Evidence map›Paper›PMID 42022538›Full record

ArticleMedComm2026

Safety and Efficacy of Lucitanib Plus Toripalimab in Advanced Solid Tumors Refractory to Standard Therapies: An Open-Label, Multicenter, Phase II Study.

Ting Zhou, Haishuang Sun, Gang Chen, Guoping Zhang, Jinsheng Wu, Shenhong Qu, Yaqian Han, Desheng Hu, Yang Ling, Yulong Zheng and 15 more

Abstract read
In one paragraph

Article in MedComm, 2026. 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

25 authors.

Ting ZhouDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer Sun Yat-sen University Cancer Center Guangzhou China.
Haishuang SunDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer Sun Yat-sen University Cancer Center Guangzhou China.
Gang ChenDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer Sun Yat-sen University Cancer Center Guangzhou China.
Guoping ZhangDepartment of Medical Oncology Yuebei People's Hospital Shaoguan China.
Jinsheng WuDepartment of Radiation Oncology The First Affiliated Hospital of Hainan Medical University Haikou China.
Shenhong QuDepartment of Otolaryngology Head and Neck The People's Hospital of Guangxi Zhuang Autonomous Region Nanning China.
Yaqian HanThe Second Department of Head and Neck Radiotherapy Hunan Cancer Hospital Changsha China.
Desheng HuDepartment of Radiotherapy Hubei Cancer Hospital Wuhan China.
Yang LingDepartment of Medical Oncology Changzhou Cancer Hospital Changzhou China.
Yulong ZhengDepartment of Medical Oncology The First Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China.
Jian LiuPhase I Clinical Trial Research Laboratory The First Affiliated Hospital, Zhejiang University School of Medicine Hangzhou China.
Lizhu LinDepartment of Oncology The First Affiliated Hospital of Guangzhou University of Chinese Medicine Guangzhou China.
Yongsheng LiDepartment of Medical Oncology Chongqing University Cancer Hospital Chongqing China.
Jianji PanDepartment of Radiotherapy Fujian Cancer Hospital Fuzhou China.
Yanyan LiuDepartment of Lymphatic Integrative Medicine Henan Cancer Hospital Zhengzhou China.
Cuiying WangDepartment of Medical Oncology Hainan Third People's Hospital Sanya China.
Guohong FuGeneral Surgery Department Hainan Third People's Hospital Sanya China.
Jian FengDepartment of Respiratory Medicine Affiliated Hospital of Nantong University Nantong China.
Jianhua ShiThe Second Ward of the Department of Internal Medicine Linyi Cancer Hospital Linyi China.
Huiming CaiHaihe Biopharma Co., Ltd Shanghai China.
Meng LiHaihe Biopharma Co., Ltd Shanghai China.
Fugen LiHaihe Biopharma Co., Ltd Shanghai China.
Yinbin WangHaihe Biopharma Co., Ltd Shanghai China.
Li ZhangDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer Sun Yat-sen University Cancer Center Guangzhou China.
Yunpeng YangDepartment of Medical Oncology, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Guangdong Provincial Clinical Research Center for Cancer Sun Yat-sen University Cancer Center Guangzhou China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lucitanib is a novel multi-target inhibitor of vascular endothelial growth factor receptor 1-3, fibroblast growth factor receptor 1-3, and platelet-derived growth factor receptor α/β. This open-label, multicenter, single-arm Phase II study evaluated lucitanib plus the anti-programmed cell death 1 (PD-1) antibody toripalimab in patients with advanced solid tumors refractory to standard therapies. Patients received lucitanib (10 mg) once daily plus toripalimab (240 mg) every 3 weeks until progression or unacceptable toxicity. The primary endpoint was investigator-assessed objective response rate (ORR) and secondary endpoints included disease control rate, duration of response, progression-free survival (PFS), overall survival, and safety. Among 131 patients across four cohorts (PD-1-treated recurrent/metastatic nasopharyngeal carcinoma [NPC], PD-1-naïve NPC, recurrent/metastatic endometrial cancer [EC], and other tumors), ORR was 34.1%, 45.8%, 38.5%, and 13.5%, respectively. Median PFS was 4.2 months (95% confidence interval [CI], 4.1-5.6), 6.5 months (95% CI, 4.0-not estimable [NE]), 5.6 months (95% CI, 2.78-11.21), and 9.7 months (95% CI, 5.4-NE). The most common Grade ≥ 3 treatment-related adverse events were hypertension (37.4%), proteinuria (10.7%), and thrombocytopenia (10.7%). Lucitanib plus toripalimab showed encouraging antitumor activity with manageable safety in heavily pretreated advanced solid tumors, supporting further randomized evaluation, particularly in NPC and EC.

Indexed as

efficacylucitanibnasopharyngeal carcinomaPhase II studysolid tumortoripalimab

Identifiers

PMID42022538
PMCPMC13097439

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.