Childhood Craniopharyngioma
Conditions
Brief summary
This phase II trial studies how well peginterferon alfa-2b works in treating younger patients with craniopharyngioma that is recurrent or cannot be removed by surgery. Peginterferon alfa-2b may interfere with the growth of tumor cells and slow the growth of craniopharyngioma.
Detailed description
PRIMARY OBJECTIVES: I. To estimate the 1-year disease stabilization rate associated with the use of Sylatron (peginterferon alfa-2b) in patients with progressive unresectable or recurrent craniopharyngiomas following surgery alone who have not received radiation therapy. II. To estimate the sustained objective response rate (partial response (PR) + complete response (CR)) to Sylatron in patients with craniopharyngiomas which progress or recur following radiation therapy. SECONDARY OBJECTIVES: I. To estimate the response rate in patients with progressive unresectable or recurrent craniopharyngioma treated with Sylatron by study stratum. II. To estimate the progression-free survival distribution for patients with unresectable or recurrent craniopharyngiomas treated with Sylatron by study stratum. III. To evaluate the toxicity profile of Sylatron in children with unresectable or recurrent craniopharyngiomas. IV. To compare the protocol specific disease assessment criteria to MacDonald criteria during the first year of treatment in stratum I and at the time of objective response and progressive disease in both strata. V. To characterize evidence of WNT pathway activation by immunohistochemistry and MAPK pathway activation by pyrosequencing in resected tumor tissue in patients with craniopharyngiomas, and correlate these results with outcome and response data. OUTLINE: Patients receive peginterferon alfa-2b subcutaneously (SC) weekly for 6 weeks. Treatment may repeat every 6 weeks for up to 18 courses in the absence of disease progression or unacceptable toxicity. After completion of study treatment, patients are followed up for 30 days.
Interventions
BIOLOGICALpeginterferon alfa-2b
Given subcutaneously (SC)
OTHERlaboratory biomarker analysis
Correlative studies
Sponsors
National Cancer Institute (NCI)
Pediatric Brain Tumor Consortium
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Months to 25 Years
Healthy volunteers
No
Inclusion criteria
* Patient must have a histologically verified diagnosis of craniopharyngioma * Stratum 1: patients with progressive unresectable or recurrent craniopharyngiomas treated with surgery alone, who have not received radiation therapy; patients with unresectable craniopharyngiomas, (i.e. residual measurable disease following surgical resection) will be enrolled at the time of progression * Stratum 2: patients with progressive or recurrent craniopharyngiomas following radiation therapy * All patients must have measurable residual disease defined as tumor measurable in two perpendicular diameters on magnetic resonance imaging (MRI) * Please note: measurements are required for both the solid and cystic components * Subjects must have recovered from the acute toxicities of all prior therapy before entering this study; for those acute baseline adverse events attributable to prior therapy, recovery is defined as a toxicity grade =\< 2, using Common Terminology Criterial for Adverse Events (CTCAE) version (v.) 4.0, unless otherwise specified in the inclusion and
Exclusion criteria
* Myelosuppressive chemotherapy (includes intra-cystic bleomycin): * Subjects must have received their last dose of known myelosuppressive anticancer chemotherapy at least three (3) weeks prior to study registration or at least six (6) weeks if nitrosourea * Subjects must have received their last dose of investigational or biologic agent \>= 7 days prior to study registration * In the event that a subject has received an investigational or biologic agent and has experienced \>= grade 2 myelosuppression, then at least three (3) weeks must have elapsed prior to registration * If the investigational or biologic agent has a prolonged half-life (\>= 7 days) then at least three (3) weeks must have elapsed prior to registration * Subjects must have completed at least 3 half-life periods from the last dose of monoclonal antibody prior to registration * Note: a list of half-lives of commonly used monoclonal antibodies is available on the Pediatric Brain Tumor Consortium (PBTC) website under Generic Forms and Templates * Stratum 1: patients must not have received radiation therapy * Stratum 2: patients must have received radiation therapy, including gamma knife