Journal
CLINICAL & TRANSLATIONAL ONCOLOGY
Volume 25, Issue 4, Pages 941-958Publisher
SPRINGER INT PUBL AG
DOI: 10.1007/s12094-022-02998-2
Keywords
Breast cancer; Neoadjuvant; Human epidermal growth factor receptor; Lapatinib; Trastuzumab; Pathological complete response
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Through a systematic review, it was found that dual anti-HER2 blockade had a higher probability of achieving pathological complete response compared to monotherapy. Furthermore, dual treatment may lead to improved survival outcomes and tumor clinical response. For neoadjuvant treatment of HER2-positive breast cancer, the use of dual blockade with trastuzumab and pertuzumab is recommended.
Background We aimed to determine the effect of dual anti-HER2 blockade compared to monotherapy on clinically important outcomes. Methods We carried out a systematic review updated until July 2022. The outcomes included pathological complete response (pCR), clinical response, event-free survival, and overall survival. Results We identified eleven randomized clinical trials (2836 patients). When comparing paclitaxel plus dual treatment versus paclitaxel plus trastuzumab or lapatinib, dual treatment was associated with a higher probability of achieving a pathological complete response (OR 2.88, 95% CI 2.02-4.10). Addition of a taxane to an anthracycline plus cyclophosphamide and fluorouracil, plus lapatinib or trastuzumab, showed that the dual treatment was better than lapatinib alone (OR 2.47, 95% CI 1.41-4.34), or trastuzumab alone (OR 1.89, 95% CI 1.13-3.16). Dual treatment may result in an increase in survival outcomes and tumour clinical response, although such benefits are not consistent for all the combinations studied. Conclusions The use of dual blockade with combinations of trastuzumab and pertuzumab can be recommended for the neoadjuvant treatment of women with HER2-positive breast cancer. PROSPERO Registration number: CRD42018110273.
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