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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00849355
Other study ID # ADOPEH-LINFMYO-2007
Secondary ID
Status Recruiting
Phase Phase 2
First received February 20, 2009
Last updated February 20, 2009
Start date August 2008
Est. completion date November 2010

Study information

Verified date February 2009
Source Asociacion Doctor Peset Para el Estudio de la Hematología
Contact Secundino Ferrer
Phone +34961622536
Email ferrer_sec@gva.es
Is FDA regulated No
Health authority Spain: Spanish Agency of Medicines
Study type Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy (and safety) of the following treatment squeme:Ciclophosphamide, Vincristine, lyposomal Doxorrubicine (Myocet) and Prednisone,combined with Rituximab in first line treatment for patients with aggresive No Hodgkin B lymphoma and cardiovascular risk


Description:

Phase II, multicenter, open , 1-arm study.


Recruitment information / eligibility

Status Recruiting
Enrollment 44
Est. completion date November 2010
Est. primary completion date November 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

1. Patients with histological diagnosis of Lymphoma no Hodgkin B CD20+ high degree of mailgnancy

2. Patients no previously treated

3. stage III o IV

4. Informed consent

5. At least one measurable injury

6. Age >18

7. ECOG 0-2

8. Life expectancy >6 months

9. Cardiovascular risk defined as:Mild-moderate systolic dysfunction,isquemic cardiopathy, diabetes mellitus, hypertension,left ventricular hypertrophy, cardiac arrhythmia, moderate pulmonar hypertension

10. adequate organic functionallity (creatinine<2mg/dl;bilirubin<2mg/dl; ALT-AST-FA<5 FSN; neutrphyls total count >1.5x 109/l and platellet count >100x1097l)

11. Use of a contraceptive method during study + 3 months -

Exclusion Criteria:

1. stage I or II with IPI=0

2. Symptomatic tumoral affection of Nervous central system

3. Lymphoma no hodgkin B indolent

4. Lymphoma no hodgkin B mantle-cell

5. Lymphoma no hodgkin T

6. lymphoprolifertaive syndrome post-transplantation or immunosuppression associated

7. cardiovacualr disease symptomatic

8. Cronic infection or acute serious

9. history of neoplasia in past 5 years

10. not able to understand the study or poor protocol adherence

11. Known Hypersensivity to any atudy drug

12. pregnant/lactant women

13. Previous participation in clinicla study in past 30 days

14. Previous treatment with antraciclines or any drug used in this study

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
RCOMP-14 + rituximab
Pretreatment: vincristine 1mg at day -6 and Methylprednisolone 100 mg from -6 to day 0. Treatment: rituximab 375m/m2 + ciclophosphamide 750 mg/m2 + Vincristine 1.4 mg/m2 + Doxorrubicine 50 mg/m2 at day 1 and every 14d. Prednisone 100 mg/d from day 1 to 5 and every 14 d.

Locations

Country Name City State
Spain hospital del Mar Barcelona
Spain Hospital Vall D'Hebrón Barcelona
Spain Hospital de Castellon Castellon
Spain Hospital de Getafe Madrid
Spain Hospital Severo Ochoa Madrid
Spain Hospital Universitario Puerta de Hierro Madrid
Spain Hospital son Llatzer Mallorca
Spain Hospital Morales Messeguer Murcia
Spain Hospital Santa Mª del Rosell Murcia
Spain H. Arnau de Vilanova Valencia
Spain Hospital general universitario de Valencia Valencia
Spain Hospital Universitario Dr. Peset Valencia

Sponsors (3)

Lead Sponsor Collaborator
Asociacion Doctor Peset Para el Estudio de la Hematología Cephalon, Pivotal S.L.

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluate treatment efficacy by measuring response to treatment at the end of study No
Secondary evaluate cardiotoxicity and tolerability At the end of study Yes
Secondary Evaluate progression free survival At the end of study No
Secondary Evaluate event free survival At the end of study No
Secondary Evaluate tumor free survival At the end of study No
Secondary Evaluate overall survival At the end of study No
Secondary Evaluate response duration At the end of study No
Secondary treatment adherence At the end of study No
Secondary time to progression At the end of the study No
Secondary dose intensity and relative dose intensity At the end of the study No