or phosphorus-32 (P32) * More than 6 months from the time of enrollment if the recurrence is predominantly solid * More than 12 months from the time of enrollment if the recurrence is predominantly cystic * At least 7 days since the completion of therapy with a hematopoietic growth agent (filgrastim, sargramostim, and erythropoietin) and 14 days for long-acting formulations * Karnofsky performance scale (KPS for \> 16 years \[yrs\] of age) or Lansky performance score (LPS for =\< 16 years of age) \>= 60 assessed within two weeks prior to registration * Age: 18 months - 25 years (Minimum weight 20 Kilogram is required to be eligible for the study, since the minimum injection volume of SYLATRON is 0.05 ml, 20 mcg, subcutaneously (SQ) as suggested by Merck) * Absolute neutrophil count (ANC) \>= 1000/ul (unsupported) * Platelets \>= 100,000/ul (unsupported) * Hemoglobin (Hg) \>= 8g/dL (unsupported) * Alanine aminotransferase (ALT) =\< 2.5 x the upper limit of institutional normal * Total bilirubin =\< x 1.5 upper limit of institutional normal * Serum creatinine =\< 1.5 x the upper limit of normal for age, or calculated creatinine clearance or nuclear glomerular filtration rate (GFR) \>= 70 ml/min/1.73 m\^2 * =\< 0.6 mg/dL (1 to \< 2 years of age) * =\< 0.8 mg/dL (2 to \< 6 years of age) * =\< 1.0 mg/dL (6 to \< 10 years of age) * =\< 1.2 mg/dL (10 to \< 13 years of age) * =\< 1.4 mg/dL (females \>= 13 years of age) * =\< 1.5 mg/dL (males 13 to \< 16 years of age) * =\< 1.7 mg/dL (males \>= 16 years of age) * All patients must have undergone at least one surgical procedure to verify the diagnosis * Patients must have evidence of radiographic progression as defined below: * Stratum 1: defined as \>= 25% increase in the product of the greatest perpendicular diameters of the tumor as a whole (solid and cystic component) AND \>= 0.4 cm increase in each of at least two dimensions of the tumor as a whole OR any new or worsening neurologic/vision deficit in conjunction with a lesser change in the solid or cystic component * Stratum 2: * For patients more than 6 months following radiation therapy (RT) (including radiosurgery or P32), progression is defined as a \>= 25% increase in the product of the greatest perpendicular diameters of the solid component AND \>= 0.4 cm increase in each of at least two dimensions of the solid component * For patients more than 12 months following RT (including radiosurgery or P32), progression is defined as \>= 25% increase in each of the product of the greatest perpendicular diameters of the solid tumor AND \>= 0.4 cm increase in each of at least two dimensions of the solid tumor; patients demonstrating isolated cyst progression more than 12 months after RT must show a continued increase in the cystic component on two serial MRI scans performed at least 4 weeks apart OR re-accumulation of the cyst following one or more cyst aspirations; patients with progressive neurologic signs and/or symptoms associated with isolated cyst formation or progression are eligible if the neurologic signs and/or symptoms do not improve within 4 weeks of cyst aspiration * Female subjects of childbearing potential must not be pregnant or breast-feeding; female subjects of childbearing potential must have a negative serum or urine pregnancy test; (pregnancy test must be repeated within 72 hours prior to the start of therapy) * Subjects of childbearing or child fathering potential must be willing to use a medically acceptable form of birth control, which includes abstinence, while being treated on this study * Ability to understand and the willingness to sign a written informed consent document
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Rate of Disease Stabilization at 1 Year (i.e., 9 Courses of Treatment) (for Stratum 1 Patients Only) | Up to 1 year | The percentage of stratum 1 patients with disease stabilization at 1 year is reported, along with a 95% exact confidence interval for the estimate of the true 1-year disease stabilization rate. |
| Sustained Objective Response (PR+CR) Rate Observed During the First Year of Treatment (for Stratum 2 Patients Only) | Up to 1 year | Objective responses had to be sustained for 3 months. The percentage of participants with sustained objective responses is reported with an exact 95% confidence interval of the true sustained objective response rate. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Sustained Objective Response (PR+CR) Rate Observed During the First Year of Treatment (for Stratum 1 Patients Only) | Up to 1 year | Objective responses had to be sustained for 3 months. The percentage of participants with sustained objective responses is reported with an exact 95% confidence interval of the true sustained objective response rate. |
