Future Directions in the Treatment of Squamous Cell Carcinoma of the Head and Neck: The Role of UFT

Article

Squamous cell carcinoma of the head and neck is a potentially curable neoplasm. Historically, the standard approach to treatment has been either surgery or radiation therapy, or a combination of the two. Over the past

ABSTRACT: Squamous cell carcinoma of the head and neck is a potentially curable neoplasm. Historically, the standard approach to treatment has been either surgery or radiation therapy, or a combination of the two. Over the past two decades, the role of chemotherapy in the curative approach to head and neck cancer has been evolving. Drugs like fluorouracil (5-FU), cisplatin (Platinol), methotrexate, paclitaxel (Taxol), docetaxel (Taxotere), and bleomycin (Blenoxane) have been investigated in both the palliative and curative settings. Multiple combination regimens have been used as neoadjuvant or induction regimens, but to date the original combination of cisplatin and fluorouracil is still the standard of therapy. UFT, a combination of uracil and tegafur (a fluorinated pyridine analogue), has been available in Japan as an oral form of treatment for squamous cell head and neck cancers. This article describes the rationale behind the use of UFT as an agent for the treatment of squamous cell carcinoma of the head and neck as well as data from ongoing investigations exploring its use in this disease.[ONCOLOGY 11(Suppl 10):86-89, 1997]

Introduction

Squamous cell carcinoma of the head and neck is a potentially curable neoplasm if it is detected while restricted to the head and neck. Stage I and II neoplasms are often curable with either radiation or surgery as the sole modality of treatment. Stage III and IV disease, however, recurs in the majority of patients despite aggressive initial management with surgery and/or radiation therapy. If the disease recurs in the head and neck region, salvage may be attempted with additional surgery or radiation, but the long-term survival after salvage is only about 20%. Metastatic recurrence of disease is not curable, except in the rare case of isolated metastatic disease managed with surgical metastasectomy. In general, therefore, patients with recurrent unresectable local disease or metastatic disease are treated without curative intent.

Chemotherapy

The role of chemotherapy in the treatment of squamous cell carcinoma of the head and neck has been evolving, with chemotherapy now playing an important role in palliative management of patients with either locally advanced or metastatic disease. The drugs used traditionally in the management of squamous cell carcinoma of the head and neck include cisplatin (Platinol), carboplatin (Paraplatin), 5-fluorouracil (5-FU), methotrexate, and bleomycin (Blenoxane).[1-6] More recently, the taxanes (docetaxel [Taxotere], paclitaxel [Taxol]) have been evaluated for their efficacy in squamous cell carcinoma of the head and neck.[7-9] Additionally, tegafur and uracil in a 1:4 molar ratio (UFT), available for years in Japan for the treatment of squamous cell carcinoma of the head and neck, is now being explored in the United States, Canada, and Europe for potential use in the management of squamous cell carcinoma of the head and neck and other malignancies.

When used individually as palliative therapy, these drugs produce overall response rates of only 15% to 40% and response durations are brief, usually less than 6 months.[8-11] Because of the low rate of response to single-agent chemotherapy, many clinical trials have concentrated on combination regimens. While response rates have been shown to be improved, studies to date have failed to reproducibly demonstrate an improvement in response duration or median survival when combination regimens are compared to standard surgery and radiation therapy.[1,12-15] On the other hand, aggressive (high dose) combination chemo- therapy for palliation has doubled the 1-year survival rate from 20% to 40%. This progress comes at a significant cost in terms of increased toxicity, hospitalization, and restricted patient eligibility.[16,17]

Combination Regimens for Induction Therapy

Beginning in the 1970s, combination chemotherapy has been studied in the induction setting in potentially curable patients with squamous cell carcinoma of the head and neck. Initial studies using combination platinum and 5-FU demonstrated that complete remission rates exceeding 50% were achievable.[4] Additionally, studies demonstrated a benefit of cisplatin over carboplatin and of infusional 5-FU over bolus 5-FU.[1,14] Further, refinement of this combination involved the addition of leucovorin as a stabilizer of the 5-fluorodeoxyuridine-1-phosphate (F-dUMP)/thymidylate synthase complex and yielded even higher overall response rates. [6,12,18,19] A recent report of an induction regimen utilizing a combination of docetaxel, 5-FU, cisplatin, and leucovorin demonstrated that pathologic response rates approaching 100% were achievable at the primary site in squamous cell carcinoma of the head and neck.[20]

Most trials using an induction regimen based on cisplatin and 5-FU have included definitive radiation therapy as an integral part of the curative treatment regimen. It is clear that patients who respond to chemotherapy have an excellent prognosis following definitive radiation therapy. Some investigators, however, attribute this chemotherapeutic response to the antineoplastic activity of the induction chemotherapy, while others view it merely as a predictor of tumor radiosensitivity.

