Zusammenfassung
Fragestellung
Ziel dieser Untersuchung war, unsere langjährigen Erfahrungen mit verschiedenen Tumorentitäten der Speicheldrüsenkarzinome zu analysieren.
Patienten
Retrospektiv wurden 155 Patienten mit Speicheldrüsenkarzinomen erfasst, welche zwischen Januar 1983 und Dezember 2002 in der Klinik für Mund-, Kiefer- und Gesichtschirurgie der Medizinischen Hochschule Hannover behandelt worden waren.
Ergebnisse
An adenoid-zystischen Karzinomen war 1,0% unserer Patienten erkrankt, 27,1% litten an Mukoepidermoidkarzinomen, 7,7% an Adenokarzinomen, 6,5% an polymorphen Adenokarzinomen und insgesamt 7,7% an weiteren Tumorentitäten mit geringeren Fallzahlen. Eine R0-Resektion wurde für 63,5% der Patienten mit hochmalignen Tumoren und für 80,0% der Patienten mit niedrigmalignen Tumoren erzielt. 26,2% der Patienten mit hochmalignen Tumoren und 13,3% der Patienten mit niedrigmalignen Tumoren erhielten eine postoperative Bestrahlung. Für das Gesamtkollektiv lagen die lokale Tumorkontrolle nach 5, 10 und 15 Jahren bei 77,5%, 66,2% und 59,0%, die regionale Tumorkontrolle nach 5, 10 und 15 Jahren bei 93,5%, 87,6% und 85,4%, die Fernmetastasenkontrolle nach 5, 10 und 15 Jahren bei 85,9%, 77,2% und 73,6% und die Überlebensrate nach 5, 10 und 15 Jahren bei 65,9%, 48,0% und 39,8%. Es gab einen signifikanten Unterschied zwischen niedrig- und hochmalignen Tumoren. Die beste Prognose zeigten polymorphe Adenokarzinome, gefolgt von niedrigmalignen Mukoepidermoidkarzinomen, adenoid-zystischen Karzinomen, Adenokarzinomen und hochmalignen Mukoepidermoidkarzinomen. Die Fallzahlen der übrigen Tumorentitäten waren zu gering, um eigene Untergruppen für statistische Auswertungen bilden zu können. Tumorentität, Tumorstadium und Resektionsstatus hatten einen signifikanten Einfluss auf die Prognose. Ein positiver Effekt für eine postoperative Bestrahlung konnte statistisch nicht nachgewiesen werden.
Schlussfolgerungen
Die Einteilung verschiedener Tumorentitäten nach ihrem Malignitätsgrad erweist sich aus prognostischer Sicht als sinnvoll, muss aber vor dem Hintergrund des Tumorstadiums betrachtet werden. Patienten mit Speicheldrüsenkarzinomen sollten zukünftig für prospektive randomisierte Studien multizentrisch erfasst werden, um die Wirksamkeit adjuvanter Behandlungsmodalitäten auch für seltene Tumorentitäten bestimmen zu können.
Abstract
Purpose
In this retrospective study we give a clinical review of our experience with different tumor entities of salivary gland cancer.
Patients
Between January 1983 and December 2002, a total of 155 patients with carcinomas of the salivary glands received initial treatment at the Department of Oral and Maxillofacial Surgery, Hanover Medical School.
Results
There were 51.0% adenoid cystic carcinomas, 27.1% mucoepidermoid carcinomas, 7.7% adenocarcinomas, 6.5% polymorphous adenocarcinomas, and altogether 7.7% other less frequent tumor entities. Complete resection was achieved for 63.5% of patients with high-grade carcinomas and for 80.0% of patients with low-grade carcinomas. Postoperative radiation was administered to 26.2% of patients with high-grade carcinomas and 13.3% of patients with low-grade carcinomas. Overall local control rates at 5, 10, and 15 years were 77.5%, 66.2%, and 59.0%. Overall regional control rates at 5, 10, and 15 years were 93.5%, 87.6%, and 85,4%. Overall distant control rates at 5, 10, and 15 years were 85.9%, 77,2%, and 73,6%. Overall survival rates at 5, 10, and 15 years were 65,9%, 48,0%, and 39,8%. There was a significant difference between patients with low-grade and high-grade carcinomas. Polymorphous adenocarcinomas showed the best prognosis, followed by low-grade mucoepidermoid carcinomas, adenoid cystic carcinomas, adenocarcinomas, and high-grade mucoepidermoid carcinomas. The number of the remaining tumor entities was too small to be divided into independent subgroups for statistical analysis. Tumor entity, tumor stage, and margin status significantly influenced prognosis. Statistically, we were not able to demonstrate a positive effect for postoperative radiation.
