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Læknablaðið - 15.09.1983, Qupperneq 64

Læknablaðið - 15.09.1983, Qupperneq 64
232 LÆKNABLADIÐ malignant tumours of the female genital tract. The sign and symptoms of the disease are non-specific and the diagnosis is most often made at surgery when most of the patients are at an advanced stage of the disease. Surgery together with chemotherapy or radiotherapy, or both in combination, is the main form of treatment. The following statements are based on the results of a study of Prognostic Factors and the Effects of Combined Treatments carried out at the University Hospital of Lund (26). Young patients with well or moderately differentiated stage Ia tumours can be treated with unilateral salpingo-oophorectomy, if wedge-resection of the unaffected ovary shows normal tissue. The value of hysterectomy in stage I is doubtful and ought only to be performed in stages II and III if this operation leads to surgical radicality or minimal residual disease. Infracolic omentectomy should be perfor- med as a staging operation. Patients primarly judged inoperable should be biopsied and reopera- ted after preoperative treatment with radiotherapy or combination chemotherapy. Postoperative treat- ment does not seem to improve cases of well differentiated tumours in stages Ia with no extracy- stic excrescences and intact tumour capsule. Accep- table results are obtained irrespective of histologic type in well or moderately differentiated tumours in stage I and Ila treated with five malphalan infusions at four weeks intervals. Chemotherapy given prior to postoperative radiotherapy gives no advantages, but chemotherapy after given radiotherapy does. In advanced poorly differentiated stage III ovarian tumours the effect of combination chemotherapy are significantly higher than the effects of radiother- apy and single drug chemotherapy. The effect of combination chemotherapy and radiotherapy on operability are much the same while the effect of single drug chemotherapy is low. In a multivariate statistical analysis, using survival as the dependent variable, the following three factors are found to be of significance: the histologic grade, the size of the residual tumour after surgery, and the stage of tumour progression. Stage Ila had the same survival rate as Stage I of this disease. The state of the tumour capsules in Stage I had no prognostic effect. Ascites did not affect survival in stages I and II. The histologic type only affects survival in patients with large residual tumours (>2 cm). A prognostic- classification is proposed for ovarian cancer, based on the above results using the tumour grading, residual tumour and the FIGO stages. HEIMILDIR 1) National Board of Health and Welfare. The Cancer Registry. Cancer Incidence in Sweden 1977. The Swedish Cancer Registry, S-106-30- Stockholm. 2) Brody S. Ovarial tumörer. Obstetrik och gyne- kologi, Stockholm, p 670, Almqvist og Wiksell 1970. 3) Fox H. Advances in the histopathology of ovarian tumours. Advances in the biosciences. Ovarian Cancer. Oxford, Pergamon Press 1980; 26: 9-26. 4) Barr W. Current problems in diagnosis and management. Advances in the biosciences. Ova- rian Cancer. Oxford, Pergamon Press 1980; 26: 3-5. 5) Sigurdsson K, Johnsson JE, Möller T. Overview of the treatment of ovarian cancer in the South Swedish Health Care Region during the 5-year- period 1974-1978. Accepted for publication, Ann Chir et Gynecol 1983. 6) Kjellgren O, Solheim F. Symptombilden vid ovarialcancer. Lakartidningen 1977; 74: 3333-5. 7) Bagshawe KD, Wass M, Searle F. Ovarian Cancer Serum Markers. Advances in the biosci- ences. Ovarian Cancer. Oxford, Pergamon Press 1980;26:57-64. 8) Day TG jr, Gallager S, Rutledge FN. Epithelial carcinom of the ovary: Prognostic importance of histologic grade. National Cancer Institute Monograph 1975; 42: 15-21. 9) Smith JP, Day TG. Review of ovarian cancer at the University of Texas Systems Cancer Center, MD Anderson Hospital and Tumor Institute. Am J Obstet Gynecol 1979; 135: 984-93. 10) Malkasian GD, Decker DG, Webb MJ. Histolo- gy of epithelial tumors of the ovary: Clinical usefulness and prognostic. Seminars in Oncolo- gy, 1975; 2: 191-201. 11) Dembo AJ, Bush RS, Beale FA, Bean HA, Pringle JF, Shergeon JFG. The Princess Marga- ret Hospital Study of ovarian cancer: Stages I, II and asymptomatic III Presentations. Cancer Treat Rep 1979; 63: 249-54. 12) Aure JC, Höeg K, Kolstad P: Clinical and histologic studies of ovarian carcinoma. Long- term Follow-up of 990 cases. Obstet Gynecol 1971;37: 1-9. 13) Webb MJ, Decker DG, Mussey E, Williams TJ. Factors influencing survival in stage I Ovarian cancer. Am J Obstet Gynecol 1973; 116: 222. 14) Bush RS, Dembo AJ. Current status of treat- ment for patients with ovarian cancer. Advan- ces in the biosciences. Ovarian cancer. Oxford, Pergamon Press 1980; 26: 115-34. 15) Purola E, Nieminen U. Does rupture of cystic carcinoma during operation influence the pro- gnosis: Ann Chir Gyn 1968; 57: 615. 16) Hudson CN, Chir M. Surgical treatment of ovarian cancer. Gynecol Oncol 1973; 1: 370. 17) Griffiths CT, Parker LM, Fuller AF jr. Role of cytoreductive surgical treatment in the mana- gement of advanced ovarian cancer. Cancer Treat Rep 1979; 63: 235. 18) Kottmeier HL. Ovarian cancer with special
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