Trial Search Results

Cabozantinib-S-Malate in Treating Younger Patients With Recurrent, Refractory, or Newly Diagnosed Sarcomas, Wilms Tumor, or Other Rare Tumors

This phase II trial studies how well cabozantinib-s-malate works in treating younger patients with sarcomas, Wilms tumor, or other rare tumors that have come back, do not respond to therapy, or are newly diagnosed. Cabozantinib-s-malate may stop the growth of tumor cells by blocking some of the enzymes needed for tumor growth and tumor blood vessel growth.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

National Cancer Institute (NCI)

Stanford Investigator(s):

Intervention(s):

  • Drug: Cabozantinib
  • Drug: Cabozantinib S-malate
  • Other: Pharmacological Study

Phase:

Phase 2

Eligibility


Inclusion Criteria:

   - Upper age limit of =< 18 years of age for medullary thyroid carcinoma (MTC), renal
   cell carcinoma (RCC) and hepatocellular carcinoma (HCC)

   - Patients must have a body surface area >= 0.35 m^2

   - Patients must have recurrent or refractory disease, or newly diagnosed disease with no
   known curative therapy or therapy proven to prolong survival with an acceptable
   quality of life; patients must have had histologic verification of one of the
   malignancies listed below at original diagnosis or at relapse:

      - Ewing sarcoma

      - Rhabdomyosarcoma (RMS)

      - Non-rhabdomyosarcoma soft tissue sarcomas (STS) including microphthalmia
      transcription factor associated STS (alveolar soft part sarcoma [ASPS] and clear
      cell sarcoma [CCS])

      - Osteosarcoma

      - Wilms tumor

      - Rare tumors

         - Medullary thyroid carcinoma (MTC)

         - Renal cell carcinoma (RCC)

         - Hepatocellular carcinoma (HCC)

         - Hepatoblastoma

         - Adrenocortical carcinoma

         - Pediatric solid tumors (including central nervous system [CNS] tumors) with
         known molecular alterations in the targets of XL184 (i.e., MET
         amplification, overexpression, activating mutation, MET translocation, MET
         exon skipping mutations, activating RET mutations, RET rearrangement,
         overexpression or activation of AXL); documentation of the alteration from a
         Clinical Laboratory Improvement Act (CLIA) certified laboratory will be
         required

            - Note: Documentation of any known tumor molecular alterations and RET
            mutation status for patients with MTC (germline) must be uploaded via
            the RAVE system

   - Patients must have radiographically measurable disease; measurable disease is defined
   as the presence of at least one lesion on magnetic resonance imaging (MRI) or computed
   tomography (CT) scan that can be accurately measured with the longest diameter a
   minimum of 10 mm in at least one dimension (CT scan slice thickness no greater than 5
   mm)

      - Note: The following do NOT qualify as measurable disease:

         - Malignant fluid collections (e.g., ascites, pleural effusions)

         - Bone marrow infiltration

         - Lesions only detected by nuclear medicine studies (e.g., bone, gallium or
         positron emission tomography [PET] scans)

         - Elevated tumor markers in plasma or cerebrospinal fluid (CSF)

         - Previously radiated lesions that have not demonstrated clear progression
         post radiation

         - Leptomeningeal lesions that do not meet the measurement parameters noted
         above

   - Patients must have a Lansky or Karnofsky performance status score of >= 50,
   corresponding to Eastern Cooperative Oncology Group (ECOG) categories 0, 1 or 2; use
   Karnofsky for patients > 16 years of age and Lansky for patients =< 16 years of age;
   patients who are unable to walk because of paralysis, but who are up in a wheelchair,
   will be considered ambulatory for the purpose of assessing the performance score

   - Patients must have fully recovered from the acute toxic effects of all prior
   chemotherapy, immunotherapy, or radiotherapy prior to entering this study

   - Patients with solid tumors must not have received myelosuppressive chemotherapy within
   3 weeks of enrollment onto this study (6 weeks if prior nitrosourea)

   - At least 7 days must have elapsed since the completion of therapy with a growth
   factor. At least 14 days must have elapsed after receiving pegfilgrastim

   - Anti-cancer agents not known to be myelosuppressive (e.g. not associated with reduced
   platelet or absolute neutrophil count [ANC] counts): >= 7 days after the last dose of
   agent

   - Antibodies: >= 21 days must have elapsed from infusion of last dose of antibody, and
   toxicity related to prior antibody therapy must be recovered to grade =< 1

