus Conference criteria
• LGG (World Health Organization [WHO] Grade 1 and 2) of the brain and spinal cord are eligible. Histologic confirmation of tumor is not necessary in the presence of consistent clinical and radiographic findings. Biopsy for histologic diagnosis is required if there is clinical suspicion for a high-grade tumor; special attention is recommended in older adolescents or young adults to the potential for malignant transformation. Patients with metastatic disease are eligible
• Patients must meet at least one of the following criteria for progression or recurrence of a previously treated target tumor: * Progression or recurrence on magnetic resonance imaging (MRI) * New or worsening neurologic symptoms attributable to the target tumor * For patients with optic pathway glioma (OPG): visual worsening, defined as worsening of visual acuity (VA) or visual fields (VF) documented within the past year by examination or history, attributable to tumor
• Patients must have two-dimensional measurable tumor > 1 cm^2
• Patients must have had at least one prior medical treatment for the target LGG
• Patients must have a performance status of equal or > than 50 using Karnofsky for patients equal or >= 16 years of age and Lansky for patients < 16 years of age
• Patients must have recovered to grade =< 1 from any acute toxicities from all prior treatments. to enroll on this study and meet time restrictions from end of prior therapy as defined below: * Myelosuppressive chemotherapy: must have received the last dose of myelosuppressive therapy at least 4 weeks prior to study registration, or at least 6 weeks if nitrosourea * Investigational/biological agent: Patient must have received the last dose of other investigational, immunotherapy, or biological agent > 14 days prior to study registration or at least 5 half-lives, whichever is greater. Bevacizumab last dose > 36 days prior to enrollment * Radiation therapy: Patients SHOULD NOT have received prior irradiation * Study specific limitations on prior therapy: There is no limit on the number of prior treatment regimens * Growth factor(s): Must not have received any hematopoietic growth factors within 7 days of study entry or > 14 days if pegylated granulocyte colony stimulating factor (GCSF) is used * Prior surgery: At the time of enrollment, must be >= 3 weeks from prior major surgery such as craniotomy, orthopedic surgery, abdominal surgery or >= 1 week from minor surgery and completely recovered. Port or central line placement is not considered a major surgery
• Hemoglobin: >= 8.0 gm/dl (may transfuse packed red blood cells [PRBCs])
• Absolute neutrophil count (ANC): >= 750/mm^3. Must be at least 7 days after last dose of growth factor or > 14 days since last dose of pegylated GCSF
• Platelet Count: >= 75,000/mm^3 (transfusion independent; >= 7 days from last transfusion)
• Serum creatinine which is less than 1.5 times upper limit of normal (ULN) for age (as per the table below) or glomerular filtration rate (GFR) > 70 ml/min/1.73 m^2 * Age: 1 month to < 6 months; Maximum serum creatinine (mg/dL): 0.4 (male); 0.4 (female) * Age: 6 months to < 1 year; Maximum serum creatinine (mg/dL): 0.5 (male); 0.5 (female) * Age: 1 to < 2 years; Maximum serum creatinine (mg/dL): 0.6 (male); 0.6 (female) * Age: 2 to < 6 years; Maximum serum creatinine (mg/dL): 0.8 (male); 0.8 (female) * Age: 6 to < 10 years; Maximum serum creatinine (mg/dL): 1 (male); 1 (female) * Age: 10 to < 13 years; Maximum serum creatinine (mg/dL): 1.2 (male); 1.2 (female) * Age: 13 to < 16 years; Maximum serum creatinine (mg/dL): 1.5 (male); 1.4 (female) * Age: >= 16 years; Maximum serum creatinine (mg/dL): 1.7 (male); 1.4 (female)
• Total bilirubin =< 1.5 x ULN (Children with diagnosis of Gilbert’s Syndrome will be allowed on the study regardless of their total and indirect bilirubin levels as long as the direct bilirubin is less than 3.1 mg/dL.)
• Serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase [ALT]) =< 5 x ULN
• Serum glutamic-oxaloacetic transaminase (SGOT) (aspartate aminotransferase [AST]) =< 5 x ULN
• No evidence of dyspnea at rest, and a pulse oximetry >= 92%
• Female patients of childbearing potential must have a negative serum or urine pregnancy test within 7 days prior to the first dose of poly-ICLC. Patient must not be pregnant or breast-feeding. Patients of childbearing or child-fathering potential must be willing to use a medically acceptable form of birth control, including abstinence, while being treated on this study and for 90 days following cessation of treatment
• Patient is able to start treatment within 7 days after enrollment
• Patients with neurological deficits must be stable for a minimum of 1 week prior to enrollment
• Patients are only eligible if complete resection of the LGG with acceptable morbidity is not feasible, or if a patient with a surgical option refuses surgery
• Patients and/or parents/legal guardians must provide written informed consent and agree that they will comply with the study

Exclusion Criteria

• Prior radiation treatment for the low-grade glioma
• Prior exposure to poly-ICLC
• Patients currently receiving other anti-tumor therapy or experimental therapy (targeted agents, chemotherapy radiation)
• Patients with a current or prior diagnosis of malignant glioma (WHO grade III or IV)
• Patients with a prior diagnosis of malignant peripheral nerve sheath tumor or other malignancy requiring treatment in the last 48 months
• Patients may not have fever (>= 38.50 degree Celsius [C]) within 3 days of enrollment
• Patients who, in the opinion of the investigator, may not be able to comply with the safety monitoring requirements of the study
• Active auto-immune illness
• Pregnant or lactating females
• Sexually active patients of reproductive potential who have not agreed to use an effective contraceptive method for the duration of their study participation and for 90 days after stopping study therapy are not eligible
• Severe unresolved infection that requires systemic intravenous (IV) antibiotics
• Patients with any significant medical illnesses that in the investigator’s opinion cannot be adequately controlled with appropriate therapy or would compromise the patient’s ability to tolerate this therapy
• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, impaired gastrointestinal function, or psychiatric illness/social situations that would limit compliance with study requirements
• Patients requiring high doses of steroids. Patients may not be on immunosuppressive therapy, including corticosteroids (with the exception of physiologic replacement, defined as =< 0.75 mg/m^2/day dexamethasone or equivalent) at time of enrollment. However, patients who require intermittent use of bronchodilators or local steroid injections will not be excluded from the study