While it has been demonstrated in a randomized setting that both induction chemotherapy followed by radiation therapy, and combined chemotherapy plus once-daily radiation therapy are superior in terms of overall survival to once daily radiation alone in the setting of unresectable locally advanced squamous cell carcinoma of the head and neck,[21,22] similar data are not available for potentially resectable disease.[23] Of interest, a small but significant group of patients with locally advanced disease can be cured with induction chemotherapy alone, but at present there is no reliable way to identify these patients.[24] Results of hyperfractionation-radiation programs have suggested increased response rates relative to daily radiation programs, but the roles of hyperfractionated or accelerated radiation used with induction therapy, or concomitant chemotherapy/hyperfractionated radiation regimens, are just beginning to be explored and should be regarded as investigational.[25]

 

Stage III and IV Disease in nonmetastatic stages III and IV squamous cell carcinoma of the head and neck, the traditional approach to curative management has included surgery and radiation therapy, with typical long-term survival rates in the range of 20% to 40%. Unfortunately, many patients who undergo curative resection are left with major, permanent functional deficits, including loss of speech and severely impaired swallowing capability. The United States Veteran’s Administration trial in 1991 and, more recently, a trial by the European Organization for the Research and Treatment of Cancer have shown in a randomized setting that induction therapy with Platinol 100 mg/m2 and infusional 5-FU (PF) 1,000 mg/m2/d ´ 5 d followed by definitive once-daily radiation therapy can preserve organ function in two thirds of surviving patients with locally advanced laryngeal cancer, without compromising overall survival in comparison with patients treated with surgery and adjuvant radiation therapy.[26,27] Overall survival in this setting, however, is still only on the order of one in three patients.

A number of currently active studies have been designed with the goal of improving on the results of the Veteran’s Administration and European Organization for the Research and Treatment of Cancer experience. As mentioned, several studies have attempted modulation of the effect of 5-FU using leucovorin, and, although multiple phase II studies have documented an increase in response rates, there are no convincing data to suggest that these leucovorin-containing regimens extend survival. As a result, explorations of alternative fluorinated pyridine analogues such as tegafur, which has been in use in Japan for a number of years, are beginning in Europe and the United States in patients with squamous cell carcinoma of the head and neck.

Tegafur, also known as Ftorafur, is effectively a 5-FU prodrug converted into 5-FU by hepatic cytochrome P-450 enzymes.[28-30] In comparison with 5-FU, tegafur has the added advantage of reliable absorption in the small intestine and thus it can be administered orally. Studies also have shown that when tegafur is administered concomitantly with uracil, there is an enhanced tumor-to-plasma concentration ratio for FdUMP, the active metabolite of tegafur. The mechanism for this enhancement appears to be uracil-mediated inhibition of the 5-FU degradative enzyme dihydrouracil dehydrogenase in tumor tissue, without significant inhibition of FdUMP binding to thymidylate synthetase. This effect of uracil on intratumor tegafur metabolism is thought to result from the different binding constants of the uracil and FdUMP moieties with respect to dihydrouracil dehydrogenase and thymidylate synthetase.[31]

A 1:4 molar ratio of tegafur to uracil has been found to result in the highest tumor-to-plasma concentration and the highest tumor kill in experimental systems.[32] Based on these observations, uracil and tegafur have been combined at this ratio for a formulation known as UFT, which has been in clinical use in Japan for many years. Combined phase II data suggest that it is an active antineoplastic agent with an activity spectrum similar to that of 5-FU.[33] Of interest, UFT activity in Japanese patients with squamous cell carcinoma of the head and neck has been reported in the range of 24% to 30%.[34,35]

