Literature DB >> 12057069

Newly diagnosed multiple myeloma.

Donna M Weber1.   

Abstract

Melphalan combined with prednisone (MP) has been accepted as the standard therapy for previously untreated multiple myeloma (MM) because most studies demonstrate only a modest survival benefit of combination chemotherapy regimens when compared with MP. There have been modest gains with more intensive myeloablative regimens in combination with blood stem cell support, particularly for patients with early primary refractory disease who subsequently achieve partial remission, and for the approximately 25% to 35% of patients achieving complete remission. To preserve the ability to adequately collect stem cells, the use of alkylating agents, such as melphalan, should be limited in the previously untreated patient with myeloma (including those older than 65 years of age) who is a candidate for myeloablative therapy. Pulse dexamethasone-containing regimens provide rapid responses and may be considered the first regimens of choice. Although vincristine/doxorubicin/dexamethasone (VAD) produces responses in approximately 50% to 70% of patients with previously untreated multiple myeloma, use early in the disease has not improved survival. Outside of a specific study protocol, this regimen may be best reserved for patients with refractory (particularly relapsing) disease. Notable exceptions include patients with renal failure or plasma cell leukemia in whom the rapid responses provided by VAD may avoid potentially permanent, serious complications. Recently, new agents with novel mechanisms of action (ie, thalidomide, immunomodulatory drugs, proteosome inhibitors) have demonstrated activity in resistant myeloma. Because these agents are likely to show activity alone or in combination, newly diagnosed patients and previously untreated patients should be considered for clinical trials. Thalidomide/dexamethasone has already produced response rates of 65% to 75% in previously untreated patients. Its ease of administration along with stem cell preservation are likely to make this, followed by myeloablative therapy with stem cell support, the treatment of choice for untreated myeloma as confirmatory studies are completed.

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Year:  2002        PMID: 12057069     DOI: 10.1007/s11864-002-0013-4

Source DB:  PubMed          Journal:  Curr Treat Options Oncol        ISSN: 1534-6277


  25 in total

1.  Impact of complete remission with intensive therapy in patients with responsive multiple myeloma.

Authors:  R Alexanian; D Weber; S Giralt; M Dimopoulos; K Delasalle; T Smith; R Champlin
Journal:  Bone Marrow Transplant       Date:  2001-05       Impact factor: 5.483

2.  Age is not a prognostic variable with autotransplants for multiple myeloma.

Authors:  D S Siegel; K R Desikan; J Mehta; S Singhal; A Fassas; N Munshi; E Anaissie; S Naucke; D Ayers; D Spoon; D Vesole; G Tricot; B Barlogie
Journal:  Blood       Date:  1999-01-01       Impact factor: 22.113

Review 3.  Standard chemotherapy for myelomatosis: an area of great controversy.

Authors:  M Boccadoro; A Pileri
Journal:  Hematol Oncol Clin North Am       Date:  1992-04       Impact factor: 3.722

4.  Prognostic features of asymptomatic multiple myeloma.

Authors:  D M Weber; M A Dimopoulos; L A Moulopoulos; K B Delasalle; T Smith; R Alexanian
Journal:  Br J Haematol       Date:  1997-06       Impact factor: 6.998

5.  Whither interferon for myeloma and other hematologic malignancies?

Authors:  R Alexanian; D Weber
Journal:  Ann Intern Med       Date:  1996-01-15       Impact factor: 25.391

Review 6.  Management of multiple myeloma.

Authors:  R Alexanian; M A Dimopoulos
Journal:  Semin Hematol       Date:  1995-01       Impact factor: 3.851

7.  Conventional induction treatments do not influence overall survival in multiple myeloma.

Authors:  M Boccadoro; A Palumbo; C Argentino; A Dominietto; R Frieri; G Avvisati; B Comotti; V M Lauta; M Liberati; F Marmont; P Musto; M Tribalto; A Pileri
Journal:  Br J Haematol       Date:  1997-02       Impact factor: 6.998

8.  Primary plasma cell leukaemia.

Authors:  M A Dimopoulos; A Palumbo; K B Delasalle; R Alexanian
Journal:  Br J Haematol       Date:  1994-12       Impact factor: 6.998

9.  Initial versus deferred melphalan-prednisone therapy for asymptomatic multiple myeloma stage I--a randomized study. Myeloma Group of Western Sweden.

Authors:  M Hjorth; L Hellquist; E Holmberg; B Magnusson; S Rödjer; J Westin
Journal:  Eur J Haematol       Date:  1993-02       Impact factor: 2.997

10.  Multiple myeloma: VMCP/VBAP alternating combination chemotherapy is not superior to melphalan and prednisone even in high-risk patients.

Authors:  M Boccadoro; F Marmont; M Tribalto; G Avvisati; A Andriani; T Barbui; M Cantonetti; M Carotenuto; B Comotti; F Dammacco
Journal:  J Clin Oncol       Date:  1991-03       Impact factor: 44.544

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  1 in total

1.  Treatment of bendamustine and prednisone in patients with newly diagnosed multiple myeloma results in superior complete response rate, prolonged time to treatment failure and improved quality of life compared to treatment with melphalan and prednisone--a randomized phase III study of the East German Study Group of Hematology and Oncology (OSHO).

Authors:  W Pönisch; P S Mitrou; K Merkle; M Herold; M Assmann; G Wilhelm; K Dachselt; P Richter; V Schirmer; A Schulze; R Subert; B Harksel; N Grobe; E Stelzer; M Schulze; A Bittrich; M Freund; R Pasold; Th Friedrich; W Helbig; D Niederwieser
Journal:  J Cancer Res Clin Oncol       Date:  2006-01-10       Impact factor: 4.553

  1 in total

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