Evidence map›Paper›PMID 42816483›Full record

ArticleSignal transduction and targeted therapy2026

Carbon nanoparticle-Fe (II) complex for ferroptosis therapy in refractory solid tumors: a phase I trial.

Huashan Shi, Ping Xie, Xiaoyu Li, Lin Lai, Qi Dang, Zehui Gou, Zhengyin Liao, Qing He, Wenhao Guo, Zhenyu Ding and 9 more

Registry-linked trialAbstract readClinical Trial, Phase I
In one paragraph

Article in Signal transduction and targeted therapy, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06048367 (Carbon Nanoparticle-Loaded Iron [CNSI-Fe), which is not on this 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.

NCT06048367 phase1completednot on this map

Carbon Nanoparticle-Loaded Iron [CNSI-Fe(II)] Dose Escalation Study for the Treatment of Advanced Solid Tumors: Phase 1 Clinical Trial

TypeinterventionalSponsorSichuan Enray Pharmaceutical Sciences CompanyRan2022 to 2025Enrolled19ConditionsAdvanced Solid Tumor, Lung Cancer, Pancreas Cancer, Breast CancerArmsCNSI-Fe(II) 30 mg, CNSI-Fe(II) 60 mg, CNSI-Fe(II) 90 mg, CNSI-Fe(II) 120 mg, CNSI-Fe(II) 150 mg
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

19 authors.

Huashan ShiDepartment of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.ORCID http://orcid.org/0000-0002-9958-9892
Ping XieSichuan Enray Pharmaceutical Sciences Company, Chengdu, China.
Xiaoyu LiClinical Trial Center, National Medical Products Administration Key Laboratory for Clinical Research and Evaluation of Innovative Drugs, West China Hospital, Sichuan University, Chengdu, China.
Lin LaiDepartment of Oncology, Hubei Key Laboratory for Translational Research in Traditional Chinese Medicine, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, China.
Qi DangPhase I Clinical Research Center, Shandong First Medical University Affiliated Tumor Hospital, Jinan, China.
Zehui GouDepartment of Medical Ultrasound, West China Hospital, Sichuan University, Chengdu, China.
Zhengyin LiaoDepartment of Abdominal Oncology, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Qing HeDepartment of Head and Neck Oncology, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Wenhao GuoDepartment of Abdominal Oncology, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Zhenyu DingDepartment of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Songpu WuDepartment of Emergency Surgery, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Yueyun ChenDepartment of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Zhen LinDepartment of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Ying WenDepartment of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Yuanfang HuangSichuan Enray Pharmaceutical Sciences Company, Chengdu, China.
Yan ChenSichuan Enray Pharmaceutical Sciences Company, Chengdu, China.
Jianqiang XuSchool of Chemical Engineering, Ocean Technology and Life Science (CEOTLS) & Panjin Institute of Industrial Technology (PIIT), Dalian University of Technology, Panjin, China.ORCID http://orcid.org/0000-0002-1289-5943
Chuying HuangDepartment of Oncology, Hubei Key Laboratory for Translational Research in Traditional Chinese Medicine, The Central Hospital of Enshi Tujia and Miao Autonomous Prefecture, Enshi, China. huangchuying2008@126.com.
Yongsheng WangDepartment of Biotherapy, Cancer Center, West China Hospital, Sichuan University, Chengdu, China. wangys75@wchscu.edu.cn.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82160490
6 · The paper itself

Abstract

We developed a novel carbon nanoparticle-Fe (II) complex prepared via suspension injection (CNSI-Fe) to induce cancer cell ferroptosis through direct intratumoral delivery of ferrous iron. Preclinical studies have demonstrated that CNSI-Fe has promising antitumour effects, thereby prompting this first-in-human, single-arm, open-label, dose-escalation phase I trial in patients with refractory solid tumors. Primary objectives included assessments of safety and tolerability and the determination of dose-limiting toxicity (DLT) and the maximum tolerated dose (MTD). Secondary objectives included the determination of preliminary antitumour efficacy and pharmacokinetics. Applying a 3 + 3 design across five doses (30-150 mg), a total of 19 enrolled patients received CNSI-Fe treatment. The MTD was not reached, and only one patient (in the 90 mg cohort) experienced DLT events. For all treated patients (n = 19), the common adverse events included injection site pain (89.5%), hypertension (52.6%), elevated serum iron levels (47.4%), and anemia (47.4%). Pharmacokinetic analysis revealed rapid iron absorption (peak time: 0.15-0.41 h) and clearance (half-life: 1.96-5.06 h), with peak serum concentrations ranging from 3520.33 to 13961.67 ng/mL. Preliminary efficacy estimates revealed an overall response rate of 10.5% and a disease control rate (DCR) of 84.2%. Notably, the DCR reached 100% in patients with lymph node and sarcoma lesions. Overall, CNSI-Fe demonstrated a favorable safety profile and promising antitumour activity (ClinicalTrials.gov identifier: NCT06048367), supporting further investigations in a phase II trial.

Indexed as

CarbonFerroptosisFerrous CompoundsNanoparticlesNeoplasmsAdultAgedFemaleHumansIronMaleMaximum Tolerated DoseMiddle AgedCarbonFerrous CompoundsIron

Identifiers

PMID42816483
PMCPMC13627718

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Registered trials

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.