Skip to main content

Table 4 Agreement between the panelists and the SBM affiliated breast surgeons for the questions related to systemic treatment

From: Management of early-stage triple-negative breast cancer: recommendations of a panel of experts from the Brazilian Society of Mastology

Questions

Panelists before brainstorming

Affiliated breast surgeons

Disagreement n (%)

Agreement

n (%)

Disagreement n (%)

Agreement n (%)

Q35. In patients with no BRCA germline mutation, platinum agents should be recommended in neoadjuvant treatment.

11 (40.7)

16 (59.3)

105 (49.1)

109 (50.9)

Q36. In patients with the BRCA germline mutation, the use of platinum agents in neoadjuvant treatment should be recommended.

11 (40.7)

16 (59.3)

39 (18.2)

175 (81.8)

Q37. In patients who will be submitted to neoadjuvant treatment, the addition of immunotherapy should be recommended as routine.

13 (48.1)

14 (51.9)

149 (69.6)

65 (30.4)

Q38. In patients who will be submitted to neoadjuvant treatment, PD-L1 status should be taken into consideration when recommending immunotherapy.

14 (51.9)

13 (48.1)

63 (29.4)

151 (70.6)

Q39. BRCA status should play a role in the decision regarding whether to recommend neoadjuvant treatment with immunotherapy.

22 (81.5)

5 (18.5)

120 (56.1)

94 (43.9)

Q40. In patients who will be submitted to neoadjuvant treatment with immunotherapy, dose-dense anthracycline-based chemotherapy should be used.

7 (25.9)

20 (74.1)

53 (24.8)

161 (75.2)

Q41. In patients with no BRCA germline mutation submitted to neoadjuvant treatment with immunotherapy and who achieve pCR, immunotherapy should be continued during adjuvant therapy.

11 (40.7)

16 (59.3)

116 (54.2)

98 (45.8)

Q42. In patients with no BRCA germline mutation submitted to neoadjuvant treatment with immunotherapy and who have residual disease, immunotherapy should be continued during adjuvant therapy.

7 (25.9)

20 (74.1)

62 (29.0)

152 (71.0)

Q43. In patients with no BRCA germline mutation submitted to neoadjuvant therapy with immunotherapy and in whom there is residual disease, the use of adjuvant immunotherapy associated with capecitabine should be suggested.

13 (48.1)

14 (51.9)

54 (25.2)

160 (74.8)

Q44. In patients with the BRCA germline mutation submitted to neoadjuvant therapy with immunotherapy and who achieve pCR, the use of adjuvant immunotherapy associated with olaparib should be suggested.

18 (66.7)

9 (33.3)

104 (48.6)

110 (51.4)

  1. SBM Brazilian Society of Mastology, pCR pathologic complete response