| Progression-free Survival (PFS) | 2 years after treatment start | PFS estimates for each stratum were estimated using the method of Kaplan and Meier. PFS was defined as the time interval from date on treatment to the earliest date of disease progression, second malignancy, or death; or to date of last contact for patients without events. One- and two-year PFS estimates are reported by stratum. Only eligible patients were included in this analysis (7 stratum 1 patients and 11 stratum 2 patients). |
Countries
United States
Participant flow
Recruitment details
Patients 18 months to 25 years with histologically confirmed craniopharyngioma were enrolled at Pediatric Brain Tumor Consortium (PBTC) member institutions. The first patient was enrolled on 4/1/2014 and the last patient was enrolled on 11/20/2017. Accrual was halted early due to lack of efficacy in stratum 2 and slow accrual in stratum 1.
Pre-assignment details
Stratum 1 patients had progressive unresectable or recurrent craniopharyngiomas treated with surgery alone. Stratum 2 patients had progressive/recurrent craniopharyngiomas following radiation. 19 patients were enrolled (7 stratum 1, 12 stratum 2); one of the stratum 2 patients was ineligible leaving 18 eligible patients (7 stratum 1, 11 stratum 2).
Participants by arm
| Arm | Count |
|---|---|
| Stratum 1 Stratum 1 patients are those with progressive unresectable or recurrent craniopharyngiomas treated with surgery alone, who had not received radiation therapy. Treatment consisted of Peginterferon alfa-2b (Sylatron) subcutaneously weekly for 6 weeks. Treatment may repeat every 6 weeks for up to 18 courses in the absence of disease progression or unacceptable toxicity. | 7 |
| Stratum 2 Stratum 2 patients are those with patients with progressive or recurrent craniopharyngiomas following radiation therapy. Treatment consisted of Peginterferon alfa-2b (Sylatron) subcutaneously weekly for 6 weeks. Treatment may repeat every 6 weeks for up to 18 courses in the absence of disease progression or unacceptable toxicity. | 11 |
| Total | 18 |
Withdrawals & dropouts
| Period | Reason | FG000 | FG001 |
|---|---|---|---|
| Overall Study | Adverse Event | 1 | 1 |
| Overall Study | Enlargement of cyst requiring drainage | 1 | 0 |
| Overall Study | Ineligible after enrollment | 0 | 1 |
| Overall Study | Lack of Efficacy | 3 | 5 |
| Overall Study | To receive alternative therapy | 1 | 2 |
| Overall Study | Weight criteria not met | 0 | 1 |
| Overall Study | Withdrawal by Subject | 0 | 1 |
Baseline characteristics
| Characteristic | Stratum 2 | Total | Stratum 1 |
|---|---|---|---|
| Age, Categorical <=18 years | 5 Participants | 12 Participants | 7 Participants |
| Age, Categorical >=65 years | 0 Participants | 0 Participants | 0 Participants |
| Age, Categorical Between 18 and 65 years | 6 Participants | 6 Participants | 0 Participants |
| Age, Continuous | 20.5 years | 13.1 years | 10.6 years |
| Race (NIH/OMB) American Indian or Alaska Native | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Asian | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Black or African American | 2 Participants | 2 Participants | 0 Participants |
| Race (NIH/OMB) More than one race | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Native Hawaiian or Other Pacific Islander | 0 Participants | 0 Participants | 0 Participants |
| Race (NIH/OMB) Unknown or Not Reported | 1 Participants | 4 Participants | 3 Participants |
| Race (NIH/OMB) White | 8 Participants | 12 Participants | 4 Participants |
| Region of Enrollment United States | 11 participants | 18 participants | 7 participants |
| Sex: Female, Male Female | 6 Participants | 10 Participants | 4 Participants |
| Sex: Female, Male Male | 5 Participants | 8 Participants | 3 Participants |
Adverse events
| Event type | EG000 affected / at risk | EG001 affected / at risk |
|---|---|---|
| deaths Total, all-cause mortality | 0 / 7 | 1 / 12 |
| other Total, other adverse events | 7 / 7 | 12 / 12 |
| serious Total, serious adverse events | 1 / 7 | 5 / 12 |
Outcome results
Primary
Rate of Disease Stabilization at 1 Year (i.e., 9 Courses of Treatment) (for Stratum 1 Patients Only)
The percentage of stratum 1 patients with disease stabilization at 1 year is reported, along with a 95% exact confidence interval for the estimate of the true 1-year disease stabilization rate.