UFT in Treatment

The Spanish experience with UFT as part of induction therapy for patients with squamous cell carcinoma of the head and neck is equally promising. Valverde and colleagues have reported their results of a randomized trial of induction chemotherapy with Platinol plus UFT (PU) vs PF, followed by definitive daily radiation therapy, as potentially curative treatment of squamous cell carcinoma of the head and neck. In this study, 67 patients with squamous cell carcinoma of the head and neck were randomized to receive either cisplatin 100 mg/m2 followed by a continuous infusion of 5-FU 1,000 mg/m2/d for 5 days or the same dose of cisplatin followed by UFT 300 mg/m2/d in divided doses orally for 20 days. Four cycles of each therapy were administered before daily radiation therapy to a total dose of 50 to 70 Gy. Response rates in the two arms were similar: In the PU arm the complete response (CR) rate was 18% and the partial response (PR) rate was 60%. Corresponding figures in the PF group were 20% CR and 52% PR. Toxicities also were comparable between the two arms. At the completion of radiation therapy, CR rates were 50% for the PF arm and 49% for the PU arm. With a median follow-up of 84 months, the investigators report a disease-free survival of 29% for the PF arm and 27% for the PU arm.[365,37]

US Trials

UFT has not yet been approved for use in the United States, but, thanks to collaborative efforts of the Bristol-Myers Squibb Pharmaceutical Company, Taiho Pharmaceutical Co., Ltd., and multiple clinical investigators in the United States, many trials are under way. The majority of these trials are focusing on neoplasms of the gastrointestinal system, but investigators at Dana-Farber/Partners Cancer Care are studying the activity and toxicity of combination UFT/leucovorin in patients with advanced squamous cell carcinoma of the head and neck.

The rationale for combining UFT with leucovorin is similar to that for combining 5-FU with leucovorin. As noted, the addition of leucovorin to PF in induction regimens for squamous cell carcinoma of the head and neck significantly enhances the antitumor activity of PF, albeit with a substantial increase in toxicity. Because the pharmacology of UFT differs somewhat from that of infusional 5-FU, it is possible that combination UFT/leucovorin may preserve the antitumor efficacy of the 5-FU/leucovorin combination, without the associated neutropenia and mucositis. Anecdotally, this seems to be the case in the hands of Japanese investigators.[38]

Additionally, because UFT/leucovorin is an oral regimen, the need for hospitalization and prolonged infusion could be eliminated for patients undergoing potentially curative or palliative treatment, resulting in reduced medical expenses and an enhanced quality of life during treatment for squamous cell carcinoma of the head and neck.

With this background, a phase II trial of UFT plus leucovorin in advanced regional or metastatic squamous cell carcinoma of the head and neck was opened to accrual at the Dana-Farber Cancer Institute in late 1996. Patients are eligible for this trial if they have had neither palliative nor induction chemotherapy in the 6 months preceding enrollment. Patients will receive UFT 300 mg/m2/d (rounded to the nearest 100 mg) plus leucovorin 90mg/day, both given orally in three divided daily doses. Treatment will be for 28 consecutive days, followed by 1 week without treatment before reinitiating therapy. The study end points are tumor response rate and toxicity. To date, two patients have been enrolled. One patient has achieved a PR following completion of one cycle of therapy, with minimal toxicity.

Conclusion

The ultimate place of UFT in the armamentarium of weapons against head and neck cancer is still uncertain. However, given the previous Japanese experience and the ongoing trials in the United States and elsewhere, a possible role for UFT should certainly be defined before the new millennium.

References:

1. Forastiere A, Metch B, Schuller D, et al: Randomized comparison of cisplatin plus fluorouracil and carboplatin plus fluorouracil vs methotrexate in advanced squamous cell carcinoma of the head and neck: A Southwest Oncology Group Study. J Clin Oncol 10:1245-1251; 1992.

2. Ervin T, Weichselbaum R, Miller D, et al: Platinum, bleomycin, methotrexate (P-B-M): A treatment for patients with advanced squamous cell carcinoma of the head and neck. Cancer Treat Rep 65:787-791, 1981.

3. DeConti R, Schoenfeld D: A randomized prospective comparison of intermittent methotrexate, methotrexate with leucovorin, and a methotrexate combination in head and neck cancer. Cancer 48:1061-1072, 1981.

4. Kish J, Weaver A, Jacobs J, et al: Cisplatin and 5-fluorouracil infusion in patients with recurrent and disseminated epidermoid cancer of the head and neck. Cancer 53:1819-1824, 1984.

5. Vokes E, Schilsky R, Weichselbaum R, et al: Induction chemotherapy with cisplatin, fluorouracil and high-dose leucovorin for locally advanced head and neck cancer: A clinical and pharmacologic analysis. J Clin Oncol 8:241-247, 1990.

