Trial Search Results
Cabozantinib for Adults With Advanced Soft Tissue Sarcoma
- Cabozantinib is a cancer treatment drug that blocks the growth of new blood vessels in tumors. It can also block a chemical on tumor cells that allows the cells to grow. A similar drug, pazopanib, is used to treat types of cancer known as sarcomas. Researchers want to see if cabozantinib can be an effective treatment for types of soft tissue sarcoma that have not responded to earlier treatments.
- To test the effectiveness of cabozantinib for soft tissue sarcomas that have not responded to standard treatments.
- Individuals at least 18 years of age who have soft tissue sarcomas that have not responded to standard treatments.
- Participants will be screened with a physical exam and medical history. Blood samples will be collected. Imaging studies and other tests will be used to study the tumor before the start of treatment.
- Participants will take cabozantinib tablets daily for 28-day cycles of treatment. The tablets should be taken whole on an empty stomach.
- Treatment will be monitored with frequent blood tests and imaging studies.
- Participants will continue to take cabozantinib for as long as the tumor does not become worse and the side effects are not too severe.
Stanford is currently not accepting patients for this trial.
National Cancer Institute (NCI)
- Drug: Cabozantinib
- INCLUSION CRITERIA:
- Patients must have histologically or cytologically confirmed soft tissue sarcoma that
is metastatic or unresectable and for which standard treatment that prolongs survival
does not exist or is no longer effective.
- Patients must have measurable disease, defined as at least one lesion that can be
accurately measured in at least one dimension (longest diameter to be recorded for
non-nodal lesions and short axis for nodal lesions) as >20 mm with conventional
techniques or as >10 mm with spiral CT scan, MRI, or calipers by clinical exam.
- Patients are allowed prior VEGFR-TKI therapy. Patients will be stratified based on
prior VEGFR-TKI therapy.
- Age greater than or equal to 18 years. Because no dosing or adverse event data are
currently available on the use of cabozantinib in patients <18 years of age, children
are excluded from this study.
- ECOG performance status less than or equal to 1 (Karnofsky >70%).
- Life expectancy > 3 months.
- Patients must have normal organ and marrow function as defined below:
- leukocytes greater than or equal to 3,000/mcL
- absolute neutrophil count greater than or equal to 1,500/mcL
- platelets greater than or equal to 100,000/mcL
- total bilirubin less than or equal to 1.5 times ULN
- AST(SGOT)/ALT(SGPT) less than or equal to 2.5 times institutional upper limit of
normal creatinine within normal institutional limits
- creatinine clearance greater than or equal to 60 mL/min/1.73 m(2) for patients with
creatinine levels above institutional normal.
- hemoglobin greater than or equal to 9 g/dL
- serum albumin greater than or equal to 2.8g/dL
- lipase <2.0 times ULN and no radiologic or clinical evidence of pancreatitis
- urine protein/creatinine ratio (UPCR) less than or equal to 1
- serum phosphorus calcium, magnesium and potassium greater than or equal to LLN
- Subjects must have blood pressure (BP) no greater than 140 mmHg (systolic) and 90
mmHg (diastolic) for eligibility. Initiation or adjustment of BP medication is
permitted prior to study entry provided that the average of three BP readings at
the time of enrollment is less than or equal to 140/90 mmHg
- Patients must be able to swallow whole tablets. Tablets must not be crushed or
- The effects of cabozantinib on the developing human fetus are unknown. For this
reason and because receptor tyrosine kinases are known to be teratogenic, women
of child-bearing potential and men must agree to use adequate contraception. All
subjects of reproductive potential must agree to use both a barrier method and a
second method of birth control during the course of the study and for 4 months
after the last dose of study drug(s).
Sexually active subjects (men and women) must agree to use medically accepted barrier
methods of contraception (e.g., male or female condom) during the course of the study and
for 4 months after the last dose of study drug(s), even if oral contraceptives are also
-Ability to understand and the willingness to sign a written informed consent document.
