Ultrasound Monitoring of Clipped Lymph Nodes to Predict Axillary Response After Chemotherapy in Breast Cancer
A Prospective Diagnostic Clinical Study Based on Longitudinal Multimodal Ultrasound Evaluation of Clipped Lymph Nodes to Assess Axillary Pathological Response After Neoadjuvant Chemotherapy in Breast Cancer
Studie Overzicht
Toestand
Studietype
Inschrijving (Geschat)
Contacten en locaties
Studiecontact
- Naam: Jingsi Mei
- Telefoonnummer: +8618825050526
- E-mail: meijs@mail.sysu.edu.cn
Studie Locaties
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Guangdong
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Guangzhou, Guangdong, China, 510000
- Sun Yat-Sen Memorial Hospital, Sun Yat-Sen University
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Contact:
- Jingsi Mei
- Telefoonnummer: +862081332066
- E-mail: meijs@mail.sysu.edu.cn
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
- Volwassen
- Oudere volwassene
Accepteert gezonde vrijwilligers
Bemonsteringsmethode
Studie Bevolking
Patients with histologically confirmed invasive breast cancer and biopsy-proven metastatic axillary lymph nodes who will receive standard neoadjuvant chemotherapy.
All enrolled patients will have a metallic clip placed in the biopsied positive lymph node before treatment, undergo longitudinal multimodal ultrasound examinations during and after NAC, and finally receive surgery with postoperative pathological evaluation of axillary lymph nodes.
Beschrijving
Inclusion Criteria:
- Female patients aged 18 years or older.
Clinical stage of breast cancer: T1-T4, N1-N3, M0.
Axillary lymph node metastasis confirmed by fine-needle aspiration (FNA) or core-needle biopsy.
Indicated for and planned to receive standard neoadjuvant chemotherapy (NAC) regimen.
The biopsy-proven metastatic lymph node is clearly visible on ultrasound and suitable for clip placement.
Completion of NAC followed by breast surgery and axillary lymph node dissection, with complete pathological results available.
Underwent multimodal ultrasound monitoring during NAC, including conventional ultrasound, elastography, and contrast-enhanced ultrasound.
Signed informed consent and willingness to complete all scheduled follow-ups.
Exclusion Criteria:
- Bilateral breast cancer.
Patients who are not suitable for neoadjuvant chemotherapy or plan to receive endocrine or targeted therapy only.
Prior breast or axillary surgery, chemotherapy, or other treatments that may affect the current therapeutic assessment.
Presence of distant metastasis or extensive axillary invasion making clip placement or evaluation difficult.
Pregnant or lactating women.
Poor image quality on ultrasound or other imaging modalities.
Inability to provide informed consent due to psychological, family, or social factors
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
Cohorten en interventies
Groep / Cohort |
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Breast cancer patients with clipped axillary lymph nodes receiving NAC and ultrasound follow-up.
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Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
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Diagnostic performance of predictive model for axillary pathological complete response (ax-pCR)
Tijdsspanne: At the time of postoperative pathological assessment (usually within 1 week after surgery)
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Area under the ROC curve (AUC), sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of the multimodal ultrasound-based predictive model for ax-pCR.
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At the time of postoperative pathological assessment (usually within 1 week after surgery)
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Diagnostic performance of predictive model for axillary pathological complete response (ax-pCR)
Tijdsspanne: At the time of postoperative pathological assessment (usually within 1 week after surgery).
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Area under the ROC curve (AUC), sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) of the multimodal ultrasound-based predictive model for ax-pCR.
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At the time of postoperative pathological assessment (usually within 1 week after surgery).
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Medewerkers en onderzoekers
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- SYSKY-2025-752-01
Plan Individuele Deelnemersgegevens (IPD)
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Informatie over medicijnen en apparaten, studiedocumenten
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