6. Dreyfuss A, Clark J, Wright J, et al. Continuous infusion high-dose leucovorin with 5-fluorouracil and cisplatin for untreated stage IV carcinoma of the head and neck. Ann Intern Med 112:167-172, 1990.

7. Fujii H, Sasaki Y, Ebihara S, et al: An early phase II study of docetaxel (Taxotere) in patients with head and neck cancer (abstract 859). Proc Am Soc Clin Oncol 14:298, 1995.

8. Dreyfuss A, Clark J, Norris CJ, et al: Docetaxel (Taxotere): An active drug for advanced, incurable squamous cell carcinoma of the head and neck. J Clin Oncol 14:1672-1678, 1996.

9. Forastiere A, Neuberg D, Taylor S IV, et al: Phase II evaluation of Taxol in advanced head and neck cancer: An Eastern Cooperative Oncology Group trial. Monogr Natl Cancer Inst 15:181-184, 1993.

10. Jacobs C: Adjuvant and neoadjuvant treatment of head and neck cancers. Semin Oncol 18:504-514, 1991.

11. Catimel G, Verwij J, Hanauske A: Docetaxel (Taxotere): An active drug for the treatment of patients with advanced squamous cell carcinoma of the head and neck. Ann Oncol 5:553-537, 1994.

12. Clark J, Busse P, Norris C, et al: Long term results of induction chemotherapy with cisplatin, 5-FU and high dose leucovorin (PFL) for squamous cell carcinoma of the head and neck (SCCHN) (abstract). Proc Am Soc Clin Oncol 15:317, 1996.

13. Jacobs C, Lyman G, Velez-Garcia E, et al: A Phase III randomized study comparing cisplatin and fluorouracil as single agents and in combination for advanced squamous cell carcinoma of the head and neck. J Clin Oncol 10:257-263, 1992.

14. Kish J, Ensley J, Jacobs J, et al: A randomized trial of cisplatin (CACP) + 5-fluorouracil (5-FU) infusion and CACP + 5-FU bolus for recurrent and advanced squamous cell carcinoma of the head and neck. Cancer 56:2740-2744, 1985.

15. Spaulding M, Fischer S, Wolf G, for the Department of Veterans Affairs Cooperative Laryngeal Cancer Study Group: Tumor response, toxicity, and survival after neoadjuvant organ-preserving chemotherapy for advanced laryngeal carcinoma. J Clin Oncol 12:1592-1599, 1994.

16. Jacobs C: Adjuvant and neoadjuvant treatment of head and neck cancers. Semin Oncol 18:504-514, 1991.

17. Forastiere A: Randomized trials of induction chemotherapy: A critical review. Hematol Oncol Clin North Am 5:725-736, 1991.

18. Pfister D, Bajorin D, Motzer R, et al: Cisplatin, fluorouracil, and leucovorin. Increased toxicity without improved response in squamous cell head and neck cancer. Arch Otolaryngol Head Neck Surg 120:89-95, 1994.

19. Vokes E, Weichselbaum R, Mick R, et al: Favorable long-term survival following induction chemotherapy with cisplatin, fluorouracil and leucovorin and concomitant chemoradiotherapy for locally advanced head and neck cancer. J Natl Cancer Inst 84:877-882, 1992.

20. Colevas A, Norris C, Busse P, et al: Taxotere(docetaxel), cisplatin (CDDP), 5-fluorouracil (5-FU) and leucovorin (LV) (TPFL) induction chemotherapy for locally advanced squamous cell carcinoma of the head and neck (SCCHN). A phase I/II study [Abstract 106]. Proc Int Congr Anti-Cancer Treat, February 3-6, 1997.

21. Merlano M, Vitale V, Rosso R, et al: Treatment of advanced squamous cell carcinoma of the head and neck with alternating chemotherapy and radiotherapy. N Engl J Med 327:1115-1121, 1992.

22. Merlano M, Benasso M, Corvo R, et al: Five year update of a randomized trial of alternating radiotherapy and chemotherapy compared with radiotherapy alone in treatment of unresectable squamous cell carcinoma of the head and neck. J Natl Cancer Inst 88:583-589, 1996.

