Background: Patients with advanced squamous cell carcinoma of the head and neck (SCC) have a depressed immune system whose function is worsened by chemotherapy. In a pilot phase II study in order to improve the immune function during chemotherapy, we combined to cisplatin (CDDP) and 5-fluorouracil (5-FU) two biological response modifiers, retinyl palmitate (R) and Thymopentin (TP-5) for the treatment of SCC. Patients and methods: Fifty patients with recurrent or metastatic SCC of the head and neck were treated with Cisplatin 24 mg/m(2) from day I to 5 and 5-FU 1,000 mg/m(2) by a 120 hour continuous infusion. Retinyl palmitate was administer ed orally 50,000 lu b.i.d and Thymopentin 50 mg subcutaneously 3 times a week. Results: Chemotherapy treatment was well tolerated with G3 hematological toxicity in 30% of patients and G2 gastrointestinal toxicity in 20% of patients. 16 patients (32%) had a complete response (CR), 13 patients had partial response (PR) (26%), (response rate 58%, 95% c.i. 43%-72%); stable disease (SD) was observed in 7 patients (14%), while 14 patients progressed (PD) (28%). Median time to progression was 12 months (range 2.8-94.5), Median overall survival was 13.5 months (range 2-104). Conclusions: The association of CDDP and 5-FU with Retinyl Palmitate and TP5 has a major activity in the treatment of advanced head and neck cancer and a relatively well tolerated toxicity.

Chemo-immunotherapy in advanced head and neck cancer. Anticancer Res 19:773-7, 1999.

REA, Silvio
1999-01-01

Abstract

Background: Patients with advanced squamous cell carcinoma of the head and neck (SCC) have a depressed immune system whose function is worsened by chemotherapy. In a pilot phase II study in order to improve the immune function during chemotherapy, we combined to cisplatin (CDDP) and 5-fluorouracil (5-FU) two biological response modifiers, retinyl palmitate (R) and Thymopentin (TP-5) for the treatment of SCC. Patients and methods: Fifty patients with recurrent or metastatic SCC of the head and neck were treated with Cisplatin 24 mg/m(2) from day I to 5 and 5-FU 1,000 mg/m(2) by a 120 hour continuous infusion. Retinyl palmitate was administer ed orally 50,000 lu b.i.d and Thymopentin 50 mg subcutaneously 3 times a week. Results: Chemotherapy treatment was well tolerated with G3 hematological toxicity in 30% of patients and G2 gastrointestinal toxicity in 20% of patients. 16 patients (32%) had a complete response (CR), 13 patients had partial response (PR) (26%), (response rate 58%, 95% c.i. 43%-72%); stable disease (SD) was observed in 7 patients (14%), while 14 patients progressed (PD) (28%). Median time to progression was 12 months (range 2.8-94.5), Median overall survival was 13.5 months (range 2-104). Conclusions: The association of CDDP and 5-FU with Retinyl Palmitate and TP5 has a major activity in the treatment of advanced head and neck cancer and a relatively well tolerated toxicity.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11697/17366
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