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Adjuvant Capecitabine for Early Breast Cancer: 15-Year Overall Survival Results From a Randomized Trial

Poikonen-Saksela Paula; Lindman Henrik; Lahdenperä Outi; Bono Petri; Ahlgren Johan; Huovinen Riikka; Nilsson Greger; Junnila Jouni; Villman Kenneth; Auvinen Päivi; Nyandoto Paul; Kataja Vesa; Jukkola Arja; Joensuu Heikki; Tanner Minna; Kellokumpu-Lehtinen Pirkko-Liisa

Adjuvant Capecitabine for Early Breast Cancer: 15-Year Overall Survival Results From a Randomized Trial

Poikonen-Saksela Paula
Lindman Henrik
Lahdenperä Outi
Bono Petri
Ahlgren Johan
Huovinen Riikka
Nilsson Greger
Junnila Jouni
Villman Kenneth
Auvinen Päivi
Nyandoto Paul
Kataja Vesa
Jukkola Arja
Joensuu Heikki
Tanner Minna
Kellokumpu-Lehtinen Pirkko-Liisa
Katso/Avaa
jco.21.02054.pdf (445.0Kb)
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LIPPINCOTT WILLIAMS & WILKINS
doi:10.1200/JCO.21.02054
URI
https://ascopubs.org/doi/full/10.1200/JCO.21.02054
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2022081155087
Tiivistelmä

PURPOSE
Few data are available regarding the influence of adjuvant capecitabine on long-term survival of patients with early breast cancer.

METHODS
The Finland Capecitabine Trial (FinXX) is a randomized, open-label, multicenter trial that evaluates integration of capecitabine to an adjuvant chemotherapy regimen containing a taxane and an anthracycline for the treatment of early breast cancer. Between January 27, 2004, and May 29, 2007, 1,500 patients with axillary node-positive or high-risk node-negative early breast cancer were accrued. The patients were randomly allocated to either TX-CEX, consisting of three cycles of docetaxel (T) plus capecitabine (X) followed by three cycles of cyclophosphamide, epirubicin, and capecitabine (CEX, 753 patients), or to T-CEF, consisting of three cycles of docetaxel followed by three cycles of cyclophosphamide, epirubicin, and fluorouracil (CEF, 747 patients). We performed a protocol-scheduled analysis of overall survival on the basis of approximately 15-year follow-up of the patients.

RESULTS
The data collection was locked on December 31, 2020. By this date, the median follow-up time of the patients alive was 15.3 years (interquartile range, 14.5-16.1 years) in the TX-CEX group and 15.4 years (interquartile range, 14.8-16.0 years) in the T-CEF group. Patients assigned to TX-CEX survived longer than those assigned to T-CEF (hazard ratio 0.81; 95% CI, 0.66 to 0.99; P = .037). The 15-year survival rate was 77.6% in the TX-CEX group and 73.3% in the T-CEF group. In exploratory subgroup analyses, patients with estrogen receptor–negative cancer and those with triple-negative cancer treated with TX-CEX tended to live longer than those treated with T-CEF.

CONCLUSION
Addition of capecitabine to a chemotherapy regimen that contained docetaxel, epirubicin, and cyclophosphamide prolonged the survival of patients with early breast cancer.

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