ASHAP - an effective salvage therapy for recurrent and refractory malignant lymphomas
Autor: | F. Fiedler, Axel R. Zander, Bernd Metzner, W. Zeller, H. J. Weh, D Braumann, D. K. Hossfeld, M. Hoffknecht, A. Hänel, S. O. Peters, N Kröger, M Hänel, William Krüger, H J Illiger, J. C. F. Schubert |
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Rok vydání: | 2000 |
Předmět: |
Adult
Male medicine.medical_specialty Adolescent medicine.medical_treatment Salvage therapy Gastroenterology Autologous stem-cell transplantation Leukocytopenia Recurrence Internal medicine Antineoplastic Combined Chemotherapy Protocols Mucositis Humans Medicine Methylprednisolone Hemisuccinate Aged Salvage Therapy Chemotherapy business.industry Lymphoma Non-Hodgkin Cytarabine Hematopoietic Stem Cell Transplantation Hematology General Medicine Middle Aged medicine.disease Hodgkin Disease Survival Analysis Lymphoma Surgery Non-Hodgkin's lymphoma Doxorubicin Female Cisplatin business medicine.drug |
Zdroj: | Annals of Hematology. 79:304-311 |
ISSN: | 1432-0584 0939-5555 |
Popis: | Background: This study was performed to examine the efficacy and toxicity of the combination of adriamycin (ADR), methylprednisolone (solumedrol), cytarabine (Ara-C), and cisplatin (CDDP) in patients with recurrent and refractory malignant lymphomas. Patients and methods: Sixty-five patients with Hodgkin's disease (HD) (n=14) or non-Hodgkin's lymphomas (NHL) (n=51) were enrolled in the study. The ASHAP therapy consisted of ADR (40 mg/m2 by continuous infusion (CI) over 96 h), methylprednisolone (500 mg i.v., days 1–5), Ara-C (2 g/m2 as a 2-h infusion on day 5), and CDDP (100 mg/m2 by CI over 96 h). Results: Twenty-five patients (38%) achieved complete remission (CR) and 20 (31%) were taken into partial remission (PR) for an overall response rate of 69%. Thirty-two patients with CR or PR following ASHAP underwent high-dose therapy (HDT) with subsequent hematopoietic stem cell transplantation. After a median follow-up of 52 months, 13 patients are in continuous CR (CCR), the 3-year event-free survival (EFS) was 30% for responders and 21% for all patients. The median overall survival (OS) was 12 months (range 0–70 months), and the OS rate after 3 years was 32%. Unfavorable prognostic factors for EFS and OS by univariate analysis were an elevated value of the serum lactate dehydrogenase and refractory lymphoma. The most frequently observed side effects following ASHAP were leukocytopenia and thrombocytopenia of World Health Organization (WHO) grades III/IV in approximately 80% of all courses. Non-hematological toxicities such as gastrointestinal side effects, infections, mucositis, renal and neurotoxicity occurred more rarely and reached WHO grades III/IV only occasionally. No treatment-related mortality with ASHAP was observed. Conclusions: ASHAP is an effective and moderately toxic salvage therapy for patients with recurrent or refractory HD and NHL. The results in patients responding to ASHAP and afterwards undergoing HDT with stem cell support are comparable with other established protocols and indicate an improvement in survival if HDT is carried out as intensification. |
Databáze: | OpenAIRE |
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