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Clinical Trials in Poland / NCT00002462
Active, not recruiting Phase 3

RT or No RT Following Chemotherapy in Treating Patients With Stage III/IV Hodgkin's Disease

NCT00002462 · tracked via the Priya Life Science Poland tracker
Phase
Phase 3
Started
1989-09
Last updated
2025-08-05

Condition(s) studied

Lymphoma

Investigational drug(s) / intervention(s)

bleomycin sulfate →doxorubicin hydrochloride →mechlorethamine hydrochlorideprednisone →procarbazine hydrochloridevinblastine sulfate →vincristine sulfate →low-LET cobalt-60 gamma ray therapylow-LET photon therapyradiation therapy

Study summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining radiation therapy with combination chemotherapy may kill more tumor cells.

PURPOSE: Randomized phase III trial to compare the effectiveness of radiation therapy with no radiation therapy following chemotherapy in treating patients with stage III or stage IV Hodgkin's disease.

Eligibility

Sex
ALL
Min age
15 Years
Max age
70 Years
Healthy volunteers
No
DISEASE CHARACTERISTICS: Histologically proven clinical or pathological Stage III/IV Hodgkin's disease Pathological Stage IIIAS disease with the spleen as the only site of subdiaphragmatic involvement excluded PATIENT CHARACTERISTICS: Age: 15 to 70 Performance status: Not specified Life expectancy: No severe limits on life expectancy due to nonmalignant disease Hematopoietic: Not specified Hepatic: Not specified Renal: Not specified Cardiovascular: No severe cardiac disease that would preclude protocol therapy Pulmonary: No severe pulmonary disease that would preclude protocol therapy Other: No severe metabolic or neurologic disease that would preclude protocol therapy No concomitant or previous second malignancy except: Nonmelanomatous skin cancer In situ carcinoma of the cervix PRIOR CONCURRENT THERAPY: No prior therapy

Primary outcome measure(s)

Trial sites (56)

FacilityCityRegionStatus
Algemeen Ziekenhuis Middelheim Antwerp Belgium
A.Z. St. Jan Bruges Belgium
Hopital Universitaire Erasme Brussels Belgium
C.H.U. Saint-Pierre Brussels (Bruxelles) Belgium
Institut Jules Bordet Brussels (Bruxelles) Belgium
Centre Hospitalier Universitaire Brugmann Brussels (Bruxelles) Belgium
Centre Hospitalier Universitaire de Tivoli La Louvière Belgium
U.Z. Gasthuisberg Leuven Belgium
U.Z. Sint-Rafael Leuven Belgium
National Cancer Institute of Egypt Cairo Egypt
Institut Bergonie Bordeaux France
Centre Regional Francois Baclesse Caen France
Centre Hospitalier General Compiègne France
Centre Georges-Francois Leclerc Dijon France
Centre Leon Berard Lyon France
Hopital Edouard Herriot Lyon France
Centre Antoine Lacassagne Nice France
Hotel Dieu de Paris Paris France
Hopital Saint Antoine Paris France
Hopital Cochin Paris France
Hopital Necker Paris France
Hopital Jules Courmont - Centre Hospitalier Lyon Sud Pierre-Bénite France
Hopital Sud Rennes France
Centre Henri Becquerel Rouen France
Centre Medico-Chirurgical Foch Suresnes France
Centre Alexis Vautrin Vandœuvre-lès-Nancy France
Institut Gustave Roussy Villejuif France
Zentralkrankenhaus Bremen Germany
Centro di Riferimento Oncologico - Aviano Aviano Italy
Dipartimente di Oncologia di Torino Turin (Torino) Italy
Leyenburg Ziekenhuis 's-Gravenhage (Den Haag, the Hague) Netherlands
Groot Ziekengasthuis 's-Hertogenbosch 's-Hertogenbosch Netherlands
Medisch Centrum Alkmaar Alkmaar Netherlands
Antoni van Leeuwenhoekhuis Amsterdam Netherlands
Integraal Kankercentrum Amsterdam Amsterdam Netherlands
Slotervaart Ziekenhuis Amsterdam Netherlands
Onze Lieve Vrouwe Gasthuis Amsterdam Netherlands
Streekziekenhuizen Gooi-Noord Blaricum Netherlands
Catharina Ziekenhuis Eindhoven Netherlands
Medisch Spectrum Twente Enschede Netherlands

+ 16 more sites — see the full list on the official registry below.

On this site

📄 Deltasone (prednisone) drug profile →

More European Organisation for Research and Treatment of Cancer - EORTC trials in Poland

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT00002462 on ClinicalTrials.gov ↗ ← All trials in Poland