Evidence map›Paper›PMID 40205403›Full record

ArticleInfectious agents and cancer2025

Clinical impact of concurrent autologous adoptive T cells immunotherapy in active COVID-19 infected cancer patients for chemotherapy.

Congcong Li, Dazhao Xu, Linyao Lu, Shu Peng, Haiyang Zhao, Chuxiong Zeng, Lina Hu, Xianzhi Guo, Li Liu, Feifei Huo and 9 more

Abstract read
In one paragraph

Article in Infectious agents and cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

19 authors.

Congcong Li *Department of Medical Oncology, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong New Area, Shanghai, 201399, China.
Dazhao Xu *Department of Medical Oncology, Beijing Zhongguancun Hospital, Chinese Academy of Sciences, Beijing, China.
Linyao LuDepartment of Medical Oncology, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong New Area, Shanghai, 201399, China.
Shu PengDepartment of Medical Oncology, Fudan University Huadong Medical Center, Shanghai, China.
Haiyang ZhaoDepartment of Medical Oncology, Beijing Zhongguancun Hospital, Chinese Academy of Sciences, Beijing, China.
Chuxiong ZengDepartment of Medical Oncology, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong New Area, Shanghai, 201399, China.
Lina HuDepartment of Medical Oncology, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong New Area, Shanghai, 201399, China.
Xianzhi GuoDepartment of Medical Oncology, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong New Area, Shanghai, 201399, China.
Li LiuDepartment of Medical Oncology, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong New Area, Shanghai, 201399, China.
Feifei HuoDepartment of Medical Oncology, Beijing Zhongguancun Hospital, Chinese Academy of Sciences, Beijing, China.
Xiumei RongDepartment of Medical Oncology, Beijing Zhongguancun Hospital, Chinese Academy of Sciences, Beijing, China.
Zhenying GengDepartment of Medical Oncology, Beijing Zhongguancun Hospital, Chinese Academy of Sciences, Beijing, China.
Ping LinDepartment of Medical Oncology, Beijing Zhongguancun Hospital, Chinese Academy of Sciences, Beijing, China.
Xinna ZhouCenter of Clinical Trials & Management, Beijing Shijitan Hospital, Capital Medical University Cancer Center, Beijing, 10038, China.
Xiaoli WangDepartment of Medical Oncology, Beijing Shijitan Hospital, Capital Medical University Cancer Center, Beijing, 10038, China.
Amy HobeikaDepartment of Surgery, Duke University Medical Center, Durham, NC, USA.
Michael A MorseDepartment of Medicine, Duke University Medical Center, Durham, NC, USA.
Herbert Kim LyerlyDepartment of Surgery, Duke University Medical Center, Durham, NC, USA. Kim.lyerly@duke.edu.
Jun RenDepartment of Medical Oncology, Fudan University Pudong Medical Center, 2800 Gongwei Road, Pudong New Area, Shanghai, 201399, China. jun.ren@duke.edu.

Funding

Pudong New Area Clinical Characteristic Discipline Project PWYts2021-11Shanghai Pudong New Area Health Commission Discipline Construction Project-Clinical Plateau Discipline PWYgy2021-01Shanghai Pudong New Area Health Commission Discipline Construction Project -Key Subject Group PWZxq2022-14
6 · The paper itself

Abstract

backgroundThe concurrent presence of COVID-19 infection in advanced cancer patients has increased the mortality since the compromised immunity was inevitably worsen. The role and clinical impact of autologous adoptive T cell immunotherapy (ACT) designed for anti-cancer treatment were not known in such circumstances. The safety and potential immune reconstitution of concurrent ACT in advanced cancer patients with active COVID-19 infection have yet unknown as well. The effect of infused ACT on the symptom severity manifestation should be summarized.

methodsIn this respectively clinical observation study, patients were non-randomized enrolled from the two centers according to the regular therapeutic plans including stage IV cancer patients for scheduled ACT, chemotherapy, cancer patients with symptomatic COVID-19 but without ACT, neither cancer or non-ACT but symptomatic cases of COVID-19 infection. We have incorporated the age-adjusted Charlson comorbidity index (aCCI) for each patient to compare the prognosis of the three groups. All patients were planned for the scheduled standard anti-cancer therapeutic considerations, chemotherapy plus ACT as planned as well as the supportive care.The clinical efficacy and impact of ACT on cancer patients within the 3 months from the peripheral blood apheresis, dendritic cell (DC) and cytokine induced killer T cell (CIK-T ) infusion and subsequent co-existence of COVID-19 infection were recorded as the primary objective. During the same period, the cancer cases without ACT and others were collected to compare the occurrence of both severe and death rate respectively.

resultsThere were 123 patients (35 of ACT, 23 of non-ACT, 65 of non-cancer) with similar aCCI. There were similar cohort-level COVID-19 in-hospital case fatality rates consistent with previously reported data for non-cancer (26.2%, 17/65) and non-ACT cancer (52.2%, 12/23) among those admitted severe cases after the adjustment.There were little overlapped adverse reactions during the ACT therapeutic period even in the presence of active COVID-19 infection. No death case was occurred (0/35) when those exposed to ACT regimen. Cancer patients receiving ACT had a shorter mean time to alleviation of symptoms compared with non-ACT and non-cancer (4.46 versus 16.88 and 17.90 days respectively) as well as the lowered severity incidence of symptoms (P = 0.0010). The infused ACT has not significant impact on peripheral blood count whereas the amount of CD3

conclusionsThese data demonstrate the clinical safety profiles while ACT infusions with active COVID-19 infection.The intervention of ACT for cancer patients could generate the benefit for symptom alleviation with improved recovery time. The concurrent ACT for advanced cancer patients during such infectious pandemic might simultaneously leverage and reduce the risk of immune compromised situation for subsequent chemotherapy complications.

Indexed as

Autologous adoptive cellular immunotherapyCOVID-19 infectionSafety.

Identifiers

PMID40205403
PMCPMC11983847

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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.