Chordoma-Natural History, Treatment and Prognosis the Florence Radiotherapy Department Experience (1956-1990) and a Critical Review of the Literature

Authors

  • Stefano M. Magrini Department of Radiotherapy, Florence, Italy
  • Maria G. Papi Department of Radiotherapy, Florence, Italy
  • Franco Marletta Department of Radiotherapy, Catania, Italy
  • Salvatore Tomaselli Department of Radiotherapy, Catania, Italy
  • Enrico Cellai Department of Radiotherapy, Florence, Italy
  • Valiano Mungai Department of Radiotherapy, Florence, Italy
  • Gianpaolo Biti Department of Radiotherapy, Florence, Italy

DOI:

https://doi.org/10.3109/02841869209089717

Abstract

Fifteen cases of chordoma, seen between 1956 and 1990 at the Florence Radiotherapy Department are reported. Twelve of them were treated with radiotherapy and surgery, while one was left untreated. We analyzed the course of the disease in the treated cases, with particular emphasis on the problem of symptom control. The natural history of the disease seemed to be only marginally affected by the treatment and new therapeutic options are strongly needed. While actuarial survival rates at 5 and 10 years were 58% and 35% respectively (owing to the slow growth rate of this neoplasm), 10 years' symptomatic progression-free, symptom-free, and disease-free survival rates were only 25%, 17% and 8% respectively.

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Published

1992-01-01

How to Cite

Magrini, S. M., Papi, M. G., Marletta, F., Tomaselli, S., Cellai, E., Mungai, V., & Biti, G. (1992). Chordoma-Natural History, Treatment and Prognosis the Florence Radiotherapy Department Experience (1956-1990) and a Critical Review of the Literature. Acta Oncologica, 31(8), 847–851. https://doi.org/10.3109/02841869209089717