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Neoadjuvant eribulin mesylate following anthracycline and taxane in triple negative breast cancer: Results from the HOPE study

Di Cosimo, Serena
•
La Verde, Nicla
•
Moretti, Anna
altro
de Braud, Filippo
2019
  • journal article

Periodico
PLOS ONE
Abstract
Background: Eribulin mesylate (E) is indicated for metastatic breast cancer patients previously treated with anthracycline and taxane. We argued that E could also benefit patients eligible for neoadjuvant chemotherapy. Methods: Patients with primary triple negative breast cancer ≥2 cm received doxorubicin 60 mg/m2 and paclitaxel 200 mg/m2 x 4 cycles (AT) followed by E 1.4 mg/m2 x 4 cycles. Primary endpoint was pathological complete response (pCR) rate; secondary and explorative endpoints included clinical/metabolic response rates and safety, and biomarker analysis, respectively. Using a two-stage Simon design, 43 patients were to be included provided that 4 of 13 patients had achieved pCR in the first stage of the study. Results: In stage I of the study 13 women were enrolled, median age 43 years, tumor size 2-5 cm in 9/13 (69%), positive nodal status in 8/13 (61%). Main grade 3 adverse event was neutropenia (related to AT and E in 4 and 2 cases, respectively). AT followed by E induced clinical complete + partial responses in 11/13 patients (85%), pCR in 3/13 (23%). Median measurements of maximum standardized uptake value (SUVmax) resulted 13, 3, and 1.9 at baseline, after AT and E, respectively. Complete metabolic response (CMR) occurred after AT and after E in 2 and 3 cases, respectively. Notably, 2 of the 5 (40%) patients with CMR achieved pCR at surgery. Immunostaining of paired pre-/post-treatment tumor specimens showed a reduction of β-catenin, CyclinD1, Zeb-1, and c-myc expression, in the absence of N-cadherin modulation. The study was interrupted at stage I due to the lack of the required patients with pCR. Conclusions: Despite the early study closure, preoperative E following AT showed clinical and biological activity in triple negative breast cancer patients. Furthermore, the modulation of β-catenin pathway core proteins, supposedly outside the domain of epithelial-mesenchymal transition, claims for further investigation.
DOI
10.1371/journal.pone.0220644
WOS
WOS:000484999400025
Archivio
https://hdl.handle.net/11368/3053158
info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85070354833
https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0220644
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6685628/
Diritti
open access
license:creative commons
license:digital rights management non definito
license uri:http://creativecommons.org/licenses/by/4.0/
license uri:iris.pri00
FVG url
https://arts.units.it/bitstream/11368/3053158/1/plose.pdf
Soggetti
  • triple negative breas...

  • eribulin

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