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Multicenter Study
. 2006 May 22;94(10):1369-74.
doi: 10.1038/sj.bjc.6603116.

Clear cell carcinoma of the ovary: a retrospective multicentre experience of 254 patients with complete surgical staging

Affiliations
Multicenter Study

Clear cell carcinoma of the ovary: a retrospective multicentre experience of 254 patients with complete surgical staging

M Takano et al. Br J Cancer. .

Abstract

A retrospective analysis was performed to evaluate the clinical characteristics and prognostic factors in the patients with clear cell carcinoma (CCC) of the ovary. After central pathological review and scanning of the medical records of nine Japanese institutions between 1992 and 2003, a total of 254 patients with CCC of the ovary were enrolled in the present study. Mean age was 52.4 years (range 23-73 years). Tumours were 13% (33/254) stage Ia, 36% (92/254) stage Ic, 13% (33/254) stage II, 30% (80/254) stage III, and 6% (16/254) stage IV. Five-year progression-free survival and overall survival was 84 and 88% in stage I, 57 and 70% in stage II, 25 and 33% in stage III and 0 and 0% in stage IV, respectively. Retroperitoneal lymph node metastasis was observed in 9% in pT1a tumours, 7% in pT1c tumours, 13% in pT2 tumours, and 58% in pT3 tumours, respectively. There was no survival benefit according to chemotherapeutic differences in the patients who received complete surgical staging procedures and conventional chemotherapy. Peritoneal cytological status was an independent prognostic factor in stage Ic patients (P=0.03) and only residual tumour diameter was an independent prognostic factor in stage III, IV patients (P=0.02). Our results suggest that cytoreductive surgery resulting in no residual tumour only could improve the prognosis of advanced CCC patients.

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Figures

Figure 1
Figure 1
Progression-free survival and overall survival of patients depending on their FIGO stage. Five-year progression-free survival and overall survival was 84 and 88% in stage I, 57 and 70% in stage II, 25 and 33% in stage III and 0 and 0% in stage IV, respectively. P-values in progression-free survival were as follows: Stage I vs stage II, P<0.01; stage II vs stage III, P<0.01; stage III vs stage IV, P=0.35. P-values in overall survival were as follows: Stage I vs stage II, P<0.01; stage II vs stage III, P<0.01; stage III vs stage IV, P=0.17.
Figure 2
Figure 2
Progression-free survival of patients with FIGO stage I patients. There is no significant difference between patients with stage Ic (capsule ruptured) and those with stage Ia (P=0.11). Survival of the patients with stage Ic (ascites/malignant washing) and Ic (ovarian surface) was significantly worse than that of stage Ic (capsule ruptured) (P=0.04).
Figure 3
Figure 3
Progression-free survival of stage III, IV patients according to the residual tumour (RT) diameter. There is no significant prognostic difference between the patients with the tumour diameter less than 1 cm and those with the tumour diameter more than 1 cm (P=0.40). The patients with no residual tumour had significantly better progression-free survival than those with the tumour less than 1 cm (P=0.04) or those with tumour diameter more than 1 cm (P<0.01), respectively. Median progression-free survival duration was 39 months in the patients with no residual tumour, 7 months in those with the tumour diameter less than 1 cm, and 5 months in those with residual tumour diameter more than 1 cm, respectively.

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