Treatment of maxillary sinus carcinoma: clinical results using the Kitasato modality

Acta Otolaryngol Suppl. 2002:(547):15-9. doi: 10.1080/000164802760057509.

Abstract

The conventional therapeutic regimen for maxillary sinus carcinoma consists of dissection of the maxilla, full-dose irradiation and extensive chemotherapy. However, the results obtained with this treatment are often poor. Even when patients recover, their quality of life is significantly reduced as a result of deformity of facial structures and swallowing and articulation dysfunctions. A retrospective analysis of 68 patients with maxillary sinus carcinoma treated with the Kitasato modality between 1975 and 1999 was conducted. All patients underwent pergingival maxillary sinus surgery combined with pre- and postoperative irradiation therapy with standardized total doses of 16 Gy; the postoperative irradiation was given in combination with regional intra-arterial infusion chemotherapy administered via the superficial temporal artery. All visible tumor lesions were removed where possible in order to preserve or facilitate cellular immunity after surgery. The cumulative 5-year survival rates were 85.7% for Stage II patients, 88.1% for Stage III, 76.6% for Stage IVA and 75.% for Stage IVB.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Antineoplastic Agents / therapeutic use*
  • Antineoplastic Protocols*
  • Carcinoma / mortality
  • Carcinoma / pathology
  • Carcinoma / therapy*
  • Combined Modality Therapy
  • Female
  • Fluorouracil / therapeutic use*
  • Hospitals, University / statistics & numerical data*
  • Humans
  • Japan
  • Male
  • Maxillary Sinus Neoplasms / mortality
  • Maxillary Sinus Neoplasms / pathology
  • Maxillary Sinus Neoplasms / therapy*
  • Middle Aged
  • Neoplasm Staging
  • Otorhinolaryngologic Surgical Procedures*
  • Outcome Assessment, Health Care / statistics & numerical data*
  • Picibanil / therapeutic use*
  • Radiotherapy Dosage
  • Retrospective Studies
  • Severity of Illness Index
  • Survival Rate

Substances

  • Antineoplastic Agents
  • Picibanil
  • Fluorouracil