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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT04581265
Other study ID # nab-PTX-sun
Secondary ID
Status Not yet recruiting
Phase Phase 2
First received
Last updated
Start date November 10, 2020
Est. completion date May 10, 2024

Study information

Verified date October 2020
Source Sun Yat-sen University
Contact Yizhuo Zhang
Phone 020-87342459
Email zhangyzh@sysucc.org.cn
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 43
Est. completion date May 10, 2024
Est. primary completion date November 10, 2023
Accepts healthy volunteers No
Gender All
Age group 1 Year to 18 Years
Eligibility Inclusion Criteria:

1. Age: 1-18 years old;

2. ECOG PS score: 0-1;

3. Patients was confirmed pathologically with malignant germ cell tumor.

4. Patients with tumor progressed, relapsed or refractory after first-line chemotherapy, and complete or partial remission was not achieved after recent treatment.

5. Have at least one measurable lesion defined by RECIST standard;

6. The estimated survival time was more than 6 months;

7. Patients must fully recover from the acute toxicity of previous anticancer chemotherapy:

8. Bone marrow function met the following criteria:

1. Absolute neutrophil count (ANC) = 1.0 × 109 / L;

2. Platelet count = 100.0 × 109 / L (not after platelet transfusion);

9. Liver and kidney function should meet the following criteria:

1. 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;

2. Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) = 2.5 × ULN;

3. Estimated glomerular filtration rate = 70 ml / min / 1.73 m2 or normal serum creatinine (CR);

10. Adequate pulmonary function: no dyspnea at rest, no exercise intolerance, pulse oxygen saturation > 94% (if there are clinical symptoms);

11. Cardiac function:

1. LVEF = 50% was detected by echocardiography;

2. There was no history of arrhythmia requiring drug intervention before enrollment;

12. Seizures that can be fully controlled without enzyme-induced anticonvulsants;

13. During the study period, they were able to comply with outpatient treatment, laboratory monitoring and necessary clinical visits;

14. 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:

1. Patients with recurrent germ cell tumor were treated by surgery alone previously;

2. Patients with immature teratoma (any grade);

3. Patients with sex cord stroma;

4. HBsAg positive patients;

5. Patients with HIV or syphilis infection;

6. Patients who had received organ transplantation before;

7. Uncontrolled active systemic bacterial, viral or fungal infections;

Study Design


Related Conditions & MeSH terms

  • Extracranial Germ Cell Tumor, Pediatric
  • Neoplasms, Germ Cell and Embryonal

Intervention

Drug:
albumin-bound paclitaxel (nab-PTX), ifosfamide and cisplatin
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.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Sun Yat-sen University

Outcome

Type Measure Description Time frame Safety issue
Primary 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. From the beginning of observation to the 2 cycles of observation(each cycle is 21 days)