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Table 2 Clinical trials evaluating the accuracy of sentinel lymph node dissection in clinically node-positive patients. Summary of trials designed to evaluate the accuracy of sentinel lymph node dissection to assess axillary nodal response to therapy in clinically node-positive patients who receive neoadjuvant chemotherapy

From: Targeting and limiting surgery for patients with node-positive breast cancer

Trial

ACOSOG Z1071 [7, 33]

SENTINA (Arm C) [9]

SN FNAC [10]

Nodal eligibility criteria

cN1-2

cN1-2

cN1-2

Endpoints reported for cN1 a

Biopsy required to confirm metastases?

Yes

No

Yes

Number of patients

cN1 = 603

592

153

cN2 = 34

Overall FNR (No IHC)

12.6 % a

14.2 %

13.4 %

FNR with IHC

8.7 % a

Not reported

8.4 %

FNR depending on mapping agents

   

One agent

20.3 %

16 %

16 %

Dual agents

10.8 %

8.6 %

5.2 %

FNR by number of SLNs

   

One SLN

31 %

24.3 %

18.2 %

Two SLNs

21.1 %

18.5 %

≥2 SLNs = 4.9 %

Three or more SLNs

9.1 %

4.9 %

  1. aLimited to patients classified as cN1 with ≥2 sentinel lymph nodes removed
  2. FNR, False negative rate; IHC, Immunohistochemistry; SLN, Sentinel lymph node