Inclusion Criteria:
1. Patients must be > 12 months and < 39 years of age at the time of study enrollment.
2. Diagnosis:
- - Cohort A: Newly Diagnosed DIPG.
- - Patients with newly-diagnosed DIPG with typical MRI findings (tumors with
a pontine epicenter and diffuse involvement of at least 2/3 of the pons)
with or without biopsy and have completed radiation therapy (RT) within 28
to 35 calendar day prior to start of therapy.
- - Patients must have started RT within 31 calendar days of radiographic
diagnosis (for non-biopsied DIPG patients only) or definitive surgery,
whichever is later.
- - If a biopsy was performed, the date of surgical biopsy will be
considered the date of definitive diagnostic surgery; if a patient
underwent two upfront surgeries [e.g., biopsy then debulking], this
is the date of the second surgery)
- Patients must have received RT, but no other anti-cancer therapy other
than surgery, and/or steroids prior to enrollment.
- - Cohort B: progressive/refractory/recurrent DIPG or H3K27-altered HGG.
- - Patients with DIPG (no biopsy required) or pathologically-confirmed (at
diagnosis or recurrence) extra-pontine H3K27-altered HGG who have
progressive, refractory or recurrent disease following frontline treatment
that included at least focal RT.
Patients with refractory disease must
have completed RT >6 months prior to study enrollment.
- - Patients with progressive disease only at the primary site(s) must have
completed RT more than 3 months prior to enrollment.
- - Patients with progressive disease only at the primary site(s) who
completed radiation therapy 3 to 6 months prior to enrollment must have
had at least one follow up MRI to confirm progression (rather than pseudo-
progression)
- Patients with progressive disease due to the development a new metastatic
site are eligible as long as eligibility criteria 3 (disease status) and 5
(prior RT) are met.
- - Patients with metastatic disease are eligible.
3. Disease Status.
- - Cohort A: patients may have any disease status but must have completed initial
radiation therapy (RT) before enrollment.
- - Cohort B: Patients must have measurable disease assessable by MRI imaging.
Patients may have metastatic disease. Lesions irradiated within the last 6
months are not considered measurable unless they show definitive progression
following RT.
4. Performance Level: Karnofsky Performance Scale score ≥ 50% for patients > 16 years
of age and Lansky Performance Scale score > 50% for patients ≤ 16 years of age
(applies to all patients) Note: Patients who are unable to walk because of
paralysis, but who are capable of using a wheelchair, will be considered ambulatory
for the purpose of assessing the performance score.
5. Prior anti-cancer therapy:
- - For Cohort A ONLY:
- Patients must not have received any prior therapy other than surgery, radiation
(focal to disease) and/or steroids (dexamethasone with goal to wean
dexamethasone throughout protocol therapy).
- - Patients must enroll and start treatment on study between 28 and 35 calendar
days post-completion of RT.
- - Patients must have started RT within 31 calendar days of initial diagnosis
(defined as the date of diagnostic biopsy or resection; if a patient underwent
two upfront surgeries [e.g., biopsy then resection or debulking], this is the
date of the second surgery).
- - Radiotherapy must have been administered at standard dose of 54 Gy for DIPG
patients.
Any variances in the radiotherapy dose within 10% of the standard
doses outlined above will be discussed with the Study Chair (or their delegate)
to confirm eligibility prior to study enrollment.
- - For Cohort B ONLY: Patients must have fully recovered from adverse events due
to prior treatment with investigational or conventional agents must have
recovered to a severity of Grade 0 or Grade 1 (per Common Terminology Criteria
for Adverse Events (CTCAE) version 5.0 or higher), with the exception of
alopecia.
Notes to the above for Cohort B: Patients with chronic Grade 2 toxicities may be
eligible per discretion of the Investigator and Sponsor (e.g., Grade 2
chemotherapy-induced neuropathy). Grade 2 or 3 toxicities from prior anti-tumor
therapy that are considered irreversible
- - defined as having been present and stable
for > 6 months (such as ifosfamide-related proteinuria) may be allowed if they are
not otherwise described in the exclusion criteria AND there is agreement to allow by
both the Investigator and Sponsor.
)
The wash out period between the prior anti-cancer chemotherapy, and first dose of
ACT001 (cycle 1 day 1) must be:
1. Myelosuppressive chemotherapy: At least 21 days after the last dose of
myelosuppressive chemotherapy (42 days if prior nitrosourea).
2. Hematopoietic growth factors: At least 14 days after the last dose of a
long-acting growth factor (e.g. Neulasta) or 7 days for short-acting growth
factor.
3. Biologic (anti-neoplastic agent): At least 7 days after the last dose of a
biologic agent. For agents that have known adverse events occurring beyond 7
days after administration, this period must be extended beyond the time during
which adverse events are known to occur. The duration of this interval must be
discussed with the study chair.
