Oxaliplatin in Treating Young Patients With Recurrent Solid Tumors That Have Not Responded to Previous Treatment

NCT ID: NCT00091182

Last Updated: 2013-06-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 180 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2004-10-31

Brief Summary

This phase II trial is studying how well oxaliplatin works in treating young patients with recurrent solid tumors that have not responded to previous treatment. Drugs used in chemotherapy, such as oxaliplatin, work in different ways to stop tumor cells from dividing so they stop growing or die.

Detailed Description

OBJECTIVES:

I. Determine the response rate in children with recurrent or refractory solid tumors treated with oxaliplatin.

II. Determine the cumulative toxicity of this drug in these patients. III. Determine the pharmacokinetic profile of this drug in these patients. IV. Determine time to progression and overall survival of patients treated with this drug.

V. Correlate the extent of oxaliplatin exposure with response in these patients.

OUTLINE: This is a multicenter study. Patients are stratified according to disease type.

Patients receive oxaliplatin IV over 2 hours on day 1. Treatment repeats every 21 days for up to 17 courses in the absence of disease progression or unacceptable toxicity.

Conditions

Childhood Central Nervous System Germ Cell Tumor; Childhood Extragonadal Germ Cell Tumor; Childhood Hepatoblastoma; Childhood Hepatocellular Carcinoma; Childhood High-grade Cerebral Astrocytoma; Childhood Low-grade Cerebral Astrocytoma; Childhood Malignant Ovarian Germ Cell Tumor; Childhood Malignant Testicular Germ Cell Tumor; Childhood Teratoma; Recurrent Adrenocortical Carcinoma; Recurrent Childhood Brain Stem Glioma; Recurrent Childhood Cerebellar Astrocytoma; Recurrent Childhood Cerebral Astrocytoma; Recurrent Childhood Ependymoma; Recurrent Childhood Liver Cancer; Recurrent Childhood Malignant Germ Cell Tumor; Recurrent Childhood Rhabdomyosarcoma; Recurrent Childhood Soft Tissue Sarcoma; Recurrent Childhood Visual Pathway and Hypothalamic Glioma; Recurrent Colon Cancer; Recurrent Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor; Recurrent Nasopharyngeal Cancer; Recurrent Neuroblastoma; Recurrent Osteosarcoma; Recurrent Rectal Cancer; Recurrent Renal Cell Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm I

Patients receive oxaliplatin IV over 2 hours on day 1. Treatment repeats every 21 days for up to 17 courses in the absence of disease progression or unacceptable toxicity.

Group Type: EXPERIMENTAL

oxaliplatin

Intervention Type: DRUG

Given IV

Interventions

oxaliplatin

Given IV

Intervention Type: DRUG

Other Intervention Names

1-OHP; Dacotin; Dacplat; Eloxatin; L-OHP

Eligibility Criteria

Inclusion Criteria

• Histologically confirmed* solid tumor, including any of the following:

• Ewing's sarcoma/peripheral primitive neuroectodermal tumor (PNET)
• Osteosarcoma
• Rhabdomyosarcoma
• Neuroblastoma
• High-grade astrocytoma
• Low-grade astrocytoma
• Glioblastoma multiforme
• Ependymoma
• Hepatoblastoma
• Germ cell tumors of any site
• Rare tumors of interest, including any of the following:

• Soft tissue sarcoma
• Hepatocellular carcinoma
• Childhood/adolescent colorectal carcinoma
• Childhood/adolescent renal cell carcinoma
• Childhood/adolescent adrenocortical carcinoma
• Childhood/adolescent nasopharyngeal carcinoma
• Recurrent disease OR refractory to conventional therapy
• Measurable disease by clinical exam, CT scan, MRI, or positron emission tomography
• Performance status - Karnofsky 50-100% (for patients over age 10)
• Performance status - Lansky 50-100% (for patients age 10 and under)
• At least 8 weeks
• Absolute neutrophil count ≥ 1,000/mm^3*
• Platelet count ≥ 75,000/mm^3* (transfusion independent)
• Hemoglobin ≥ 8.0 g/dL* (RBC transfusions allowed)
• Granulocytopenia, anemia, and/or thrombocytopenia due to bone marrow metastases or extensive prior radiotherapy allowed provided the above hematological criteria are met
• Bilirubin ≤ 3 mg/dL
• Creatinine based on age as follows:

• ≤ .8 mg/dL (for patients age 5 and under)
• ≤ 1.0 mg/dL (for patients age 6 to 10)
• ≤ 1.2 mg/dL (for patients age 11 to 15)
• ≤1.5 mg/dL (for patients age 16 to 21)
• Creatinine clearance or radioisotope glomerular filtration rate > 20 mL/min
• No uncontrolled seizure disorder
• No uncontrolled infection
• CNS toxicity ≤ grade 2
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective contraception
• Recovered from prior immunotherapy
• At least 7 days since prior anticancer biologic therapy
• More than 1 week since prior growth factors
• At least 6 months since prior allogeneic stem cell transplantation

• No evidence of active graft-vs-host disease
• No concurrent immunomodulating agents
• Recovered from prior chemotherapy
• No prior oxaliplatin
• Prior carboplatin or cisplatin allowed
• More than 3 weeks since prior myelosuppressive chemotherapy (6 weeks for nitrosoureas)
• No other concurrent anticancer chemotherapy
• Concurrent dexamethasone for CNS tumors allowed provided patient has been on a stable or decreasing dose for ≥ 1 week before study entry
• Recovered from prior radiotherapy
• At least 2 weeks since prior local palliative radiotherapy (small port)
• At least 6 months since prior craniospinal radiotherapy
• At least 6 months since prior radiotherapy to ≥ 50% of the pelvis
• At least 6 weeks since other prior substantial radiotherapy to the bone marrow
• Concurrent radiotherapy to localized painful lesions allowed provided ≥ 1 measurable lesion is not irradiated
• No other concurrent investigational agents
• No other concurrent anticancer agents

• Maximum Eligible Age: 21 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Orren Beaty

Role: PRINCIPAL_INVESTIGATOR

Children's Oncology Group

Locations

Children's Oncology Group

Arcadia, California, United States

Countries

United States

Other Identifiers

ADVL0421

Identifier Type: -

Identifier Source: secondary_id

COG-ADVL0421

Identifier Type: -

Identifier Source: secondary_id

CDR0000384560

Identifier Type: -

Identifier Source: secondary_id

U10CA098543

Identifier Type: NIH

Identifier Source: secondary_id

View Link

NCI-2012-01815

Identifier Type: -

Identifier Source: org_study_id