Publication:
Efficacy of Chemotherapy for ER-Negative and ER-Positive Isolated Locoregional Recurrence of Breast Cancer: Final Analysis of the CALOR Trial

cris.virtual.author-orcid0000-0002-3383-9449
cris.virtualsource.author-orcid4ef85fd1-beae-44f7-8237-a1e0aeb109ff
datacite.rightsopen.access
dc.contributor.authorWapnir, Irene L.
dc.contributor.authorPrice, Karen N.
dc.contributor.authorAnderson, Stewart J.
dc.contributor.authorRobidoux, André
dc.contributor.authorMartín, Miguel
dc.contributor.authorNortier, Johan W.R.
dc.contributor.authorPaterson, Alexander H.G.
dc.contributor.authorRimawi, Mothaffar F.
dc.contributor.authorLáng, István
dc.contributor.authorBaena-Cañada, José Manuel
dc.contributor.authorThürlimann, Beat
dc.contributor.authorMamounas, Eleftherios P.
dc.contributor.authorGeyer, Charles E.
dc.contributor.authorGelber, Shari
dc.contributor.authorCoates, Alan S.
dc.contributor.authorGelber, Richard D.
dc.contributor.authorRastogi, Priya
dc.contributor.authorRegan, Meredith M.
dc.contributor.authorWolmark, Norman
dc.contributor.authorAebi, Stefan
dc.date.accessioned2024-10-25T14:22:14Z
dc.date.available2024-10-25T14:22:14Z
dc.date.issued2018
dc.description.abstractPurpose Isolated locoregional recurrence (ILRR) predicts a high risk of developing breast cancer distant metastases and death. The Chemotherapy as Adjuvant for LOcally Recurrent breast cancer (CALOR) trial investigated the effectiveness of chemotherapy (CT) after local therapy for ILRR. A report at 5 years of median follow-up showed significant benefit of CT for estrogen receptor (ER)-negative ILRR, but additional follow-up was required in ER-positive ILRR. Patients and Methods CALOR was an open-label, randomized trial for patients with completely excised ILRR after unilateral breast cancer. Eligible patients were randomly assigned to receive CT or no CT and stratified by prior CT, hormone receptor status, and location of ILRR. Patients with hormone receptor-positive ILRR received adjuvant endocrine therapy. Radiation therapy was mandated for patients with microscopically involved margins, and anti-human epidermal growth factor receptor 2 therapy was optional. End points were disease-free survival (DFS), overall survival, and breast cancer-free interval. Results From August 2003 to January 2010, 162 patients were enrolled: 58 with ER-negative and 104 with ER-positive ILRR. At 9 years of median follow-up, 27 DFS events were observed in the ER-negative group and 40 in the ER-positive group. The hazard ratios (HR) of a DFS event were 0.29 (95% CI, 0.13 to 0.67; 10-year DFS, 70% v 34%, CT v no CT, respectively) in patients with ER-negative ILRR and 1.07 (95% CI, 0.57 to 2.00; 10-year DFS, 50% v 59%, respectively) in patients with ER-positive ILRR ( Pinteraction = .013). HRs were 0.29 (95% CI, 0.13 to 0.67) and 0.94 (95% CI, 0.47 to 1.85), respectively, for breast cancer-free interval ( Pinteraction = .034) and 0.48 (95% CI, 0.19 to 1.20) and 0.70 (95% CI, 0.32 to 1.55), respectively, for overall survival ( Pinteraction = .53). Results for the three end points were consistent in multivariable analyses adjusting for location of ILRR, prior CT, and interval from primary surgery. Conclusion The final analysis of CALOR confirms that CT benefits patients with resected ER-negative ILRR and does not support the use of CT for ER-positive ILRR.
dc.description.numberOfPages7
dc.description.sponsorshipUniversitätsklinik für Medizinische Onkologie
dc.identifier.doi10.7892/boris.114144
dc.identifier.pmid29443653
dc.identifier.publisherDOI10.1200/JCO.2017.76.5719
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/160198
dc.language.isoen
dc.publisherAmerican Society of Clinical Oncology
dc.relation.ispartofJournal of clinical oncology
dc.relation.issn0732-183X
dc.relation.organizationClinic of Medical Oncology
dc.subject.ddc600 - Technology::610 - Medicine & health
dc.titleEfficacy of Chemotherapy for ER-Negative and ER-Positive Isolated Locoregional Recurrence of Breast Cancer: Final Analysis of the CALOR Trial
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.endPage1079
oaire.citation.issue11
oaire.citation.startPage1073
oaire.citation.volume36
oairecerif.author.affiliationUniversitätsklinik für Medizinische Onkologie
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unibe.date.licenseChanged2019-10-24 18:59:56
unibe.description.ispublishedpub
unibe.eprints.legacyId114144
unibe.journal.abbrevTitleJ CLIN ONCOL
unibe.refereedtrue
unibe.subtype.articlejournal

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