Nivolumab and Tovorafenib for Treatment of Craniopharyngioma in Children and Young Adults (PNOC029)

Investigational Treatment for Craniopharyngioma, a Type of Brain Tumor, in Children and Young Adults

S
Scott Coven

Primary Investigator

Enrolling By Invitation
1 year - 39 years
All
Phase 2
56 participants needed
2 Locations

Brief description of study

The current study assesses the tolerability and efficacy of combination therapy with PD-1 (nivolumab) and pan-RAF-kinase (Tovorafenib) inhibition for the treatment of children and young adults with craniopharyngioma.

THIS STUDY IS ENROLLING BY INVITATION ONLY - Consistent with most oncology trials, patients are not actively “recruited,” but are screened by their physician for appropriate clinical trial(s) at the time of their routine clinic visit. Occasionally, a patient may be a self-referral or physician referral, but are still screened for appropriate clinical trials at the time of their routine clinic visit. PI and staff may send copies of relevant consent forms to these patients to look over prior to actually consenting or enrolling them. This may take place at the patient's visit at which the consent is presented or the patient's next visit to the outpatient hematology/oncology clinic. 

Interested in participating? For more information about this research study or other cancer-related clinical trials at IU Simon Comprehensive Cancer Center, please contact:

IU Clinical Trials Office 

Email: iutrials@iu.edu 

Phone: (317) 278-5632

Detailed description of study

Participants will be divided into 2 Groups (newly diagnosed craniopharyngioma, recurrent craniopharyngioma without histological diagnosis) with 3 treatment arms within each group (Neoadjuvant nivolumab, Neoadjuvant Tovorafenib, Neoadjuvant combination nivolumab plus Tovorafenib). There will also be a separate Non-biopsy/resection arm within the Recurrent Craniopharyngioma group.

Participants will be randomized in a 1:1:1 and will receive one dose of assigned drug prior to planned biopsy or resection. Participants with measurable disease will then continue on combination maintenance therapy. Participants may continue treatment for up to 24 months total and will be followed up for 3 years after enrollment into the study.

Eligibility of study

You may be eligible for this study if you meet the following criteria:

  • Conditions: Craniopharyngioma, Riley
  • Age: 1 year - 39 years
  • Gender: All