Conclusion
Grading is important, but should be considered in the context of stage. In the future, patients with salivary gland carcinomas should be randomized for prospective multicenter clinical trials, which could provide reliable information about adjuvant treatment modalities and their results even for rare subtypes of salivary gland cancer.
Literatur
Avery CM, Moody AB, McKinna FE, Taylor J, Henk JM, Langdon JD (2000) Combined treatment of adenoid cystic carcinoma of the salivary glands. Int J Oral Maxillofac Surg 29:277–279
Bensadoun RJ, Blanc-Vincent MP, Chauvel P, Dassonville O, Gory-Delabaere G, Demard F (2001) Malignant tumours of the salivary glands. Br J Cancer 84 (Suppl 2):42–48
Brown JS (1999) Prognostic factors in oral, oropharyngeal and salivary gland cancer. In: Booth PW, Schendel SA, Hausamen J-E (eds) Maxillofacial surgery, vol 1. Livingstone, Edinburgh, pp 291–308
Callender DL, Frankenthaler RA, Luna MA, Lee SS, Goepfert H (1992) Salivary gland neoplasms in children. Arch Otolaryngol Head Neck Surg 118:472–476
Colmenero C, Patron M, Sierra I (1991) Acinic cell carcinoma of the salivary glands. J Craniomaxillofac Surg 19:260–266
Frierson HF, El-Naggar AK, Welsh JB, et al (2002) Large scale molecular analysis identifies genes with altered expression in salivary adenoid cystic carcinoma. Am J Pathol 161:1315–1323
Garden AS, Weber RS, Morrison WH (1995) The influence of positive margins and nerve invasion in adenoid cystic carcinoma of the head and neck treated with surgery and radiation. Int J Radiat Oncol Biol Phys 32:619–626
Guzzo M, Andreola S, Sirizzotti G, Cantu G (2002) Mucoepidermoid carcinoma of the salivary glands: clinicopathologic review of 108 patients treated at the National Cancer Institute of Milan. Ann Surg Oncol 9:688–695
Hicks MJ, El-Naggar AK, Flaitz CM, Luna MA, Batsakis JG (1995) Histocytologic grading of mucoepidermoid carcinoma of major salivary glands in prognosis and survival: a clinicopathologic and flow cytometric investigation. Head Neck 17:89–95
Hill ME, Constenla DO, A’Hern RP, et al (1997) Cisplatin and 5-fluorouracil for symptom control in advanced salivary adenoid cystic carcinoma. Oral Oncol 33:275–278
Huang M, Ma D, Sun K, Yu G, Guo C, Gao F (1997) Factors influencing survival rate in adenoid cystic carcinoma of the salivary glands. Int J Oral Maxillofac Surg 26:435–439
Huber PE, Debus J, Latz D, Zierhut D, Bischof M, Wannenmacher M, Engenhart-Cabillic R (2001) Radiotherapy for advanced adenoid cystic carcinoma: neutrons, photons or mixed beam? Radiother Oncol 59:161–167
Jansisyanont P, Blanchaert Jr RH, Ord RA (2002) Intraoral minor salivary gland neoplasm: a single institution experience of 80 cases. Int J Oral Maxillofac Surg 31:257–261
Kaplan EL, Meier P (1958) Nonparametric estimation from incomplete observations. J Am Stat Assoc 53:457–481
Khan AJ, DiGiovanna MP, Ross DA, Sasaki CT, Carter D, Son YH, Haffty BG (2001) Adenoid cystic carcinoma: a retrospective clinical review. Int J Cancer 96:149–158
Kokemüller H, Eckardt A, Brachvogel P, Hausamen J-E (2003) Adenoid cystic carcinoma of the major and minor salivary glands: retrospective analysis of 74 patients. Mund Kiefer GesichtsChir 7:94–101
