کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
2135902 1087646 2011 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Age at transplantation and outcome after autologous stem cell transplantation in elderly patients with multiple myeloma
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی تحقیقات سرطان
پیش نمایش صفحه اول مقاله
Age at transplantation and outcome after autologous stem cell transplantation in elderly patients with multiple myeloma
چکیده انگلیسی

BACKGROUND AND OBJECTIVEThe optimal treatment of patients with multiple myeloma (MM) is not well defined, in part because these patients are underrepresented in clinical studies. Autologous stem cell transplantation (auto-SCT) after high-dose melphalan chemotherapy can result in a prolonged response duration and survival in patients under 65 years of age.DESIGN AND SETTINGSingle-center, retrospective study of patients treated at Paoli-Calmettes Institute Cancer Centre, between January 1994 and January 2007 (96 months)PATIENTS AND METHODSWe compared the outcome of elderly (age > 65 years) patients with younger patients aged between 60 and 65 years with MM.RESULTSWe compared 82 elderly patients with 104 younger patients. Except for age, both groups had comparable demographic features, disease characteristics, and prognostic factors. Induction VAD chemotherapy was comparable between the elderly (87%) and younger (94%) group. Prior to auto-SCT, the calculated hematopoietic cell transplantation-specific co-morbidity index was also comparable. With a median follow-up of 41 months (range, 5-227 months) after auto-SCT, 120 patients were still alive. Disease progression (n = 40; 61%) was the main cause of death, and it was comparable in the two groups. Auto-SCT-related mortality was 3.8% (n = 4/104) in younger and 3.7% (n = 3/82) in older patients. Comparing younger/older subjects, progression-free survival was significantly higher in the younger group (P < .0001). However, disease response rates after the first auto-SCT was comparable and overall survival (OS) was also comparable (57% vs. 54% at 5 years, P = NS; 32% vs. 24% at 10 years, P = NS). In a Cox multivariate analysis model, none of the relevant characteristics was shown to be a critical prognostic feature for OS.CONCLUSIONSAge was insignificant for both OS and transplant-related mortality. We conclude that there is no biological justification for an age-discriminate policy for MM therapy. Physiologic aging is likely more important than chronologic aging.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Hematology/Oncology and Stem Cell Therapy - Volume 4, Issue 1, January–March 2011, Pages 30–36
نویسندگان
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