High-dose chemotherapy with hematopoietic stem-cell rescue for multiple myeloma.

BACKGROUND High-dose therapy with supporting autologous stem-cell transplantation remains a controversial treatment for cancer. In multiple myeloma, first-line regimens incorporating high-dose therapy yield higher remission rates than do conventional-dose treatments, but evidence that this translates into improved survival is limited. METHODS In this multicenter study, the Medical Research Council Myeloma VII Trial, we randomly assigned 407 patients with previously untreated multiple myeloma who were younger than 65 years of age to receive either standard conventional-dose combination chemotherapy or high-dose therapy and an autologous stem-cell transplant. RESULTS Among the 401 patients who could be evaluated, the rates of complete response were higher in the intensive-therapy group than in the standard-therapy group (44 percent vs. 8 percent, P<0.001). The rates of partial response were similar (42 percent and 40 percent, respectively; P=0.72), and the rates of minimal response were lower in the intensive-therapy group than in the standard-therapy group (3 percent vs. 18 percent, P<0.001). Intention-to-treat analysis showed a higher rate of overall survival (P=0.04 by the log-rank test) and progression-free survival (P<0.001) in the intensive-therapy group than in the standard-therapy group. As compared with standard therapy, intensive treatment increased median survival by almost 1 year (54.1 months [95 percent confidence interval, 44.9 to 65.2] vs. 42.3 months [95 percent confidence interval, 33.1 to 51.6]). There was a trend toward a greater survival benefit in the group of patients with a poor prognosis, as defined by a high beta2-microglobulin level (more than 8 mg per liter). CONCLUSIONS High-dose therapy with autologous stem-cell rescue is an effective first-line treatment for patients with multiple myeloma who are younger than 65 years of age.

[1]  A. Newland,et al.  INFUSION OF VINCRISTINE AND DOXORUBICIN WITH ORAL DEXAMETHASONE AS FIRST-LINE THERAPY FOR MULTIPLE MYELOMA , 1989, The Lancet.

[2]  J. Baars,et al.  Overall and event-free survival are not improved by the use of myeloablative therapy following intensified chemotherapy in previously untreated patients with multiple myeloma: a prospective randomized phase 3 study. , 2002, Blood.

[3]  G. Morgan,et al.  Autologous stem cell transplantation for malignancy: a systematic review of the literature. , 2000, Clinical and laboratory haematology.

[4]  J. Rossi,et al.  A Prospective, Randomized Trial of Autologous Bone Marrow Transplantation and Chemotherapy in Multiple Myeloma , 1996 .

[5]  D. Vesole,et al.  High-dose therapy in multiple myeloma. , 2003, Blood.

[6]  T. Mcelwain,et al.  HIGH-DOSE INTRAVENOUS MELPHALAN FOR PLASMA-CELL LEUKAEMIA AND MYELOMA , 1983, The Lancet.

[7]  G. Morgan,et al.  The impact of attaining a minimal disease state after high‐dose melphalan and autologous transplantation for multiple myeloma , 2001, British journal of haematology.

[8]  R. Bataille,et al.  Chromosome 13 abnormalities identified by FISH analysis and serum beta2-microglobulin produce a powerful myeloma staging system for patients receiving high-dose therapy. , 2001, Blood.

[9]  B. Barlogie,et al.  Total therapy with tandem transplants for newly diagnosed multiple myeloma. , 1999, Blood.

[10]  P. Ravaud,et al.  High-dose therapy and autologous peripheral blood stem cell transplantation in multiple myeloma: up-front or rescue treatment? Results of a multicenter sequential randomized clinical trial. , 1998, Blood.

[11]  I. Maclennan,et al.  Combined chemotherapy with ABCM versus melphalan for treatment of myelomatosis , 1992, The Lancet.

[12]  T. Hickish,et al.  High-dose melphalan and autologous bone marrow transplantation as consolidation in previously untreated myeloma. , 1994, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[13]  H. Johnsen,et al.  Impact on survival of high-dose therapy with autologous stem cell support in patients younger than 60 years with newly diagnosed multiple myeloma: a population-based study. Nordic Myeloma Study Group. , 2000, Blood.

[14]  B. Barlogie,et al.  Predicting long‐term (≥ 5 years) event‐free survival in multiple myeloma patients following planned tandem autotransplants , 2002, British journal of haematology.

[15]  J. Child EVOLVING STRATEGIES FOR THE TREATMENT OF MYELOMATOSIS , 1994, British journal of haematology.

[16]  B. Barlogie,et al.  Superiority of tandem autologous transplantation over standard therapy for previously untreated multiple myeloma. , 1997, Blood.

[17]  J. Cuzick,et al.  The prognostic value of serum beta 2 microglobulin compared with other presentation features in myelomatosis. , 1985, British Journal of Cancer.

[18]  S. Jagannath,et al.  CRITERIA FOR EVALUATING DISEASE RESPONSE AND PROGRESSION IN PATIENTS WITH MULTIPLE MYELOMA TREATED BY HIGH‐DOSE THERAPY AND HAEMOPOIETIC STEM CELL TRANSPLANTATION , 1998, British journal of haematology.

[19]  M. Slevin,et al.  Multiple myeloma treated with high dose intravenous melphalan , 1987, British journal of haematology.

[20]  J. San-Miguel,et al.  Remission status defined by immunofixation vs. electrophoresis after autologous transplantation has a major impact on the outcome of multiple myeloma patients , 2000, British journal of haematology.

[21]  K. Fields,et al.  High-Dose Therapy and Stem Cell Transplantation. , 1998, Cancer control : journal of the Moffitt Cancer Center.

[22]  M. Gore,et al.  INTENSIVE TREATMENT OF MULTIPLE MYELOMA AND CRITERIA FOR COMPLETE REMISSION , 1989, The Lancet.

[23]  E. Montserrat,et al.  Survival of multiple myeloma patients who are potential candidates for early high-dose therapy intensification/ autotransplantation and who were conventionally treated. , 1996, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.