Nab-PTX, Ifosfamide and Cisplatin in the Treatment of Pediatric Extracranial Germ Cell Tumor.
Primary Purpose
Extracranial Germ Cell Tumor, Pediatric
Status
Not yet recruiting
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
albumin-bound paclitaxel (nab-PTX), ifosfamide and cisplatin
Sponsored by
About this trial
This is an interventional treatment trial for Extracranial Germ Cell Tumor, Pediatric
Eligibility Criteria
Inclusion Criteria:
- Age: 1-18 years old;
- ECOG PS score: 0-1;
- Patients was confirmed pathologically with malignant germ cell tumor.
- Patients with tumor progressed, relapsed or refractory after first-line chemotherapy, and complete or partial remission was not achieved after recent treatment.
- Have at least one measurable lesion defined by RECIST standard;
- The estimated survival time was more than 6 months;
- Patients must fully recover from the acute toxicity of previous anticancer chemotherapy:
Bone marrow function met the following criteria:
- Absolute neutrophil count (ANC) ≥ 1.0 × 109 / L;
- Platelet count ≥ 100.0 × 109 / L (not after platelet transfusion);
Liver and kidney function should meet the following criteria:
- Bilirubin (the sum of bound and unconjugated) ≤ 1.5 × upper limit of normal value (ULN) (corresponding to age). Patients with confirmed Gilbert's syndrome can be classified according to the researcher;
- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN;
- Estimated glomerular filtration rate ≥ 70 ml / min / 1.73 m2 or normal serum creatinine (CR);
- Adequate pulmonary function: no dyspnea at rest, no exercise intolerance, pulse oxygen saturation > 94% (if there are clinical symptoms);
Cardiac function:
- LVEF ≥ 50% was detected by echocardiography;
- There was no history of arrhythmia requiring drug intervention before enrollment;
- Seizures that can be fully controlled without enzyme-induced anticonvulsants;
- During the study period, they were able to comply with outpatient treatment, laboratory monitoring and necessary clinical visits;
- Parents / guardians of child or adolescent subjects have the ability to understand, agree and sign the study informed consent form (ICF) and the applicable child consent form before starting any program related procedures; subject has the ability to express consent (when applicable) with the consent of parents / guardians.
Exclusion Criteria:
Patients with any of the following items will not be enrolled in this study:
- Patients with recurrent germ cell tumor were treated by surgery alone previously;
- Patients with immature teratoma (any grade);
- Patients with sex cord stroma;
- HBsAg positive patients;
- Patients with HIV or syphilis infection;
- Patients who had received organ transplantation before;
- Uncontrolled active systemic bacterial, viral or fungal infections;
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
nab-PTX, ifosfamide and cisplatin
Arm Description
albumin-bound paclitaxel (nab-PTX), ifosfamide and cisplatin in the treatment of pediatric advanced, recurrent or refractory extracranial germ cell tumor.
Outcomes
Primary Outcome Measures
overall response rate,ORR
Percentage of participants who experienced an overall response (overall response rate,ORR) of albumin-binding paclitaxel, ifosfamide, cisplatin regimen in the treatment of advanced, recurrent and refractory children with extracranial germ cell tumor.
Secondary Outcome Measures
Full Information
NCT ID
NCT04581265
First Posted
September 13, 2020
Last Updated
October 6, 2020
Sponsor
Sun Yat-sen University
1. Study Identification
Unique Protocol Identification Number
NCT04581265
Brief Title
Nab-PTX, Ifosfamide and Cisplatin in the Treatment of Pediatric Extracranial Germ Cell Tumor.
Official Title
A Multicenter Phase II Clinical Study of Albumin-bound Paclitaxel (Nab-PTX), Ifosfamide and Cisplatin in the Treatment of Pediatric Advanced, Recurrent or Refractory Extracranial Germ Cell Tumor.
Study Type
Interventional
2. Study Status
Record Verification Date
October 2020
Overall Recruitment Status
Not yet recruiting
Study Start Date
November 10, 2020 (Anticipated)
Primary Completion Date
November 10, 2023 (Anticipated)
Study Completion Date
May 10, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sun Yat-sen University
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
The purpose is to evaluate the effectiveness and safety of albumin-bound paclitaxel (nab-PTX), ifosfamide and cisplatin in the treatment of children patients with advanced, recurrent or refractory extracranial germ cell tumor.
