Randomized Controlled Trial of Neo-adjuvant Progesterone and Vitamin D3 in Women With Large Operable Breast Cancer and Locally Advanced Breast Cancer
Locally Advanced Breast Cancer and Large Operable Breast Cancer

About this trial
This is an interventional treatment trial for Locally Advanced Breast Cancer and Large Operable Breast Cancer
Eligibility Criteria
Inclusion Criteria:
- Unilateral breast cancer
- Large operable breast cancer/LOBC (T3N0M0 or T3N1M0) and Locally advanced breast cancer/LABC (T3N1-2M0; T2N2M0)
- Age <70 years
- Fit for CT
Exclusion Criteria:
- Prior IB or EB
- Metastatic breast cancer
- Renal failure or deranged RFT
- Hypoparathyroidism
- Pregnant or lactating mothers or women of childbearing age not practicing contraception
- Patient on any of the following drugs: Magnesium-containing antacids, Digitalis, Phenytoin barbiturates, Thiazide diuretics.
- Previous history of other cancers except cured skin and cervical carcinoma in situ.
Sites / Locations
- Tata Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
No Intervention
Active Comparator
Active Comparator
Active Comparator
No additional treatment
Inj. Proluton
Inj. Arachitol
Inj. Proluton and Inj. Arachitol
No Injection Vit D3 or Injection Progesterone prior to chemotherapy cycle
Injection Progesterone 500 mg deep IM before each cycle of NACT (for total 4 cycles) and one injection before surgery.
Injection Arachitol (Vitamin D3) 300,000 I.U/ml IM before each cycle of NACT (for total 4 cycles) and one injection before surgery.
Injection Arachitol (Vitamin D3) 300,000 I.U/ml IM and Injection Progesterone 500 mg deep IM before each cycle of NACT (for total 4 cycles) and one injection before surgery.