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Profil bibliographique

V. Valero

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

12Publications signalées
1Citations signalées
1Affiliations récentes

Les institutions déclarées

Les domaines associés

Advanced Breast Cancer TherapiesBreast Cancer Treatment StudiesHER2/EGFR in Cancer ResearchCancer Immunotherapy and BiomarkersChemokine receptors and signaling

Les publications récentes

2026 conference-abstract OpenAlex

Abstract 3763: CCR7 expression and spatial distribution in inflammatory breast cancer: A baseline characterization for therapeutic targeting

S. Shivhare, Caren I. Sanchez, Richard Larson, Lacey E. Dobrolecki et autres

Abstract Purpose: Inflammatory breast cancer (IBC) is a rare, highly aggressive subtype marked by rapid proliferation, extensive angio-/lymphangiogenesis, and early metastasis. CCR7, a chemokine receptor involved in immune trafficking, promotes tumor migration toward lymphatics via CCL19/CCL21. This study provides an integrated genomic, …

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0 citations Cancer Research
2026 conference-abstract OpenAlex

Abstract PS4-12-26: Neosaci-io: neoadjuvant sacituzumab govitecan (sg) + pembrolizumab (pb) in patients (pts) with early-stage tnbc experiencing suboptimal response to keynote-522

Clinton Yam, T. Iwase, B. Nelson, R. L. Bassett et autres

Abstract Background: Pts with residual disease (non-pCR) after the KEYNOTE-522 regimen face a 30-40% risk of recurrence within 3 years, underscoring the urgent need for more effective therapies. In preliminary analyses, we identified that ≤80% tumor reduction after 4 cycles of paclitaxel+carboplatin …

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1 citation Clinical Cancer Research
2026 conference-abstract OpenAlex

Abstract PS4-07-22: Chemotherapy Decision Making and Outcomes in Very Early-Stage Triple Negative Breast Cancer

E. R. Lopez, A. Singareeka Raghavendra, Sarah Pasyar, B. Lim et autres

Abstract BACKGROUND The benefit of chemotherapy in very early-stage triple-negative breast cancer (TNBC) remains unclear, as these patients have historically been excluded from clinical trials. Guidelines recommend consideration of chemotherapy for T1b tumors (0.6-1 cm) and is not recommend for T1a tumors …

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0 citations Clinical Cancer Research
2026 conference-abstract OpenAlex

Abstract PS4-01-10: Characterizing CCR7 Gene Amplification and Protein Expression in Inflammatory and non-inflammatory Breast Cancer

S. Shivhare, C. Sanchez, R. Larson, L. Dobrolecki et autres

Abstract Purpose: Inflammatory breast cancer (IBC) is a rare yet exceptionally aggressive subtype that accounts for a disproportionate number of breast cancer deaths. A significant barrier to effective treatment is its ability to invade the lymphatic system and evade immune suppression. Emerging …

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0 citations Clinical Cancer Research
2026 conference-abstract OpenAlex

Abstract PS1-09-12: Trop2 expression and therapeutic opportunities in inflammatory breast cancer

S. Murray, A. Nasrazadani, Clinton Yam, A. Alexander et autres

Abstract Background: Inflammatory breast cancer (IBC) is a rare and aggressive subtype with poor outcomes, particularly in patients with residual disease post-neoadjuvant therapy. Antibody-drug conjugates (ADCs), such as sacituzumab govitecan (SG), have shown efficacy in hard-to-treat subtypes like TNBC and HR+/HER2- disease. …

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0 citations Clinical Cancer Research
2026 conference-abstract OpenAlex

Abstract PD7-03: Circulating Immune Correlates of Pathological Response to Neoadjuvant Pembrolizumab plus Chemotherapy in High-Risk, Early-Stage Triple-Negative Breast Cancer

Clinton Yam, Anastasia Radko, L. Huo, S. Akshara et autres

Abstract Background: The incorporation of immune checkpoint inhibitors, specifically pembrolizumab (anti-PD-1), into neoadjuvant therapy, has improved outcomes for patients with stage II-III triple-negative breast cancer (TNBC). However, due to the risk of of immune-related adverse events, there remains a critical need to …

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0 citations Clinical Cancer Research
2026 conference-abstract OpenAlex

