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Table 3 pCR analyses in the ITT populations

From: Comparing efficacy and safety of P013, a proposed pertuzumab biosimilar, with the reference product in HER2-positive breast cancer patients: a randomized, phase III, equivalency clinical trial

 

P013

Reference pertuzumab

Difference (95% Confidence interval)

Total pCR (ITT)

60 (56.07)

68 (63.55)

−0.07 (− 0.21, 0.06)

  1. For ITT analysis, patients with missing assessments were considered to be nonresponders
  2. Difference = P013- Reference pertuzumab
  3. pCR Pathological complete response