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Randomized study on adjuvant chemotherapy in stage I high-risk ovarian cancer with evaluation of DNA-ploidy as prognostic instrument

Tropé, C (författare)
Norwegian Radium Hospital
Kaern, J (författare)
Hogberg, T (författare)
Lund University,Lunds universitet
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Abeler, V (författare)
Hagen, B (författare)
Kristensen, G (författare)
Onsrud, M (författare)
Pettersen, E (författare)
Rosenberg, P (författare)
Sandvei, R (författare)
Sundfor, K (författare)
Vergote, I (författare)
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 (creator_code:org_t)
Elsevier BV, 2000
2000
Engelska 8 s.
Ingår i: Annals of oncology : official journal of the European Society for Medical Oncology. - : Elsevier BV. - 0923-7534. ; 11:3, s. 8-281
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • PURPOSE: Adjuvant chemotherapy versus observation and chemotherapy at progression was evaluated in 162 patients in a prospective randomized multicenter study. We also evaluated DNA-measurements as an additional prognostic factor.PATIENTS AND METHODS: Patients received adjuvant carboplatin AUC 7 every 28 days for six courses (n = 81) or no adjuvant treatment (n = 81). Eligibility included surgically staged and treated patients with FIGO stage I disease, grade 1 aneuploid or grade 2 or 3 non-clear cell carcinomas or clear cell carcinomas. Disease-free (DFS) and disease-specific (DSS) survival were end-points.RESULTS: Median follow-up time was 46 months and progression was observed in 20 patients in the treatment group and 19 in the control group. Estimated five-year DFS and DSS were 70% and 86% in the treatment group and 71% and 85% in the control group. The hazard ratio was 0.98 (95% confidence interval (95% CI): 0.52-1.83) regarding DFS and 0.94 (95% CI: 0.37-2.36) regarding DSS. No significant differences in DFS or DSS could be seen when the log-rank test was stratified for prognostic variables. Therefore, data from both groups were pooled for the analysis of prognostic factors. DNA-ploidy (P = 0.003), extracapsular growth (P = 0.005), tumor rupture (P = 0.04), and WHO histologic grade (P = 0.04) were significant independent prognostic factors for DFS with P < 0.0001 for the model in the multivariate Cox analysis. FIGO substage (P = 0.01), DNA ploidy (P < 0.05), and histologic grade (P = 0.05) were prognostic for DSS with a P-value for the model < 0.0001.CONCLUSIONS: Due to the small number of patients the study was inconclusive as regards the question of adjuvant chemotherapy. The survival curves were superimposable, but with wide confidence intervals. DNA-ploidy adds objective independent prognostic information regarding both DFS and DSS in early ovarian cancer.

Nyckelord

Adenocarcinoma/drug therapy
Adult
Aged
Analysis of Variance
Antineoplastic Agents/therapeutic use
Carboplatin/therapeutic use
Chemotherapy, Adjuvant
DNA, Neoplasm/genetics
Female
Humans
Middle Aged
Neoplasm Staging
Ovarian Neoplasms/drug therapy
Ploidies
Prognosis
Prospective Studies
Risk Factors
Survival Analysis

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