| Eligibility |
Inclusion Criteria:
- Be >/= 18 years of age
- Have a histological diagnosis (fresh or archived tumor biopsy sample) of locally
advanced/metastatic or recurrent operable chondrosarcoma (conventional grade 2 or 3
only) confirmed by central pathology review
- Patients with low grade (grade 1) and dedifferentiated chondrosarcoma are
ineligible
- Patients with biopsy proven low grade (grade 1) pelvic chondrosarcoma are
ineligible unless they have radiological imaging consistent with higher grade
disease in which case they will be deemed potentially eligible. In such cases the
pre-treatment biopsy should be taken where feasible from the area of presumed
higher-grade disease to confirm grade 2 or 3 disease to confirm eligibility
- Patients without confirmation of grade 2 or 3 disease will not be eligible for
the study unless in the case where radiology features are consistent with high
grade disease but a biopsy confirmation of this is not technically feasible. Such
cases should be discussed with the principal investigator before enrollment onto
the study
- Have a documented IDH1 gene mutation (from a fresh tumor biopsy or from archived tumor
tissue) confirmed by a CLIA approved laboratory.
- Have an ECOG OS score of 0 to 2.
- Have expected survival of >/= 4 months.
- Have at least one measurable lesion as defined by RECIST 1.1, subjected who have
received prior local therapy are eligible provided the measurable disease falls
outside of the treatment field or within the field and has shown >/=20% growth in size
since post-treatment assessment.
- Have documented radiographic disease progression within the preceding 4 months before
study entry (date ICF signed).
Have recovered from toxicities associated with prior anti-cancer therapy to baseline unless
stabilized under medical management (see washout time from different therapies in Exclusion
Criteria section).
- Have adequate bone marrow functions as evidenced by:
- Absolute neutrophil count >/=1,500/mm^3 or 100 x 10^9/L.
- Hemoglobin >/=8/dL.
- Platelets >/=100,000/mm^3 or 100 x 10^9/L.
- Have adequate hepatic function as evidenced by:
- Serum total bilirubin </=2 x upper limit of normal (ULN), unless considered due
to Gilbert's disease.
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) </=5 x ULN.
- Have adequate renal function as evidenced by:
- Serum creatinine <1.5 x ULN OR
- creatinine clearance >/= 50ml/min based on the cockcroft-gault glomerular
filtration rate (GFR) estimation:
- (140 Age) x (weight in kg) x (0.85 if female)/72 x serum creatinine
- Be able to understand and willing to sign the informed consent form and to comply with
scheduled visits, treatment plans, procedures and laboratory tests, including serial
peripheral blood sampling and urine sampling, during the study. A legally authorized
representative may consent on behalf of a subject who is otherwise unable to provide
informed consent if acceptable to and approved by the site's Institutional Review
Board (IRB)
- Be able to swallow oral medication.
- Female subjects with reproductive potential must have a negative serum or urine
pregnancy test prior to the start of therapy, or a confirmation from an obstetrician
in case of equivocal serum pregnancy results. Females of reproductive potential are
defined as sexually mature women who have not undergone a hysterectomy, bilateral
oophorectomy, or tubal occlusion or who have not been naturally postmenopausal (i.e.,
who have not menstruated) for at least 24 consecutive months (i.e., have not had
menses at any time in the preceding 24 consecutive months). Women of reproductive
potential, as well as fertile men and their partners who are female with reproductive
potential, must agree to use 2 effective forms of contraception (including at least 1
barrier form) from the time of giving informed consent throughout the study and for 90
days (both females and males) following the last dose of study drug. Effective forms
of contraception are defined as hormonal oral contraceptive, injectables, patches,
intrauterine devices, intrauterine hormone-releasing systems bilateral tubal ligation,
condoms with spermicide, or male partner sterilization.
Exclusion Criteria:
- Received a prior IDH1 inhibitor.
- Received systemic anticancer therapy or an investigational agent < 3 week prior to the
Day 1 (washout from prior immune based anticancer therapy is 4 weeks).
- Received radiotherapy or other local intervention to metastatic sites of disease <2
weeks prior to Day 1.
- Underwent major surgery within 4 weeks of Day 1 or have not recovered from clinically
significant post-surgery toxicities.
- Have known symptomatic brain metastasis requiring steroids. Subject with previously
diagnosed brain metastases are eligible if they completed their treatment and have
recovered from the acute effects of radiation therapy or surgery prior to study entry,
have discontinued corticosteroid treatment for these metastases for at least 4 weeks
and have a radiographically stable disease for a least 3 months prior to study entry.
*Note: up to 10mg per day of prednisolone or equivalent will be allowed,
- Has another concurrent active cancer requiring therapeutic intervention.
- Are pregnant or breastfeeding.
- Are taking known strong CYP3A4 inducers or sensitive CYP3A4 substrate medications with
a narrow therapeutic window unless they can be transferred to other medication within
>/=5 half-lives prior to dosing
- Are taking p-glycoprotein (P-gp) transporter-sensitive substrate medications with a
narrow therapeutic window, unless they can be transferred to other medications within
>/= half-lives prior to dosing, or unless the medications can be properly monitored
during the study.
- Have an active infection requiring systemic anti-infective therapy or with an
unexplained fever > 38.5 degrees C within 7 days of Day 1 (at the discretion of the
investigator, subjects with tumor fever may be enrolled).
- Have any known hypersensitivity to any components of AG-120.
- Have significant active cardiac disease within 6 months prior to the start of study
treatment, including New York Heart Association Class II or IV congestive heart
failure: myocardial infraction: unstable angina; and/or stroke.
- Have LVEP <40% by ECHO and/or MUGA scan obtained within 28 days prior to the start of
the study treatment.
- Have a heart-rate corrected QT interval [using Frederica's Formula] (QTcF) >/=450msec
or other factor that increase the risk of QT prolongation or arrhythmic events (e.g.,
heart failure, hypokalemia, family history of long QT interval syndrome). Bundle
branch block and prolonged QTcF interval are permitted with approval of the principal
investigator.
- Are taking medications known to prolong the QT interval, unless they can have
transferred to other medications within >/= half-lives prior to dosing, or unless the
medications can be properly monitored during the study (If equivalent medication is
not available, QTcF should be closely monitored).
- Have known active hepatitis B (HBV) or hepatitis C (HCV) infections, known positive
human immunodeficiency virus (HIV) antibody results, or acquired immunodeficiency
syndrome (AIDS) related illness. Subjects with a sustained viral response to HCV or
immunity to prior HBV infection will be permitted. Subjects with chronic HBV that is
adequately suppressed per institutional practice will be permitted.
- Have any other acute or chronic medical or psychiatric condition, including recent or
active suicidal ideation or behavior, or a laboratory abnormality that may increase
the risk associated with study participation or investigational product administration
or may interfere with the interpretation of study results and, in the judgment of the
investigator, would make the subject inappropriate for entry into this study.
- Have known active inflammatory gastrointestinal disease, previous gastric resection,
or lap band dysphagia, short bowel syndrome, gastroparesis or other conditions that
limit ingestion or gastrointestinal absorption of drugs administered orally.
- Has a known medical history of progressive multifocal leukoencephalopathy (PML)
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