A randomized controlled clinical study on the prevention of anthracycline chemotherapy-induced cardiotoxicity by Bifidobacterium lactis V9 in breast cancer patients

Li Shiqi, Suriguga, Zhang Jiao, Niu Luying, Cai Zhihui

Electronic Journal of Metabolism and Nutrition of Cancer ›› 2026, Vol. 13 ›› Issue (3) : 391-399.

PDF(1309 KB)
PDF(1309 KB)
Electronic Journal of Metabolism and Nutrition of Cancer ›› 2026, Vol. 13 ›› Issue (3) : 391-399. DOI: 10.16689/j.cnki.cn11-9349/r.2026.03.010
Original Articles

A randomized controlled clinical study on the prevention of anthracycline chemotherapy-induced cardiotoxicity by Bifidobacterium lactis V9 in breast cancer patients

  • 1Li Shiqi, 1Suriguga, 2Zhang Jiao, 2Niu Luying, 3Cai Zhihui
Author information +
History +

Abstract

Objective This study aimed to evaluate the effect of Bifidobacterium lactis V9 (B. lactis V9) on preventing anthracycline-induced cardiotoxicity in breast cancer patients. Method From June 2023 to September 2025, breast cancer patients who underwent anthracycline-based chemotherapy after surgery at the People's Hospital of Inner Mongolia Autonomous Region were enrolled. According to the random number table method, the patients were randomly divided into an observation group (50 cases) and a control group(51 cases). The observation group received a standardized anthracycline chemotherapy regimen combined with B. lactis V9, while the control group was given the same standardized chemotherapy regimen plus a matched placebo. Both groups received four treatment cycles, with each cycle lasting 21 days. The incidence of abnormal 12-lead electrocardiograms before and after treatment was recorded in both groups. Additionally, changes in N-terminal pro-brain natriuretic peptide (NT-proBNP), creatine kinase (CK), creatine kinase isoenzyme (CK-MB), and left ventricular ejection fraction (LVEF) via routine echocardiography were detected and documented at three time points: before the first cycle of treatment, after the 2nd cycle, and after the 4th cycle. Result At the end of treatment, the incidence of ECG abnormalities was higher in the control group than in the observation group, and the difference was statistically significant (54.90% vs 24.00%, P < 0.05). Intra-group comparisons of NT-proBNP levels before and after treatment showed no significant changes in either group (P >0.05); however, after 4 treatment cycles, NT-proBNP levels in the observation group were lower than those in the control group, and the difference was statistically significant (P < 0.05).CK levels in the observation group first decreased and then increased, however, there was no statistically significant difference between the two groups compared to the control group (P >0.05). There were no significant changes in CK-MB levels between or within the two groups (P >0.05). During the treatment period, LVEF levels in the observation group first decreased and then increased, whereas LVEF levels in the control group decreased compared to pre-treatment levels (P < 0.05). After 4 treatment cycles, the LVEF levels in the observation group were higher than those in the control group (P < 0.05). Conclusion B. lactis V9 may offer some degree of benefit in preventing anthracycline-induced cardiac toxicity in breast cancer patients undergoing chemotherapy.

Key words

Breast cancer / Probiotics / Bifidobacterium lactis V9 / Anthracyclines / Cardiotoxicity / Randomization / Chemotherapy / Prevention

Cite this article

Download Citations
Li Shiqi, Suriguga, Zhang Jiao, Niu Luying, Cai Zhihui. A randomized controlled clinical study on the prevention of anthracycline chemotherapy-induced cardiotoxicity by Bifidobacterium lactis V9 in breast cancer patients[J]. Electronic Journal of Metabolism and Nutrition of Cancer. 2026, 13(3): 391-399 https://doi.org/10.16689/j.cnki.cn11-9349/r.2026.03.010