   - >= 2 weeks must have elapsed since local palliative radiation therapy (XRT) (small
   port); >= 6 weeks must have elapsed since treatment with therapeutic doses of
   M-Iodobenzylguanidine (MIBG); >= 3 months must have elapsed if prior craniospinal XRT
   was received, if >= 50% of the pelvis was irradiated, or if total-body irradiation
   (TBI) was received; >= 6 weeks must have elapsed if other substantial bone marrow
   irradiation was given

      - Subjects should not have any clinically relevant ongoing complications from prior
      radiation therapy (i.e., radiation esophagitis or other inflammation of the
      viscera)

   - No evidence of active graft versus (vs.) host disease and >= 2 months must have
   elapsed since transplant

   - Not previously received XL184 or another MET/HGF inhibitor (tivantinib or crizotinib);
   there are no limits on number of prior therapeutic regimens; patients who have been
   treated with prior VEGF pathway, or RET inhibitors (except XL184) may be eligible

   - Peripheral absolute neutrophil count (ANC) >= 1000/uL for patients with solid tumors
   without bone marrow involvement

   - Platelet count >= 100,000/uL (transfusion independent, defined as not receiving
   platelet transfusions within a 7 day period prior to enrollment) for patients with
   solid tumors without bone marrow involvement

   - Hemoglobin >= 8.0 g/dL (may receive red blood cell [RBC] transfusions) for patients
   with solid tumors without bone marrow involvement

   - Peripheral absolute neutrophil count (ANC) >= 750/uL for patients with solid tumors
   and known bone marrow metastatic disease

   - Platelet count >= 50,000/uL for patients with solid tumors and known bone marrow
   metastatic disease

   - Hemoglobin >= 8.0 g/dL for patients with solid tumors and known bone marrow metastatic
   disease

   - Transfusions are permitted to meet both the platelet and hemoglobin criteria; patients
   must not be known to be refractory to red blood cell or platelet transfusions

   - Creatinine clearance or radioisotope glomerular filtration rate (GFR) >= 70
   mL/min/1.73 m^2 or a serum creatinine based on age/gender as follows:

      - 2 to < 6 years of age

         - Male and female: 0.8 (maximum serum creatinine [mg/dL])

      - 6 to < 10 years of age

         - Male and female: 1 (maximum serum creatinine [mg/dL])

      - 10 to < 13 years of age

         - Male and female: 1.2 (maximum serum creatinine [mg/dL])

      - 13 to < 16 years of age

         - Male 1.5 (maximum serum creatinine [mg/dL])

         - Female: 1.4 (maximum serum creatinine [mg/dL])

      - >= 16 years of age

         - Male: 1.7 (maximum serum creatinine [mg/dL])

         - Female: 1.4 (maximum serum creatinine [mg/dL])

   - Urine protein: =< 30 mg/dl in urinalysis or =< 1+ on dipstick, unless quantitative
   protein is < 1000 mg in a 24 hour (h) urine sample

   - Total bilirubin =< 1.5 x upper limit of normal (ULN) for age

   - Serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase [ALT]) =< 135
   U/L (3 x ULN) (for the purpose of this study, the ULN for SGPT is 45 U/L)

   - Serum albumin >= 2.8 g/dL

   - No history of congenital prolonged corrected QT (QTc) syndrome, New York Heart
   Association (NYHA) class III or IV congestive heart failure (CHF)

   - No clinically significant cardiac arrhythmias, stroke or myocardial infarction within
   6 months prior to enrollment

   - QTc =< 480 msec; Note: Patients with grade 1 prolonged QTc (450- 480 msec) at the time
   of study enrollment should have correctable causes of prolonged QTc addressed if
   possible (i.e., electrolytes, medications)

   - Patients with a known seizure disorder who are receiving non-enzyme inducing
   anticonvulsants and have well-controlled seizures may be enrolled

   - CNS toxicity =< grade 2 with the exception of decreased tendon reflex (DTR); any grade
   of DTR is eligible

   - A blood pressure (BP) =< the 95th percentile for age, height, and gender for pediatric
   patients < 18 years old and =< 140/90 mmHg for patients >= 18 years old; patients
   should not be receiving medication for treatment of hypertension (except patients with
   Wilms tumor and RCC who may be eligible if on stable doses of no more than one
   anti-hypertensive medication with a baseline BP =< ULN for pediatric patients and =<
   140/90 for adult patients); please note that 3 serial blood pressures should be
   obtained and averaged to determine baseline BP

