Evidence map›Paper›PMID 36059640›Full record

ArticleFrontiers in oncology2022

Case report: B7-H3 CAR-T therapy partially controls tumor growth in a basal cell carcinoma patient.

Gang Hu, Guangchao Li, Wei Wen, Wen Ding, Zhao Zhou, Yongwei Zheng, Taoyuan Huang, Junnan Ren, Rongyi Chen, Dingheng Zhu and 3 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
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

13 authors.

Gang HuDepartment of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
Guangchao LiResearch and Development Department Guangzhou Bio-Gene Technology Co., Ltd., Guangzhou, China.
Wei WenDepartment of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
Wen DingResearch and Development Department Guangzhou Bio-Gene Technology Co., Ltd., Guangzhou, China.
Zhao ZhouResearch and Development Department Guangzhou Bio-Gene Technology Co., Ltd., Guangzhou, China.
Yongwei ZhengResearch and Development Department Guangzhou Bio-Gene Technology Co., Ltd., Guangzhou, China.
Taoyuan HuangDepartment of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
Junnan RenDepartment of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
Rongyi ChenDepartment of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
Dingheng ZhuDepartment of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
Renliang HeDepartment of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
Yunsheng LiangDepartment of Dermatology, Dermatology Hospital, Southern Medical University, Guangzhou, China.
Min LuoResearch and Development Department Guangzhou Bio-Gene Technology Co., Ltd., Guangzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

B7-H3 is over-expressed in multiple types of solid tumors, making it an ideal target for chimeric antigen receptor (CAR)-T therapy. Here, we first report a case of multiple basal cell carcinoma (BCC) patient treated with humanized monoclonal anti-B7-H3 CAR-T cells through direct intratumoral injection. After three dose-escalated injections, the lesion in the abdomen decreased by 40% in volume, shrank from bulging to flat, but was not eradicated completely. The large lesion in the forehead became dry from original ulcer and bleeding. The adverse events observed were itching, myalgia, and redness. Immunohistochemistry analysis demonstrated that B7-H3-positive tumor cells and B7-H3 expression intensity were reduced after injections of CAR-T cells. The number of infiltrating CD3 T cells increased significantly but mainly located outside the tumor region. Subsequently, high levels of TGF-β in the tumor area were observed, suggesting that solid tumor microenvironment may hinder the infiltration and effect of CAR-T cells. In summary, in this particular case report, intratumoral injection of B7-H3 CAR-T cells partially controls tumor growth in the BCC patient with minor adverse events. The efficacy and safety of B7-H3 CAR-T therapy need to be further investigated with a larger cohort of patients. Although only one clinical case is reported here, the anti-B7-H3 CAR-T cell therapy should be considered as a treatment option for solid tumors in the future. This clinical trial was registered at the Chinese Clinical Trial Registry (www.chictr.org.cn) with registration number ChiCTR2100044386.

Indexed as

B7-H3basal cell carcinomasCAR-T cell therapyCD276intratumoral injectionskin cancers

Identifiers

PMID36059640
PMCPMC9428555

What OpenQuestion 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 OpenQuestion graph.