Evidence map›Paper›PMID 36503490›Full record

ArticleMilitary Medical Research2022

Nanomedicine-boosting icaritin-based immunotherapy of advanced hepatocellular carcinoma.

Yi Lu, Yue Gao, Huan Yang, Yong Hu, Xin Li

Erratum issuedOpen access · diamondAbstract read
In one paragraph

Article in Military Medical Research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
8.1field-weighted citation impact, top 2% 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.

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

45 citing papers in PubMed, 48 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Journal of pharmaceutical analysis · 2025
    Review
  17. Article
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 3 institutions in 1 country.

Yi Lu *Department of Polymeric Materials, School of Materials Science and Engineering, Tongji University, Shanghai, 201804, China.
Yue Gao *College of Chemistry, Chemical Engineering and Biotechnology, Donghua University, Shanghai, 201620, China.
Huan YangSchool of Pharmacy, Jiangsu University, Zhenjiang, 212013, Jiangsu, China.
Yong HuDepartment of Polymeric Materials, School of Materials Science and Engineering, Tongji University, Shanghai, 201804, China. yonghu@tongji.edu.cn.
Xin LiDepartment of Polymeric Materials, School of Materials Science and Engineering, Tongji University, Shanghai, 201804, China. xin_li1991@foxmail.com.ORCID http://orcid.org/0000-0002-7837-7874
Tongji University · CNDonghua University · CNJiangsu University · CN

Funding

China Scholarship Council 201908320330Chinesisch-Deutsche Zentrum für Wissenschaftsförderung GZ1505Fundamental Research Funds for the Central Universities 22120220075National Natural Science Foundation of China 52103181National Natural Science Foundation of China 81873196
6 · The paper itself

Abstract

Traditional treatments for advanced hepatocellular carcinoma (HCC), such as surgical resection, transplantation, radiofrequency ablation, and chemotherapy are unsatisfactory, and therefore the exploration of powerful therapeutic strategies is urgently needed. Immunotherapy has emerged as a promising strategy for advanced HCC treatment due to its minimal side effects and long-lasting therapeutic memory effects. Recent studies have demonstrated that icaritin could serve as an immunomodulator for effective immunotherapy of advanced HCC. Encouragingly, in 2022, icaritin soft capsules were approved by the National Medical Products Administration (NMPA) of China for the immunotherapy of advanced HCC. However, the therapeutic efficacy of icaritin in clinical practice is impaired by its poor bioavailability and unfavorable in vivo delivery efficiency. Recently, functionalized drug delivery systems including stimuli-responsive nanocarriers, cell membrane-coated nanocarriers, and living cell-nanocarrier systems have been designed to overcome the shortcomings of drugs, including the low bioavailability and limited delivery efficiency as well as side effects. Taken together, the development of icaritin-based nanomedicines is expected to further improve the immunotherapy of advanced HCC. Herein, we compared the different preparation methods for icaritin, interpreted the HCC immune microenvironment and the mechanisms underlying icaritin for treatment of advanced HCC, and discussed both the design of icaritin-based nanomedicines with high icaritin loading and the latest progress in icaritin-based nanomedicines for advanced HCC immunotherapy. Finally, the prospects to promote further clinical translation of icaritin-based nanomedicines for the immunotherapy of advanced HCC were proposed.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsAdjuvants, ImmunologicChinaHumansImmunotherapyTumor MicroenvironmentAdjuvants, ImmunologicAdvanced hepatocellular carcinomaClinical translationIcaritinImmunotherapyNanomedicine

Identifiers

PMID36503490
PMCPMC9743634
OpenAlexW4311118648

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.