Systemic Therapy for Patients With Advanced Human Epidermal Growth Factor Receptor 2-Positive Breast Cancer: American Society of Clinical Oncology Clinical Practice Guideline

被引:267
作者
Giordano, Sharon H. [1 ]
Temin, Sarah [3 ]
Kirshner, Jeffrey J. [4 ]
Chandarlapaty, Sarat [5 ]
Crews, Jennie R. [7 ]
Davidson, Nancy E. [8 ,9 ]
Esteva, Francisco J. [6 ]
Gonzalez-Angulo, Ana M. [1 ]
Krop, Ian
Levinson, Jennifer
Lin, Nancy U. [10 ]
Modi, Shanu [5 ]
Patt, Debra A. [2 ]
Perez, Edith A. [11 ]
Perlmutter, Jane
Ramakrishna, Naren [12 ]
Winer, Eric P. [10 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[2] Texas Oncol, Austin, TX USA
[3] Amer Soc Clin Oncol, Alexandria, VA 22314 USA
[4] Hematol Oncol Associates Cent New York, East Syracuse, NY USA
[5] Mem Sloan Kettering Canc Ctr, New York, NY 10021 USA
[6] NYU, Inst Canc, New York, NY USA
[7] PeaceHealth St Joseph Canc Ctr, Bellingham, WA USA
[8] Univ Pittsburgh, Inst Canc, Pittsburgh, PA USA
[9] Univ Pittsburgh, Med Ctr, Ctr Canc, Pittsburgh, PA USA
[10] Dana Farber Canc Inst, Boston, MA 02115 USA
[11] Mayo Clin, Jacksonville, FL USA
[12] Univ Florida, Orlando Hlth, Hlth Canc Ctr, Orlando, FL USA
关键词
LAPATINIB PLUS CAPECITABINE; PHASE-II; TRASTUZUMAB; WOMEN; COMBINATION; SURVIVAL; PROGNOSIS; DISEASE; RECOMMENDATIONS; PERTUZUMAB;
D O I
10.1200/JCO.2013.54.0948
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose To provide evidence-based recommendations to practicing oncologists and others on systemic therapy for patients with human epidermal growth factor receptor 2 (HER2) -positive advanced breast cancer. Methods The American Society of Clinical Oncology convened a panel of medical oncology, radiation oncology, guideline implementation, and advocacy experts and conducted a systematic literature review from January 2009 to October 2012. Outcomes of interest included overall survival, progression-free survival (PFS), and adverse events. Results A total of 16 trials met the systematic review criteria. The CLEOPATRA trial found survival and PFS benefits for docetaxel, trastuzumab, and pertuzumab in first-line treatment, and the EMILIA trial found survival and PFS benefits for trastuzumab emtansine (T-DM1) in second-line treatment. T-DM1 also showed a third-line PFS benefit. One trial reported on duration of HER2-targeted therapy, and three others reported on endocrine therapy for patients with HER-positive advanced breast cancer. Recommendations HER2-targeted therapy is recommended for patients with HER2-positive advanced breast cancer, except for those with clinical congestive heart failure or significantly compromised left ventricular ejection fraction, who should be evaluated on a case-by-case basis. Trastuzumab, pertuzumab, and taxane for first-line treatment and T-DM1 for second-line treatment are recommended. In the third-line setting, clinicians should offer other HER2-targeted therapy combinations or T-DM1 (if not previously administered) and may offer pertuzumab, if the patient has not previously received it. Optimal duration of chemotherapy is at least 4 to 6 months or until maximum response, depending on toxicity and in the absence of progression. HER2-targeted therapy can continue until time of progression or unacceptable toxicities. For patients with HER2-positive and estrogen receptor-positive/progesterone receptor-positive breast cancer, clinicians may recommend either standard first-line therapy or, for selected patients, endocrine therapy plus HER2-targeted therapy or endocrine therapy alone. (c) 2014 by American Society of Clinical Oncology
引用
收藏
页码:2078 / U148
页数:23
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