Evidence map›Paper›PMID 35727633›Full record

ArticleThe Journal of clinical investigation2022

Phase I study of adjuvant immunotherapy with autologous tumor-infiltrating lymphocytes in locally advanced cervical cancer.

He Huang, Cai-Ping Nie, Xiu-Feng Liu, Bin Song, Jian-Hui Yue, Jing-Xiao Xu, Jia He, Kui Li, Yan-Ling Feng, Ting Wan and 13 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase I
In one paragraph

Article in The Journal of clinical investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04443296 (Study of Tumor Infiltrating Lymphocytes Following Concurrent Chemoradiotherapy in the Treatment of Patients With Cervical Carcinoma), which is not on this map. Cited by 44 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 3 pooled it
4.8field-weighted citation impact, top 4% of its field
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.

NCT04443296 phase1unknown statusnot on this map

Study of Tumor Infiltrating Lymphocytes Following Concurrent Chemoradiotherapy in the Treatment of Patients With Cervical Carcinoma

TypeinterventionalSponsorSun Yat-sen UniversityRan2019 to 2022Enrolled10ConditionsCervical CarcinomaArmsCCRT+TIL
3 · Its place in the literature

Who cites it

44 citing papers in PubMed, 3 syntheses or guidelines pooled it, 51 citations in OpenAlex.

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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

23 authors at 2 institutions in 2 countries.

He HuangState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Cai-Ping NieState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Xiu-Feng LiuState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Bin SongBGI-Shenzhen, Shenzhen, China.
Jian-Hui YueBGI-Shenzhen, Shenzhen, China.
Jing-Xiao XuState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Jia HeState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Kui LiState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Yan-Ling FengState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Ting WanState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Min ZhengState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Yan-Na ZhangState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Wei-Jun YeState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Jun-Dong LiState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Yan-Fang LiState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Jun-Yun LiState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Xin-Ping CaoState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Zhi-Min LiuState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Xiao-Shi ZhangState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Qing LiuState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Xi ZhangBGI-Shenzhen, Shenzhen, China.
Ji-Hong LiuState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Jiang LiState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine.
Sun Yat-sen University · CNBGI Group (China) · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUNDAdoptive cell therapy (ACT) with tumor-infiltrating lymphocytes (TILs) has achieved remarkable clinical efficacy in metastatic cancers such as melanoma and cervical cancer (CC). Here, we explored the safety, feasibility, and preliminary tumor response and performed translational investigations of adjuvant immunotherapy using infusion of autogenous TILs (auto-TILs) following concurrent chemoradiotherapy (CCRT) in patients with CC who had locally advanced disease.METHODSTwenty-seven patients with CC with stage III-IV disease were recruited in this single-center, phase I study. TILs were isolated from lesions in the uterine cervix and generated under good manufacturing practice (GMP) conditions and then infused after CCRT plus i.m. IL-2 injections.RESULTSTILs from 20 of the 27 patients were successfully expanded, with a feasibility of 74.1%. Twelve patients received TILs following CCRT. Adverse events (AEs) were primarily attributable to CCRT. Only 1 (8.3%) patient experienced severe toxicity with a grade 3 hypersensitivity reaction after TIL infusion. No autoimmune AEs, such as pneumonitis, hepatitis, or myocarditis, occurred, and there were no treatment-related mortalities. Nine of 12 patients (75.0%) attained a complete response, with a disease control duration of 9-22 months. Translational investigation showed that the transcriptomic characteristics of the infused TIL products and some immune biomarkers in the tumor microenvironment and serum of patients with CC at baseline were correlated with the clinical response.CONCLUSIONTIL-based ACT following CCRT was safe in an academic center setting, with potentially effective responses in patients with locally advanced CC. "Hot" inflammatory immune environments were beneficial to the clinical efficacy of TIL-based ACT as adjuvant therapy.TRIAL REGISTRATIONClinicalTrials.gov NCT04443296.FUNDINGNational Key R&D Program; Sci-Tech Key Program of the Guangzhou City Science Foundation; the Guangdong Province Sci-Tech International Key Program; the National Natural Science Foundation of China.

Indexed as

ImmunotherapyUterine Cervical NeoplasmsChemoradiotherapyFemaleHumansLymphocytes, Tumor-InfiltratingMelanomaTumor MicroenvironmentAdaptive immunityCancerClinical TrialsOncology

Identifiers

PMID35727633
PMCPMC9337833
OpenAlexW4283275383

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.