   - International normalized ratio (INR) =< 1.5

   - Serum amylase =< 1.5 ULN

   - Serum lipase =< 1.5 ULN

Exclusion Criteria:

   - Pregnant or breast-feeding women will not be entered on this study due to risks of
   fetal and teratogenic adverse events as seen in animal/human studies; pregnancy tests
   must be obtained in girls who are post-menarchal; males or females of reproductive
   potential may not participate unless they have agreed to use two methods of birth
   control- a medically accepted barrier method of contraceptive method (e.g., male or
   female condom) and a second effective method of birth control-during protocol therapy
   and for at least 4 months after the last dose of XL184; abstinence is an acceptable
   method of birth control

   - Growth factors that support platelet or white cell number or function must not have
   been administered within the 7 days prior to enrollment (14 days if pegfilgrastim)

   - Patients requiring corticosteroids who have not been on a stable or decreasing dose of
   corticosteroid for the 7 days prior to enrollment are not eligible; if used to modify
   immune adverse events related to prior therapy, >= 14 days must have elapsed since
   last dose of corticosteroid

   - Previous treatment with XL184 (cabozantinib) or another MET/HGF inhibitor (tivantinib,
   crizotinib)

   - Patients who are currently receiving another investigational drug are not eligible

   - Patients who are currently receiving other anti-cancer agents are not eligible

   - Patients who are receiving cyclosporine, tacrolimus or other agents to prevent either
   graft-versus-host disease post bone marrow transplant or organ rejection
   post-transplant are not eligible for this trial

   - Patients must not be receiving any of the following potent CYP3A4 inducers or
   inhibitors: erythromycin, clarithromycin, ketoconazole, azithromycin, itraconazole,
   grapefruit juice or St. John's wort

   - Concomitant anticoagulation with oral anticoagulants (e.g., warfarin, direct thrombin,
   and Factor Xa inhibitors) or platelet inhibitors (e.g., clopidogrel) are prohibited

      - Note: Low-dose aspirin for cardioprotection (per local applicable guidelines) and
      low dose, low molecular weight heparins (LMWH) are permitted; anticoagulation
      with therapeutic doses of LMWH is allowed in subjects without radiographic
      evidence of brain metastasis, who are on a stable dose of LMWH for at least 6
      weeks before first dose of study treatment, and who have had no complications
      from a thromboembolic event or the anticoagulation regimen

   - Patients must not have received enzyme-inducing anticonvulsants within 14 days prior
   to enrollment

   - Patients who are receiving drugs that prolong QTc are not eligible

   - Patients who are unable to swallow intact tablets are not eligible

   - Patients who have an uncontrolled infection are not eligible

   - Patients who in the opinion of the investigator may not be able to comply with the
   safety monitoring requirements of the study are not eligible

   - Patients with active bleeding are not eligible; specifically, no clinically
   significant gastrointestinal (GI) bleeding, GI perforation, intra-abdominal abscess or
   fistula for 6 months prior to enrollment, no hemoptysis or other signs of pulmonary
   hemorrhage for 3 months prior to enrollment; patients with evidence of an acute
   intracranial or intratumoral hemorrhage on CT or MRI are not eligible (patients with
   evidence of resolving hemorrhage will be eligible); in patients with CNS tumors, an
   MRI with ECHO gradient sequences would be required to exclude presence of petechial
   hemorrhages

   - Patients who have had or are planning to have the following invasive procedures are
   not eligible:

      - Major surgical procedure, laparoscopic procedure, or open biopsy within 28 days
      prior to enrollment

      - Central line placement or subcutaneous port placement is not considered major
      surgery but must be placed at least 3 days prior to enrollment for external lines
      (e.g., Hickman or Broviac catheter, peripherally inserted central catheter
      [PICC]) and at least 7 days prior to enrollment for a subcutaneous port

      - Core biopsy within 7 days prior to enrollment

      - Fine needle aspirate within 7 days prior to enrollment

      - Surgical or other wounds must be adequately healed prior to enrollment

      - NOTE: For purposes of this study, bone marrow aspirate and biopsy are not
      considered surgical procedures and therefore are permitted within 14 days prior
      to start of protocol therapy

   - Patients who have had significant traumatic injury within 28 days prior to enrollment
   are not eligible

   - Patients with any medical or surgical conditions that would interfere with
   gastrointestinal absorption of the study drug are not eligible

Ages Eligible for Study

2 Years - 30 Years

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Richard Fu
650-497-8815
Not Recruiting