Inclusion Criteria:
Newly Diagnosed Participants:
  • Newly diagnosed craniopharyngioma diagnosis based on imaging characteristics and central radiology review. Participants will initially be screened within confines of a screening consent and only those participants with findings consistent with craniopharyngioma and without findings suggesting an indeterminate lesion or lesion of an alternative diagnosis (including abnormal tumor markers found in blood or cerebral spinal fluid (CSF), if completed as part of standard of care (SOC) work-up or if lesion concerning for alternate diagnosis) will move ahead with enrollment on the treatment protocol. Additionally, for participants that have undergone initial biopsy to confirm diagnosis, are within 4 weeks of radiographic diagnosis, and are planned to undergo follow up second surgery for additional tumor resection as per standard of care recommendations, these participants will also be considered eligible.
  • Participants must be surgical candidates for biopsy or resection and planned for standard of care biopsy or resection.
Recurrent Participants:
  • Recurrent craniopharyngioma, as based on histologic confirmation at time of initial diagnosis (participants with Adamantinomatous craniopharyngioma (ACP) will only be eligible for the recurrent arm).
  • Recurrent craniopharyngioma without prior histologic confirmation will initially be screened within confines of a screening consent and only those participants with findings consistent with craniopharyngioma and without findings suggesting an indeterminate lesion or lesion of an alternative diagnosis (including abnormal tumor markers found in blood or CSF, if completed as part of SOC work-up or if lesion concerning for alternate diagnosis) will move ahead with enrollment on the treatment protocol.
  • Participants should be surgical candidates for biopsy or resection. If participants are not surgical candidates, but have available archival tumor tissue, they will be enrolled into the exploratory cohort and must be willing to provide a minimum of 10-20 paraffin embedded unstained slides OR 1 block with tumor content of 40% or greater is required. Participants who do not meet this criteria may be discussed on a case-by-case basis with the Study Chair(s).
  • Participants can have been previously treated with surgical resection alone, cyst drainage and biopsy alone, radiation therapy, other systemic therapies, or any combination thereof.
  • Prior Therapy:
    • Had their last dose of myelosuppressive chemotherapy >= 21 days prior to study registration (>=42 days if nitrosourea therapy).
    • Had their last dose of hematopoietic growth factor >=14 days (long-acting growth factor) or >=7 days (short-acting growth factor) prior to study registration, or beyond the time during which adverse events (AEs) are known to occur.
    • Had their last dose of biologic (anti-neoplastic agent) >=7 days prior to study registration, or beyond the time during which AEs are known to occur.
    • Had their last dose of monoclonal antibodies >=21 days prior to study registration. Radiation
  • Had their last fraction of local irradiation to primary tumor >=12 weeks prior to
    registration; investigators are reminded to review potentially eligible cases to avoid confusion with pseudo-progression.
  • At least 14 days after local palliative radiation (small-port).
All Participants:
  • Age 1 to 39 years.
  • Participants continuing on maintenance therapy after standard of care biopsy/resection must have measurable disease, as defined as lesions that can be accurately measured in two dimensions (longest diameter to be recorded) with a minimum size of no less than double the slice thickness. Previously irradiated lesions are considered non-measurable except in cases of documented progression of the lesion since the completion of radiation therapy. Participants without measurable disease may continue on study and will be followed for study endpoints, but will not be included as part of target accrual.
  • Performance Score: Karnofsky >= 50 for participants > 16 years of age and Lansky >= 50 for participants <= 16 years of age. Participants who are unable to walk because of paralysis, but who are up in a wheelchair, will be considered ambulatory for the purpose of assessing the performance score.
  • Corticosteroids: Participants who are receiving dexamethasone must be on a stable or decreasing dose for at least 1 week prior to registration. The participant steroid dose should be no more than a steroid-equivalent of dexamethasone 0.1 mg/kg/day (or maximum 4mg/day; whichever is the lower dose) at time of enrollment. Participants that have been stable on physiologic hormone replacement for hypopituitarism are allowed.
  • Organ Function Requirements:
    • Adequate Bone Marrow Function defined as:
      • Peripheral absolute neutrophil count (ANC) >=1000/mm3.
      • Platelet count >= 100,000/mm3 (transfusion independent, defined as not receiving platelet transfusions for at least 7 days prior to enrollment).
    • Adequate Renal Function defined as-
      ---A serum creatinine < 1.5 Upper Limit normal (ULN) based on age and gender.
    • Adequate Liver Function defined as-
      • Bilirubin (sum of conjugated + unconjugated) <= 1.5 x upper limit of normal (ULN) for age (except in participants with documented Gilbert syndrome).
      • Serum glutamic-pyruvic transaminase (SGPT)((alanine aminotransferase (ALT)) <= 3 x ULN.
      • Serum albumin >=2 g/dL (20g/L).
    • Adequate Neurologic Function defined as participants with seizure disorder may be
      enrolled if well controlled. Participants on non-enzyme inducing anticonvulsants may be excluded pending interaction(s) with study drug.
    • Adequate Pancreatic Function defined as serum lipase <= 1.5 x ULN at baseline.
    • Adequate Pulmonary Function defined as no evidence of dyspnea at rest, no exercise intolerance due to pulmonary insufficiency, and a pulse oximetry of > 92% while breathing room air.
  • The effects of Tovorafenib and nivolumab on the developing human fetus are unknown.
    For this reason, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry, for the duration of study participation and 6 months after completion of Tovorafenib and/or nivolumab administration, whichever is later. Should a woman become pregnant or suspect she is pregnant while she or her partner is participating in this study, she should inform her treating physician immediately.
  • A legal parent/guardian or participants must be able to understand, and willing to sign, a written informed consent and assent document, as appropriate.
Exclusion Criteria:
Newly Diagnosed Participants:
  • Participants should not have undergone any previous tumor-directed therapy.
Recurrent Participants:
  • Participants who have had chemotherapy or radiotherapy within 3 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or those who have not recovered from acute adverse events due to agents administered more than 4 weeks earlier.
  • Participants must be at least 1 week since the completion of therapy with a biologic or small molecule agent. For any agent with known adverse events that can occur beyond 1 week after administration, the period prior to enrollment must be beyond the time during which adverse events are known to occur. Such participants should also be discussed with study chairs.
  • Participants should not have previously received any RAS-pathway directed therapy combined with PD-1 inhibition. However, individual therapy with either of these individual agents will be allowed. Such subjects should be discussed with study chairs.
All Participants:
  • Rapidly progressive symptoms that require urgent surgery or radiation therapy, which would prevent central review and or preclude participation with tumor-directed medical management alone.
  • Uncontrolled symptoms of neuroendocrine dysfunction such as diabetes insipidus, hypothyroidism, panhypopituitarism (participants can be on supplemental medications for hormonal repletion; however, should be on controlled doses for at least 2 weeks prior to enrollment).
  • Participants with a history or current evidence of central serous retinopathy (CSR), retinal vein occlusion (RVO), or ophthalmopathy present at baseline who would be considered a risk factor for CSR or RVO.
  • Clinically significant active cardiovascular disease, or history of myocardial infarction, or deep vein thrombosis/pulmonary embolism within 6 months prior to registration, ongoing cardiomyopathy, or current prolonged QT interval corrected for heart rate by Fridericia's formula (QTcF) interval > 440 ms based on triplicate ECG average.
  • History of allergic reactions attributed to compounds of similar chemical or biologic composition to Tovorafenib or nivolumab or other agents used in study.
  • History of pneumonitis within the last 5 years or history of thoracic radiation, including prior craniospinal irradiation (CSI) or have radiation fields that overlap the lung.
  • Nausea and vomiting >= Grade 2, malabsorption requiring supplementation, or significant bowel or stomach resection that would preclude adequate absorption.
  • Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection.
  • Participants who are receiving any other investigational agents.
  • Participants who have received a live / attenuated vaccine within 30 days of registration.
  • Participants with a known disorder that affects their immune system, such as HIV or Hepatitis B or C, an auto-immune disorder disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids, or immunosuppressive drugs). Replacement therapy (e.g. thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment. Note: Participants that are currently using inhaled, intranasal, ocular, topical or other non-oral or non-IV steroids are not necessarily excluded from the study but need to be discussed with the study chair.
  • Participants with a >= Grade 2 hypothyroidism due to history of autoimmunity are not eligible. (Note: Hypothyroidism due to previous irradiation or thyroidectomy will not impact eligibility).
  • Participants who have received prior solid organ or bone marrow transplantation are not eligible.
  • Women of childbearing potential must not be pregnant or breast-feeding.
  • Current treatment with a strong cytochrome P4502C8(CYP2C8) inhibitor or inducer other than those allowed per Section 5.6.1. Medications that are substrates of CYP2C8 are allowed but should be used with caution.
  • Participants with inability to return for follow-up visits or obtain follow-up studies required to assess toxicity to therapy.