23. Paccagnella A, Orlando A, Marchiori C, et al: Phase III trial of initial chemotherapy in stage III-IV head and neck cancer: A study by the Gruppo di Studio sui Tumori della Testa e del Collo. J Natl Cancer Inst 86:265-272, 1994.

24. Laccourreye O, Brasnu D, Bassok V, et al: Cisplatin-fluorouracil exclusive chemotherapy for T1-T3N0 glottic squamous cell carcinoma complete clinical responders: Five-year results. J Clin Oncol 14:2331-2336, 1996.

25. Parsons J, Mendenhall W, Stringer S, et al: Twice-a-day radiotherapy for squamous cell carcinoma of the head and neck: The University of Florida experience. Head Neck 15:87-96, 1993.

26. Lefebvre J, Chevalier D, Luboinski B, et al: Larynx preservation in pyriform sinus cancer: Preliminary results of a European organization for Research and Treatment of Cancer phase III trial. J Natl Cancer Inst 88:890-898, 1996.

27. Department of Veterans Affairs Laryngeal Cancer Study Group: Induction chemotherapy plus radiation compared with surgery plus radiation in patients with advanced laryngeal cancer. N Engl J Med 324:1685-1690, 1991.

28. Au J, Freidman M, Sadeed W: Pharmacokinetics and metabolism of Ftorafur in man. Cancer Treat Rep 63:343-350, 1979.

29. Anttila M, Slotaniemi E, Kairaluoma M: Pharmacokinetics of Ftorafur after intravenous and oral administration. Cancer Chemother Pharmacol 10:150-153, 1983.

30. Benvenuto J, Lu K, Hall S: Disposition and metabolism of 1-(tetrahydro-2-furanyl)-5-fluorouracil (Ftorafur) in humans. Cancer Res 38:3867-3870, 1978.

31. Ikenaka K, Shirasaka T, Kitano S: Effect of uracil on metabolism of 5-fluorouracil in vitro. Gann 70:353-359, 1979.

32. Fujii S, Ikenaka M, Fukushima M: Effect of coadministration of uracil or cytosine on the antitumor activity of clinical doses of 1-(2-tetrahydrofuryl)-5-fluorouracil and level of 5-fluorouracil in rodents. Gann 70:209-214, 1979.

33. Ota K: Report on nationwide pooled data and cohort investigation in UFT phase II study. Cancer Chemother Pharmacol 22:333-338, 1988.

34. Mukai H, Kawashima K: Clinical results with UFT in malignant oral cavity cancer. Jpn J Clin Exp Med 62:303-307, 1985.

35. Inuyama Y, Takeda C: Phase II study of UFT for head and neck cancer. Jpn J Cancer Chemother 12:479-484, 1985.

36. Valverde J, Gonzalez J, Dominguez S, et al: Neoadjuvant chemotherapy with cisplatin and 5-fluorouracil versus cisplatin and Ftorafur-uracil (UFT) in advanced squamous head and neck cancer (abstract 909). Proc Am Soc Clin Oncol 12:281, 1993.

37. Gonzalez-Larriba J: Neoadjuvant chemotherapy with cisplatin plus 5-FU versus cisplatin plus UFT in advanced squamous head and neck cancer. Oncology 11(9) [supp 10]):90-97, 1997.

38. Taguchi T: Japanese experience with UFT. Oncology 11(9) [supp 10]):30-34, 1997.

Recent Videos
Haydar Frangoul, MD, the medical director of pediatric hematology/oncology at Sarah Cannon Research Institute and Pediatric Transplant and Cellular Therapy Program at TriStar Centennial
David Barrett, JD, the chief executive officer of ASGCT
Georg Schett, MD, vice president research and chair of internal medicine at the University of Erlangen – Nuremberg
David Barrett, JD, the chief executive officer of ASGCT
Bhagirathbhai R. Dholaria, MD, an associate professor of medicine in malignant hematology & stem cell transplantation at Vanderbilt University Medical Center
Caroline Diorio, MD, FRCPC, FAAP, an attending physician at the Cancer Center at Children's Hospital of Philadelphia
R. Nolan Townsend; Sandi See Tai, MD; Kim G. Johnson, MD
Daniela van Eickels, MD, PhD, MPH, the vice president and head of medical affairs for Bristol Myers Squibb’s Cell Therapy Organization
Paul Melmeyer, MPP, the executive vice president of public policy & advocacy at MDA
Related Content
© 2024 MJH Life Sciences

All rights reserved.