Kowalski PJ, Paulino AF (2002) Perineural invasion in adenoid cystic carcinoma: its causation/promotion by brain-derived neurotrophic factor. Hum Pathol 33:933–936
Leverstein H, van der Wal JE, Tiwari RM, Tobi H, van der Waal I, Metha DM, Snow GB (1998) Malignant epithelial parotid gland tumours: analysis and results in 65 previously untreated patients. Br J Surg 85:1267–1272
Maciejewsky A, Szymczyk C, Wierzgon J (2002) Outcome of surgery for adenoid cystic carcinoma of head and neck region. J Craniomaxillofac Surg 30:59–61
Nascimento AG, Amaral AL, Prado LA, Kligerman J, Silviera TR (1986) Mucoepidermoid carcinoma of salivary glands: a clinicopathologic study of 46 cases. Head Neck 8:409–417
Numata T, Muto H, Shiba K, Nagata H, Terada N, Konno A (2000) Evaluation of the validity of the 1997 International Union Against Cancer TNM classification of major salivary gland carcinoma. Cancer 89:1664–1669
Ribeiro Kde C, Kowalski LP, Saba LM, de Camargo B (2002) Epithelial salivary glands neoplasms in children and adolescents: a forty-four-year experience. Med Pediatr Oncol 39:594–600
Sadeghi A, Hanson D, Juillard G, Mackintosh R, Calcaterra TC, Parker RG (1986) Major salivary gland tumors: treatment results and prognostic factors. Laryngoscope 96:1139–1144
Sato S, Kawamura H (1991) Acinic cell tumor of the hard palate. Int J Oral Maxillofac Surg 20:130–132
Seiferth G (1997) Diagnosis and prognosis of salivary gland tumors. An interpretation of new revised WHO classification. Mund Kiefer GesichtsChir 1:252–267
Speight PM, Barrett AW (2002) Salivary gland tumours. Oral Dis 8:229–240
Spiro RH (1985) Salivary neoplasms: overview of a 35 year experience with 2807 patients. Head Neck 8:177–184
Spiro RH, Huvos AG (1992) Stage means more than grade in adenoid cystic carcinoma. Am J Surg 164:623–628
Sun CX, He RG, Cheung LK, et al (2002) The biological behavior of human adenoid cystic carcinoma cells transduced with interleukin-2-gene. Int J Oral Maxillofac Surg 31:650–656
UICC (1997) TNM-classification of malignant tumours. Wiley & Sons, New York, pp 44–46
Umeda M, Nishimatsu N, Yokoo S, Shibuya Y, Fujioka M, Komori T (2000) The role of radiotherapy for patients with adenoid cystic carcinoma of the salivary gland. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 89:724–729
Vander Poorten VL, Balm AJ, Hilgers FJ, Tan IB, Keus RB, Hart AA (2000) Stage as major long term outcome predictor in minor salivary gland carcinoma. Cancer 89:1195–1204
Vered M, Braunstein E, Buchner A (2002) Immunohistochemical study of epidermal growth factor receptor in adenoid cystic carcinoma of salivary gland origin. Head Neck 24:632–636
Wahlberg P, Anderson H, Biorklund A, Moller T, Perfekt R (2002) Carcinoma of the parotid and submandibular glands—a study of survival in 2465 patients. Oral Oncol 38:706–713
Author information
Authors and Affiliations
Corresponding author
Rights and permissions
About this article
Cite this article
Kokemüller, H., Brüggemann, N., Brachvogel, P. et al. Maligne epitheliale Speicheldrüsentumoren. Mund Kiefer GesichtsChir 8, 191–201 (2004). https://doi.org/10.1007/s10006-004-0531-2
Published:
Issue Date:
DOI: https://doi.org/10.1007/s10006-004-0531-2