| Eligibility |
Inclusion Criteria:
1. Patients with histologically proven supratentorial WHO grade IV glioma (glioblastoma
or gliosarcoma) will be eligible for the study.
2. Patients must have shown unequivocal evidence for tumor recurrence or progression by
MRI scan and should have failed radiation therapy. The scan done prior to study entry
documenting progression will be reviewed by the treating physician to document changes
in tumor dimension to confirm recurrence. Patients with prior therapy that included
interstitial brachytherapy or stereotactic radiosurgery must have confirmation of true
progressive disease rather than radiation necrosis.
3. (2. continued) Patients with prior therapy that included interstitial brachytherapy,
Gliadel wafers or stereotactic radiosurgical procedures must have confirmation of true
progressive disease rather than radiation necrosis. Such confirmation may be using
advanced imaging studies (e.g. PET scans, diffusion-perfusion MRI, SPECT etc) or if
available, surgical sampling and histological confirmation (surgery is not required).
4. Patients may have had up to 2 prior relapses.
5. All patients must sign an IRB approved informed consent indicating their awareness of
the investigational nature of this study. Patients must have signed an authorization
for the release of their protected health information.
6. The baseline on-study MRI should be performed within 14 days (+ 3 working days) prior
to registration and on a steroid dosage that has been stable or decreasing for at
least 5 days. If the steroid dose is increased between the date of imaging and the
initiation of therapy (or at that time), a new baseline MRI is required. The same type
of scan, i.e., MRI, must be used throughout the period of protocol treatment for tumor
measurement.
7. Patients who have undergone recent resection of recurrent or progressive tumor will be
eligible as long as they have recovered from the effects of surgery. Evaluable or
measurable disease following resection of recurrent tumor is not mandated for
eligibility into the study. To best assess the extent of residual measurable disease
post-operatively, a MRI should be done no later than 96 hours in the immediate
post-operative period or 4-6 weeks post-operatively.
8. Patients must be 18 years old or older.
9. Patients must have a Karnofsky performance status equal or greater than 60.
10. Patients must have recovered from the toxic effects of prior therapy to < grade 2 non
hematological or grade 2 or lesser hematological toxicity per CTC ver 4 (except deep
vein thrombosis): 4 weeks from prior cytotoxic therapy and/or at least two weeks from
vincristine, 6 weeks from nitrosoureas, 3 weeks from procarbazine administration, and
1 week for non-cytotoxic agents, e.g., interferon, tamoxifen, cis-retinoic acid, etc.
(radiosensitizer does not count). Patients who receive anticancer agents for
non-therapeutic purposes unrelated to this study
11. (10. continued) (such as presurgically for obtaining pharmacology data for the agent)
will be eligible to enter the study provided they have recovered from the toxic
effects of the agent if any. Any questions related to the definition of non-cytotoxic
agents should be directed to the Study Chair.
12. Patients must have adequate bone marrow function (ANC = or > 1,500/mm^3 and platelet
count of = or > 100,000/mm^3), adequate liver function (SGPT = or < 3 times upper
limit of normal and alkaline phosphatase = or < 2 times upper limit of normal,
bilirubin = or <1.5 mg/dl), adequate renal function (BUN and creatinine = or <1.5
times upper limit of normal) and normal serum amylase and lipase prior to starting
therapy. Elevated cholesterol and triglycerides are not a contraindication to study
enrollment, but should be managed as clinically appropriate by the treating physician.
13. Patients must be willing and able to comply with the FDA mandated iPLEDGE program for
treatment with isotretinoin (cRA). Patients must sign specific informed consents for
treatment with cRA, as mandated by iPLEDGE guidelines. Women of childbearing potential
must not be pregnant, must not be breast-feeding and must practice adequate
contraception during and one month after participation in the study. Male and Female
patients on treatment with vorinostat must agree to use an adequate method of
contraception for the duration of the study, and for 30 days after the last dose of
study medication.
14. Prior treatment with dose dense regimens of temozolomide is not allowed (e.g, 7 days
on/7 days off, 21 day/28 day and daily low dose continuous dosing). However, prior
treatment with standard day 1-5 dosing in the adjuvant setting and low dose daily
dosing as part of chemoradiation therapy are allowed
15. Prior treatment with isotretinoin is allowed because the trial is based on the
hypothesis that HDAC inhibition will potentially overcome resistance to retinoids.
Exclusion Criteria:
1. Patients with a history of any other cancer (except non-melanoma skin cancer or
carcinoma in-situ of the cervix or bladder), unless in complete remission and off of
all therapy for that disease for a minimum of 3 years.
2. Patients must not have: a) active infection; b) disease that will obscure toxicity or
dangerously alter drug metabolism, especially liver disease; c) serious intercurrent
medical illness; d) prior treatment with HDAC inhibitors. However, patients who have
received anticancer agents for non-therapeutic purposes (for eg., as part of a
pharmacology study without therapeutic intent) will remain eligible for enrollment
into the study.
3. Prior treatment with bevacizumab is not allowed.
4. Patients receiving valproic acid (VPA), an anticonvulsant drug with HDAC inhibitor
properties, will be excluded, unless they are switched to an alternative agent prior
to treatment initiation. No wash out period is required.
5. Patients on previous treatment with carboplatin.
6. Patients with a known allergy to any component of vorinostat, or a known allergy to
temozolomide and/or isotretinoin.
7. Patient must be able to tolerate the procedures required in this study including
periodic blood sampling, study related assessments, and management at the treating
institution for the duration of the study. Inability to comply with protocol or study
procedures (for example, an inability to swallow tablets) will be an exclusion
criterion.
8. Patients receiving treatment with other antiepileptic medications will not be
excluded. Vorinostat is not metabolized by cytochrome P450 3A4 (CYP 3A4). However,
vorinostat may potentially suppress CYP 3A4 activity. Therefore, patients should
preferably be treated with non-enzyme inducing anti-epileptic medications to avoid any
potential interactions with vorinostat.
9. (8. continued) However, the use of non-enzyme inducing anti-epileptic medications is
not mandatory. If enzyme-inducing antiepileptic drugs are used, monitoring of drug
levels should be considered, as considered clinically appropriate by the treating
physician.
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