Pathologic Complete Response After Neoadjuvant Chemotherapy and Long-Term Outcomes Among Young Women With Breast Cancer

被引:103
作者
Spring, Laura [1 ]
Greenup, Rachel [2 ]
Niemierko, Andrzej [1 ]
Schapira, Lidia [3 ]
Haddad, Stephanie [1 ]
Jimenez, Rachel [1 ]
Coopey, Suzanne [1 ]
Taghian, Alphonse [1 ]
Hughes, Kevin S. [1 ]
Isakoff, Steven J. [1 ]
Ellisen, Leif W. [1 ]
Smith, Barbara L. [1 ]
Specht, Michelle [1 ]
Moy, Beverly [1 ]
Bardia, Aditya [1 ]
机构
[1] Harvard Med Sch, Massachusetts Gen Hosp, Ctr Canc, Lawrence House 304,10 North Grove St, Boston, MA 02114 USA
[2] Duke Univ, Durham, NC USA
[3] Stanford Univ, Palo Alto, CA 94304 USA
来源
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK | 2017年 / 15卷 / 10期
关键词
OVARIAN SUPPRESSION; RECEPTOR STATUS; ADJUVANT; SURVIVAL; THERAPY; AGE; SUBTYPE; RATES;
D O I
10.6004/jnccn.2017.0158
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Breast cancer in young women is associated with an aggressive tumor biology and higher risk of recurrence. Pathologic complete response (pCR) after neoadjuvant therapy has been shown to be a surrogate marker for disease-free survival (DFS) and overall survival (OS), but the association between pCR and survival outcomes in young women with breast cancer is not well described. Methods: This study included women aged <= 40 years at diagnosis who received neoadjuvant chemotherapy (NAC) for stage II-III invasive breast cancer between 1998 and 2014 at Massachusetts General Hospital. Outcomes were compared between patients who achieved pCR (ypT0/is, ypN0) and those with residual disease. Results: A total of 170 young women were included in the analytical data set, of which 53 (31.2%) achieved pCR after NAC. The 5-year DFS rate for patients with and without pCR was 91% versus 60%, respectively (P<.01), and the OS rate was 95% versus 75%, respectively (P<.01). Among patients with pCR, no difference was seen in OS irrespective of baseline clinical stage (P=.6), but among patients with residual disease after NAC, a significant difference in OS based on baseline clinical stage was observed (P<.001). Conclusions: Our results suggest pCR after NAC is strongly associated with significantly improved DFS and OS in young women with breast cancer, and perhaps even more so than baseline stage. However, the significantly higher mortality for patients who did not attain pCR highlights the need for better therapies, and the neoadjuvant trial design could potentially serve as an efficient method for rapid triage and escalation/de-escalation of therapies to improve outcomes for young women with breast cancer.
引用
收藏
页码:1216 / 1223
页数:8
相关论文
共 29 条
[1]   Poor outcome of hormone receptor-positive breast cancer at very young age is due to tamoxifen resistance: Nationwide survival data in Korea - A report from the Korean Breast Cancer Society [J].
Ahn, Sei Hyun ;
Son, Byung Ho ;
Kim, Seok Won ;
Kim, Seung Il ;
Jeong, Joon ;
Ko, Seung-Sang ;
Han, Wonshik .
JOURNAL OF CLINICAL ONCOLOGY, 2007, 25 (17) :2360-2368
[2]   Breast Cancer Before Age 40 Years [J].
Anders, Carey K. ;
Johnson, Rebecca ;
Litton, Jennifer ;
Phillips, Marianne ;
Bleyer, Archie .
SEMINARS IN ONCOLOGY, 2009, 36 (03) :237-249
[3]   Response to Neoadjuvant Systemic Therapy for Breast Cancer in BRCA Mutation Carriers and Noncarriers: A Single-Institution Experience [J].
Arun, Banu ;
Bayraktar, Soley ;
Liu, Diane D. ;
Barrera, Angelica M. Gutierrez ;
Atchley, Deann ;
Pusztai, Lajos ;
Litton, Jennifer Keating ;
Valero, Vicente ;
Meric-Bernstam, Funda ;
Hortobagyi, Gabriel N. ;
Albarracin, Constance .
