局部晚期三阴性乳腺癌强化新辅助铂基化疗方案

M. Stenina, E. Glazkova, M. Frolova, A. Rumyantsev, A. Petrovsky, O.V. Krochina, Y. Vishnevskaya, O. Trofimova, A.A. Avalian, O. Gorbacheva, S. Tjulandin
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摘要

三阴性乳腺癌(TNBC)的高增殖潜能决定了强化新辅助化疗方案的重要性。患者和方法:80例局部晚期TNBC (IIIA、IIIB、IIIC期)患者纳入了一项非随机单臂II期研究。所有患者均接受新辅助化疗:阿霉素40 mg/m2 IV,紫杉醇160 mg/m2 IV,顺铂50 mg/m2 IV;第1天给药。计划进行8个疗程,间隔2周(有集落刺激因子),然后进行手术治疗和病理评估。主要终点为病理完全缓解率(pCR);第二个终点是5年总生存期(OS)、无病生存期(DFS)和毒性。统计假设:预计采用新的强化新辅助化疗方案将使pCR的发生率从40%增加到60%。考虑到1型误差(α = 0.05)和2型误差(β = 0.02)的水平,77名患者必须纳入研究。在这些条件下,研究的有效性为80%。结果:pCR检出率为62.5% (95% CI 50,9 - 73,1);5年OS - 74%, 5年DFS - 69%。主要毒性为:贫血(98.7%,包括3 - 37.5%);中性粒细胞减少症(85.0%,其中gr. 3-4 - 57.5%);发热性中性粒细胞减少症(3.7%);恶心(100%,包括3 - 3.8%),多神经病变(50.0%,包括3 - 8.7%)。结论:pCR检出率为62.5%,符合统计假设,该指标的规定频率大于60%。该方案疗效高,毒性可控,可作为局部晚期TNBC新辅助化疗的可能选择之一
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Intensified neoadjuvant platinum based chemotherapy regimen for locally advanced triple negative breast cancer
Introduction: The high proliferative potential of triple negative breast cancer (TNBC) determines the importance of intensifying neoadjuvant chemotherapy regimens. Patients and methods: 80 patients (pts) with locally advanced TNBC (stages IIIA, IIIB, IIIC) were included in a nonrandomized single-arm phase II study. All pts received neoadjuvant chemotherapy: doxorubicin 40 mg/m2 IV, paclitaxel 160 mg/m2 IV, cisplatin 50 mg/m2 IV; all drugs were administered on the 1st day. It was planned to conduct 8 courses with an interval of 2 weeks (with colony-stimulating factors) followed by surgical treatment and pathological assessment. The primary end point was the rate of pathological complete response (pCR); the second end points were 5-year overall survival (OS), disease-free survival (DFS) and toxicity. Statistical hypothesis: it was expected that the use of a new intensified regimen of neoadjuvant chemotherapy would increase the incidence of pCR from 40% to 60%. Given the level of type 1 error (α = 0,05) and type 2 error (β = 0,2), 77 pts had to be included in the study. Under these conditions, the power of the study was 80%. Results: the rate of pCR was 62.5% (95% CI 50,9–73,1); 5-year OS – 74%, 5-year DFS – 69%. The main toxicity was: anemia (98.7% pts, including gr. 3 – 37,5% pts); neutropenia (85.0% pts, including gr. 3–4 – 57,5% pts; febrile neutropenia – 3,7% pts); nausea (100% pts, including gr. 3 – 3,8% pts), polyneuropathy (50.0% pts, including gr. 3 – 8,7% pts). Conclusion: the rate of pCR was 62.5%, which corresponds to the statistical hypothesis with the stated frequency of this indicator of more than 60%. High efficacy and controlled toxicity allow us to consider the studied regimen as one of the possible options for neoadjuvant chemotherapy for locally advanced TNBC
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