# Real-world validation of ECOG performance status and neutrophil-to-lymphocyte ratio in second-line paclitaxel plus ramucirumab for advanced gastric cancer

**Authors:** Hong Cheng, Lulu Sun, Xinyue Wang, Yixia Wang, Yu Chen, Kejin Cai, Xiaoli Hou

PMC · DOI: 10.1515/biol-2025-1191 · Open Life Sciences · 2026-02-24

## TL;DR

This study confirms that ECOG performance status and neutrophil-to-lymphocyte ratio predict outcomes in patients with advanced gastric cancer treated with paclitaxel and ramucirumab.

## Contribution

Validates ECOG and NLR as prognostic factors in real-world use of paclitaxel-ramucirumab for advanced gastric cancer.

## Key findings

- Median overall survival was 8.3 months and progression-free survival was 4.2 months.
- ECOG 0–1 and low neutrophil-to-lymphocyte ratio were associated with longer survival.
- Treatment showed manageable toxicity with grade ≥3 events in 33% of patients.

## Abstract

Advanced gastric cancer (AGC) has a poor prognosis; better second-line options are needed. We retrospectively reviewed 130 AGC patients treated at one center with paclitaxel 80 mg/m2 (days 1, 8, 15) plus ramucirumab 8 mg/kg (days 1, 15) every 28 days after failure of platinum/fluoropyrimidine therapy. Kaplan–Meier curves estimated overall (OS) and progression-free survival (PFS); Cox models identified prognostic factors. Median OS was 8.3 months (95 % CI 6.9–9.7) and median PFS 4.2 months (95 % CI 3.3–5.1); 12-month OS was 31.8 %. Objective response and disease-control rates were 19.2 % and 50.0 %, respectively. Grade ≥ 3 toxicity occurred in 33 % of patients, mainly neutropenia (19 %) and neuropathy (14 %). Multivariable analysis linked longer OS to ECOG 0–1 (HR 0.54, p = 0.011) and a low neutrophil-to-lymphocyte ratio (HR 0.59, p = 0.017). In this real-world single-center cohort, paclitaxel plus ramucirumab provided clinically meaningful benefit with manageable toxicity. ECOG performance status and NLR confirmed their prognostic value in this real-world cohort. Further multicenter studies may refine patient selection and optimize outcomes. Clinically, ECOG and NLR can be used to communicate prognosis, tailor follow-up/supportive care, and stratify patients in routine practice receiving paclitaxel–ramucirumab.

## Linked entities

- **Chemicals:** paclitaxel (PubChem CID 36314)
- **Diseases:** gastric cancer (MONDO:0001056)

## Full-text entities

- **Genes:** CSF3 (colony stimulating factor 3) [NCBI Gene 1440] {aka C17orf33, CSF3OS, GCSF}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, KDR (kinase insert domain receptor) [NCBI Gene 3791] {aka CD309, FLK1, VEGFR, VEGFR2}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, VEGFA (vascular endothelial growth factor A) [NCBI Gene 7422] {aka L-VEGF, MVCD1, VEGF, VPF}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}
- **Diseases:** PD (MESH:D010300), NLR (MESH:D015467), inflammation (MESH:D007249), lymphopenia (MESH:D008231), cancer (MESH:D009369), fatigue (MESH:D005221), AGC (MESH:D013274), non-melanoma skin cancer (MESH:D012878), Proteinuria (MESH:D011507), neutrophilia (MESH:C563010), Hypertension (MESH:D006973), hematologic and non-hematologic toxicities (MESH:D006402), death (MESH:D003643), neutropenia (MESH:D009503), metastasis (MESH:D009362), Toxicities (MESH:D064420), peritoneal (MESH:D010538), gastrointestinal-cancer (MESH:D005770), peripheral neuropathy (MESH:D010523), heart failure (MESH:D006333), neuropathy (MESH:D009422), MSI-H (MESH:D000848)
- **Chemicals:** Platinum (MESH:D010984), Ramucirumab (MESH:C543333), trastuzumab (MESH:D000068878), Paclitaxel (MESH:D017239), irinotecan (MESH:D000077146), ECOG (-), fruquintinib (MESH:C000591844), sintilimab (MESH:C000632826), taxanes (MESH:D043823), docetaxel (MESH:D000077143), creatinine (MESH:D003404), taxane (MESH:C080625), nivolumab (MESH:D000077594)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

32 references — full list in the complete paper: https://tomesphere.com/paper/PMC12927453/full.md

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Source: https://tomesphere.com/paper/PMC12927453