- Patients who have had anticancer therapy, including kinase inhibitors or any
investigational agent within 4 weeks or 5 half-lives (whichever is shorter) (6 weeks
for nitrosoureas or mitomycin C) prior to entering the study or those who have not
recovered to baseline from adverse events (except alopecia and other non-clinically
significant AEs). Patients who have received prior cabozantinib or inhibitors of c-MET
or HGF are ineligible.
- The subject has received radionuclide treatment within 6 weeks of the first dose of
- The subject has received radiation therapy within 4 weeks (greater than or equal to 2
weeks for palliative radiation therapy)
- Patients with active brain metastases or carcinomatous meningitis or epidural disease
are excluded from this clinical trial. Subjects with brain metastases previously
treated with whole brain radiation or radiosurgery or subjects with epidural disease
previously treated with radiation who are asymptomatic and have remained stable for 4
weeks and do not require steroid treatment for at least 2 weeks before starting study
treatment are eligible. Neurosurgical resection of brain metastases or brain biopsy is
permitted if completed at least 3 months before starting study treatment. Baseline
brain imaging with contrast-enhanced CT or MRI scans for subjects with known brain
metastases is required to confirm eligibility.
- Eligibility of subjects receiving any medications or substances known to affect or
with the potential to affect the activity of cabozantinib will be determined following
review of their cases by the Principal Investigator. Patients who are taking
enzyme-inducing anticonvulsant agents are not eligible.
- Patients with refractory nausea and vomiting, chronic gastrointestinal diseases (e.g.,
inflammatory bowel disease), or significant bowel resection that could interfere with
- Uncontrolled intercurrent illness including, but not limited to symptomatic congestive
heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric
illness/social situations that would limit compliance with study requirements.
- Pregnant women are excluded from this study because cabozantinib has the potential for
teratogenic or abortifacient effects. Because there is an unknown but potential risk
for adverse events in nursing infants secondary to treatment of the mother with
cabozantinib, breastfeeding should be discontinued if the mother is treated with
- Strong inhibitors and inducers of CYP3A4 can affect levels of cabozantinib and should
be avoided whenever possible or switched to alternatives. Subjects requiring chronic
concomitant treatment of strong CYP3A4 inducers (e.g., dexamethasone, phenytoin,
carbamazepine, rifampin, rifabutin, rifapentin, phenobarbital, and St. John s Wort)
are not eligible for this study. Because the lists of these agents are constantly
changing, it is important to regularly consult a frequently-updated list such as
http://medicine.iupui.edu/clinpharm/ddis/; medical reference texts such as the
Physicians Desk Reference may also provide this information. As part of the
enrollment/informed consent procedures, the patient will be counseled on the risk of
interactions with other agents, and what to do if new medications need to be
prescribed or if the patient is considering a new overthe-counter medicine or herbal
- HIV-positive patients on combination antiretroviral therapy are ineligible because of
the potential for pharmacokinetic interactions with cabozantinib. Appropriate studies
will be undertaken in patients receiving combination antiretroviral therapy when
- The subject requires concomitant treatment, in therapeutic doses, with anticoagulants
such as warfarin or warfarin-related agents, heparin, thrombin or Factor Xa
inhibitors, or antiplatelet agents (e.g., clopidogrel). Low dose aspirin (less than or
equal to 81 mg/day), low-dose warfarin (less than or equal to 1 mg/day), and
prophylactic low molecular weight heparin (LMWH) are permitted. (Please note that
there may be cases in which patients on study require anticoagulation for DVT/PE
management; this does not necessitate taking
the patient off study.)
- The subject has experienced any of the following
- clinically-significant gastrointestinal bleeding within 6 months before the first
dose of study treatment
- hemoptysis of greater than or equal to 0.5 teaspoon (2.5 mL) of red blood within
3 months before the first dose of study treatment
- any other signs indicative of pulmonary hemorrhage within 3 months before the
first dose of study treatment
- The subject has radiographic evidence of cavitating pulmonary lesion(s).
