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Phase II study of docetaxel in advanced soft tissue sarcomas.

Publication ,  Journal Article
Edmonson, JH; Ebbert, LP; Nascimento, AG; Jung, SH; McGaw, H; Gerstner, JB
Published in: Am J Clin Oncol
December 1996

Because of its unusual mechanism of action, docetaxel was selected for study in advanced soft tissue sarcomas of adults as part of a search for new active antisarcoma agents. Patients at least 18 years old with measurable histologically proven advanced nonosseous sarcomas were enrolled if they had ECOG performance status of < or = 2 and satisfactory leukocyte and platelet counts, and hepatic and renal function. Patients with Kaposi's sarcoma, mesothelioma, meningioma, embryonal rhabdomyosarcoma, and extraosseous Ewing's sarcoma were excluded, as were patients with brain or leptomeningeal metastases. Other specific contraindications to participation included other active cancer, previous or concurrent cancer chemotherapy or immunotherapy, and known allergy to the drug vehicle, polysorbate 80. Women of childbearing potential were required to have a negative pregnancy test. Following premedication with dexamethasone and diphenhydramine hydrochloride, docetaxel 100 mg/m2 as a concentrated solution containing 40 mg/ml in polysorbate 80 was infused over 1 h in 250 ml of either dextrose 5% in water or 0.9% saline. Treatment was repeated at 3-week intervals using standard definitions for objective responses. Up to two separate 25% toxicity directed dose reductions were permitted. Between May and December 1993, nine men and nine women registered (median age, 44 years). They received a total of 51 cycles of docetaxel (median, 2.5 cycles). Toxicity included moderate leukopenia (median first cycle nadir, 1.5 x 10(9)/L) but no significant thrombocytopenia. Alopecia, diarrhea, nausea, vomiting, and anorexia were common side effects. Fever, minor skin rashes, stomatitis, and edema were also observed. One drug-related death occurred in a neutropenic patient. One partial regression was observed (5.9%, 95% C.I. 0.15-28.7%) among the 17 eligible patients in a patient with metastatic uterine leiomyosarcoma.

Duke Scholars

Published In

Am J Clin Oncol

DOI

ISSN

0277-3732

Publication Date

December 1996

Volume

19

Issue

6

Start / End Page

574 / 576

Location

United States

Related Subject Headings

  • Vomiting
  • Uterine Neoplasms
  • Taxoids
  • Sarcoma
  • Remission Induction
  • Premedication
  • Patient Selection
  • Paclitaxel
  • Oncology & Carcinogenesis
  • Nausea
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Edmonson, J. H., Ebbert, L. P., Nascimento, A. G., Jung, S. H., McGaw, H., & Gerstner, J. B. (1996). Phase II study of docetaxel in advanced soft tissue sarcomas. Am J Clin Oncol, 19(6), 574–576. https://doi.org/10.1097/00000421-199612000-00008
Edmonson, J. H., L. P. Ebbert, A. G. Nascimento, S. H. Jung, H. McGaw, and J. B. Gerstner. “Phase II study of docetaxel in advanced soft tissue sarcomas.Am J Clin Oncol 19, no. 6 (December 1996): 574–76. https://doi.org/10.1097/00000421-199612000-00008.
Edmonson JH, Ebbert LP, Nascimento AG, Jung SH, McGaw H, Gerstner JB. Phase II study of docetaxel in advanced soft tissue sarcomas. Am J Clin Oncol. 1996 Dec;19(6):574–6.
Edmonson, J. H., et al. “Phase II study of docetaxel in advanced soft tissue sarcomas.Am J Clin Oncol, vol. 19, no. 6, Dec. 1996, pp. 574–76. Pubmed, doi:10.1097/00000421-199612000-00008.
Edmonson JH, Ebbert LP, Nascimento AG, Jung SH, McGaw H, Gerstner JB. Phase II study of docetaxel in advanced soft tissue sarcomas. Am J Clin Oncol. 1996 Dec;19(6):574–576.

Published In

Am J Clin Oncol

DOI

ISSN

0277-3732

Publication Date

December 1996

Volume

19

Issue

6

Start / End Page

574 / 576

Location

United States

Related Subject Headings

  • Vomiting
  • Uterine Neoplasms
  • Taxoids
  • Sarcoma
  • Remission Induction
  • Premedication
  • Patient Selection
  • Paclitaxel
  • Oncology & Carcinogenesis
  • Nausea