Please use this identifier to cite or link to this item:
https://hdl.handle.net/2445/215185
Full metadata record
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Falo Zamora, Catalina | - |
dc.contributor.author | Azcarate, Juan | - |
dc.contributor.author | Fernández González, Sergi | - |
dc.contributor.author | Perez, Xavier | - |
dc.contributor.author | Petit, Anna | - |
dc.contributor.author | Perez Montero, Héctor | - |
dc.contributor.author | Vethencourt, Andrea | - |
dc.contributor.author | Vazquez, Silvia | - |
dc.contributor.author | Laplana, Maria | - |
dc.contributor.author | Ales, Miriam | - |
dc.contributor.author | Stradella, Agostina | - |
dc.contributor.author | Fullana, Bartomeu | - |
dc.contributor.author | Pla Farnós, Maria Jesús | - |
dc.contributor.author | Gumà i Garcia, Anna Maria | - |
dc.contributor.author | Ortega, Raul | - |
dc.contributor.author | Varela, M. | - |
dc.contributor.author | Pérez, Diana | - |
dc.contributor.author | Ponton, Jose Luis | - |
dc.contributor.author | Cobo, Sara | - |
dc.contributor.author | Benítez, Ana | - |
dc.contributor.author | Campos, Miriam | - |
dc.contributor.author | Fernández, Adela | - |
dc.contributor.author | Villanueva, Rafael | - |
dc.contributor.author | Obadia, Verónica | - |
dc.contributor.author | Recalde, Sabela | - |
dc.contributor.author | Soler-Monsó, Teresa | - |
dc.contributor.author | López Ojeda, Anna | - |
dc.contributor.author | Martinez, Evelyn | - |
dc.contributor.author | Ponce i Sebastià, Jordi | - |
dc.contributor.author | Pernas, Sònia | - |
dc.contributor.author | Gil-Gil, Miguel | - |
dc.contributor.author | García Tejedor, María Amparo | - |
dc.date.accessioned | 2024-09-16T17:12:08Z | - |
dc.date.available | 2024-09-16T17:12:08Z | - |
dc.date.issued | 2024-06-30 | - |
dc.identifier.issn | 2072-6694 | - |
dc.identifier.uri | https://hdl.handle.net/2445/215185 | - |
dc.description.abstract | Introduction: Neoadjuvant chemotherapy in breast cancer offers the possibility to facilitate breast and axillary surgery; it is a test of chemosensibility in vivo with significant prognostic value and may be used to tailor adjuvant treatment according to the response. Material and Methods: A retrospective single-institution cohort of 482 stage II and III breast cancer patients treated with neoadjuvant chemotherapy based on anthracycline and taxans, plus antiHEr2 in Her2-positive cases, was studied. Survival was calculated at 5 and 10 years. Kaplan-Meier curves with a log-rank test were calculated for differences according to age, BRCA status, menopausal status, TNM, pathological and molecular surrogate subtype, 20% TIL cut-off, surgical procedure, response to chemotherapy and the presence of vascular invasion. Results: The pCR rate was 25.3% and was greater in HER2 (51.3%) and TNBC (31.7%) and in BRCA carriers (41.9%). The factors independently related to patient survival were pathology and molecular surrogate subtype, type of surgery, response to NACT and vascular invasion. BRCA status was a protective prognostic factor without reaching statistical significance, with an HR 0.5 (95%CI 0.1-1.4). Mastectomy presented a double risk of distant recurrence compared to breast-conservative surgery (BCS), supporting BCS as a safe option after NACT. After a mean follow-up of 126 (SD 43) months, luminal tumors presented a substantial difference in survival rates calculated at 5 or 10 years (81.2% compared to 74.7%), whereas that for TNBC was 75.3 and 73.5, respectively. The greatest difference was seen according to the response in patients with pCR, who exhibited a 10 years DDFS of 95.5% vs. 72.4% for those patients without pCR, p < 0001. This difference was especially meaningful in TNBC: the 10 years DDFS according to an RCB of 0 to 3 was 100%, 80.6%, 69% and 49.2%, respectively, p < 0001. Patients with a particularly poor prognosis were those with lobular carcinomas, with a 10 years DDFS of 42.9% vs. 79.7% for ductal carcinomas, p = 0.001, and patients with vascular invasion at the surgical specimen, with a 10 years DDFS of 59.2% vs. 83.6% for those patients without vascular invasion, p < 0.001. Remarkably, BRCA carriers presented a longer survival, with an estimated 10 years DDFS of 89.6% vs. 77.2% for non-carriers, p = 0.054. Conclusions: Long-term outcomes after neoadjuvant chemotherapy can help patients and clinicians make well-informed decisions. | - |
dc.format.extent | 22 p. | - |
dc.format.mimetype | application/pdf | - |
dc.language.iso | eng | - |
dc.publisher | MDPI | - |
dc.relation.isformatof | Reproducció del document publicat a: https://doi.org/10.3390/cancers16132421 | - |
dc.relation.ispartof | Cancers, 2024, vol. 16, num.13 | - |
dc.relation.uri | https://doi.org/10.3390/cancers16132421 | - |
dc.rights | cc-by (c) Falo, C. et al., 2024 | - |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | - |
dc.source | Articles publicats en revistes (Bioquímica i Biomedicina Molecular) | - |
dc.subject.classification | Càncer de mama | - |
dc.subject.classification | Quimioteràpia | - |
dc.subject.classification | Pronòstic mèdic | - |
dc.subject.other | Breast cancer | - |
dc.subject.other | Chemotherapy | - |
dc.subject.other | Prognosis | - |
dc.title | Breast cancer patient’s outcomes after neoadjuvant chemotherapy and surgery at 5 and 10 years for stage II–III disease | - |
dc.type | info:eu-repo/semantics/article | - |
dc.type | info:eu-repo/semantics/publishedVersion | - |
dc.identifier.idgrec | 749548 | - |
dc.date.updated | 2024-09-16T17:12:08Z | - |
dc.rights.accessRights | info:eu-repo/semantics/openAccess | - |
Appears in Collections: | Articles publicats en revistes (Bioquímica i Biomedicina Molecular) Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL)) Articles publicats en revistes (Ciències Clíniques) |
Files in This Item:
File | Description | Size | Format | |
---|---|---|---|---|
863844.pdf | 4.62 MB | Adobe PDF | View/Open |
This item is licensed under a
Creative Commons License