A phase II trial of cisplatin, methotrexate, levofolinic acid, and 5-fluorouracil in the treatment of patients with locally advanced, metastatic squamous cell carcinoma of the head and neck
Article first published online: 19 NOV 2000
Copyright © 1999 American Cancer Society
Volume 85, Issue 4, pages 952–959, 15 February 1999
How to Cite
Caponigro, F., Comella, P., Marcolin, P., Spena, F. R., Biglietto, M., Cartenì, G., De Lucia, L., Avallone, A., Gravina, A. and Comella, G. (1999), A phase II trial of cisplatin, methotrexate, levofolinic acid, and 5-fluorouracil in the treatment of patients with locally advanced, metastatic squamous cell carcinoma of the head and neck. Cancer, 85: 952–959. doi: 10.1002/(SICI)1097-0142(19990215)85:4<952::AID-CNCR25>3.0.CO;2-N
- Issue published online: 19 NOV 2000
- Article first published online: 19 NOV 2000
- Manuscript Revised: 8 SEP 1998
- Manuscript Accepted: 8 SEP 1998
- Manuscript Received: 18 MAY 1998
- folinic acid;
- head and neck carcinoma
Induction chemotherapy in locoregionally advanced squamous cell carcinoma of the head and neck (SCCHN) might improve survival with respect to radiation therapy alone. Furthermore, chemotherapy represents the only therapeutic option in metastatic head and neck carcinoma.
To improve further the results that could be obtained with an induction regimen of cisplatin (CDDP) plus 5-fluorouracil (5-FU), the authors treated 50 patients with locally advanced or metastatic SCCHN with a combination of CDDP 65 mg/m2 on Day 1, methotrexate 500 mg/m2 on Day 1, levofolinic acid 250 mg/m2 on Day 2, and 5-FU 800 mg/m2 on Day 2. Cycles were repeated every 2 weeks. The authors' aim was to increase the activity of CDDP plus 5-FU (PF) using a regimen that combined the three most active drugs in SCCHN and provided an adequate biochemical modulation of 5-FU, which was administered as an intravenous bolus infusion.
Forty objective responses were observed among 50 evaluable patients (80%; 95% confidence interval [C.I.], 66–90%), including 7 complete responses (14%; 95% C.I., 5–27%), and 33 partial responses (66%; 95% C.I., 51–79%). Locoregional treatment, consisting of radiotherapy or surgery, was given at the end of chemotherapy. On completion of induction chemotherapy and locoregional treatment, 42 of 46 patients (91%) were rendered disease free. After a median follow-up of 20 months, the median duration of response was 10 months, the median failure free survival was 10 months, and the median overall survival was 21 months. The treatment was generally well tolerated. Grade 3–4 neutropenia occurred in 25 patients (50%), but it was febrile in only 3 patients. Nausea and vomiting were well managed with serotonin-3 blocking agents. Severe mucositis was seldom observed and easily manageable, and it never required hospitalization.
The high level of activity, the manageable toxicity, and the noteworthy survival data of this regimen compare favorably with most of the drug combinations used worldwide to treat similar patient populations, with the additional advantage of significantly lower cost. Cancer 1999;85:952–9. © 1999 American Cancer Society.