2002
CTOS Annual Meeting Posters
— Medical Onology
GEMCITABINE
AND DOCETAXEL IN SARCOMA
[Abstract
ID: 80]
Category:
Medical Oncology
Authors:
Kirsten M. Leu1, Mark Zalupski1, Vernon Sondak1,
Krisinda Snyder1, Laurence H. Baker1
Author Institutions:
1University of Michigan Comprehensive Cancer Center,
MI, United States
Presenter:
Kirsten M. Leu
kmleu@umich.edu
Correspondent:
Kirsten M. Leu
kmleu@umich.edu
Ann Arbor MI United States 48109-0948
Ph: 734/936-3983
Fax: 734/93607376
Objectives: A
recent clinical trial of the combination of gemcitabine and docetaxel
reported favorable results in patients with unresectable, predominantly
uterine leiomyosarcoma (LMS). The objective of this report is to
describe additional experience with this combination in a variety
of histologic subtypes of sarcoma.
Methods: A retrospective
chart review of 24 consecutively treated patients was performed.
Results: Twenty
four patients with a median age of 52.5 years (range 22-70) were
treated with gemcitabine 675 mg/m2 on days 1 and 8 and docetaxel
100 mg/m2 on day 8 of a 21-day cycle. Nineteen patients had previously
received adriamycin, ifosfamide, or both. Eighteen patients had
metastatic disease, 4 had locally recurrent disease, and 2 patients
presenting with their original diagnosis were unable to receive
adriamycin and/or ifosfamide for medical reasons. Patients received
a median of 6 cycles of chemotherapy (range, 2-8 cycles); 5 continue
on treatment at the time of this report. Responses occurred in 6/10
LMS from various primary sites, 2/2 angiosarcomas, 1/2 osteosarcomas,
1/2 malignant peripheral nerve sheath tumors, 0/2 synovial sarcomas,
1/2 malignant fibrous histiocytomas, 1/1 Ewing’s sarcoma, 1/1 high
grade sarcoma, not otherwise specified, 0/1 chondrosarcoma, and
0/1 liposarcoma. We observed 5 complete responses and 8 partial
responses for an overall response rate of 54%. We are currently
confirming these responses using the RECIST criteria.
Conclusions:
The combination of gemcitabine with docetaxel is a potentially
useful therapy for a variety of sarcomas. We look forward to participating
in a multicenter clinical trial of this promising combination.
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