Incidence and prognostic impact of HER2-positivity loss after dual HER2-directed neoadjuvant therapy for HER2+breast cancer

被引:5
作者
LeVee, Alexis [1 ,2 ]
Spector, Kellie [1 ,3 ]
Larkin, Brigid [1 ]
Dezem, Felipe [4 ]
Plummer, Jasmine [4 ]
Dadmanesh, Farnaz [5 ]
Patil, Sujata [6 ]
McArthur, Heather L. L. [1 ,7 ]
机构
[1] Cedars Sinai Med Ctr, Dept Med, Los Angeles, CA USA
[2] City Hope Comprehens Canc Ctr, Dept Med Oncol & Therapeut Res, Duarte, CA USA
[3] Olive View UCLA Med Ctr, Dept Med, Los Angeles, CA USA
[4] Cedars Sinai Med Ctr, Ctr Bioinformat & Funct Genom, Dept Biomed Sci, Los Angeles, CA USA
[5] Cedars Sinai Med Ctr, Dept Pathol, Los Angeles, CA USA
[6] Cleveland Clin, Taussig Canc Inst, Dept Quantitat Hlth Sci, Cleveland, OH USA
[7] Univ Texas Southwestern, Dept Med, Dallas, TX 75390 USA
关键词
breast cancer; discordance; dual; HER2; neoadjuvant therapy; BREAST-CANCER; HORMONE-RECEPTORS; CHEMOTHERAPY; HER2; TRASTUZUMAB; AMPLIFICATION; PACLITAXEL; EXPRESSION;
D O I
10.1002/cam4.5817
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Loss of HER2 "positivity" can occur in patients with residual disease after neoadjuvant treatment, but the incidence of HER2-positivity loss after neoadjuvant dual HER2-targeted treatment plus chemotherapy, the current standard-of-care for most early stage HER2-positive breast cancers, is not well described. Previous studies that report the HER2 discordance rate after neoadjuvant treatment also do not include the novel HER2-low category. In this retrospective study, we determine the incidence and prognostic impact of HER2-positivity loss, including the evolution to HER2-low disease, after neoadjuvant dual HER2-targeted therapy with chemotherapy.Methods: Clinicopathologic data for patients with stage I-III HER2+ breast cancer diagnosed between 2015 and 2019 were reviewed in this single institution retrospective study. Patients who received dual HER2-targeted treatment with chemotherapy were included, and HER2 status before and after neoadjuvant therapy was interrogated.Results: A total of 163 female patients were included in the analysis with a median age of 50 years. A pathologic complete response (pCR as defined by ypT0/is) was achieved in 102 (62.5%) of 163 evaluable patients. Among the 61 patients with residual disease after neoadjuvant therapy, 36 (59.0%) had HER2-positive and 25 (41.0%) had HER2-negative residual disease. Of the 25 patients with HER2-negative residual disease, 22 (88%) of patients were classified as HER2-low. After a median follow-up of 3.3 years, patients who retained HER2-positivity after neoadjuvant treatment had a 3-year IDFS rate of 91% (95% CI, 91%-100%), while patients who lost HER2-positivity had a 3-year IDFS rate of 82% (95% CI, 67%-100%).Conclusion: Almost half of patients with residual disease following neoadjuvant dual HER2-targeted therapy plus chemotherapy lost HER2-positivity. The loss of HER2-positivity may not confer negative prognostic impact, although the results were limited by short follow-up time. Further research on the HER2 status after neoadjuvant treatment may help guide treatment decisions in the adjuvant setting.
引用
收藏
页码:10647 / 10659
页数:13
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