A Clinical Trial Using Metronomic Oral Low-dose Cyclophosphamide Alternating With Low-dose Oral Methotrexate With Continuous Celecoxib and Weekly Vinblastine in Children and Adolescents With Relapsed or Progressing soliD Tumours.

NCT ID: NCT01285817

Last Updated: 2023-03-13

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 79 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-01-12
• Study Completion Date: 2023-03-09

Brief Summary

To establish the anti-tumour effect of this metronomic combination regimen defined by progression-free survival (PFS) after two cycles of treatment (4 months) and 12 months of treatment, as well as response rate after any number of cycles of treatment ("best response").

To define the safety profile of the combination. To characterize pharmacodynamics of the drug combination with the use of angiogenic markers (CEP, CEC, microparticles).

Detailed Description

Multi-center, combination phase II study, open-label, non-comparative, non-randomized.

All progressive or recurrent solid tumours will be included in the Phase II study, provided there are no curative options anymore.

Total expected number of patients (minimum maximum): 54 to 90 (2-stage design)

Conditions

Survival Without Progression

Study Design

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

Study Groups

traetment

Group Type: EXPERIMENTAL

celecoxib, Vinblastine, Cyclophosphamide , methotrexate ,

Intervention Type: DRUG

Interventions

celecoxib, Vinblastine, Cyclophosphamide , methotrexate ,

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• Patients must have a histologically or cytologically confirmed malignant solid tumour.
• Progression or recurrence of the tumour radiologically established or confirmed within the 4 weeks prior to inclusion.
• Disease must be considered refractory to any line of conventional therapy or for which no effective conventional treatment exists.
• Age: ≥4 to 21 years of age at study entry
• Life expectancy: at least 8 weeks
• ECOG Performance status ≤ 1 or Lansky-Play Scale ≥ 70%
• Written informed consent of parent/guardian and patient assent
• Wash out of 4 weeks in case of prior chemotherapy, 6 weeks if treatment included nitrosoureas, 2 weeks in case of vincristine alone; 6 weeks in case of prior radiotherapy (except palliative radiotherapy on non measurable lesions).
• Patients must have recovered from the acute toxic effects of all prior therapy before enrolment into the study
• Able to comply with scheduled follow-up and with management of toxicity
• All patients with reproductive potential must practice an effective method of birth control while on study.
• Female patients aged > 12 years must have a negative pregnancy test within 7 days before study treatment.
• Capable of swallowing oral medication

Exclusion Criteria

• Pregnant and breast feeding women.
• Uncontrolled intercurrent illness or active infection
• Inability to swallow oral medication.
• Patients on anticonvulsants will be allowed on study

• Minimum Eligible Age: 4 Years
• Maximum Eligible Age: 21 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Assistance Publique Hopitaux De Marseille

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

BERNARD BELAIGUES

Role: STUDY_DIRECTOR

Assistance Publique hôpitaux de Marseille

Locations

Assistance Publique Hopitaux de Marseille

Marseille, , France

Countries

France

References

Verschuur A, Heng-Maillard MA, Dory-Lautrec P, Truillet R, Jouve E, Chastagner P, Leblond P, Aerts I, Honore S, Entz-Werle N, Sirvent N, Gentet JC, Corradini N, Andre N. Metronomic Four-Drug Regimen Has Anti-tumor Activity in Pediatric Low-Grade Glioma; The Results of a Phase II Clinical Trial. Front Pharmacol. 2018 Sep 27;9:00950. doi: 10.3389/fphar.2018.00950. eCollection 2018.

Reference Type: DERIVED

PMID: 30319400 (View on PubMed)

Andre N, Abed S, Orbach D, Alla CA, Padovani L, Pasquier E, Gentet JC, Verschuur A. Pilot study of a pediatric metronomic 4-drug regimen. Oncotarget. 2011 Dec;2(12):960-5. doi: 10.18632/oncotarget.358.

Reference Type: DERIVED

PMID: 22156656 (View on PubMed)

Other Identifiers

2010-021792-81

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

2010-12

Identifier Type: -

Identifier Source: org_study_id