4. Immunotherapy: At least 42 days after the completion of any type of
immunotherapy, e.g. tumor vaccines.
5. Monoclonal antibodies: > 21 days must have elapsed from the infusion of last
dose of antibody and toxicity related to antibody therapy must be recovered to
Grade ≤ 1. 6. Radiation therapy:
- - For Cohort B, patients with refractory disease must have received their
last fraction of frontline craniospinal or focal RT > 6 months prior to
study enrollment.
Patients that have received re-irradiation for
progression must have received their last fraction of focal radiation >6
weeks or craniospinal radiation >6 weeks prior to study enrollment.
7. Stem Cell Transplant: Patients must be ≥ 3 months since autologous stem cell
transplant. Patients who received allogenic stem cell transplant or solid organ
transplant are not eligible for study. 6. Organ Function Requirements (applies to all patients)
1. 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)
2.
Adequate renal function defined as:
- - Creatinine clearance or radioisotope GFR > 70 mL/min/1.73 m² or.
- - A serum creatinine based on age/gender as follows (Schwartz et al.
J.
Peds, 106:522, 1985): Age Maximum Serum Creatinine (mg/dL) Male Female 2
to < 6 years 0.8 0.8 6 to < 10 years 1.0 1.0 10 to < 13 years 1.2 1.2 13
to < 16 years 1.5 1.4 ≥ 16 years 1.7 1.4. 3. Adequate liver function defined as:
- - total bilirubin within normal institutional limits.
- - AST (serum glutamic-oxaloacetic transaminase [SGOT]) / ALT (serum
glutamic-oxaloacetic transaminase [SGPT]) ≤ 2.5 × institutional upper
limit of normal.
- - Serum albumin ≥ 2 g/dL.
4. Adequate cardiac function defined as:
- - Ejection fraction of ≥ 50% by echocardiogram.
- - QTc ≤ 480 msec (by Bazett formula)
5.
For Cohort B: Adequate neurologic function defined as:
- - Patients with seizure disorders may be enrolled if seizures are well-
controlled.
Well controlled is defined by no increase in seizure frequency
in the 7 days prior to enrollment.
- - Patients with neurological deficits should have deficits that are stable
for at least the 7 days prior to enrollment.
7. Informed Consent: All patients and/or their parents or legally authorized
representatives must sign a written informed consent. Assent, when appropriate, will
be obtained according to institutional guidelines.
8. Life expectancy of ≥ 3 months.
9. Absence of other clinically significant concomitant active medical disorder, based
on the investigator's judgement.
Exclusion Criteria:
A patient who meets any of the following exclusion criteria will not be eligible in the
study (Applies to both cohorts except where noted below):
1. Cohort A only: Patients with metastatic disease.
2. Concomitant medications:
- - Corticosteroids:
- Cohort A - Patients receiving corticosteroids are eligible regardless of
dosing.
- - Cohort B - Patients receiving corticosteroids who have been on a stable or
decreasing dose of corticosteroid for at least 7 days prior to enrollment
are eligible.
- - Anti-cancer Agents: Patients who are currently receiving other anti-cancer
agents are not eligible (Refer study inclusion criteria relating to anti-cancer
therapies)
- Cohort A - Patients that have received any anti-cancer treatment other
than RT are not eligible.
- - Investigational Drugs: Patients who are currently receiving another
investigational drug are not eligible.
- - Anticonvulsants should be used as clinically indicated.
The use of enzyme
inducing anticonvulsants is not permitted.
- - LHRH agonist / antagonists are not permitted.
- - High Dose Biotin (B7) supplements are not permitted.
3. Concomitant medications used with caution: selective serotonin reuptake inhibitor
(SSRI) such as Lexapro, Fluoxetine (Prozac), fluvoxamine (Luvox), paroxetine
(Paxil), sertraline (Zoloft), citalopram (Celexa), and escitalopram should be used
with caution.
4. Infection: Patients who currently have an uncontrolled infection (in the opinion of
the PI) are not eligible.
5. Patients who have received a prior solid organ transplantation are not eligible.
6. Pregnant or breast-feeding women will not be entered on this study due to unknown
risks of fetal and teratogenic adverse events as seen in animal/human studies.
Pregnancy tests must be obtained in girls who are postmenarchal. Males or females of
reproductive potential may not participate unless they have agreed to use an
effective contraceptive method.
7. Patients of childbearing or child fathering potential must agree to use adequate
contraceptive methods (hormonal or barrier method of birth control; abstinence)
while being treated on this study and for 3 months after completing therapy. Note:
The definition of effective contraception will be based on the judgement of the
principal investigator or a designated associate.
8. Patients who are in the opinion of the investigator may not be able to comply with
the safety monitoring requirements of the study are not eligible.
9. Patients who have previously received either ACT001 or parthenolide are not
eligible.
