Evidence map›Paper›PMID 39883265›Full record

Trial reportInvestigational new drugs2025

Anti-PD-L1 envafolimab combined with anti-VEGF suvemcitug in pretreated solid tumors and hepatocellular carcinoma: an open-label phase II study with safety run-in stage.

Lixia Ma, Yu Zhang, Yong Fang, Chunyi Hao, Qingxia Fan, Da Jiang, Liqin Lu, Fang Su, Chen Yang, Zhenru Liu and 4 more

Registry-linked trialAbstract readClinical Trial, Phase IIMulticenter Study
PubMed Publisher
In one paragraph

Trial report in Investigational new drugs, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05148195 (An Open Label, Multi-cohort, Multicenter Phase II Study to Evaluate the Efficacy and Safety of Envofolimab in Combination With BD0801 Injection With/Without Chemotherapy in Patients With Advanced Solid Tumors), which is not on this map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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.

NCT05148195 phase2terminatednot on this map

An Open Label, Multi-cohort, Multicenter Phase II Study to Evaluate the Efficacy and Safety of Envofolimab in Combination With BD0801 Injection With/Without Chemotherapy in Patients With Advanced Solid Tumors

TypeinterventionalSponsorJiangsu Simcere Pharmaceutical Co., Ltd.Ran2021 to 2023Enrolled86ConditionsAdvanced Solid TumorArmsEnvofolimab, BD0801, Docetaxel, Irinotecan, Leucovorin calcium
3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Review
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

14 authors.

Lixia MaDepartment of Internal Medicine, Jilin Cancer Hospital, Changchun, China.
Yu ZhangDepartment of Oncology, Mianyang Central Hospital, Mianyang, China.
Yong FangMedical Oncology Dept, Sir Run Run Shaw Hospital, Zhejiang University School of Medicine, Hangzhou, China.
Chunyi HaoDepartment of Hepato-Pancreato-Biliary Surgery, Key Laboratory of Carcinogenesis and Translational Research, MinistryofEducation/Beijing), Peking University Cancer Hospital and Institute, Beijing, China.
Qingxia FanOncology Department, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Da JiangDepartment of Medical Oncology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, China.
Liqin LuDepartment of Medical Oncology, Zhejiang Provincial People's Hospital, Hangzhou, China.
Fang SuDepartment of Medical Oncology, The First Affiliated Hospital of Bengbu Medical College, Bengbu, China.
Chen YangClinical Science, Shandong Simcere Biopharmaceutical Co., Ltd, Shandong, China.
Zhenru LiuClinical Science, Shandong Simcere Biopharmaceutical Co., Ltd, Shandong, China.
Ji TianClinical Science, Shandong Simcere Biopharmaceutical Co., Ltd, Shandong, China.
Xiyang SunClinical Pharmacology, Shandong Simcere Biopharmaceutical Co., Ltd, Shandong, China.
Shuguang SunClinical Statistics, Shandong Simcere Biopharmaceutical Co., Ltd, Shandong, China.
Ying ChengDepartment of Internal Medicine, Jilin Cancer Hospital, Changchun, China. jl.cheng@163.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundImmune checkpoint inhibitors (ICIs) combined with anti-vascular endothelial growth factor (VEGF) have been the standard first-line treatment of hepatocellular carcinoma (HCC). However, the efficacy of this combination in post-line treatment is still unknown. This study aimed to evaluate the efficacy and safety of the combination of anti-PD-L1 envafolimab and novel humanized anti-VEGF suvemcitug as second-line treatment for patients with HCC.

methodsThis open-label, prospective phase II clinical study (NCT05148195) comprised safety run-in stage and dose expansion stage of HCC cohort. Eligible patients were aged ≥ 18 years and had undergone at least a prior line of treatment. Patients received fixed-dose envafolimab and suvemcitug until termination of disease progression, unacceptable toxicities, or withdrawal. The primary endpoint of safety run-in stage was recommended dose (RD), and dose expansion stage was objective response rate (ORR).

resultsAs of August 10, 2023, no dose-limiting toxicity was observed in six patients in the safety-run-in stage, and 2 mg/kg dose every 3 weeks was declared the RD of suvemcitug. Among 20 patients with HCC, the median age was 54.5 (range, 42-70) years. Of these patients, 20 (100.0%) received ≥ one prior line treatment, with 20 (100%) received tyrosine kinase inhibitor (TKI) treatment and 8 (40.0%) received prior ICI treatment. The ORR was 10.0% (95% confidence interval (CI), 1.2-31.7), DCR was 65.0% (95% CI, 40.8-84.6), and DoR was not reached (NR). With a median follow-up of 13.9 months, the median progression-free survival (PFS) and median overall survival (OS) were 4.3 months (95% CI, 1.4-8.1) and 10.7 months (95% CI, 6.0-not evaluable [NE]), respectively. Treatment-related adverse events (TRAEs) of grade ≥ 3 occurred in 40% patients, with proteinuria (20.0%, 4/20) being the most frequent. The ORR of no lung metastasis, prior first-line treatment and IO naïve treatment subgroup was 16.7%.

conclusionsThe combination of envafolimab and suvemcitug showed a tolerable safety profile and promising antitumor activity in HCC patients who failed later-line treatment.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsCarcinoma, HepatocellularImmune Checkpoint InhibitorsLiver NeoplasmsNeoplasmsVascular Endothelial Growth Factor AAdultAgedB7-H1 AntigenFemaleHumansMaleMiddle AgedProspective StudiesAntibodies, Monoclonal, HumanizedB7-H1 AntigenCD274 protein, humanImmune Checkpoint InhibitorsVascular Endothelial Growth Factor AAnti-angiogenesisEnvafolimabHepatocellular carcinomaImmune checkpoint inhibitorSuvemcitug

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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.