Evidence map›Paper›PMID 41331488›Full record

Observational studyEuropean journal of medical research2025

Real-world application of surufatinib in the treatment of neuroendocrine tumors: a multi-center retrospective study in China.

Xiaoli Gao, Caitong Zhao, Fangxu Liu, Renzheng Chen, Xiang Yu, Jiahe Zhao, Yingchun Li, Jian Ming, Shuang Zhang, Bona Liu

Abstract readMulticenter StudyObservational Study
In one paragraph

Observational study in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Xiaoli Gao *Department of Oncology, The General Hospital of Northern Theater Command, Shenyang, China.
Caitong Zhao *Department of Quality Control, The General Hospital of Northern Theater Command, Shenyang, China.
Fangxu Liu *Department of Cardiac Surgery, The General Hospital of Northern Theater Command, Shenyang, China.
Renzheng ChenDepartment of Emergency, The 967, Hospital of Joint Logistics Support Force of Chinese PLA, Dalian, China.
Xiang YuDepartment of Clinical Pharmacy, Shenyang Pharmaceutical University, Shenyang, China.
Jiahe ZhaoDepartment of Internal Medicine, Flushing Hospital Medical Center, Flushing, NY, USA.
Yingchun LiDepartment of Pathology, The General Hospital of Northern Theater Command, Shenyang, China.
Jian MingDepartment of Pathology, The General Hospital of Northern Theater Command, Shenyang, China. mjjgc7878@hotmail.com.
Shuang ZhangDepartment of Military Medical and Casualty Administration, The General Hospital of Northern Theater Command, Shenyang, China. jiejie65165@163.com.
Bona LiuDepartment of Oncology, The General Hospital of Northern Theater Command, Shenyang, China. apbnaliu@sina.com.

Funding

the Liaoning Province Science and Technology Plan-Joint Fund Project No. 2023-MSLH-157the Liaoning Province Science and Technology Plan-Key Technology Research Project No. 2024JH2/102600297
6 · The paper itself

Abstract

Recently, the incidence of neuroendocrine tumors (NETs), characterized by neuroendocrine differentiation, has increased. Their heterogeneous origins and biological behaviors complicate diagnosis and treatment. Surufatinib, a novel oral tyrosine kinase inhibitor with dual anti-angiogenic and immunomodulatory properties, has shown promising efficacy against NETs in recent clinical trials. However, comparative data on the prognostic impact of surufatinib treatment remain limited. We investigated risk factors associated with mortality and tumor progression in patients with NETs, and aimed to provide insights into the administration of surufatinib to improve the clinical outcomes of these patients. In this multi-center, observational study, we retrospectively analyzed 373 patients diagnosed with NETs and followed up for 1 year. All patients received anti-tumor treatments during their hospitalization, including chemotherapy, radiotherapy, surgery, and immunosuppressants. Among them, 93 patients received surufatinib. Logistic regression was performed to identify potential risk factors, which were subsequently adjusted for confounding variables using a Cox proportional hazards regression model. Multivariable analysis revealed that surufatinib use was an independent risk factor for death (OR 0.36, P = 0.006) and disease progression (OR 0.44, P = 0.005). Survival analysis showed significantly higher overall (HR 0.44, 95% CI 0.26-0.76, P = 0.003) and progression-free survival (HR 0.56, 95% CI 0.37-0.84, P = 0.005) among patients treated with surufatinib than those in patients not receiving treatment. A higher proportion of patients in the surufatinib treatment cohort experienced proteinuria (9 [3.2%] vs. 10 [10.8%], P = 0.010) and increased blood bilirubin levels (25 [8.9%] vs. 16 [17.2%], P = 0.027), however, no significant differences were observed in the severity of adverse reactions. Surufatinib showed clinically meaningful efficacy in patients with NETs and exhibited a generally manageable safety profile.

Indexed as

Antineoplastic AgentsNeuroendocrine TumorsProtein Kinase InhibitorsAdultAgedChinaFemaleHumansMaleMiddle AgedRetrospective StudiesAntineoplastic AgentsProtein Kinase InhibitorsEfficacyNeuroendocrine tumorsRisk factorsSafetySurufatinib

Identifiers

PMID41331488
PMCPMC12802006

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.