Kin Takanori, Ohtani Shoichiro, Maeda Reina, Ueno Ayako, Fujihara Miwa, Takamatsu Yuri, Kajiwara Yukiko, Ito Mitsuya, Kawasaki Kensuke, Abe Keisuke, Sakata Yasuhiko, Hiraki Koichi
Department of Breast Surgery, Hiroshima City Hiroshima Citizens Hospital, 7-33 Motomachi, Naka-ku, Hiroshima-shi, Hiroshima 730-8518, Japan.
Department of Breast and Endocrine Surgery, Okayama University, 2-5-1 Shikata-cho, Kita-ku, Okayama-shi, Okayama 700-0914, Japan.
World J Oncol. 2020 Oct;11(5):197-203. doi: 10.14740/wjon1333. Epub 2020 Oct 15.
The aim of this phase II study was to evaluate combined nab-paclitaxel (nab-PTX) with sequential anthracycline-based therapy as a neoadjuvant chemotherapy.
We enrolled 41 patients with advanced breast cancer (stage IIA - IIIC). All patients were to receive three-weekly nab-PTX (260 mg/m) for four cycles followed by three-weekly 5-fluorouracil, epirubicin and cyclophosphamide (FEC) for four cycles. Trastuzumab administration was permitted in human epidermal growth factor receptor 2 (HER2)-positive patients.
The overall pathological complete response (pCR) rate was 24% (10 of 41). In patients with luminal A, luminal B (HER2-), luminal B (HER2+), triple-negative and HER2, the pCR rates were 0% (0/2), 7% (1/14), 42% (3/7), 25% (4/16) and 100% (2/2), respectively. The most significant toxicities of nab-PTX were grade 2/3 peripheral sensory neuropathy (24%) and grade 3/4 neutropenia (26%). Febrile neutropenia was not observed in any patient. The most significant toxicities of FEC were grade 3/4 neutropenia (24%) and grade 3 febrile neutropenia (9%). One patient died of sepsis secondary to pneumonia during FEC treatment.
Neoadjuvant chemotherapy using nab-PTX with trastuzumab every 3 weeks followed by FEC was suitably tolerated and associated with a high pCR rate of 55% for patients with HER2-positive breast cancer.
本II期研究的目的是评估纳米白蛋白结合型紫杉醇(nab-PTX)联合序贯蒽环类药物治疗作为新辅助化疗的效果。
我们纳入了41例晚期乳腺癌患者(IIA-IIIC期)。所有患者接受每三周一次的nab-PTX(260mg/m²),共四个周期,随后接受每三周一次的5-氟尿嘧啶、表柔比星和环磷酰胺(FEC),共四个周期。人表皮生长因子受体2(HER2)阳性患者可使用曲妥珠单抗。
总体病理完全缓解(pCR)率为24%(41例中的10例)。在luminal A、luminal B(HER2阴性)、luminal B(HER2阳性)、三阴性和HER2亚型患者中,pCR率分别为0%(0/2)、7%(1/14)、42%(3/7)、25%(4/16)和100%(2/2)。nab-PTX最显著的毒性是2/3级周围感觉神经病变(24%)和3/4级中性粒细胞减少(26%)。未观察到任何患者发生发热性中性粒细胞减少。FEC最显著的毒性是3/4级中性粒细胞减少(24%)和3级发热性中性粒细胞减少(9%)。1例患者在FEC治疗期间死于肺炎继发的败血症。
每3周使用nab-PTX联合曲妥珠单抗,随后使用FEC的新辅助化疗耐受性良好,HER2阳性乳腺癌患者的pCR率高达55%。