Treatment of Waldenstrom's Macroglobulinemia with Rituximab: Prognostic Factors for Response and Progression
العنوان: | Treatment of Waldenstrom's Macroglobulinemia with Rituximab: Prognostic Factors for Response and Progression |
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المؤلفون: | Dimitra Gika, A. Zomas, A A Meletios Dimopoulos, Donna M. Weber, Marie C. Kyrtsonis, Gerassimos A. Pangalis, Athanasios Anagnostopoulos, Constantinos Zervas, N. Anagnostopoulos, Raymond Alexanian |
المصدر: | Leukemia & Lymphoma. 45:2057-2061 |
بيانات النشر: | Informa UK Limited, 2004. |
سنة النشر: | 2004 |
مصطلحات موضوعية: | Male, Oncology, Cancer Research, medicine.medical_specialty, Disease-Free Survival, Antibodies, Monoclonal, Murine-Derived, Risk Factors, immune system diseases, hemic and lymphatic diseases, Internal medicine, Humans, Medicine, Aged, Analysis of Variance, business.industry, Remission Induction, Antibodies, Monoclonal, Macroglobulinemia, Blood Proteins, Hematology, Middle Aged, Prognosis, medicine.disease, Lymphoma, Leukemia, Immunology, Disease Progression, Female, Rituximab, Waldenstrom Macroglobulinemia, business, medicine.drug |
الوصف: | Recent data have suggested that rituximab is an active agent for the treatment of Waldenstrom's macroglobulinemia (WM). However, the patients that are more likely to benefit have not been clearly defined. In order to address this question we evaluated 52 patients who were treated with single-agent rituximab in the context of prospective studies. Several clinical and laboratory variables were assessed for their correlation with response and time to progression. Twenty-three (44%) patients achieved a partial response after treatment with rituximab. Previously untreated and pretreated patients had the same probability for response. Higher response rates were noted in patients with serum monoclonal protein40 g/l, with serum albuminor = 35 g/l and with kappa light chain. The median time to progression for all patients was 13.8 months. A multivariate analysis indicated that elevated serum monoclonal protein levels and low serum albumin were the dominant variables associated with shorter progression. Presence of two, one or none of these adverse prognostic factors was associated with time to progression of 3.6 months, 11 months and more than 40 months, respectively. We conclude that rituximab is an effective treatment modality for patients with WM. Patients with both low levels of monoclonal protein and normal albumin are the best candidates for treatment with standard dose rituximab. |
تدمد: | 1029-2403 1042-8194 |
DOI: | 10.1080/10428190410001723287 |
URL الوصول: | https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d0b90dc69f11b59112107f78825ea55 https://doi.org/10.1080/10428190410001723287 |
رقم الانضمام: | edsair.doi.dedup.....3d0b90dc69f11b59112107f78825ea55 |
قاعدة البيانات: | OpenAIRE |
تدمد: | 10292403 10428194 |
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DOI: | 10.1080/10428190410001723287 |