Impact of Neoadjuvant Chemotherapy on Breast Cancer Subtype: Does Subtype Change and, if so, How?: IHC Profile and Neoadjuvant Chemotherapy

被引:22
作者
De la Cruz, Lucy M. [1 ]
Harhay, Michael O. [2 ]
Zhang, Paul [3 ]
Ugras, Stacy [1 ]
机构
[1] Univ Penn Hlth Syst, Dept Surg, Div Endocrine & Oncol Surg, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Biostat Epidemiol & Informat, Philadelphia, PA 19104 USA
[3] Hosp Univ Penn, Dept Pathol, 3400 Spruce St, Philadelphia, PA 19104 USA
关键词
HORMONE-RECEPTOR STATUS; PROGESTERONE-RECEPTOR; PREOPERATIVE CHEMOTHERAPY; ESTROGEN-RECEPTOR; PROGNOSTIC VALUE; KI-67; METAANALYSIS; EXPRESSION; EVOLUTION; THERAPY;
D O I
10.1245/s10434-018-6608-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundBreast cancer subtype, as determined by the expression of estrogen receptor (ER) and progesterone receptor (PR), together defined as hormone receptor (HR) status, and the HER2/neu receptor (HER2), is important in predicting prognosis and guiding therapy. Knowledge regarding how tumors evolve during treatment and whether subtype is influenced by neoadjuvant chemotherapy (nCT) is limited. The purpose of this study was to compare the HR and HER2 status between core needle biopsy and residual tumor after surgery of breast cancer patients treated with nCT and to evaluate the impact of status change on therapeutic management.MethodsAfter institutional review board approval, we performed a retrospective review of all patients with a diagnosis of breast cancer who received nCT and had their initial biopsy and post-nCT surgical specimens evaluated for tumor subtype between January 2009 and December 2014 at our institution. Immunohistochemistry (IHC) of ER, PR, HER2, and fluorescence in situ hybridization for HER2 expression, when indicated, was performed using identical technique and measured by a single pathologist who specializes in breast pathology. Pre- and post-nCT subtype was cross-tabulated to assess change. Standard diagnostic metrics were computed.ResultsFifty-two patients with 54 cancers were identified to have their initial biopsy and post-nCT surgical specimens evaluated for tumor subtype in identical fashion. There was a complete pathologic response after nCT in 23 cancers (42.6%). Residual disease was noted in 31 cancers (57.4%). Five of these (16.1%) had a change in tumor subtype, of which four changes were based on IHC. HR status changed from positive to negative in two cases and from negative to positive in one case. HER2 status changed from positive to negative in one case and from negative to positive in one case. Subtype change led to treatment change in all five cases, with either the addition or discontinuation of adjuvant therapies.ConclusionsPatients with breast cancer may experience alterations in their tumor subtype after nCT. At our institution, this led to a change in adjuvant treatment in 100% of such patients. This implies that retesting receptor status of residual tumors after nCT should be routinely performed to tailor adjuvant therapy after nCT.
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收藏
页码:3535 / 3540
页数:6
相关论文
共 20 条
[1]   Inference of Tumor Evolution during Chemotherapy by Computational Modeling and In Situ Analysis of Genetic and Phenotypic Cellular Diversity [J].
Almendro, Vanessa ;
Cheng, Yu-Kang ;
Randles, Amanda ;
Itzkovitz, Shalev ;
Marusyk, Andriy ;
Ametller, Elisabet ;
Gonzalez-Farre, Xavier ;
Munoz, Montse ;
Russnes, Hege G. ;
Helland, Aslaug ;
Rye, Inga H. ;
Borresen-Dale, Anne-Lise ;
Maruyama, Reo ;
van Oudenaarden, Alexander ;
Dowsett, Mitchell ;
Jones, Robin L. ;
Reis-Filho, Jorge ;
Gascon, Pere ;
Goenen, Mithat ;
Michor, Franziska ;
Polyak, Kornelia .
CELL REPORTS, 2014, 6 (03) :514-527
[2]   Molecular Profiling of the Residual Disease of Triple-Negative Breast Cancers after Neoadjuvant Chemotherapy Identifies Actionable Therapeutic Targets [J].
Balko, Justin M. ;
Giltnane, Jennifer M. ;
Wang, Kai ;
Schwarz, Luis J. ;
Young, Christian D. ;
Cook, Rebecca S. ;
Owens, Phillip ;
Sanders, Melinda E. ;
Kuba, Maria G. ;
Sanchez, Violeta ;
Kurupi, Richard ;
Moore, Preston D. ;
Pinto, Joseph A. ;
Doimi, Franco D. ;
Gomez, Henry ;
Horiuchi, Dai ;
Goga, Andrei ;
Lehmann, Brian D. ;
Bauer, Joshua A. ;
Pietenpol, Jennifer A. ;
Ross, Jeffrey S. ;
Palmer, Gary A. ;
Yelensky, Roman ;
Cronin, Maureen ;
Miller, Vincent A. ;
Stephens, Phillip J. ;
Arteaga, Carlos L. .
