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Spots Global Cancer Trial Database for Multi Centre Trial of DSMM for Newly Diagnosed Multiple Myeloma up to 60 Years

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Trial Identification

Brief Title: Multi Centre Trial of DSMM for Newly Diagnosed Multiple Myeloma up to 60 Years

Official Title: Multizentrische Therapiestudie Des Multiplen Myeloms DSMM V Therapieoptimierungs-Studie Der Deutschen Studiengruppe Multiples Myelom für Patienten Bis 60 Jahre im Stadium II/III

Study ID: NCT00546988

Study Description

Brief Summary: The study is evaluating whether risk-stratification by the means of a chromosomal aberration provides a tool to discriminate between standard and high risk. Risk-adapted therapy is based on allogeneic stem-cell transplantation for high-risk subjects instead of a second autograft in patients with deletion of chromosome 13 who have an HLA-identical stem cell donor available.

Detailed Description: The DSMM V protocol is to compare a consolidation treatment for standard-risk patients not displaying del(13) at initial diagnosis following two cycles of high-dose melphalan 200 mg/m² each supported by autologous stem cell retransfusion with interferon versus PEG-interferon. Patients with del(13) are screened for availability of a fully HLA-matched related or unrelated donor. If patient's informed consent is obtained additionally, he is scheduled to undergo an allogeneic SCT following the first cycle of high-dose melphalan. All other subjects are to proceed to a second course of high-dose melphalan similar to the standard-risk group. Initial cytoreduction is foreseen with four cycles of anthracycline-dexamethasone combination followed by combination therapy with ifosfamide/epirubicine/etoposide for stem-cell collection.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Medizinische Univ.-Klinik Graz, Graz, , Austria

Klin. Abt. für Onkologie, AKH Wien, Vienna, , Austria

Staedtisches Klinikum, Augsburg, , Germany

Dept. of Hematology/Oncology, Charité Berlin, Berlin, , Germany

Charité University Medicine, Berlin, , Germany

University Hospital, Erlangen, , Germany

Krankenhaus Nordwest, Frankfurt, , Germany

Freiburg University Hospital, Freiburg, , Germany

Georg August University Hospital, Gottingen, , Germany

Ernst-Moritz Arndt University Hospital, Greifswald, , Germany

Martin-Luther University Hospital, Halle/Saale, , Germany

University Hospital Eppendorf, Hamburg, , Germany

Hannover Medical School, Hannover, , Germany

Saarland University Hospital, Homburg/Saar, , Germany

Schleswig-Holstein University Hospital, Lubeck, , Germany

Mainz University Hospital, Mainz, , Germany

Dept. of Internal Medicine A, University Muenster, Muenster, , Germany

Dept. of Internal Medicine, Ludwig-Maximilian-University Munich, Munich, , Germany

Klinikum rechts der Isar, Munich, , Germany

Nuremberg Central Hospital, Nuremberg, , Germany

Oldenburg Hospital, Oldenburg, , Germany

University Hospital, Regensburg, , Germany

Katharinenhospital, Stuttgart, , Germany

Diakonissenkrankenhaus, Stuttgart, , Germany

Tubingen University Hospital, Tubingen, , Germany

Dept. of Internal Medicine III, University of Ulm, Ulm, , Germany

Ulm University Hospital, Ulm, , Germany

Horst-Schmidt-Kliniken, Wiesbaden, , Germany

Dept. of Internal Medicine II, University of Wuerzburg, Wuerzburg, , Germany

Contact Details

Name: Hermann Einsele, M.D.

Affiliation: Wuerzburg University Hospital, Dept. of Hematology and Oncology

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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