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A medical records based retrospective study for the correlation between MyD88 expression and neoadjuvant chemotherapy response in breast cancer

A medical records based retrospective study for the correlation between MyD88 expression and neoadjuvant chemotherapy response in breast cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027537
Enrollment
Unknown
Registered
2019-11-17
Start date
2019-11-30
Completion date
Unknown
Last updated
2019-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

breast cancer

Interventions

Case series:paclitaxel-containing neoadjuvant chemotherapy

Sponsors

Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment, Chongqing University Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Women aged 18 to 70 years; 2. Pathologically confirmed invasive breast cancer before neoadjuvant chemotherapy.Patients with stageI-IIIB clinical evaluation and indications of neoadjuvant chemotherapy according to NCCN guidelines; 3. Neoadjuvant chemotherapy including AC-TTACTCATTP (Her2 positive patients can be combined with trastuzumab); 4. In preoperative examination, no evidence of metastasis was found in clinical or imaging studies; 5. Modified radical mastectomy or Breast conserving surgery was performed after neoadjuvant chemotherapy, and postoperative specimens were evaluated using the standard miller-payne (MP) system; 6. Eastern Cooperative Oncology Group(ECOG) Performance Status <=1; 7. Complete clinicopathological data; 8. Signed Informed Consent Form(ICF).

Exclusion criteria

Exclusion criteria: 1. Any prior (ipsilateral or contralateral) history of breast cancer other than lobular carcinoma in situ (LCIS); 2. Any metastasis; 3. Other systemic and local treatments, such as endocrine therapy and radiotherapy, other than those allowed by the program; 4. Other malignant tumors, excluding cured cervical carcinoma in situ, skin basal cell carcinoma; 5. Neoadjuvant chemotherapy was not completed; 6. Incomplete medical records or missing pathological specimens.

Design outcomes

Primary

MeasureTime frame
Pathological remission rate;

Secondary

MeasureTime frame
Objective Response Rate;

Contacts

Public ContactFaliang Xu

Chongqing Key Laboratory of Translational Research for Cancer Metastasis and Individualized Treatment, Chongqing University Cancer Hospital

flxu88@163.com+86 13101300516

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026