# Effect of compound kushen injection on immune function in patients with primary liver cancer: a systematic review and meta-analysis

**Authors:** Yu Xiong, Yutong Cai, Chenxi Li, Qian Yan, Xiongwen Wang, Xiaoying Zhang

PMC · DOI: 10.3389/fphar.2026.1715798 · Frontiers in Pharmacology · 2026-02-19

## TL;DR

This study reviews evidence that combining compound kushen injection with standard treatment improves immune function and reduces side effects in liver cancer patients.

## Contribution

A systematic review and meta-analysis of CKI's impact on immune markers and treatment outcomes in primary liver cancer.

## Key findings

- CKI combined with conventional treatment increased CD3+, CD4+, CD4+/CD8+ ratio, and NK cell levels in PLC patients.
- CKI improved objective response rate, disease control rate, and one-year survival while reducing treatment-related adverse reactions.
- No significant change in CD8+ levels was observed with CKI combination therapy.

## Abstract

Primary liver cancer (PLC) is the third leading cause of cancer mortality worldwide. The heterogeneity of PLC and the complex immunosuppressive microenvironment make it difficult for single treatment regimens to meet patient needs. Therefore, it is crucial to find effective combination treatment strategies that enhance immune function in PLC therapy.

To systematically evaluate the effect of compound kushen injection (CKI) on enhancing immune function in PLC patients and its role in treatment efficacy and related adverse reactions.

Relevant Chinese and English electronic databases were searched to include randomized controlled trials (RCTs) assessing the impact of CKI on immune function in PLC patients published before June 2025. The quality of the included studies was assessed using the Cochrane risk of bias assessment tool. Statistical analyses, Sensitivity analysis and publication bias assessment were conducted using Stata 18.0 software.

A total of 2,359 patients from 25 RCTs were included (1,185 in the experimental group and 1,174 in the control group). Compared to conventional treatment alone, the combination of CKI and conventional treatment significantly enhanced immune function, as evidenced by increased CD3+ levels, CD4+ levels, CD4+/CD8+ ratio, and natural killer (NK) cell levels, while CD8+ levels showed no statistical significance. Additionally, CKI improved the objective response rate (ORR) and disease control rate (DCR), reduced AFP levels, increased KPS scores and the one-year overall survival period, reduced treatment-related adverse reactions, including nausea and vomiting, hepatic dysfunction, myelosuppression, fever, and pain.

Existing evidence suggests that the combined use of CKI and conventional treatment may positively impact immune function, therapeutic effect and treatment-related adverse reactions in patients with PLC. However, the reliability of these conclusions is limited by the absence of disease staging stratification analysis and long-term follow-up data, which are essential for confirming the long-term efficacy and safety of the combined treatment.

https://www.crd.york.ac.uk/PROSPERO/view/CRD420251112494, identifier CRD420251112494.

## Linked entities

- **Diseases:** primary liver cancer (MONDO:0002691)

