Breast Cancer Research and Treatment

, Volume 133, Issue 1, pp 237–246 | Cite as

Dose-dependent change in biomarkers during neoadjuvant endocrine therapy with fulvestrant: results from NEWEST, a randomized Phase II study

  • Irene KuterEmail author
  • Julia M. W. Gee
  • Roberto Hegg
  • Christian F. Singer
  • Rajendra A. Badwe
  • Elizabeth S. Lowe
  • Ugochi A. Emeribe
  • Elizabeth Anderson
  • Francisco Sapunar
  • Pauline Finlay
  • Robert I. Nicholson
  • José Bines
  • Nadia Harbeck
Clinical trial


NEWEST (Neoadjuvant Endocrine Therapy for Women with Estrogen-Sensitive Tumors) is the first study to compare biological and clinical activity of fulvestrant 500 versus 250 mg in the neoadjuvant breast cancer setting. We hypothesized that fulvestrant 500 mg may be superior to 250 mg in blocking estrogen receptor (ER) signaling and growth. A multicenter, randomized, open-label, Phase II study was performed to compare fulvestrant 500 mg (500 mg/month plus 500 mg on day 14 of month 1) versus fulvestrant 250 mg/month for 16 weeks prior to surgery in postmenopausal women with ER+ locally advanced breast cancer. Core biopsies at baseline, week 4, and surgery were assessed for biomarker changes. Primary endpoint: change in Ki67 labeling index (LI) from baseline to week 4 determined by automated computer imaging system (ACIS). Secondary endpoints: ER protein expression and function; progesterone receptor (PgR) expression; tumor response; tolerability. ER and PgR were examined retrospectively using the H score method. A total of 211 patients were randomized (fulvestrant 500 mg: n = 109; 250 mg: n = 102). At week 4, fulvestrant 500 mg resulted in greater reduction of Ki67 LI and ER expression versus 250 mg (−78.8 vs. −47.4% [p < 0.0001] and −25.0 vs. −13.5% [p = 0.0002], respectively [ACIS]); PgR suppression was not significantly different (−22.7 vs. −17.6; p = 0.5677). However, H score detected even greater suppression of ER (−50.3 vs. −13.7%; p < 0.0001) and greater PgR suppression (−80.5 vs. −46.3%; p = 0.0018) for fulvestrant 500 versus 250 mg. At week 16, tumor response rates were 22.9 and 20.6% for fulvestrant 500 and 250 mg, respectively, with considerable decline in all markers by both ACIS and H score. No detrimental effects on endometrial thickness or bone markers and no new safety concerns were identified. This provides the first evidence of greater biological activity for fulvestrant 500 versus 250 mg in depleting ER expression, function, and growth.


Estrogen receptor-positive breast cancer Fulvestrant 500 mg Faslodex® Neoadjuvant Biomarkers 



The authors gratefully acknowledge the collaboration of the Munich Study Centre, Munich, Germany, and would like to thank Sandra Cuscó, PhD, from Complete Medical Communications, who provided medical writing support funded by AstraZeneca. Final approval of the manuscript lay solely with the authors. The NEWEST study was funded by AstraZeneca.

Conflict of interests

Irene Kuter, Jose Bines and Nadia Harbeck have acted as consultants to or in advisory roles to AstraZeneca. Julia Gee and Robert Nicholson have received research funding from AstraZeneca. Elizabeth Lowe and Ugochi Emeribe are employees of AstraZeneca and hold stock ownership with AstraZeneca. Elizabeth Anderson and Francisco Sapunar are former employees of AstraZeneca. Elizabeth Anderson holds stock ownership with AstraZeneca. Roberto Hegg, Christian Singer and Rajendra Badwe have no conflicts of interest to disclose.

Supplementary material

10549_2011_1947_MOESM1_ESM.doc (1.2 mb)
Supplementary material 1 (DOC 1183 kb)


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Copyright information

© Springer Science+Business Media, LLC. 2012

Authors and Affiliations

  • Irene Kuter
    • 1
    Email author
  • Julia M. W. Gee
    • 2
  • Roberto Hegg
    • 3
  • Christian F. Singer
    • 4
  • Rajendra A. Badwe
    • 5
  • Elizabeth S. Lowe
    • 6
  • Ugochi A. Emeribe
    • 6
  • Elizabeth Anderson
    • 7
  • Francisco Sapunar
    • 7
  • Pauline Finlay
    • 2
  • Robert I. Nicholson
    • 2
  • José Bines
    • 8
  • Nadia Harbeck
    • 9
    • 10
  1. 1.Massachusetts General HospitalBostonUSA
  2. 2.Tenovus Centre for Cancer Research, Welsh School of PharmacyCardiff UniversityCardiffUK
  3. 3.School of MedicineUniversity of Sao Paulo and Hospital Pérola ByingtonSao PauloBrazil
  4. 4.Division of Special GynaecologyMedical University of ViennaViennaAustria
  5. 5.Tata Memorial HospitalMumbaiIndia
  6. 6.AstraZenecaWilmingtonUSA
  7. 7.Formerly AstraZeneca PharmaceuticalsMacclesfieldUK
  8. 8.Instituto de CâncerRio de JaneiroBrazil
  9. 9.Frauenklinik der Technischen Universität MünchenMunichGermany
  10. 10.Breast Centre, Department of Obstetrics and GynaecologyUniversity of CologneCologneGermany

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