Know Cancer

or
forgot password

Evaluation of Sentinel Lymph Node Detection After Neoadjuvant Chemotherapy for Large Operable Breast Cancer


N/A
18 Years
N/A
Open (Enrolling)
Female
Breast Cancer

Thank you

Trial Information

Evaluation of Sentinel Lymph Node Detection After Neoadjuvant Chemotherapy for Large Operable Breast Cancer


Inclusion Criteria:



- T2-T3 operable infiltrating breast carcinoma

- No allergy to Patent Blue

- Pre-operative diagnosis of unilateral infiltrating breast carcinoma.

- Patient planned to be treated by NAC.

- Informed consent.

- Surgery available 4 to 6 weeks after the last chemotherapy course (radical or
conservative surgery)

Exclusion Criteria:

- pT4d (inflammatory breast cancer)

- Locally advanced or metastatic breast cancer

- Any previous chemotherapy of contra-lateral breast cancer.

- Breast cancer local relapse

- Previous surgical removal of breast Cancer.

- Inadequate biopsy for pathological analysis.

- Dementia or altered mental disorder

- Pregnant woman or breast feeding or without efficacious contraceptive method.

- Contra-indication to NAC NAC interrupted due to progressive disease.

Type of Study:

Interventional

Study Design:

Allocation: Non-Randomized, Intervention Model: Parallel Assignment, Masking: Open Label

Outcome Measure:

false-negative rate for the Sentinel Lymph Node Detection

Outcome Time Frame:

5 years

Safety Issue:

No

Authority:

France : Afssaps

Study ID:

BRD 09/9-G

NCT ID:

NCT01221688

Start Date:

July 2010

Completion Date:

Related Keywords:

  • Breast Cancer
  • Sentinel lymph node biopsy (SLNB)
  • large operable breast cancer
  • neoadjuvant chemotherapy
  • patients with large operable breast cancer after neoadjuvant chemotherapy (NAC)
  • Breast Neoplasms

Name

Location