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Table 2 Multivariate analysis of clinicopathological model, Model 2 (the early-treatment model) and Model 3 (the posttreatment model)

From: An integrated deep learning model for the prediction of pathological complete response to neoadjuvant chemotherapy with serial ultrasonography in breast cancer patients: a multicentre, retrospective study

 

Clinicopathological model

p-value

Model 2

p-value

Model 3

p-value

OR

95%CI

OR

95%CI

OR

95%CI

Ki67

  Negative

Reference

        

  Positive

1.436

0.783–2.633

0.240

1.716

0.815–3.615

0.153

1.985

0.858–4.594

0.107

ER

  Negative

Reference

        

  Positive

0.742

0.333–1.657

0.465

0.559

0.212–1.470

0.236

0.700

0.242–2.024

0.509

PR

  Negative

Reference

        

  Positive

0.990

0.427–2.302

0.984

0.701

0.258–1.904

0.484

0.768

0.231–2.548

0.664

Her2

  Negative

Reference

        

  Positive

0.937

0.078–11.320

0.959

1.062

0.369–3.055

0.911

1.036

0.063–16.92

0.980

Subtype

  Triple-negative

Reference

        

  HER2(+)

2.047

0.161–25.97

0.578

1.375

0.083–22.90

0.823

1.271

0.075–21.44

0.867

  HER2(−)&HR(+)

1.194

0.361–3.945

0.770

1.275

0.305–5.331

0.738

1.378

0.272–6.987

0.697

P0-Signature

–

–

–

2.357

1.531–3.629

 < 0.001

1.881

1.222–2.894

0.004

P1-Signature

–

–

–

2.455

1.721–3.502

 < 0.001

2.094

1.468–2.987

 < 0.001

P2-Signature

–

–

–

–

–

–

2.097

1.543–2.849

 < 0.001

  1. Model 2 was built based on the P0-Signature plus the P1-Signature. And Model 3 was based on Model 2 plus the P2-Signature
  2. ER estrogen receptor, PR progesterone receptor, HER2 human epidermal growth factor receptor, P0 Phase 0 (pretreatment), P1 Phase 1 (early-stage treatment, namely, during the first–second cycle of the neoadjuvant chemotherapy), P2 Phase 2 (posttreatment), OR odds ratio, 95%CI 95% confidence interval