Overview

Temozolomide, Cixutumumab, and Combination Chemotherapy in Treating Patients With Metastatic Rhabdomyosarcoma

Status:
Completed
Trial end date:
2016-06-01
Target enrollment:
0
Participant gender:
All
Summary
This randomized pilot clinical trial is studying the side effects and how well giving temozolomide and cixutumumab together with combination chemotherapy works in treating patients with metastatic rhabdomyosarcoma. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as cixutumumab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Giving temozolomide and cixutumumab together with combination chemotherapy may kill more tumor cells.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
National Cancer Institute (NCI)
Treatments:
Antibodies
Antibodies, Monoclonal
Camptothecin
Cyclophosphamide
Dacarbazine
Dactinomycin
Doxorubicin
Etoposide
Etoposide phosphate
Ifosfamide
Irinotecan
Isophosphamide mustard
Liposomal doxorubicin
Podophyllotoxin
Temozolomide
Vincristine
Criteria
Inclusion Criteria:

- Patients must be eligible for, and enrolled on D9902 prior to enrollment on ARST08P1

- Patients with newly diagnosed, biopsy-proven metastatic rhabdomyosarcoma or
ectomesenchymoma (stage IV, clinical group IV) are eligible for this study; patients
with stage IV, clinical group IV RMS with parameningeal and paraspinal primary tumors,
including those with intracranial extension (ICE) are eligible for ARST08P1; ICE is
defined by contrast magnetic resonance imaging (MRI) showing that the primary tumor
touches, displaces, invades, distorts, or otherwise causes signal abnormality of the
dura in brain or spinal cord in contiguity to the primary site; ICE is also presumed
to exist if the cerebrospinal fluid (CSF) cytopathology is positive for tumor at
diagnosis

- Patients must have a performance status corresponding to Eastern Cooperative Oncology
Group (ECOG) scores of 0, 1, or 2; use Karnofsky for patients > 16 years of age and
Lansky for patients =< 16 years of age

- No prior chemotherapy or radiotherapy except for use of corticosteroids or emergent
radiation therapy; patients requiring emergency radiation are eligible

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

- 0.4 mg/dL (for patients 1 to 5 months of age)

- 0.5 mg/dL (for patients 6 to 11 months of age)

- 0.6 mg/dL (for patients 1 year of age)

- 0.8 mg/dL (for patients 2 to 5 years of age)

- 1.0 mg/dL (for patients 6 to 9 years of age)

- 1.2 mg/dL (for patients 10 to 12 years of age)

- 1.5 mg/dL (males) or 1.4 mg/dL (females) (for patients 13 to 15 years of age)

- 1.7 mg/dL (males) or 1.4 mg/dL (females) (for patients >= 16 years of age)

- Patients with urinary tract obstruction by tumor must meet the renal function criteria
listed above AND must have unimpeded urinary flow established via decompression of the
obstructed portion of the urinary tract

- Total bilirubin =< 1.5 x upper limit of normal (ULN) for age, unless there is evidence
of biliary obstruction by the tumor

- Shortening fraction >= 27% by echocardiogram (ECHO) OR ejection fraction >= 50% by
radionuclide angiogram

- Absolute neutrophil count (ANC) >= 750/uL; abnormal blood counts are permissible if
there is bone marrow biopsy or aspirate proven bone marrow involvement by
rhabdomyosarcoma

- Platelet count >= 75,000/uL; abnormal blood counts are permissible if there is bone
marrow biopsy or aspirate proven bone marrow involvement by rhabdomyosarcoma

- Sexually active patients of childbearing potential must agree to use effective
contraception during therapy (Pilots 1 and 2) and for at least 3 months after the last
dose of IMC-A12 (Pilots 1)

Exclusion Criteria:

- Female patients who are pregnant are not eligible

- Female patients who are breastfeeding are not eligible; female patients who are
lactating must agree to stop breastfeeding to participate in this study

- Patients receiving growth hormone therapy are not eligible

- Patients with known type I or type II diabetes mellitus are not eligible for
enrollment on Pilot 1

- Patients with evidence of uncontrolled infection are not eligible

- All patients and/or their parents or legal guardians must sign a written informed
consent

- All institutional, Food and Drug Administration (FDA), and National Cancer Institute
(NCI) requirements for human studies must be met