Skip to content
Open access

Real-world treatment patterns and survival outcomes in HER2-positive metastatic gastric cancer

Aug 2026 · Akademik Gastroenteroloji Dergisi · Vol 25, pp. 100-108 · 0 citations · 12 references

TL;DR

Human epidermal growth factor receptor 2-positive metastatic gastric cancer remains associated with poor survival and limited real-world access to novel agents, and there is an ongoing need for more effective therapies and better implementation of new treatments in routine practice.

Abstract

Background and Aims: Despite the evolution in management of metastatic human epidermal growth factor receptor-2 gastric cancer over the past decade, challenges remain in accessing new therapies in some parts of the world. We aimed to describe real-world treatment patterns, attrition, and survival outcomes in patients with human epidermal growth factor receptor 2-positive metastatic gastric cancer. Materials and Methods: This retrospective cohort study included patients aged ≥ 18 years with human epidermal growth factor receptor 2-positive metastatic gastric cancer who received at least one line of systemic antineoplastic therapy between January 1, 2015, and December 30, 2024. The primary outcome of the study was to define treatment choices and attrition rates in real-world clinical practice. Secondary endpoints were progression-free survival across treatment lines and overall survival. Results: Thirty-nine patients were included; median age was 65.5 years (min - max, 24.2 - 82.9), and 74.4% were male. The most common first-line regimens were oxaliplatin + 5-fluorouracil plus trastuzumab (38.5%) and docetaxel + cisplatin + 5-fluorouracil plus trastuzumab (25.6%); 15.4% did not receive trastuzumab, and no patient received pembrolizumab as first-line treatment. Median first-line progression-free survival was 7.49 months (95% CI 5.56 - 9.42), and median overall survival was 16.53 months (95% CI 12.56 - 20.49). Overall, 68.4% of patients received second-line therapy, 41.0% received third-line therapy, and 10.3% proceeded to fourth-line treatment. Second-line treatment was predominantly irinotecan + 5-fluorouracil-based, while paclitaxel was the most frequent third-line regimen. Median progression-free survival was 3.35 months (95% CI 3.02 - 3.68) in the second line and 2.69 months (95% CI 2.28 - 3.10) in the third-line setting. Disease progression was the leading cause of treatment discontinuation across all lines. Conclusion: Human epidermal growth factor receptor-2-positive metastatic gastric cancer remains associated with poor survival and limited real-world access to novel agents. There is an ongoing need for more effective therapies and better implementation of new treatments in routine practice.

Read PDF

Similar papers

Open access Sep 2026

Real-world treatment patterns and associated outcomes in patients with HER2-positive unresectable or metastatic breast cancer: the HER2 REAL Study.

BACKGROUND The HER2 REAL (NCT04857619) retrospective study explored treatment practices and survival outcomes in patients with human epidermal growth factor receptor 2 (HER2)-positive unresectable breast cancer/metastatic breast cancer (mBC) in routine clinical care across six countries. METHODS Adult patients (≥18 y...

S. C. Lee, C. Barrios, W. Chung et al. · 0 citations
Sep 2026

Real-world outcomes of ribociclib treatment in HR-positive/HER2-negative metastatic breast cancer: efficacy, safety, and prognostic factors.

BACKGROUND This study evaluated the real-world efficacy, safety, and prognostic factors associated with progression-free survival (PFS) in patients with HR-positive/HER2-negative metastatic breast cancer treated with ribociclib. RESEARCH DESIGN AND METHODS This retrospective single-center study included 110 patients...

Salih Karatlı, D. Yazılıtaş, Mustafa Altınbaş · 0 citations
Review Open access Sep 2026

Treatment patterns and clinical outcomes among patients with metastatic castration-resistant prostate cancer: a multinational retrospective medical record review.

In a population where few had received treatment intensification for metastatic hormone-sensitive prostate cancer, real-world outcomes were aligned with those observed previously and in clinical trials, however, there remains significant need to broaden access to effective systemic therapy in mCRPC and to find new trea...

Robert J. Jones, Katherine Houghton, A. Niyazov et al. · 0 citations
Open access Sep 2026

Real-world treatment landscape and clinical outcomes in first-line advanced or metastatic gastroesophageal adenocarcinoma in the United States

Abstract Background Contemporary real-world evidence in advanced gastric, gastroesophageal junction, or esophageal adenocarcinoma (GC/GEJC/EAC) remains limited. This study evaluated real-world treatment patterns and clinical outcomes in patients with advanced GC/GEJC/EAC treated with first-line therapy in the United St...

Jin Gu, S. Mhatre, D. O. Koralek et al. · 0 citations
Open access Sep 2026

Use of Metronomic Chemotherapy in Hormone Receptor‐Positive/HER2‐Negative Metastatic Breast Cancer: A Retrospective Multicenter Study

ABSTRACT Purpose The optimal chemotherapy strategy after progression on cyclin‐dependent kinase 4/6 inhibitors (CDK4/6i) in hormone receptor‐positive/human epidermal growth factor receptor 2‐negative (HR+/HER2−) metastatic breast cancer remains a matter of controversy. This study evaluated the efficacy of metronomic ch...

Lara Laini, D. Cosentini, M. Laganà et al. · 0 citations
Open access Sep 2026

A multicenter retrospective study on the clinical features of patients with human epidermal growth factor receptor 2-positive colorectal cancer (HGCSG2304).

BACKGROUND In metastatic colorectal cancer (mCRC), human epidermal growth factor receptor 2 (HER2)-positive disease is a molecular subtype for targeted therapy; however, real-world data remain limited. METHODS A multicenter retrospective study of patients with HER2-positive mCRC diagnosed between 2010 and 2023 at 14...

S. Kaneko, K. Sawada, K. Hatanaka et al. · 0 citations

We use cookies to run the site and, with your consent, for analytics and to show ads. See our Cookie Policy.