TY - JOUR
T1 - Ki67 proliferation index as a tool for chemotherapy decisions during and after neoadjuvant aromatase inhibitor treatment of breast cancer
T2 - Results from the American college of surgeons oncology group Z1031 trial (alliance)
AU - Ellis, Matthew J.
AU - Suman, Vera J.
AU - Hoog, Jeremy
AU - Goncalves, Rodrigo
AU - Sanati, Souzan
AU - Creighton, Chad J.
AU - DeSchryver, Katherine
AU - Crouch, Erika
AU - Brink, Amy
AU - Watson, Mark
AU - Luo, Jingqin
AU - Tao, Yu
AU - Barnes, Michael
AU - Dowsett, Mitchell
AU - Budd, G. Thomas
AU - Winer, Eric
AU - Silverman, Paula
AU - Esserman, Laura
AU - Carey, Lisa
AU - Ma, Cynthia X.
AU - Unzeitig, Gary
AU - Pluard, Timothy
AU - Whitworth, Pat
AU - Babiera, Gildy
AU - Guenther, J. Michael
AU - Dayao, Zoneddy
AU - Ota, David
AU - Leitch, Marilyn
AU - Olson, John A.
AU - Allred, D. Craig
AU - Hunt, Kelly
N1 - Publisher Copyright:
© 2017 by American Society of Clinical Oncology.
PY - 2017/4/1
Y1 - 2017/4/1
N2 - Purpose To determine the pathologic complete response (PCR) rate in estrogen receptor (ER)-positive primary breast cancer triaged to chemotherapy when the protein encoded by the MKI67 gene (Ki67) level was.10%after 2 to 4weeks of neoadjuvant aromatase inhibitor (AI) therapy. A second objectivewas to examine risk of relapse using the Ki67-based Preoperative Endocrine Prognostic Index (PEPI). Methods The American College of Surgeons Oncology Group (ACOSOG) Z1031A trial enrolled postmenopausal women with stage II or III ER-positive (Allred score, 6 to 8) breast cancer whose treatment was randomly assigned to neoadjuvant AI therapy with anastrozole, exemestane, or letrozole. For the trial ACOSOG Z1031B, the protocol was amended to include a tumor Ki67 determination after 2 to 4 weeks of AI. If the Ki67 was. 10%, patients were switched to neoadjuvant chemotherapy. A PCR rate of. 20% was the predefined efficacy threshold. In patients who completed neoadjuvant AI, stratified Cox modeling was used to assess whether time to recurrence differed by PEPI = 0 score (T1 or T2, N0, Ki67, 2.7%, ER Allred. 2) versus PEPI. 0 disease. Results Only two of the 35 patients in ACOSOG Z1031B who were switched to neoadjuvant chemotherapy experienced a PCR (5.7%; 95% CI, 0.7% to 19.1%). After 5.5 years of median follow-up, four (3.7%) of the 109 patients with a PEPI = 0 score relapsed versus 49 (14.4%) of 341 of patients with PEPI. 0 (recurrence hazard ratio [PEPI = 0 v PEPI. 0], 0.27; P = .014; 95% CI, 0.092 to 0.764). Conclusion Chemotherapy efficacy was lower than expected in ER-positive tumors exhibiting AI-resistant proliferation. The optimal therapy for these patients should be further investigated. For patients with PEPI = 0 disease, the relapse risk over 5 years was only 3.6% without chemotherapy, supporting the study of adjuvant endocrine monotherapy in this group. These Ki67 and PEPI triage approaches are being definitively studied in the ALTERNATE trial (Alternate Approaches for Clinical Stage II or III Estrogen Receptor Positive Breast Cancer Neoadjuvant Treatment in Postmenopausal Women: A Phase III Study; clinical trial information: NCT01953588).
AB - Purpose To determine the pathologic complete response (PCR) rate in estrogen receptor (ER)-positive primary breast cancer triaged to chemotherapy when the protein encoded by the MKI67 gene (Ki67) level was.10%after 2 to 4weeks of neoadjuvant aromatase inhibitor (AI) therapy. A second objectivewas to examine risk of relapse using the Ki67-based Preoperative Endocrine Prognostic Index (PEPI). Methods The American College of Surgeons Oncology Group (ACOSOG) Z1031A trial enrolled postmenopausal women with stage II or III ER-positive (Allred score, 6 to 8) breast cancer whose treatment was randomly assigned to neoadjuvant AI therapy with anastrozole, exemestane, or letrozole. For the trial ACOSOG Z1031B, the protocol was amended to include a tumor Ki67 determination after 2 to 4 weeks of AI. If the Ki67 was. 10%, patients were switched to neoadjuvant chemotherapy. A PCR rate of. 20% was the predefined efficacy threshold. In patients who completed neoadjuvant AI, stratified Cox modeling was used to assess whether time to recurrence differed by PEPI = 0 score (T1 or T2, N0, Ki67, 2.7%, ER Allred. 2) versus PEPI. 0 disease. Results Only two of the 35 patients in ACOSOG Z1031B who were switched to neoadjuvant chemotherapy experienced a PCR (5.7%; 95% CI, 0.7% to 19.1%). After 5.5 years of median follow-up, four (3.7%) of the 109 patients with a PEPI = 0 score relapsed versus 49 (14.4%) of 341 of patients with PEPI. 0 (recurrence hazard ratio [PEPI = 0 v PEPI. 0], 0.27; P = .014; 95% CI, 0.092 to 0.764). Conclusion Chemotherapy efficacy was lower than expected in ER-positive tumors exhibiting AI-resistant proliferation. The optimal therapy for these patients should be further investigated. For patients with PEPI = 0 disease, the relapse risk over 5 years was only 3.6% without chemotherapy, supporting the study of adjuvant endocrine monotherapy in this group. These Ki67 and PEPI triage approaches are being definitively studied in the ALTERNATE trial (Alternate Approaches for Clinical Stage II or III Estrogen Receptor Positive Breast Cancer Neoadjuvant Treatment in Postmenopausal Women: A Phase III Study; clinical trial information: NCT01953588).
UR - http://www.scopus.com/inward/record.url?scp=85016622416&partnerID=8YFLogxK
U2 - 10.1200/JCO.2016.69.4406
DO - 10.1200/JCO.2016.69.4406
M3 - Article
C2 - 28045625
AN - SCOPUS:85016622416
SN - 0732-183X
VL - 35
SP - 1061
EP - 1069
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
IS - 10
ER -