CANCER DISCOVERY, 2014, 4 (02) :232-245
[3]   Estrogen Receptor and Progesterone Receptor As Predictive Biomarkers of Response to Endocrine Therapy: A Prospectively Powered Pathology Study in the Tamoxifen and Exemestane Adjuvant Multinational Trial [J].
Bartlett, John M. S. ;
Brookes, Cassandra L. ;
Robson, Tammy ;
van de Velde, Cornelis J. H. ;
Billingham, Lucinda J. ;
Campbell, Fiona M. ;
Grant, Margaret ;
Hasenburg, Annette ;
Hille, Elysee T. M. ;
Kay, Charlene ;
Kieback, Dirk G. ;
Putter, Hein ;
Markopoulos, Christos ;
Kranenbarg, Elma Meershoek-Klein ;
Mallon, Elizabeth A. ;
Dirix, Luc ;
Seynaeve, Caroline ;
Rea, Daniel .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (12) :1531-1538
[4]   Evaluation of ER, PgR, HER-2 and Ki-67 as predictors of response to neoadjuvant anthracycline chemotherapy for operable breast cancer [J].
Burcombe, RJ ;
Makris, A ;
Richman, PI ;
Daley, FM ;
Noble, S ;
Pittam, M ;
Wright, D ;
Allen, SA ;
Dove, J ;
Wilson, GD .
BRITISH JOURNAL OF CANCER, 2005, 92 (01) :147-155
[5]   Neoadjuvant therapy for treatment of breast cancer: the way forward, or simply a convenient option for patients? [J].
Chatterjee, Abhishek ;
Erban, John K. .
GLAND SURGERY, 2017, 6 (01) :119-124
[6]   Prognostic Value of a Positive-to-negative Change in Hormone Receptor Status after Neoadjuvant Chemotherapy in Patients with Hormone Receptor-positive Breast Cancer [J].
Chen, Sheng ;
Chen, Can-Ming ;
Yu, Ke-Da ;
Zhou, Ruo-Ji ;
Shao, Zhi-Ming .
ANNALS OF SURGICAL ONCOLOGY, 2012, 19 (09) :3002-3011
[7]   Outcomes After Oncoplastic Breast-Conserving Surgery in Breast Cancer Patients: A Systematic Literature Review [J].
De La Cruz, Lucy ;
Blankenship, Stephanie A. ;
Chatterjee, Abhishek ;
Geha, Rula ;
Nocera, Nadia ;
Czerniecki, Brian J. ;
Tchou, Julia ;
Fisher, Carla S. .
ANNALS OF SURGICAL ONCOLOGY, 2016, 23 (10) :3247-3258
[8]   Effect of preoperative chemotherapy on the outcome of women with operable breast cancer [J].
Fisher, B ;
Bryant, J ;
Wolmark, N ;
Mamounas, E ;
Brown, A ;
Fisher, ER ;
Wickerham, DL ;
Begovic, M ;
DeCillis, A ;
Robidoux, A ;
Margolese, RG ;
Cruz, AB ;
Hoehn, JL ;
Lees, AW ;
Dimitrov, NV ;
Bear, HD .
JOURNAL OF CLINICAL ONCOLOGY, 1998, 16 (08) :2672-2685
[9]   Intratumor Heterogeneity and Branched Evolution Revealed by Multiregion Sequencing [J].
Gerlinger, Marco ;
Rowan, Andrew J. ;
Horswell, Stuart ;
Larkin, James ;
Endesfelder, David ;
Gronroos, Eva ;
Martinez, Pierre ;
Matthews, Nicholas ;
Stewart, Aengus ;
Tarpey, Patrick ;
Varela, Ignacio ;
Phillimore, Benjamin ;
Begum, Sharmin ;
McDonald, Neil Q. ;
Butler, Adam ;
Jones, David ;
Raine, Keiran ;
Latimer, Calli ;
Santos, Claudio R. ;
Nohadani, Mahrokh ;
Eklund, Aron C. ;
Spencer-Dene, Bradley ;
Clark, Graham ;
Pickering, Lisa ;
Stamp, Gordon ;
Gore, Martin ;
Szallasi, Zoltan ;
Downward, Julian ;
Futreal, P. Andrew ;
Swanton, Charles .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (10) :883-892
[10]   Change in the hormone receptor status following administration of neoadjuvant chemotherapy and its impact on the long-term outcome in patients with primary breast cancer [J].
Hirata, T. ;
Shimizu, C. ;
Yonemori, K. ;
Hirakawa, A. ;
Kouno, T. ;
Tamura, K. ;
Ando, M. ;
Katsumata, N. ;
Fujiwara, Y. .
BRITISH JOURNAL OF CANCER, 2009, 101 (09) :1529-1536