Abstract GS3-05: Evaluation of the Sensitivity to Endocrine Therapy (SETER/PR) assay to predict benefit from extended endocrine therapy in the NRG/NSABP B-42 trial

E. P. Mamounas, Hanna Bandos, K. J. Sweeney, K. M. Tran et autres

Abstract Background: SETER/PR index of sensitivity to endocrine therapy (ET) measures endocrine receptor-related transcription from fixed paraffin-embedded tissue and is highly reproducible within and between laboratories. SETER/PR index is correlated with receptor ligand binding activity and predicts early pharmacodynamic response to ET …

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0 citations Clinical Cancer Research
2026 conference-abstract OpenAlex

Abstract PS1-07-23: Outcome After Locoregional Recurrences For Definitively Treated Non-Metastatic Inflammatory Breast Cancer

E. Onwubiko, Megumi Kai, M. C. Stauder, S. X. Sun et autres

Abstract Purpose: This study examines the clinical outcomes for Inflammatory Breast Cancer (IBC) patients who develop locoregional recurrence (LRR) after tri-modality therapy (TMT), including systemic therapy, modified radical mastectomy and post-mastectomy radiation therapy (PMRT). While LRR is uncommon after standard trimodal therapy …

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0 citations Clinical Cancer Research
2026 conference-abstract OpenAlex

Abstract PS5-08-21: Prospective breast cancer clinical validation study of an ultrasensitive, tumor-informed, whole genome, circulating tumor DNA assay to detect molecular residual disease and predict recurrence of high-risk early breast cancer treated with standard (neo)adjuvant therapy; NSABP B-64/EXActDNA/003/NCT06401421

Mark Basik, Emilia J. Diego, G. Tang, S. Puhalla et autres

Abstract Background: Detection of occult micrometastatic cancer—molecular residual disease (MRD)—in patients following treatment for high-risk phenotypes of early breast cancer using circulating tumor DNA (ctDNA) is associated with a high risk of recurrence. An ultra-sensitive, tumor-informed, whole-genome, minor-allele-enriched sequencing through recognition oligonucleotides …

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0 citations Clinical Cancer Research
2026 conference-abstract OpenAlex

Abstract PS1-09-19: Real world outcomes of sacituzumab govitecan in hormone receptor-positive and triple-negative breast cancer: Impact of prior therapy

A. Singareeka Raghavendra, Z. WANG, R. Bssett, S. Damodaran et autres

Abstract Background: The antibody-drug conjugate sacituzumab govitecan (SG) is approved for patients with metastatic triple-negative breast cancer (mTNBC) and hormone receptor (HR)+/Human epidermal growth factor receptor 2 (HER2)- metastatic breast cancer (mBC). The impact of HER2-low status on treatment outcomes remains unclear. …

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0 citations Clinical Cancer Research
2026 conference-abstract OpenAlex

Abstract PS5-02-03: Clinical Outcomes of Trastuzumab Emtansine (T-DM1) Following Trastuzumab Deruxtecan (T-DXd) in Metastatic Breast Cancer: A Single-Center Experience

V. Valero, Z. WANG, R. L. Bassett, R. K. MURTHY et autres

Abstract Background: HER2-positive metastatic breast cancer (MBC) remains an oncological challenge afterdisease progression to pertuzumab-trastuzumab, and fam-trastuzumab deruxtecan. Data on treatmentoutcomes with T-DM1 following progression on trastuzumab deruxtecan (T-DXd) remain limited. This study evaluates the clinical outcomes of patients with HER2-positive MBC …

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0 citations Clinical Cancer Research
2026 conference-abstract OpenAlex

Abstract PD2-02: Stability of Estrogen receptor (ER), Progesterone receptor (PR), and Human epidermal growth factor receptor 2 (HER2) in Residual Invasive Tumor after Neoadjuvant Therapy in Inflammatory Breast Cancer

S. Krishnamurthy, R. S. Tidwell, Megumi Kai, L. Villareal et autres

Abstract Background: Current guidelines do not mandate routine evaluation of ER, PR, and HER2 in residual tumor after neoadjuvant therapy (NAT), including chemotherapy, targeted therapy, and immune checkpoint inhibitors, in breast cancer. There are no studies that evaluated the stability of these …

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0 citations Clinical Cancer Research

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