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Dedifferentiated chordoma. Response to aggressive chemotherapy in two cases.

AbstractBACKGROUND:
Dedifferentiated chordoma is an unusual and aggressive variant of chordoma which is likely to metastasize. Few reports exist of treatment of these tumors with chemotherapy.
METHODS:
In 1988, two patients with dedifferentiated sacral chordomas were seen at the University of Chicago Hospitals. Both developed metastatic disease less than a year after sacral resection and radiation therapy. These patients' diagnoses, courses, and treatments were reviewed along with the literature on chemotherapy in both conventional and dedifferentiated chordomas.
RESULTS:
Both patients obtained complete remissions, one to a six-drug regimen and the other to ifosfamide.
CONCLUSIONS:
A trial of reasonably aggressive chemotherapy is warranted in patients with metastatic dedifferentiated chordoma. The optimum regimen is unclear, but agents active in high-grade sarcomas are logical choices.
AuthorsG F Fleming, P S Heimann, J K Stephens, M A Simon, M K Ferguson, R S Benjamin, B L Samuels
JournalCancer (Cancer) Vol. 72 Issue 3 Pg. 714-8 (Aug 01 1993) ISSN: 0008-543X [Print] United States
PMID8334623 (Publication Type: Case Reports, Journal Article, Review)
Topics
  • Adult
  • Antineoplastic Combined Chemotherapy Protocols (therapeutic use)
  • Bone Neoplasms (pathology)
  • Chordoma (drug therapy, pathology, secondary)
  • Female
  • Humans
  • Lung Neoplasms (drug therapy, pathology, secondary)
  • Neoplasm Recurrence, Local (surgery)
  • Sacrum

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