Clinical Experience with Simultaneous Mixed Infusion of Trastuzumab and Pertuzumab in the Neo-Peaks Study (JBCRG-20 Sub-Study).

Q4 Medicine Japanese Journal of Cancer and Chemotherapy Pub Date : 2024-09-01
Hiroko Bando, Hiroyuki Yasojima, Kazushige Ishida, Kokoro Kobayashi, Hiroi Kasai, Masahiro Kashiwaba, Shinji Ohno, Satoshi Morita, Masakazu Toi, Norikazu Masuda
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Abstract

Dual human epidermal growth factor receptor 2(HER2)blockade with trastuzumab(H)and pertuzumab(P)combined with docetaxel and carboplatin(TCb)is a standard neoadjuvant therapy for HER2-positive breast cancer patients. We conducted this sub-study using data from the investigator-initiated randomized phase 2 JBCRG-20(Neo-peaks)study to evaluate the safety of simultaneous mixed HP infusion in Japanese patients, as there have been no data to date. A total of 204 patients in groups A-C received TCbHP, TCbHP followed by trastuzumab emtansine(T-DM1)+P, and T-DM1+P, respectively. Of the 103 patients in groups A and B who received H and P by sequential infusion in cycle 1, the 17(median age 59; range 29-69 years)who did not experience an infusion reaction(IF)received these agents as a mixed, single-bag infusion from cycle 2 onwards. No cases of IF were observed, thus 71 mixed doses were safely administered. Administration time was reduced to 60 min from cycle 3 onwards. Furthermore, in the group B patients, mixed HP infusion did not affect their subsequent treatment(i. e. 4 cycles of T-DM1+P). Simultaneous administration of H and P enables a reduced administration time, which would benefit both patients and healthcare providers.

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Neo-Peaks研究(JBCRG-20子研究)中同时混合输注曲妥珠单抗和帕妥珠单抗的临床经验。
曲妥珠单抗(H)和百妥珠单抗(P)联合多西他赛和卡铂(TCb)的双重人类表皮生长因子受体 2(HER2)阻断疗法是 HER2 阳性乳腺癌患者的标准新辅助疗法。我们利用研究者发起的随机 2 期 JBCRG-20(Neo-peaks)研究的数据开展了这项子研究,以评估在日本患者中同时混合输注 HP 的安全性,因为迄今为止还没有相关数据。A-C组共204名患者分别接受了TCbHP、TCbHP后曲妥珠单抗(T-DM1)+P和T-DM1+P治疗。A组和B组的103名患者在第一周期接受了H和P的序贯输注,其中17名患者(中位年龄59岁;范围29-69岁)未出现输注反应(IF),他们从第二周期起接受了这些药物的混合单袋输注。没有观察到 IF 病例,因此安全地使用了 71 种混合剂量。从第 3 个周期开始,给药时间缩短至 60 分钟。此外,在 B 组患者中,混合输注 HP 不会影响其后续治疗(即 4 个周期的 T-DM1+P 治疗)。同时输注 H 和 P 可以缩短给药时间,这对患者和医护人员都有好处。
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