## Full-text entities

- **Genes:** CD8A (CD8 subunit alpha) [NCBI Gene 925] {aka CD8, CD8alpha, IMD116, Leu2, p32}, LAG3 (lymphocyte activating 3) [NCBI Gene 3902] {aka CD223}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, FGL1 (fibrinogen like 1) [NCBI Gene 2267] {aka HFREP1, HP-041, HPS, LFIRE-1, LFIRE1}, TNF receptor-associated factor 6 [NCBI Gene 222344], TRAF2 (TNF receptor associated factor 2) [NCBI Gene 7186] {aka MGC:45012, RNF117, TRAP, TRAP3}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, CD28 (CD28 molecule) [NCBI Gene 940] {aka IMD123, Tp44}, PDCD1LG2 (programmed cell death 1 ligand 2) [NCBI Gene 80380] {aka B7DC, Btdc, CD273, PD-L2, PDCD1L2, PDL2}, MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609] {aka MRTL, MYCC, bHLHe39, c-Myc}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, NPPB (natriuretic peptide B) [NCBI Gene 4879] {aka BNP, Iso-ANP}, RIPK1 (receptor interacting serine/threonine kinase 1) [NCBI Gene 8737] {aka AIEFL, IMD57, RIP, RIP-1, RIP1}, CD86 (CD86 molecule) [NCBI Gene 942] {aka B7-2, B7.2, B70, BU63, CD28LG2, CD86 v6}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, CEACAM3 (CEA cell adhesion molecule 3) [NCBI Gene 1084] {aka CD66D, CEA, CGM1, CGM1a, W264, W282}, PTGS2 (prostaglandin-endoperoxide synthase 2) [NCBI Gene 5743] {aka COX-2, COX2, GRIPGHS, PGG/HS, PGHS-2, PHS-2}, SMAD2 (SMAD family member 2) [NCBI Gene 4087] {aka CHTD8, JV18, JV18-1, LDS6, MADH2, MADR2}, AFP (alpha fetoprotein) [NCBI Gene 174] {aka AFPD, FETA, HPAFP}, CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IL10 (interleukin 10) [NCBI Gene 3586] {aka CSIF, GVHDS, IL-10, IL10A, TGIF}, IFNG (interferon gamma) [NCBI Gene 3458] {aka IFG, IFI, IMD69}, TNNI3 (troponin I3, cardiac type) [NCBI Gene 7137] {aka CMD1FF, CMD2A, CMH7, RCM1, TNNC1, cTnI}, IL2RA (interleukin 2 receptor subunit alpha) [NCBI Gene 3559] {aka CD25, IDDM10, IL2R, IMD41, TCGFR, p55}, TNFRSF1A (TNF receptor superfamily member 1A) [NCBI Gene 7132] {aka CD120a, FPF, TBP1, TNF-R, TNF-R-I, TNF-R55}, SMAD3 (SMAD family member 3) [NCBI Gene 4088] {aka HSPC193, HsT17436, JV15-2, LDS1C, LDS3, MADH3}, TRADD (TNFRSF1A associated via death domain) [NCBI Gene 8717] {aka Hs.89862}, TGFBR1 (transforming growth factor beta receptor 1) [NCBI Gene 7046] {aka AAT5, ACVRLK4, ALK-5, ALK5, ESS1, LDS1}, DCR (Down syndrome chromosome region) [NCBI Gene 1637] {aka DSCR}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, RELA (RELA proto-oncogene, NF-kB subunit) [NCBI Gene 5970] {aka AIF3BL3, CMCU, NFKB3, p65}, GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], IL12B (interleukin 12B) [NCBI Gene 3593] {aka CLMF, CLMF2, IL-12B, IMD28, IMD29, NKSF}, CHKA (choline kinase alpha) [NCBI Gene 1119] {aka CHK, CK, CKI, EK, NEDMIMS}, JAK2 (Janus kinase 2) [NCBI Gene 3717] {aka JTK10}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, MYD88 (MYD88 innate immune signal transduction adaptor) [NCBI Gene 4615] {aka IMD68, MYD88D, WM1}, CD80 (CD80 molecule) [NCBI Gene 941] {aka B7, B7-1, B7.1, BB1, CD28LG, CD28LG1}, ICAM1 (intercellular adhesion molecule 1) [NCBI Gene 3383] {aka BB2, CD54, P3.58}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, ENO2 (enolase 2) [NCBI Gene 2026] {aka HEL-S-279, NSE}, SMAD7 (SMAD family member 7) [NCBI Gene 4092] {aka CRCS3, MADH7, MADH8}
- **Diseases:** lung cancer (MESH:D008175), chills (MESH:D023341), cancers (MESH:D009369), gastrointestinal reactions (MESH:D005767), immune dysfunction (MESH:D007154), liver cirrhosis (MESH:D008103), abdominal pain (MESH:D015746), systemic damage (MESH:D057772), hepatic dysfunction (MESH:D008107), inflammatory (MESH:D007249), flushing (MESH:D005483), metastasis (MESH:D009362), carcinogenic (MESH:D011230), pain (MESH:D010146), CL (MESH:D002971), viral infection (MESH:D014777), metabolic abnormalities (MESH:D008659), HCC (MESH:D006528), cardiotoxic injury (MESH:D066126), cancer pain (MESH:D000072716), esophageal cancer (MESH:D004938), fever (MESH:D005334), non-small cell lung cancer (MESH:D002289), liver tumors (MESH:D008113), vomiting (MESH:D014839), autoimmune thyroid diseases (MESH:D013967), nausea and vomiting (MESH:D020250), rashes (MESH:D005076), breast cancer (MESH:D001943), bleeding (MESH:D006470), triple-negative breast cancer (MESH:D064726), abdominal distension (MESH:D000007), lymph node metastasis (MESH:D008207), gastric cancer (MESH:D013274), nausea (MESH:D009325), fatigue (MESH:D005221), gastrointestinal tumors (MESH:D005770), damage to liver, kidney (MESH:D056486), chest tightness (MESH:D002637), heart functions (MESH:D006331), cholangiocarcinoma (MESH:D018281)
- **Chemicals:** Matrine (MESH:D000093842), paclitaxel (MESH:D017239), Oxymatrine (MESH:C037573), CT (-), Cisplatin (MESH:D002945), DEN (MESH:D004052), Gemcitabine (MESH:D000093542), alcohol (MESH:D000438), sorafenib (MESH:D000077157), alkaloids (MESH:D000470), Oxaliplatin (MESH:D000077150), ethanol (MESH:D000431), 125I (MESH:C000614960), 5-FU (MESH:D005472), Folinic acid (MESH:D002955), camrelizumab (MESH:C000631724)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Sophora flavescens (species) [taxon 49840], Smilax goeringii (species) [taxon 299607]
- **Cell lines:** Hepa1-6 — Mus musculus (Mouse), Hepatocellular carcinoma of the mouse, Cancer cell line (CVCL_0327), NK-92MI — Homo sapiens (Human), Natural killer cell lymphoblastic leukemia/lymphoma, Cancer cell line (CVCL_2142), HepG2 — Homo sapiens (Human), Hepatoblastoma, Cancer cell line (CVCL_0027), MCF-7 — Homo sapiens (Human), Invasive breast carcinoma of no special type, Cancer cell line (CVCL_0031)

## Full text

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## Figures

15 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12960130/full.md

## References

69 references — full list in the complete paper: https://tomesphere.com/paper/PMC12960130/full.md

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Source: https://tomesphere.com/paper/PMC12960130