Evidence map›Paper›PMID 39362847›Full record

Trial reportSignal transduction and targeted therapy2024

Neoadjuvant toripalimab plus axitinib for clear cell renal cell carcinoma with inferior vena cava tumor thrombus: NEOTAX, a phase 2 study.

Liangyou Gu, Cheng Peng, Qiyang Liang, Qingbo Huang, Deqiang Lv, Houming Zhao, Qi Zhang, Yu Zhang, Peng Zhang, Shichao Li and 8 more

Abstract readClinical Trial, Phase II
In one paragraph

Trial report in Signal transduction and targeted therapy, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

18 authors.

Liangyou Gu *Department of Urology, Chinese PLA General Hospital, Beijing, China.
Cheng Peng *Department of Urology, Chinese PLA General Hospital, Beijing, China.
Qiyang Liang *Department of Urology, Chinese PLA General Hospital, Beijing, China.
Qingbo Huang *Department of Urology, Chinese PLA General Hospital, Beijing, China.
Deqiang LvDepartment of Urology, Chinese PLA General Hospital, Beijing, China.
Houming ZhaoDepartment of Urology, Chinese PLA General Hospital, Beijing, China.
Qi ZhangChina National Center for Bioinformation, Beijing, China.
Yu ZhangDepartment of Urology, Chinese PLA General Hospital, Beijing, China.
Peng ZhangDepartment of Urology, Chinese PLA General Hospital, Beijing, China.
Shichao LiDepartment of Urology, Chinese PLA General Hospital, Beijing, China.
Junnan XuDepartment of Urology, Chinese PLA General Hospital, Beijing, China.
Luyao ChenDepartment of Urology, The First Affiliated Hospital of Nanchang University, Nanchang, China.
Yongpeng XieDepartment of Urology, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
Jinhang LiDepartment of Pathology, Chinese PLA General Hospital, Beijing, China.
Gang GuoDepartment of Urology, Chinese PLA General Hospital, Beijing, China.
Xu ZhangDepartment of Urology, Chinese PLA General Hospital, Beijing, China. xzhang301@163.com.
Baojun WangDepartment of Urology, Chinese PLA General Hospital, Beijing, China. baojun40009@126.com.
Xin MaDepartment of Urology, Chinese PLA General Hospital, Beijing, China. urologist@foxmail.com.

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82273412National Natural Science Foundation of China (National Science Foundation of China) 82372704National Natural Science Foundation of China (National Science Foundation of China) 82373169
6 · The paper itself

Abstract

The potential benefit of neoadjuvant toripalimab plus axitinib in cases with clear cell renal cell carcinoma (ccRCC) and inferior vena cava tumor thrombus (IVC-TT) remains unclear. NEOTAX was a phase 2 study to investigate the efficacy and safety of neoadjuvant toripalimab plus axitinib in patients with ccRCC and IVC-TT (ChiCTR2000030405). The primary endpoint was the down-staging rate of IVC-TT level. Secondary endpoints included change in TT length, response rate, percentage change in surgical approach, surgical morbidity, progression-free survival (PFS), safety, and biomarker analyses. In all, 25 patients received study treatment, 44.0% (11/25) patients had a reduction in thrombus level, and none experienced an increase in Mayo level. The median change in tumor thrombus length was -2.3 cm (range: -7.1 to 1.1 cm). Overall, 61.9% (13/21) patients experienced changes in surgical strategy compared with planned surgery, three patients experienced major complications. The median PFS was 25.3 months (95% CI: 17.0-NE). The 1-year PFS was 89.1% (95% CI: 62.7-97.2). No any of grade 4 or 5 treatment-related adverse event was identified. Biopsy samples of non-responders exhibited increased T cytotoxic cell infiltration, but these cells were predominantly PD-1 positive. Biopsy samples of responders exhibited lower T helper cells, however, their subtype, regulatory T cells remained unchanged. In surgical samples of the TT, non-responders exhibited increased CD8T_01_GZMK_CXCR4 subset T cells. NEOTAX met preset endpoints proving that toripalimab in combination with axitinib downstages IVC-TT in a significant proportion of patients leading to simplification in the procedure of surgery.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsAxitinibCarcinoma, Renal CellKidney NeoplasmsNeoadjuvant TherapyVena Cava, InferiorAdultAgedFemaleHumansMaleMiddle AgedAntibodies, Monoclonal, HumanizedAxitinibtoripalimab

Identifiers

PMID39362847
PMCPMC11450193

What OpenQuestion holds

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LicenceCC BY
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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.