Clinical outcomes according to molecular subtypes in stage II-III breast cancer patients treated with neoadjuvant chemotherapy followed by surgery and radiotherapy

被引:12
|
作者
Kim, Hakyoung [1 ]
Park, Won [1 ]
Huh, Seung Jae [1 ]
Choi, Doo Ho [1 ]
Noh, Jae Myoung [1 ]
Im, Young-Hyuck [2 ]
Ahn, Jin Seok [2 ]
Park, Yeon Hee [2 ]
Nam, Seok Jin [3 ]
Kim, Seok Won [3 ]
Lee, Jeong Eon [3 ]
Cho, Eun Yoon [4 ]
机构
[1] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Radiat Oncol, 81 Irwon Ro, Seoul 06351, South Korea
[2] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Med, Seoul, South Korea
[3] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Surg, Seoul, South Korea
[4] Sungkyunkwan Univ, Sch Med, Samsung Med Ctr, Dept Pathol, Seoul, South Korea
关键词
breast cancer; molecular subtypes; neo-adjuvant chemotherapy; radiotherapy; INTERNATIONAL EXPERT CONSENSUS; PARALLEL HER2-NEGATIVE COHORT; CONTROLLED SUPERIORITY TRIAL; GENE-EXPRESSION PROFILES; ADJUVANT CHEMOTHERAPY; PRIMARY THERAPY; TRASTUZUMAB; CLASSIFICATION; MULTICENTER; HIGHLIGHTS;
D O I
10.1111/ajco.12652
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: We evaluated the tumor response and clinical outcomes according to molecular subtypes in stage II-III breast cancer patients who received neo-adjuvant chemotherapy (NAC) followed by surgery and radiotherapy. Methods: We retrospectively analyzed 329 patients with clinical stage II-III breast cancer who received NAC followed by surgery and radiotherapy. Luminal A and B, HER2-enriched and triple-negative subgroups were identified. Results: The overall pathologic complete response (pCR) rate after NAC was 20.1% and the HER2-enriched subgroup had the highest pCR rate (43.6%), whereas luminal A showed the lowest rate of pCR (4.6%). The median follow-up duration was 55 months (range, 5-98 months). The 5-year overall survival (OS) and disease-free survival (DFS) rates were 88.9% and 72.9%, respectively. In subgroup analysis, according to the pathologic response (pCR vs non-pCR), the triple-negative subtype exhibited a significant difference in 5-year OS rate (100.0% vs 71.6%, P = 0.005) and 5-year DFS rate (93.1% vs 55.1%, P < 0.001). A distinct survival difference according to molecular subtype was found, particularly in the non-pCR group (5-year OS and DFS, P < 0.001, respectively). Conclusions: The non-pCR group showed significantly decreased 5-year OS and DFS rates compared to the pCR group, especially in triple negative and HER2-enriched breast cancer patients. A significant difference in survival rates and molecular subtypes was found in patients who failed to attain pCR.
引用
收藏
页码:329 / 336
页数:8
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