Journal of Clinical Oncology, Vol 14, 2306-2310, Copyright © 1996 by American Society of Clinical Oncology
Phase II study of paclitaxel therapy for unresectable biliary tree carcinomas
DV Jones Jr, R Lozano, A Hoque, A Markowitz and YZ Patt
Department of Gastrointestinal Medical Oncology and Digestive Diseases, University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
PURPOSE: To evaluate the efficacy of paclitaxel administered to patients
with unresectable adenocarcinomas of the gallbladder and biliary tree over
3 hours every 21 days. PATIENTS AND METHODS: Fifteen patients with
unresectable and/or metastatic carcinoma of the gallbladder and bile ducts
received intravenous paclitaxel over 3 hours after premedication with
dexamethasone, diphenhydramine, and cimetidine. Treatment was repeated
every 21 days, and one complete course of therapy was comprised of two such
21-day treatment cycles. The initial dose of paclitaxel was 170 mg/m2, and
this was elevated to 200 mg/m2 due to tolerance within the initial patient
cohort. RESULTS: All patients were assessable for both toxicity and
response: 11 with bile duct cancer and four with gall-bladder carcinoma.
Forty-three cycles of therapy were delivered during the trial (median,
two), and one patient remains on treatment. No complete or partial
responses were noted, although two patients achieved minor responses that
lasted 2 and 2+ months, respectively. There were no deaths on this study,
and all but one of the patients is still alive. The therapy was well
tolerated, and hematologic and mucosal toxic effects were moderate and
readily reversible, although significant neuromuscular adverse effects were
noted. CONCLUSION: These findings indicate that paclitaxel, administered on
this schedule, is tolerable, but is unlikely to have activity in metastatic
carcinomas of the biliary tree. It is unclear whether a different regimen
of paclitaxel, or another taxane, may have activity in these neoplasms.