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Efficacy and safety of TC dose-dense chemotherapy as first-line treatment of epithelial ovarian cancer: a single-institution retrospective cohort study (CROSBI ID 285054)

Prilog u časopisu | izvorni znanstveni rad | međunarodna recenzija

Vrdoljak, Josip ; Boban, Toni ; Petrić Miše, Branka ; Boraska Jelavić, Tihana ; Bajić, Željko ; Tomić, Snježana ; Vrdoljak, Eduard Efficacy and safety of TC dose-dense chemotherapy as first-line treatment of epithelial ovarian cancer: a single-institution retrospective cohort study // Japanese journal of clinical oncology, 49 (2019), 4; 347-353. doi: 10.1093/jjco/hyz011

Podaci o odgovornosti

Vrdoljak, Josip ; Boban, Toni ; Petrić Miše, Branka ; Boraska Jelavić, Tihana ; Bajić, Željko ; Tomić, Snježana ; Vrdoljak, Eduard

engleski

Efficacy and safety of TC dose-dense chemotherapy as first-line treatment of epithelial ovarian cancer: a single-institution retrospective cohort study

Background: The optimal first-line therapy of advanced ovarian cancer still remains questionable: standard paclitaxel–carboplatin (TC), dose-dense TC, intraperitoneal chemotherapy or TC plus bevacizumab. In this study, we present the real-life results of dose-dense treatment of the singleinstitution on Caucasian population. Methods: A retrospective cohort study was used on consecutive samples of 74 patients treated with the conventional 3-weekly TC protocol (2008–11) and on 70 treated with TC dose-dense protocol (2012–16). The primary endpoint of this study was overall survival (OS). Secondary endpoints were progression free-survival (PFS) and toxicity. We made adjustments for age, pathohistological type, tumor grade, stage and postoperative residual disease by Cox regression. Results: After adjustment for pre-planned clinical and sociodemographic factors, patients treated with dose-dense protocol showed a significantly lower hazard for dying from any cause, than patients treated with conventional protocol (HR = 0.50 ; 95% CI 0.26–0.98 ; P = 0.042). Median OS, at 60 months follow-up had not been reached in the dose- dense group, while in the standard treatment group was 48 months (95% CI 33–62). Unadjusted PFS was significantly longer in the dosedense group (HR = 0.58 ; 95% CI 0.38–0.88 ; P = 0.011), but not after the adjustment (P = 0.096). Generally, the level of toxicity was similar in both groups of patients. The need for blood transfusions and usage of filgrastim was significantly higher in the TC dd group. The incidence of neutropenia and thrombocytopenia Grade 3 or 4 were not significantly different in both regimens. Conclusions: Our retrospective study has shown the superior efficacy and comparable toxicity of dose- dense chemotherapy regimen over the conventional regimen in treatment of ovarian cancer on Caucasian population at a single-institution.

dose-dense, chemotherapy, ovarian cancer, paclitaxel, carboplatin

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Podaci o izdanju

49 (4)

2019.

347-353

objavljeno

0368-2811

1465-3621

10.1093/jjco/hyz011

Povezanost rada

nije evidentirano

Poveznice
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