Phase 2 study of PVAG (prednisone, vinblastine, doxorubicin, gemcitabine) in elderly patients with early unfavorable or advanced stage Hodgkin lymphoma

Author:

Böll Boris12,Bredenfeld Henning2,Görgen Helen2,Halbsguth Teresa12,Eich Hans T.23,Soekler Martin4,Markova Jana5,Keller Ulrich6,Graeven Ullrich7,Kremers Stephan8,Geissler Michael9,Trenn Guido10,Fuchs Michael12,von Tresckow Bastian12,Eichenauer Dennis A.12,Borchmann Peter12,Engert Andreas12

Affiliation:

1. Department I of Internal Medicine, University Hospital Cologne, Cologne, Germany;

2. German Hodgkin Study Group, Cologne, Germany;

3. Department of Radiotherapy, University Hospital Cologne, Cologne, Germany;

4. Department II of Internal Medicine, Eberhard-Karls-University Tübingen, Tübingen, Germany;

5. Department of Clinical Hematology, University Hospital Kralovske and Vinohrady, Third Faculty of Medicine, Charles University Prague, Prague, Czech Republic;

6. Department III of Internal Medicine, Klinikum Rechts der Isar, Technische Universität Munich, Munich, Germany;

7. Department I of Internal Medicine, Klinikum Maria Hilf Mönchengladbach, Mönchengladbach, Germany;

8. Department of Hematology-Oncology, Caritas Hospital Lebach, Lebach, Germany;

9. Department of Oncology, Hospital Esslingen, Esslingen, Germany; and

10. Department of Internal Medicine, Knappschaftskrankenhaus Bottrop, Bottrop, Germany

Abstract

Abstract Approximately 20% of all Hodgkin lymphoma (HL) patients are older than 60 years and have a poor prognosis, mainly because of increased treatment-related toxicity resulting in reduced overall dose intensity and more treatment-related mortality. To possibly improve the treatment of elderly HL patients, the German Hodgkin Study Group developed a new regimen, PVAG (prednisone, vinblastine, doxorubicin, and gemcitabine). In this multicenter phase 2 study, elderly HL patients in early unfavorable and advanced stages received 6 to 8 cycles of PVAG and additional radiotherapy if they were not in complete remission (CR) after chemotherapy. Endpoints included feasibility, acute toxicity, and response rate. Fifty-nine patients 60 to 75 years of age (median, 68 years) were eligible for analysis; 93% had advanced stage disease. WHO grade 3/4 toxicities were documented in 43 patients; 46 patients responded with CR/CR uncertain (78%). Within 37 months median observation time, 15 progressions or relapses and 17 deaths were observed, of which 8 were related to HL and 1 was the result of treatment-related toxicity. The 3-year estimates for overall survival and progression-free survival were 66% (95% CI, 50%-78%) and 58% (95% CI, 43%-71%), respectively. We conclude that PVAG is safe and feasible in elderly HL patients. This trial was registered at www.clinicaltrials.gov as #NCT00147875.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference31 articles.

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3. A prospectively randomized trial carried out by the German Hodgkin Study Group (GHSG) for elderly patients with advanced Hodgkin's disease comparing BEACOPP baseline and COPP-ABVD (study HD9elderly).;Ballova;Ann Oncol,2005

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