Evidence map›Paper›PMID 41782961›Full record

ArticleMedComm2026

Efficacy and Safety of DNV3 (a Lymphocyte-activation Gene 3-blocking Antibody) Combined With Toripalimab and Chemotherapy in Advanced Melanoma: An Open-label, Single-arm Clinical Trial.

Jing Lin, Lizhu Chen, Ling Chen, Dingyi Wang, Yuping Lu, Huishan Zhang, Ping Chen, Wei Yan, Zuoxiang Xiao, Yu Chen

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. Cited by 1 paper, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed, 1 pooled it
–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

1 citing paper in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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.

Jing LinDepartment of Medical Oncology Clinical Oncology School of Fujian Medical University Fujian Cancer Hospital, NHC Key Laboratory of Cancer Metabolism Fuzhou China.ORCID https://orcid.org/0000-0002-9025-1721
Lizhu ChenDepartment of Medical Oncology Clinical Oncology School of Fujian Medical University Fujian Cancer Hospital, NHC Key Laboratory of Cancer Metabolism Fuzhou China.ORCID https://orcid.org/0000-0002-9881-2976
Ling ChenDepartment of Medical Oncology Clinical Oncology School of Fujian Medical University Fujian Cancer Hospital, NHC Key Laboratory of Cancer Metabolism Fuzhou China.
Dingyi WangDepartment of Phase I Clinical Trial Ward Clinical Oncology School of Fujian Medical University Fujian Cancer Hospital Fuzhou China.
Yuping LuDepartment of Medical Oncology Clinical Oncology School of Fujian Medical University Fujian Cancer Hospital, NHC Key Laboratory of Cancer Metabolism Fuzhou China.
Huishan ZhangDepartment of Phase I Clinical Trial Ward Clinical Oncology School of Fujian Medical University Fujian Cancer Hospital Fuzhou China.
Ping ChenDepartment of Medical Oncology Clinical Oncology School of Fujian Medical University Fujian Cancer Hospital, NHC Key Laboratory of Cancer Metabolism Fuzhou China.
Wei YanDepartment of Medical Oncology Clinical Oncology School of Fujian Medical University Fujian Cancer Hospital, NHC Key Laboratory of Cancer Metabolism Fuzhou China.
Zuoxiang XiaoDepartment of Clinical Research Center Zhejiang Shimai Pharmaceutical Co., Ltd Hangzhou Zhejiang Province China.
Yu ChenDepartment of Medical Oncology Clinical Oncology School of Fujian Medical University Fujian Cancer Hospital, NHC Key Laboratory of Cancer Metabolism Fuzhou China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the remarkable therapeutic advances achieved with immune checkpoint inhibitors in advanced melanoma, treatment options remain limited for patients with refractory subtypes. This study evaluated a novel combination of DNV3 (anti-LAG-3), toripalimab (anti-PD-1), and chemotherapy (nab-paclitaxel/cisplatin) in 27 Asian patients with unresectable or metastatic melanoma (77.8% [21/27] previously treated with anti-PD-[L]1 and 22.2% [6/27] treatment-naïve mucosal melanoma; subtypes: 13 mucosal, 6 acral, 5 cutaneous, and 3 of unknown primary origin). The regimen achieved an overall response rate (ORR) of 44.4%, which was further elevated to 54.5% in the subgroup of 11 patients with hepatic metastases. Notably, it also demonstrated substantial efficacy in anti-PD-(L)1-resistant cases, with a 42.9% ORR and a median progression-free survival (PFS) of 7.36 months. Among treatment-naïve mucosal melanoma, the ORR reached 50%. At data cutoff, median overall survival remained unreached in all cohorts. Grade ≥3 treatment-related adverse events initially occurred in 55.6% of participants; subsequent dose modification of nab-paclitaxel (from 260 mg/m

Indexed as

chemo‐immunotherapyLAG‐3 inhibitormucosal melanomaPD‐1 refractory melanomatoripalimab

Identifiers

PMID41782961
PMCPMC12954137

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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.