Long-term remission of paraprotein-induced immunotactoid glomerulopathy after high-dose therapy and autologous blood stem cell transplantation

2007 ◽  
Vol 86 (12) ◽  
pp. 927-930 ◽  
Author(s):  
Mathias Witzens-Harig ◽  
Rüdiger Waldherr ◽  
Joerg Beimler ◽  
Martin Zeier ◽  
Jochen Hansmann ◽  
...  
2012 ◽  
Vol 91 (9) ◽  
pp. 1419-1425 ◽  
Author(s):  
Gabriela B. Thoennissen ◽  
Nils H. Thoennissen ◽  
Fleur Fritz ◽  
Andreas Hilbig ◽  
Andrea Kerkhoff ◽  
...  

2005 ◽  
Vol 23 (36) ◽  
pp. 9227-9233 ◽  
Author(s):  
Jean-Paul Fermand ◽  
Sandrine Katsahian ◽  
Marine Divine ◽  
Veronique Leblond ◽  
Francois Dreyfus ◽  
...  

Purpose To study the impact of high-dose therapy (HDT) with autologous stem-cell support in patients with symptomatic multiple myeloma (MM) between the ages of 55 and 65 years. Patients and Methods One hundred ninety patients between 55 and 65 years old who had newly diagnosed stage II or III MM were randomly assigned to receive either conventional chemotherapy (CCT; ie, monthly courses of a regimen of vincristine, melphalan, cyclophosphamide, and prednisone) or HDT and autologous blood stem-cell transplantation (using either melphalan alone 200 mg/m2 intravenous [IV] or melphalan 140 mg/m2 IV plus busulfan 16 mg/kg orally as pretransplantation cytoreduction). Results Within a median follow-up of 120 months, median event-free survival (EFS) times were 25 and 19 months in the HDT and CCT groups, respectively. Median overall survival (OS) time was 47.8 months in the HDT group compared with 47.6 months in the CCT group. A trend to better EFS (P = .07) was observed in favor of HDT, whereas OS curves were not statistically different (P = .91). The period of time without symptoms, treatment, and treatment toxicity (TwiSTT) was significantly longer for the HDT patients than for the CCT patients (P = .03). Conclusion With a median follow-up time of approximately 10 years, this randomized trial confirmed a benefit of HDT in terms of EFS and TwiSTT but did not provide evidence for superiority of HDT over CCT in OS of patients aged 55 to 65 years with symptomatic newly diagnosed MM.


Blood ◽  
2002 ◽  
Vol 99 (8) ◽  
pp. 3057-3059 ◽  
Author(s):  
Arnaud Jaccard ◽  
Bruno Royer ◽  
Dominique Bordessoule ◽  
Jean-Claude Brouet ◽  
Jean-Paul Fermand

Abstract We treated 5 patients with polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy, and skin changes (POEMS) syndrome and multifocal bone lesions or diffuse bone marrow plasmacytic infiltration with high-dose therapy (HDT) and autologous blood stem cell transplantation. In all cases, the treatment produced remission of plasma cell proliferation associated with marked improvement in the patients' performance status, neurologic symptoms, and other manifestations of the syndrome. HDT with stem cell support should be investigated further as a therapeutic option in patients with POEMS syndrome and disseminated plasma cell dyscrasia.


2019 ◽  
Vol 55 (5) ◽  
pp. 891-905 ◽  
Author(s):  
Hanne Skjerven Bersvendsen ◽  
Hege Sagstuen Haugnes ◽  
Alv A. Dahl ◽  
Unn-Merete Fagerli ◽  
Øystein Fluge ◽  
...  

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