JOURNAL OF CLINICAL ONCOLOGY, 2011, 29 (28) :3739-3746
[4]   Neoadjuvant Therapy as a Platform for Drug Development and Approval in Breast Cancer [J].
Bardia, Aditya ;
Baselga, Jose .
CLINICAL CANCER RESEARCH, 2013, 19 (23) :6360-6370
[5]   I-SPY 2: An Adaptive Breast Cancer Trial Design in the Setting of Neoadjuvant Chemotherapy [J].
Barker, A. D. ;
Sigman, C. C. ;
Kelloff, G. J. ;
Hylton, N. M. ;
Berry, D. A. ;
Esserman, L. J. .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 2009, 86 (01) :97-100
[6]   Neoadjuvant Therapy in Breast Cancer as a Basis for Drug Approval [J].
Berry, Donald A. ;
Hudis, Clifford A. .
JAMA ONCOLOGY, 2015, 1 (07) :875-876
[7]   Response to neo-adjuvant chemotherapy in women with BRCA1-positive breast cancers [J].
Byrski, T. ;
Gronwald, J. ;
Huzarski, T. ;
Grzybowska, E. ;
Budryk, M. ;
Stawicka, M. ;
Mierzwa, T. ;
Szwiec, M. ;
Wisniowski, R. ;
Siolek, M. ;
Narod, S. A. ;
Lubinski, J. .
BREAST CANCER RESEARCH AND TREATMENT, 2008, 108 (02) :289-296
[8]   Role of endocrine responsiveness and adjuvant therapy in very young women (below 35 years) with operable breast cancer and node negative disease [J].
Colleoni, M. ;
Rotmensz, N. ;
Peruzzotti, G. ;
Maisonneuve, P. ;
Orlando, L. ;
Ghisini, R. ;
Viale, G. ;
Pruneri, G. ;
Veronesi, P. ;
Luini, A. ;
Intra, M. ;
Cardillo, A. ;
Torrisi, R. ;
Rocca, A. ;
Goldhirsch, A. .
ANNALS OF ONCOLOGY, 2006, 17 (10) :1497-1503
[9]   Pathological complete response and long-term clinical benefit in breast cancer: the CTNeoBC pooled analysis [J].
Cortazar, Patricia ;
Zhang, Lijun ;
Untch, Michael ;
Mehta, Keyur ;
Costantino, Joseph P. ;
Wolmark, Norman ;
Bonnefoi, Herve ;
Cameron, David ;
Gianni, Luca ;
Valagussa, Pinuccia ;
Swain, Sandra M. ;
Prowell, Tatiana ;
Loibl, Sibylle ;
Wickerham, D. Lawrence ;
Bogaerts, Jan ;
Baselga, Jose ;
Perou, Charles ;
Blumenthal, Gideon ;
Blohmer, Jens ;
Mamounas, Eleftherios P. ;
Bergh, Jonas ;
Semiglazov, Vladimir ;
Justice, Robert ;
Eidtmann, Holger ;
Paik, Soonmyung ;
Piccart, Martine ;
Sridhara, Rajeshwari ;
Fasching, Peter A. ;
Slaets, Leen ;
Tang, Shenghui ;
Gerber, Bernd ;
Geyer, Charles E., Jr. ;
Pazdur, Richard ;
Ditsch, Nina ;
Rastogi, Priya ;
Eiermann, Wolfgang ;
von Minckwitz, Gunter .
LANCET, 2014, 384 (9938) :164-172
[10]   Breast Cancer Statistics, 2015: Convergence of Incidence Rates Between Black and White Women [J].
DeSantis, Carol E. ;
Fedewa, Stacey A. ;
Sauer, Ann Goding ;
Kramer, Joan L. ;
Smith, Robert A. ;
Jemal, Ahmedin .
CA-A CANCER JOURNAL FOR CLINICIANS, 2016, 66 (01) :31-42