Updated on 10 Jun 2025. Study ID: PHO-UCSF-PNOC029, 16352

This study investigates the use of investigational medications for treating craniopharyngioma in children and young adults. Craniopharyngioma is a type of brain tumor that can affect hormone levels and vision. The study will look at how well the treatment works and if it is safe for the participants.

Participants will be divided into groups based on their diagnosis and treatment needs. They may receive either nivolumab, Tovorafenib, or a combination of both before surgery. After surgery, some participants will continue with a maintenance treatment for up to 24 months. A placebo is not used in this study.

  • Who can participate: Children and young adults aged 1 to 39 years with either newly diagnosed or recurrent craniopharyngioma can participate. Participants must be surgical candidates for biopsy or resection, and meet specific health criteria.
  • Study details: Participants will be assigned to different treatment arms and receive medication before their surgery. Those with measurable disease may continue with maintenance therapy after surgery. All participants will be monitored for three years following their enrollment.
  • Study timelines: The study will last up to 24 months.
Please visit our main page to search for other studies you may be interested in. If you need help finding a study or have any questions, please contact us at inhealth@iu.edu

Interested in the study?

This study is accepting only persons who receive care at a certain clinic or doctor or who are part of an invited group. Questions about this study can be directed to the study team listed in the description or contact your doctor to see if you are eligible.

Accepting referrals by invitation only