Adjuvant Capecitabine for Early Breast Cancer: 15-Year Overall Survival Results From a Randomized Trial
| dc.contributor.author | Joensuu Heikki | |
| dc.contributor.author | Kellokumpu-Lehtinen Pirkko-Liisa | |
| dc.contributor.author | Huovinen Riikka | |
| dc.contributor.author | Jukkola Arja | |
| dc.contributor.author | Tanner Minna | |
| dc.contributor.author | Ahlgren Johan | |
| dc.contributor.author | Auvinen Päivi | |
| dc.contributor.author | Lahdenperä Outi | |
| dc.contributor.author | Villman Kenneth | |
| dc.contributor.author | Nyandoto Paul | |
| dc.contributor.author | Nilsson Greger | |
| dc.contributor.author | Poikonen-Saksela Paula | |
| dc.contributor.author | Kataja Vesa | |
| dc.contributor.author | Bono Petri | |
| dc.contributor.author | Junnila Jouni | |
| dc.contributor.author | Lindman Henrik | |
| dc.contributor.organization | fi=kliininen syöpätautioppi|en=Clinical Oncology| | |
| dc.contributor.organization | fi=lääketieteellinen tiedekunta|en=Faculty of Medicine| | |
| dc.contributor.organization | fi=tyks, vsshp|en=tyks, varha| | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.13290506867 | |
| dc.contributor.organization-code | 1.2.246.10.2458963.20.74978886054 | |
| dc.converis.publication-id | 175602963 | |
| dc.converis.url | https://research.utu.fi/converis/portal/Publication/175602963 | |
| dc.date.accessioned | 2022-10-28T14:38:40Z | |
| dc.date.available | 2022-10-28T14:38:40Z | |
| dc.description.abstract | <p>PURPOSE<br>Few data are available regarding the influence of adjuvant capecitabine on long-term survival of patients with early breast cancer.</p><p>METHODS<br>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.<br></p><p>RESULTS<br>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.</p><p>CONCLUSION<br>Addition of capecitabine to a chemotherapy regimen that contained docetaxel, epirubicin, and cyclophosphamide prolonged the survival of patients with early breast cancer.<br></p> | |
| dc.format.pagerange | 1051 | |
| dc.format.pagerange | 1057+ | |
| dc.identifier.eissn | 1527-7755 | |
| dc.identifier.jour-issn | 0732-183X | |
| dc.identifier.olddbid | 189443 | |
| dc.identifier.oldhandle | 10024/172537 | |
| dc.identifier.uri | https://www.utupub.fi/handle/11111/44568 | |
| dc.identifier.url | https://ascopubs.org/doi/full/10.1200/JCO.21.02054 | |
| dc.identifier.urn | URN:NBN:fi-fe2022081155087 | |
| dc.language.iso | en | |
| dc.okm.affiliatedauthor | Huovinen, Riikka | |
| dc.okm.affiliatedauthor | Lahdenperä, Outi | |
| dc.okm.affiliatedauthor | Dataimport, tyks, vsshp | |
| dc.okm.discipline | 3122 Cancers | en_GB |
| dc.okm.discipline | 3122 Syöpätaudit | fi_FI |
| dc.okm.internationalcopublication | international co-publication | |
| dc.okm.internationality | International publication | |
| dc.okm.type | A1 ScientificArticle | |
| dc.publisher | LIPPINCOTT WILLIAMS & WILKINS | |
| dc.publisher.country | United States | en_GB |
| dc.publisher.country | Yhdysvallat (USA) | fi_FI |
| dc.publisher.country-code | US | |
| dc.relation.doi | 10.1200/JCO.21.02054 | |
| dc.relation.ispartofjournal | Journal of Clinical Oncology | |
| dc.relation.issue | 10 | |
| dc.relation.volume | 40 | |
| dc.source.identifier | https://www.utupub.fi/handle/10024/172537 | |
| dc.title | Adjuvant Capecitabine for Early Breast Cancer: 15-Year Overall Survival Results From a Randomized Trial | |
| dc.year.issued | 2022 |
Tiedostot
1 - 1 / 1