Efficacy and Safety of Paclitaxel Plus Ramucirumab as Second-Line Therapy in Advanced Gastric Cancer: A Retro-Prospective Single-Centre Study.

The Gulf journal of oncology Pub Date : 2025-09-01
Varun Goel, Arpit Jain, Nivedita Patnaik, Dharmistha Basu, Shaifali Goel, Akanksha Jaju, Vineet Talwar, Shivendra Singh
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Abstract

Background: Advanced gastric cancer (AGC) has limited treatment options beyond first-line therapy. The combination of paclitaxel and ramucirumab is an approved second-line regimen. This study evaluates the real-world efficacy and safety of this combination in Indian patients.

Aim: To assess the effectiveness and tolerability of paclitaxel plus ramucirumab in advanced gastric/gastroesophageal junction adenocarcinoma in a real-world setting.

Materials and methods: This retro-prospective study included 85 patients with AGC treated between January 2020 and December 2024 at a tertiary cancer centre in North India. Patients received paclitaxel 80 mg/m² on days 1, 8, and 15, and ramucirumab 8 mg/kg on days 1 and 15 of a 28-day cycle. The primary endpoint was progression-free survival (PFS); secondary endpoints included overall survival (OS), objective response rate (ORR), disease control rate (DCR), and safety.

Results: The median age was 58 years; 71% were male. ECOG PS 0-1 was present in 70%. Prior gastrectomy was reported in 36%. Median PFS was 5.1 months, and OS was 9.3 months. ORR was 27%, and DCR was 66%. Common grade 3/4 adverse events included neutropenia (19%), neuropathy (13%), and hypertension (9%).

Conclusion: Paclitaxel plus ramucirumab is effective and well-tolerated as second-line treatment in Indian AGC patients. Outcomes mirror global data and support its continued use in resource-limited settings.

紫杉醇联合Ramucirumab作为二线治疗晚期胃癌的疗效和安全性:一项回顾性前瞻性单中心研究
背景:晚期胃癌(AGC)在一线治疗之外的治疗选择有限。紫杉醇联合ramucirumab是一种被批准的二线治疗方案。本研究评估了这种组合在印度患者中的实际疗效和安全性。目的:在现实世界中评估紫杉醇联合ramucirumab治疗晚期胃/胃食管交界处腺癌的有效性和耐受性。材料和方法:这项回顾性前瞻性研究纳入了2020年1月至2024年12月在印度北部三级癌症中心接受治疗的85例AGC患者。患者在28天周期的第1、8和15天接受紫杉醇80 mg/ m2,在第1和15天接受ramucirumab 8 mg/kg。主要终点是无进展生存期(PFS);次要终点包括总生存期(OS)、客观缓解率(ORR)、疾病控制率(DCR)和安全性。结果:中位年龄58岁;71%为男性。70%出现ECOG PS 0-1。36%的患者曾做过胃切除术。中位PFS为5.1个月,OS为9.3个月。ORR为27%,DCR为66%。常见的3/4级不良事件包括中性粒细胞减少(19%)、神经病变(13%)和高血压(9%)。结论:紫杉醇联合ramucirumab作为印度AGC患者的二线治疗有效且耐受性良好。结果反映了全球数据,并支持在资源有限的情况下继续使用。
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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