- The subject has tumor in contact with, invading, or encasing any major blood vessels
- The subject has evidence of tumor invading the GI tract (esophagus, stomach, small or
large bowel, rectum or anus), or any evidence of endotracheal or endobronchial tumor
within 28 days before the first dose of cabozantinib
- The subject has uncontrolled, significant intercurrent or recent illness including,
but not limited to, the following conditions:
1. Cardiovascular disorders including:
1. Congestive heart failure (CHF): New York Heart Association (NYHA) Class III
(moderate) or Class IV (severe) at the time of screening
2. Concurrent uncontrolled hypertension defined as sustained BP > 140 mm Hg
systolic, or > 90 mm Hg diastolic despite optimal antihypertensive treatment
within 7 days of the first dose of study treatment
3. Any history of congenital long QT syndrome
4. Any of the following within 6 months before the first dose of study
- unstable angina pectoris
- clinically-significant cardiac arrhythmias
- stroke (including TIA, or other ischemic event)
- myocardial infarction
- thromboembolic event requiring therapeutic anticoagulation (Note:
subjects with a venous filter (e.g. vena cava filter) are not eligible
for this study)
2. Gastrointestinal disorders particularly those associated with a high risk of
perforation or fistula formation including:
1. Any of the following within 28 days before the first dose of study treatment
- intra-abdominal tumor/metastases invading GI mucosa
- active peptic ulcer disease,
- inflammatory bowel disease (including ulcerative colitis and Crohn s
disease), diverticulitis, cholecystitis, symptomatic cholangitis or
- malabsorption syndrome
2. Any of the following within 6 months before the first dose of study
- abdominal fistula
- gastrointestinal perforation
- bowel obstruction or gastric outlet obstruction
- intra-abdominal abscess. Note: Complete resolution of an
intra-abdominal abscess must be confirmed prior to initiating treatment
with cabozantinib even if the abscess occurred more that 6 months
before the first dose of study treatment.
3. Other disorders associated with a high risk of fistula formation including PEG
tube placement within 3 months before the first dose of study therapy
4. Other clinically significant disorders such as:
1. serious non-healing wound/ulcer/bone fracture within 28 days before the
first dose of study treatment
2. history of organ transplant, including allogeneic bone marrow transplant
3. concurrent uncompensated hypothyroidism or thyroid dysfunction within 7 days
before the first dose of study treatment
4. history of major surgery as follows:
i. Major surgery within 3 months of the first dose of cabozantinib if there were
no wound healing complications or within 6 months of the first dose of
cabozantinib if there were wound complications
ii. Minor surgery within 1 months of the first dose of cabozantinib if there were
no wound healing complications or within 3 months of the first dose of
cabozantinib if there were wound complications
In addition, complete wound healing from prior surgery must be confirmed at least
28 days before the first dose of cabozantinib irrespective of the time from
- The subject is unable to swallow tablets
- The subject has a corrected QT interval calculated by the Fridericia formula (QTcF)
>500 ms within 28 days before enrollment. Note: if initial QTcF is found to be > 500
ms, two additional EKGs separated by at least 3 minutes should be performed. If the
average of these three consecutive results for QTcF is less than or equal to 500 ms,
the subject meets eligibility in this regard.
- The subject is unable or unwilling to abide by the study protocol or cooperate fully
with the investigator or designee.
- The subject has had evidence within 2 years of the start of study treatment of another
malignancy which required systemic treatment.
- Patients should not have any clinical evidence of an active infection at the time of
INCLUSION OF WOMEN AND MINORITIES:
Both men and women of all races and ethnic groups are eligible for this trial.
Ages Eligible for Study
18 Years - 120 Years
Genders Eligible for Study