2022
DOI: 10.1016/j.annonc.2022.07.176
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141MO Pathological response and early survival data according to TNBCtype4 classifier in operable triple-negative breast cancer (TNBC) treated with neoadjuvant carboplatin and docetaxel

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Cited by 3 publications
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“…A retrospective analysis of the I-SPY2 trial also showed that FOXC1 and Ki67-based biomarkers could perfectly predict the poor response to an immune checkpoint inhibitor-based NAC regimen using durvalumab in patients with primary TNBC 29 . The BLIS subtype showed downregulation of immune-regulating and cytokine pathways and had the worst outcome 7,10 . However, the BLIS subtype has high chromosomal instability and constitutes 65% of TNBC with homologous recombination deficiency, a predictive biomarker for response to DNA-damaging agents or poly (ADP-ribose) polymerase (PARP) inhibitors 9 .…”
Section: Discussionmentioning
confidence: 99%
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“…A retrospective analysis of the I-SPY2 trial also showed that FOXC1 and Ki67-based biomarkers could perfectly predict the poor response to an immune checkpoint inhibitor-based NAC regimen using durvalumab in patients with primary TNBC 29 . The BLIS subtype showed downregulation of immune-regulating and cytokine pathways and had the worst outcome 7,10 . However, the BLIS subtype has high chromosomal instability and constitutes 65% of TNBC with homologous recombination deficiency, a predictive biomarker for response to DNA-damaging agents or poly (ADP-ribose) polymerase (PARP) inhibitors 9 .…”
Section: Discussionmentioning
confidence: 99%
“…29 The BLIS subtype showed downregulation of immune-regulating and cytokine pathways and had the worst outcome. 7,10 However, the BLIS subtype has high chromosomal instability and constitutes 65% of TNBC with homologous recombination deficiency, a predictive biomarker for response to DNA-damaging agents or poly (ADP-ribose) polymerase (PARP) inhibitors. 9 Furthermore, the BLIS subtype had a higher vascular endothelial growth factor signature score than the other subtypes, suggesting that anti-angiogenesis therapy might be a therapy of choice for patients with the BLIS subtype.…”
Section: Discussionmentioning
confidence: 99%
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“…Unlike advanced or metastatic TNBC [ 40 ], PD-L1 expression was not associated with an improved pCR rate or EFS in the KEYNOTE-522 trial. Other immune-related markers, such as tumor-infiltrating lymphocytes (TIL), are currently being investigated [ 48 , 49 ], and follow-up of these results is needed. Second, the backbone chemotherapy regimen of the KEYNOTE-522 trial consisted of three weekly paclitaxel–carboplatin cycles followed by anthracycline and cyclophosphamide.…”
Section: Introductionmentioning
confidence: 99%