Journal of Clinical Oncology, Vol 12, 1164-1168, Copyright © 1994 by American Society of Clinical Oncology
Cisplatin plus doxorubicin plus cyclophosphamide in metastatic or recurrent thymoma: final results of an intergroup trial. The Eastern Cooperative Oncology Group, Southwest Oncology Group, and Southeastern Cancer Study Group
Sr Loehrer PJ, K Kim, SC Aisner, R Livingston, LH Einhorn, D Johnson and R Blum
Department of Medicine, Indiana University Medical Center, Indianapolis 46202.
PURPOSE: The purpose of this study was to evaluate the impact of cisplatin,
doxorubicin, and cyclophosphamide (PAC) in patients with advanced thymoma
with respect to response rate, duration of remission, and overall survival.
PATIENTS AND METHODS: Assessable patients with thymoma (n = 29) or thymic
carcinoma (n = 1) with metastatic or locally progressive recurrent disease
following radiotherapy were treated with intravenous cisplatin (50 mg/m2),
doxorubicin (50 mg/m2), and cyclophosphamide (500 mg/m2) with normal saline
hydration. Courses were repeated every 3 weeks for a maximum of eight
cycles of therapy. RESULTS: Toxicity, which was primarily hematologic, was
mild, with only one patient developing a fever associated with neutropenia.
Three complete responses (CRs) and 12 partial responses (PRs) were observed
(CR+PR rate, 50%; 95% confidence interval, 31.3% to 68.7%). Ten patients
had stable disease. The median duration of response was 11.8 months (range,
0.9 to 70.5+), the time to treatment failure 18.4 months (range, 0.8 to
91.9+), and median survival time 37.7 months (range, 2 to 91.9+).
CONCLUSION: This trial demonstrates that objective response rates and
prolonged survival can be achieved in patients with advanced thymoma.

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