Anti-angiogenetic Therapy With Radiotherapy for Pediatric Neuroblastoma

NCT ID: NCT02615106

Last Updated: 2016-06-14

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2015-11-30
• Study Completion Date: 2018-11-30

Brief Summary

The purpose of this study is to evaluate the safety and efficacy of Radiotherapy plus Endostar(Recombinant Human Endostatin) in patients with Pediatric Neuroblastoma.

Detailed Description

Clinical data proved that Endostar was a wild spectrum and safe antiangiogenesis factor which could suppress almost 65 kinds of tumor mass in animal models and affect about 12 percent human genome. So investigators design Radiotherapy plus Endostar to treat Pediatric Neuroblastoma to research the RR and safety. Investigators believe this treatment regimen may be a new approach to the pediatric neuroblastoma patients.

Conditions

Neuroblastoma

Study Design

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

Study Groups

Endostar Combined With Radiotherapy

Drug: Endostar Endostar 7.5 mg/m2/day, day 1-14 Radiation: 21.6Gy/12Fx to the tumor bed and 36Gy/20Fx to the tumor

Group Type: EXPERIMENTAL

Endostar

Intervention Type: DRUG

7.5 mg/m2/day, day 1-14

21.6Gy/12Fx to the tumor bed and 36Gy/20Fx to the tumor

Intervention Type: RADIATION

21.6Gy/12Fx to the tumor bed and 36Gy/20Fx to the tumor

Interventions

Endostar

7.5 mg/m2/day, day 1-14

Intervention Type: DRUG

21.6Gy/12Fx to the tumor bed and 36Gy/20Fx to the tumor

21.6Gy/12Fx to the tumor bed and 36Gy/20Fx to the tumor

Intervention Type: RADIATION

Other Intervention Names

recombinant human endostatin

Eligibility Criteria

Inclusion Criteria

• Participants must have histologically confirmed neuroblastoma or ganglioneuroblastoma or elevated urinary catecholamine metabolites.
• Life expectancy of greater than 12 months.
• ECOG performance status ≤2
• Diagnostic Imaging MRI and/or CT of the area to be treated within 8 weeks of any treatment. Baseline bone marrow biopsy and bone scan (with 99mTc-diphosphonate or MIBG scan (131I-MIBG or 123I-MIBG) from time of original diagnosis is required.
• Because radiation is known to be teratogenic, women of child-bearing potential and men must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) prior to study entry and for the duration of study participation. Should a woman become pregnant or suspect she is pregnant while participating in this study, she should inform her treating physician immediately.
• Ability of the patient or the patient's legal guardian to understand and the willingness to sign a written informed consent document.
• Participants or their legal guardian must sign consent prior to the initiation of radiation therapy.

Exclusion Criteria

• Patients will be ineligible if any prior therapeutic radiation therapy > 500 cGy has been delivered.
• Patients will be ineligible if chemotherapy was completed ≥ 1 year from the planned start date of radiation therapy or if the patient is referred for radiation therapy after a relapse following a regimen with chemotherapy alone.
• Individuals with a history of a different malignancy are ineligible except for the following circumstances. Individuals with a history of other malignancies are eligible if they have been disease-free for at least 5 years and are deemed by the investigator to be at low risk for recurrence of that malignancy. Individuals with the following cancers are eligible if diagnosed and treated within the past 5 years: cervical cancer in situ, and basal cell or squamous cell carcinoma of the skin.
• Pregnant females are excluded. Women of childbearing age/menstruating must have a negative pregnancy test prior to initiation of radiation therapy.

• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

OTHER

Sponsor Role: lead

Responsible Party

Chuanying Zhu

doctor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

mawei jiang, MD

Role: PRINCIPAL_INVESTIGATOR

The Department of Radiation Oncology, Xin Hua Hospital affiliated to Shanghai Jiaotong University School of Medicine

Locations

The Department of Radiation Oncology, Xin Hua Hospital Affiliated to Shanghai Jiao Tong University School of Medicine

Shanghai, Shanghai Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

chuanying zhu, MD

Role: CONTACT

sdnanhai123@163.com

862125076994

Facility Contacts

Chuanying zhu, MD

Role: primary

sdnanhai123@163.com

862125076994

Other Identifiers

SanghaiXinhua-001

Identifier Type: -

Identifier Source: org_study_id