Evidence map›Paper›PMID 41469556›Full record

ArticleBiological procedures online2025

Effect of the Addition of Xianglian Granules to PD-1 Monoclonal Antibodies in Pancancer Patients.

Tingting Wu, Shiying Li, Hui Shuang, Yun Li, Shujuan Fu, Haiyan Jiang, Shiqiang Zhang, Boqian Du, Junqiang Lv, Xiaoting Xia and 8 more

Abstract read
In one paragraph

Article in Biological procedures online, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

18 authors.

Tingting Wu *Oncology Department, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China.
Shiying Li *Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Hui Shuang *Oncology Department, Songjiang Fangta Chinese Medicine Hospital, Shanghai, China.
Yun LiOncology Department, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China.
Shujuan FuOncology Department, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China.
Haiyan JiangOncology Department, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China.
Shiqiang ZhangOncology Department, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China.
Boqian DuOncology Department, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China.
Junqiang LvOncology Department, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China.
Xiaoting XiaOncology Department, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China.
Shengcheng CaoOncology Department, Songjiang Fangta Chinese Medicine Hospital, Shanghai, China.
Liping YaoOncology Department, Songjiang Fangta Chinese Medicine Hospital, Shanghai, China.
Pingsheng PanOncology Department, Songjiang Fangta Chinese Medicine Hospital, Shanghai, China.
Siqi FengShanghai University of Traditional Chinese Medicine, Shanghai, China.
Cunya LiShanghai University of Traditional Chinese Medicine, Shanghai, China.
Zhangjie ZhouOncology Department, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China. 455432398@qq.com.
Jian ChenInstitute of Vascular Anomalies, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China. alexandercj@126.com.
Yi ZhongOncology Department, Shanghai TCM-Integrated Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, 230 Baoding Road, Hongkou District, Shanghai, 200082, China. zhongzixian2000@163.com.

Funding

Shanghai Hospital of Integrative Medicine, Shanghai University of Traditional Chinese Medicine RCPY0050AShanghai Municipal Health System 2024ZDXK0026Shanghai Science and Technology Commission 19401971600,21YF14444,22Y31920104Shanghai University of Traditional Chinese Medicine 23KFL089Shanghai University of Traditional Chinese Medicine KECJ2024174the Shandong Provincial Foundation for Rural Revitalization Zhang Xiulan, Ren Nianrongthe Shanghai Hongkou District Health Committee Hongwei1903-02,HKZYY-2024-24,HKQGYQY-ZYY-2022-17
6 · The paper itself

Abstract

backgroundWith the successive listing of immune checkpoint inhibitors in China, a new era of immunotherapy for malignant tumors has opened. However, this study has several limitations. Xianglian granule (XG), a Chinese herbal formula, has been proven to have a therapeutic effect on tumors in animal experiments. Our aim was to evaluate the efficacy and safety of XG combined with programmed death ligand 1 (PD-1) in pancancer patients through a randomized, double-blind, controlled trial.

methodsPatients with cancer who received PD-1 monoclonal antibody therapy were randomized to the XG or control group according to the blinded method for 9 weeks. The primary endpoint was the overall survival (OS) rate, and the secondary endpoint was the incidence rate of immune-related adverse events (irAEs). Related biological markers were observed.

resultsA total of 91 patients were included in the study. The 3-year OS rates of the XG group and the control group were 35.56% and 15.22%, respectively (P = 0.0012). The lactate dehydrogenase (LDH) level in the XG group was lower than that in the other groups, especially in the lung cancer patients (P = 0.06, P = 0.03). The two groups showed similar safety. The incidence rate of irAEs was 22.2% in the XG group and 32.6% in the control group (P = 0.27). In addition, XG can reduce D-lactic acid (D-LA) and diamine oxidase (DAO) contents (P = 0.012, P < 0.001). The B lymphocyte count and percentage of the XG group increased (P = 0.04, P = 0.035), and the interleukin-2 level decreased (P = 0.045). The Cox regression results suggested that the potential factors of the prognostic model might be XG treatment, D-LA and B lymphocyte count (P = 0.002, P < 0.001, P = 0.001).

conclusionXG had efficacy-enhancing and toxicity-reducing effects on pancancer patients when combined with a PD-1 monoclonal antibody. The mechanisms may be related to the participation of the intestinal barrier, B lymphocytes and interleukin-2. D-LA and B lymphocytes may be potential factors in the prognostic model of pancancer patients treated with immunotherapy.

Indexed as

ImmunotherapyIntestinal barrierPancancerPD-1 monoclonal antibodyXianglian granules

Identifiers

PMID41469556
PMCPMC12754985

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Registered trials

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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.