Detailed Description
Children patients with advanced, recurrent or refractory extracranial germ cell tumor were treated with albumin-bound paclitaxel (nab-PTX), ifosfamide and cisplatin . This is a multi-center and single arm phase II clinical study.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Extracranial Germ Cell Tumor, Pediatric
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
43 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
nab-PTX, ifosfamide and cisplatin
Arm Type
Experimental
Arm Description
albumin-bound paclitaxel (nab-PTX), ifosfamide and cisplatin in the treatment of pediatric advanced, recurrent or refractory extracranial germ cell tumor.
Intervention Type
Drug
Intervention Name(s)
albumin-bound paclitaxel (nab-PTX), ifosfamide and cisplatin
Intervention Description
Participants received a single dose of albumin-bound paclitaxel (nab-PTX) 270mg/m2/d, administered intravenously (IV) on Day 1; Ifosfamide 1.2g/m2/d administered intravenously (IV) on Day 2-6; Cisplatin 20mg/m2/d administered intravenously (IV) on Day 2-6.
Primary Outcome Measure Information:
Title
overall response rate,ORR
Description
Percentage of participants who experienced an overall response (overall response rate,ORR) of albumin-binding paclitaxel, ifosfamide, cisplatin regimen in the treatment of advanced, recurrent and refractory children with extracranial germ cell tumor.
Time Frame
From the beginning of observation to the 2 cycles of observation(each cycle is 21 days)
10. Eligibility
Sex
All
Minimum Age & Unit of Time
1 Year
Maximum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age: 1-18 years old;
ECOG PS score: 0-1;
Patients was confirmed pathologically with malignant germ cell tumor.
Patients with tumor progressed, relapsed or refractory after first-line chemotherapy, and complete or partial remission was not achieved after recent treatment.
Have at least one measurable lesion defined by RECIST standard;
The estimated survival time was more than 6 months;
Patients must fully recover from the acute toxicity of previous anticancer chemotherapy:
Bone marrow function met the following criteria:
Absolute neutrophil count (ANC) ≥ 1.0 × 109 / L;
Platelet count ≥ 100.0 × 109 / L (not after platelet transfusion);
Liver and kidney function should meet the following criteria:
Bilirubin (the sum of bound and unconjugated) ≤ 1.5 × upper limit of normal value (ULN) (corresponding to age). Patients with confirmed Gilbert's syndrome can be classified according to the researcher;
Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN;
Estimated glomerular filtration rate ≥ 70 ml / min / 1.73 m2 or normal serum creatinine (CR);
Adequate pulmonary function: no dyspnea at rest, no exercise intolerance, pulse oxygen saturation > 94% (if there are clinical symptoms);
Cardiac function:
LVEF ≥ 50% was detected by echocardiography;
There was no history of arrhythmia requiring drug intervention before enrollment;
Seizures that can be fully controlled without enzyme-induced anticonvulsants;
During the study period, they were able to comply with outpatient treatment, laboratory monitoring and necessary clinical visits;
Parents / guardians of child or adolescent subjects have the ability to understand, agree and sign the study informed consent form (ICF) and the applicable child consent form before starting any program related procedures; subject has the ability to express consent (when applicable) with the consent of parents / guardians.
Exclusion Criteria:
Patients with any of the following items will not be enrolled in this study:
Patients with recurrent germ cell tumor were treated by surgery alone previously;
Patients with immature teratoma (any grade);
Patients with sex cord stroma;
HBsAg positive patients;
Patients with HIV or syphilis infection;
Patients who had received organ transplantation before;
Uncontrolled active systemic bacterial, viral or fungal infections;
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yizhuo Zhang
Phone
020-87342459
Email
zhangyzh@sysucc.org.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yizhuo Zhang
Organizational Affiliation
Sun Yat-sen University CancerCenter
Official's Role
Principal Investigator
12. IPD Sharing Statement
Learn more about this trial
Nab-PTX, Ifosfamide and Cisplatin in the Treatment of Pediatric Extracranial Germ Cell Tumor.
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