Time frame: Up to 1 year
Population: This primary outcome measure only relates to stratum 1 patients.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Stratum 1 | Rate of Disease Stabilization at 1 Year (i.e., 9 Courses of Treatment) (for Stratum 1 Patients Only) | 28.6 percentage of participants |
Primary
Sustained Objective Response (PR+CR) Rate Observed During the First Year of Treatment (for Stratum 2 Patients Only)
Objective responses had to be sustained for 3 months. The percentage of participants with sustained objective responses is reported with an exact 95% confidence interval of the true sustained objective response rate.
Time frame: Up to 1 year
Population: Only eligible stratum 2 patients are included in this analysis. This is a \*secondary\* outcome measure for stratum 1 patients and is therefore reported as a separate outcome measure.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Stratum 2 | Sustained Objective Response (PR+CR) Rate Observed During the First Year of Treatment (for Stratum 2 Patients Only) | 0.0 percentage of participants |
Secondary
Progression-free Survival (PFS)
PFS estimates for each stratum were estimated using the method of Kaplan and Meier. PFS was defined as the time interval from date on treatment to the earliest date of disease progression, second malignancy, or death; or to date of last contact for patients without events. One- and two-year PFS estimates are reported by stratum. Only eligible patients were included in this analysis (7 stratum 1 patients and 11 stratum 2 patients).
Time frame: 2 years after treatment start
Population: The one ineligible stratum 2 patient enrolled on the study was excluded from this analysis, leaving 7 stratum 1 patients and 11 stratum 2 patients.
| Arm | Measure | Group | Value (NUMBER) |
|---|---|---|---|
| Stratum 1 | Progression-free Survival (PFS) | PFS at 1 year | 83.3 percentage of participants |
| Stratum 1 | Progression-free Survival (PFS) | PFS at 2 years | 27.8 percentage of participants |
| Stratum 2 | Progression-free Survival (PFS) | PFS at 1 year | 68.2 percentage of participants |
| Stratum 2 | Progression-free Survival (PFS) | PFS at 2 years | 34.1 percentage of participants |
Secondary
Sustained Objective Response (PR+CR) Rate Observed During the First Year of Treatment (for Stratum 1 Patients Only)
Objective responses had to be sustained for 3 months. The percentage of participants with sustained objective responses is reported with an exact 95% confidence interval of the true sustained objective response rate.
Time frame: Up to 1 year
Population: The seven stratum 1 patients are included in this analysis. This outcome measure was a \*primary\* outcome measure for stratum 2 patients and is therefore reported as a separate outcome measure for stratum 2.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Stratum 1 | Sustained Objective Response (PR+CR) Rate Observed During the First Year of Treatment (for Stratum 1 Patients Only) | 14.3 percentage of participants |