Ki67 measured after neoadjuvant chemotherapy for primary breast cancer

  • Gunter von Minckwitz
  • Wolfgang D Schmitt
  • Sibylle Loibl
  • Berit M Müller
  • Jens U Blohmer
  • Bruno V Sinn
  • Holger Eidtmann
  • Wolfgang Eiermann
  • Bernd Gerber
  • Hans Tesch
  • Jörn Hilfrich
  • Jens Huober
  • Tanja Fehm
  • Jana Barinoff
  • Thomas Rüdiger
  • Erhard Erbstoesser
  • Peter A Fasching
  • Thomas Karn
  • Volkmar Müller
  • Christian Jackisch
  • Carsten Denkert

Related Research units

Abstract

PURPOSE: The value of Ki67 measured on residual disease after neoadjuvant chemotherapy is not sufficiently described.

EXPERIMENTAL DESIGN: Participants of the GeparTrio study with primary breast cancer randomly received neoadjuvant response-guided [8 cycles TAC (docetaxel/doxorubicin/cyclophosphamide) in responding and TAC-NX (vinorelbine/capecitabine) in nonresponding patients] or conventional (6 cycles TAC) chemotherapy according to interim response assessment. Ki-67 levels were centrally measured immunohistochemically after neoadjuvant treatment if tumor tissue was available. Here, we analyze 1,151 patients having a pathologic complete response (pCR; n, 484), or residual disease with low (0-15%), intermediate (15.1-35%), or high (35.1-100%) posttreatment Ki67 levels in 488, 77, and 102 patients, respectively.

RESULTS: Patients with high posttreatment Ki67 levels showed higher risk for disease relapse (P < 0.0001) and death (P < 0.0001) compared with patients with low or intermediate Ki67 levels. Patients with low Ki67 levels showed a comparable outcome to patients with a pCR (P = 0.211 for disease-free and P = 0.779 for overall survival). Posttreatment Ki67 levels provided more prognostic information than pretreatment Ki67 levels or changes of Ki67 from pre- to posttreatment. Information on pCR plus posttreatment Ki67 levels surmount the prognostic information of pCR alone in hormone-receptor-positive disease [hazard ratios (HR), 1.82-5.88] but not in hormone-receptor-negative disease (HR: 0.61-1.73). Patients with conventional and response-guided treatment did not show a different distribution of posttreatment Ki67 (P = 0.965).

CONCLUSIONS: Posttreatment Ki67 levels provide prognostic information for patients with hormone-receptor-positive breast cancer and residual disease after neoadjuvant chemotherapy. Levels were not prognostic for outcome after response-guided chemotherapy. High posttreatment Ki67 indicates the need for innovative postneoadjuvant treatments.

Bibliographical data

Original languageEnglish
ISSN1078-0432
DOIs
Publication statusPublished - 15.08.2013
PubMed 23812670