Oral Versus Intravenous Melphalan and Prednisone Treatment in Multiple Myeloma Stage II: A randomized study from the Myeloma Group of Central Sweden

Authors

  • A. Österborg Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • A. Åhre Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • M. Björkholm Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • M. Björeman Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • G. Brenning Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • G. Gahrton Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • G. Grimfors Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • H. Gyllenhammar Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • R. Hast Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • B. Johansson Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • G. Juliusson Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • M Järnmark Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • A. Killander Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • E. Kimby Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • R. Lerner Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • B. Nilsson Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • C. Paul Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • B. Simonsson Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • A.-M. Stalfelt Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • B. Smedmyr Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • E. Svedmyr Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • A.-M. Udén Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • B. Wadman Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • E. Ösby Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden; Departments of Medicine, Danderyd Hospital, Danderyd, Södersjukhuset, Stockholm, Huddinge Hospital, Huddinge, Academic Hospital, Uppsala, and Region Hospital, Örebro, Sweden
  • H. Mellstedt Department of Oncology (Radiumhemmet), Department of Biostatistics, Department of Medicine, Karolinska Hospital, Stockholm, Sweden

DOI:

https://doi.org/10.3109/02841869009092991

Keywords:

Multiple myeloma, melphalan, intravenous, oral, randomized study

Abstract

Eighty-one previously untreated patients with multiple myeloma stage II entered a randomized trial comparing oral melphalan (0.25 mg/kg/day; n = 40) with intravenous melphalan (0.125 mg/kg/day; n = 41) in combination with oral prednisone (2 mg/kg/day). The courses were given for 4 days and repeated every sixth week. The treatment groups were well comparable with regard to major prognostic factors. There was no statistically significant difference in the response rates, the response duration times and the survival times. No significant difference in non-hematological and hematological toxicity was noted. Since intravenous administration of melphalan did not result in a substantial increase in response rate or survival, this study supports the use of oral melphalan/prednisone as first-line therapy for patients with multiple myeloma.

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Published

1990-01-01

How to Cite

Österborg, A., Åhre, A., Björkholm, M., Björeman, M., Brenning, G., Gahrton, G., … Mellstedt, H. (1990). Oral Versus Intravenous Melphalan and Prednisone Treatment in Multiple Myeloma Stage II: A randomized study from the Myeloma Group of Central Sweden. Acta Oncologica, 29(6), 727–731. https://doi.org/10.3109/02841869009092991