Trastuzumab Deruxtecan or Ramucirumab plus Paclitaxel in Gastric Cancer.

IF 96.2 1区 医学 Q1 MEDICINE, GENERAL & INTERNAL
Kohei Shitara, Eric Van Cutsem, Mahmut Gümüş, Sara Lonardi, Christelle de la Fouchardière, Clélia Coutzac, Jeroen Dekervel, Daniel Hochhauser, Lin Shen, Wasat Mansoor, Bo Liu, Lorenzo Fornaro, Min-Hee Ryu, Jeeyun Lee, Cátia Faustino, Jean-Philippe Metges, Josep Tabernero, Fábio Franke, Yelena Y Janjigian, Fabricio Souza, Lori Jukofsky, Yumin Zhao, Takahiro Kamio, Aziz Zaanan, Filippo Pietrantonio
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引用次数: 0

Abstract

Background: On the basis of phase 2 studies, trastuzumab deruxtecan was approved for patients with human epidermal growth factor receptor 2 (HER2)-positive metastatic gastric cancer or gastroesophageal junction adenocarcinoma who had previously received trastuzumab-based therapy. Ramucirumab plus paclitaxel is also a standard second-line treatment option regardless of HER2 status.

Methods: We conducted an international, randomized, phase 3 trial comparing second-line trastuzumab deruxtecan at a dose of 6.4 mg per kilogram of body weight with ramucirumab plus paclitaxel in patients with HER2-positive metastatic gastric cancer or gastroesophageal junction adenocarcinoma confirmed on tumor biopsy conducted after the patient had progression while receiving trastuzumab-based therapy. The primary end point was overall survival. Secondary end points included progression-free survival, confirmed objective response (complete or partial response lasting ≥4 weeks), disease control, duration of response, and safety.

Results: Among 494 patients who had undergone randomization, overall survival was significantly longer with trastuzumab deruxtecan than with ramucirumab plus paclitaxel (median, 14.7 vs. 11.4 months; hazard ratio for death, 0.70; 95% confidence interval, 0.55 to 0.90; P = 0.004). Significant results were also seen with regard to progression-free survival (hazard ratio for disease progression or death, 0.74; 95% CI, 0.59 to 0.92) and confirmed objective response (in 44.3% of the patients in the trastuzumab deruxtecan group vs. 29.1% of those in the ramucirumab-paclitaxel group). The incidence of drug-related adverse events of any grade was 93.0% with trastuzumab deruxtecan and 91.4% with ramucirumab plus paclitaxel; the incidence of drug-related adverse events of grade 3 or higher was 50.0% and 54.1%, respectively. Adjudicated drug-related interstitial lung disease or pneumonitis occurred in 13.9% of the patients who received trastuzumab deruxtecan (grade 1 or 2 in 33 patients and grade 3 in 1) and in 1.3% of those who received ramucirumab plus paclitaxel (grade 3 in 2 patients and grade 5 in 1).

Conclusions: Trastuzumab deruxtecan led to significantly longer overall survival than ramucirumab plus paclitaxel among patients with HER2-positive metastatic gastric cancer or gastroesophageal junction adenocarcinoma. Adverse events were common in both groups. Events of interstitial lung disease or pneumonitis with trastuzumab deruxtecan, a known risk, were mainly low-grade. (Funded by Daiichi Sankyo and AstraZeneca; DESTINY-Gastric04 ClinicalTrials.gov number, NCT04704934.).

曲妥珠单抗、德鲁西替康或Ramucirumab联合紫杉醇治疗胃癌。
背景:在2期研究的基础上,曲妥珠单抗德鲁西替康被批准用于先前接受过曲妥珠单抗为基础治疗的人表皮生长因子受体2 (HER2)阳性转移性胃癌或胃食管交界处腺癌患者。无论HER2状态如何,Ramucirumab +紫杉醇也是标准的二线治疗选择。方法:我们进行了一项国际、随机、3期试验,比较了在接受曲妥珠单抗为基础的治疗后发生进展的her2阳性转移性胃癌或胃食管结腺癌患者中,每公斤体重6.4 mg剂量的二线曲妥珠单抗德鲁西替康与ramucirumab加紫杉醇的疗效。主要终点为总生存期。次要终点包括无进展生存期、确认的客观缓解(完全或部分缓解持续≥4周)、疾病控制、缓解持续时间和安全性。结果:在接受随机分组的494例患者中,曲妥珠单抗德鲁西替康组的总生存期明显长于拉穆单抗加紫杉醇组(中位,14.7个月vs 11.4个月;死亡风险比0.70;95%置信区间为0.55 ~ 0.90;p = 0.004)。在无进展生存方面也有显著的结果(疾病进展或死亡的风险比,0.74;95% CI, 0.59 - 0.92)和证实的客观缓解(曲妥珠单抗-德鲁德替康组44.3%的患者vs.雷默单抗-紫杉醇组29.1%的患者)。任何级别的药物相关不良事件的发生率,曲妥珠单抗德鲁西替康组为93.0%,拉穆单抗联合紫杉醇组为91.4%;3级及以上药物相关不良事件发生率分别为50.0%和54.1%。在接受曲妥珠单抗德鲁西替康治疗的患者中,13.9%的患者发生了药物相关性间质性肺病或肺炎(33例患者为1级或2级,1例为3级),而接受拉穆单抗加紫杉醇治疗的患者中,这一比例为1.3%(2例患者为3级,1例为5级)。结论:在her2阳性转移性胃癌或胃食管交界腺癌患者中,曲妥珠单抗德鲁西替康的总生存期明显长于ramucirumab加紫杉醇。不良事件在两组中都很常见。服用曲妥珠单抗后发生间质性肺病或肺炎的风险主要为低级别。(由Daiichi Sankyo和AstraZeneca资助;DESTINY-Gastric04 ClinicalTrials.gov编号:NCT04704934)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
New England Journal of Medicine
New England Journal of Medicine 医学-医学:内科
CiteScore
145.40
自引率
0.60%
发文量
1839
审稿时长
1 months
期刊介绍: The New England Journal of Medicine (NEJM) stands as the foremost medical journal and website worldwide. With an impressive history spanning over two centuries, NEJM boasts a consistent publication of superb, peer-reviewed research and engaging clinical content. Our primary objective revolves around delivering high-caliber information and findings at the juncture of biomedical science and clinical practice. We strive to present this knowledge in formats that are not only comprehensible but also hold practical value, effectively influencing healthcare practices and ultimately enhancing patient outcomes.
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