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Preoperative Chemotherapy in Advanced Resectable Head and Neck Cancer: Final Report of the Southwest Oncology Group
WILLARD E. FEE, JR, MD
Stanford, Calif
Arch Otolaryngol Head Neck Surg. 1989;115(2):139.
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At the Triological Society section meeting of the combined otolaryngology spring meeting in Palm Beach, Fla, Dr Schuller and colleagues reported on the final report of a prospective, randomized study comparing standard therapy (surgery plus postoperative radiation) with induction chemotherapy, which included the administration of cisplatin, 50 mg/m2 intravenously (IV) on day 1; methotrexate, 40 mg/m2 IV on day 1; bleomycin, 15 U/m2 IV on days 1 and 8; and vincristine sulfate, 2 mg IV on day 1 for three courses, with 21 days between courses, and an additional 21 days after chemotherapy rest, prior to surgery. Of the 175 patients entered into the study, 158 were eligible for the study, and of these, 76 were randomized to receive standard treatment and 82 were randomized to receive chemotherapy. All patients had operable stage III or stage IV epidermoid carcinoma of the head and neck. The overall chemotherapy
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