Health Condition 1: C509- Malignant neoplasm of breast of unspecified site
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1. Treatment naïve non-metastatic breast cancer patients receiving/received neoadjuvant chemotherapy 2. For prospective group: patients consenting to participate in the study
Exclusion criteria
Exclusion criteria: 1. Breast cancer patients with previous history of surgery or radiotherapy to chest and axilla. 2. Metastatic breast cancer at presentation. 3. Patients not consenting to participate in the study. 4. Patients having incomplete records.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To develop a predictive nomogram to predict pathological complete response in treatment naïve non metastatic breast cancer patients receiving neoadjuvant chemotherapyTimepoint: From enrollment to final histopathology (06 months) | — |
Secondary
| Measure | Time frame |
|---|---|
| To validate the predictive nomogram developed to identify the patients having a likelihood of achieving pathological complete response in treatment naïve non metastatic breast cancer patients receiving neoadjuvant chemotherapyTimepoint: 01 month;To study the factors predicting pathological complete response in treatment naïve non metastatic breast cancer patients receiving neoadjuvant chemotherapyTimepoint: 06 months | — |
Countries
India
Contacts
All India Institute of Medical Sciences, New Delhi