References

[1] 吴疆,张志仁.抗肿瘤药物所致心血管毒性的研究进展[J].中国医刊,2020,55(10):1077-1081.
[2] SPERLONGANO S, VERDE G, GUARNACCLA N, et al. Echocardiographic monitoring in cancer therapy: clinical guidance for cardiologists and oncologists[J]. Heart Fail Rev,2025,30(6):1591-1602.
[3] 崔健嫦,李勇,黄积雄,等.右心室应变评价蒽环类药物对乳腺癌患者右心室功能的影响[J].中国临床医生杂志,2023,51(10):1170-1172.
[4] WEI J J, LAN G Z, ZHANG W F, et al. Targeting FDX1 by trilobatin to inhibit cuproptosis in doxorubicin-induced cardiotoxicity[J]. Br J Pharmacol,2025,182(11):2409-2425.
[5] LI N, WANG L, LI L, et al. The correlation between gut microbiome and atrial fibrillation: pathophysiology and therapeutic perspectives[J]. Mil Med Res,2023;10(1):51.
[6] TANG W H W, LI D Y, HAZEN S L. Dietary metabolism, the gut microbiome, and heart failure[J]. Nat Rev Cardiol,2019,16(3):137-154.
[7] ABU-ELSAAD N M, ABD ELHAMEED A G, EL-KAREF A, et al. Yogurt containing the probacteria Lactobacillus acidophilus combined with natural antioxidants mitigates doxorubicin-induced cardiomyopathy in rats[J]. J Med Food,2015,18(9):950-959.
[8] STEWART L K, SMOAK P, HYDOCK D S, et al. Milk and kefir maintain aspects of health during doxorubicin treatment in rats[J]. J Dairy Sci,2019,102(3):1910-1917.
[9] LIU R, FAN C, LIU X,et al . Evaluating cardioprotective strategies for anthracycline-induced cardiotoxicity in breast cancer: insights from a systematic review and network meta-analysis[J]. Cardio-oncol, 2025;11(1):65.
[10] 王瑞平.随机对照临床试验设计中的样本量估算方法[J].上海医药,2023,44(1):48-52.
[11] SCHNEIDER C, RYFFEL C, STÜTZ L, et al. Supervised exercise training in patients with cancer during anthracycline-based chemotherapy to mitigate cardiotoxicity: a randomized controlled trial[J]. Front Cardiovasc Med,2023,10:1283153.
[12] 刘文慧,杨青澍,常佩芬.加拿大心血管病学会《临床实践更新:QT间期延长患者管理共识》解读[J].临床药物治疗杂志,2024,22(5):12-17.
[13] FULVIO M, FABIO A, CHARLOTTEl V, et al. Supportive care in older lymphoma patients to reduce toxicity and preserve quality of life[J]. Cancers,2023,15(22):5381.
[14] ZHAO L, XING C, SUN W, et al. Lactobacillus supplementation prevents cisplatin-induced cardiotoxicity possibly by inflammation inhibition[J]. Cancer Chemoth Pharm,2018,82(6):999-1008.
[15] SUN Z, CHEN, WWANG J, et al. Complete genome sequence of probiotic Bifidobacterium animalis subsp. lactis strain V9[J]. J Bacteriol,2010,192(15):4080-4081.
[16] YAN Y, LIU C, ZHAO S, et al. Probiotic bifidobacterium lactis V9 attenuates hepatic steatosis and inflammation in rats with non-alcoholic fatty liver disease[J]. AMB Express,2020,10(1):101.
[17] LU X, ZHAO Y, CHEN C, et al. BNP as a marker for early prediction of anthracycline-induced cardiotoxicity in patients with breast cancer[J]. Oncol Lett, 2019;18(5):4992-5001.
[18] BHAGAT A A, KALOGEROPOULOS A P, BAER L, et al. Biomarkers and strain echocardiography for the detection of subclinical cardiotoxicity in breast cancer patients receiving anthracyclines[J]. J Pers Med,2023,13(12):1710.
[19] BHAGAT A, KLEINERMAN E S. Anthracycline-Induced cardiotoxicity: causes, mechanisms, and prevention[J]. Adv Exp Med Biol,2020,1257:181-192.
[20] 中国食品科学技术学会益生菌分会.益生菌健康新功能的科学证据[J].中国食品学报,2025,25(7):468-482.
[21] SAMPSELI K, HAO D, REIMER R A, et al. The gut microbiota: a potential gateway to improved health outcomes in breast cancer treatment and survivorship[J]. Int J Mol Sci,2020,21(23):9239.
[22] SU N, SUN J, ZHANG G, et al. New advances in medical imaging technology for the evaluation of anthracycline-induced cardiotoxicity[J]. Chi Med J,2022,135(16):1883-1885.
[23] KITTIWARAWUT A, VORASETTAKARNKIG Y, TANASANVIMON S,et al. Serum NT-proBNP in the early detection of doxorubicin-induced cardiac dysfunction[J]. Asia Pac J Clin Onco,2013,9(2):155-161.
[24] SANDAMALI J A N, HEWAWASAM R P, FERNANDO M A C S S, et al. Electrocardiographic and biochemical analysis of anthracycline induced cardiotoxicity in breast cancer patients from Southern Sri Lanka[J]. BMC Cancer,2023,23(1):210.
[25] LIU C, CHENG B, ZHAO G, et al. Process analysis of anthracycline adverse reactions in breast cancer patients with postoperative chemotherapy[J]. J Invest Med,2022,70(6):1352-1357.
[26] 买泓,吴春农.右丙亚胺预防化疗药物心脏毒性的临床研究[J].中西医结合心脑血管病杂志,2018,16(17):2542-2545.
[27] ZHEN J, ZHOU Z, HE M, et al. The gut microbial metabolite trimethylamine N-oxide and cardiovascular diseases[J]. Front Endocrinol,2023,14:1085041.
[28] KUNIKA, FREY N, RANGREZ A Y, et al. Exploring the involvement of gut microbiota in cancer therapy-induced cardiotoxicity[J]. Int J Mol Sci, 2023,24(8):7261.
[29] 赵媛,于世杰,饶本强.粪菌移植在肿瘤治疗中的应用进展[J].中国肿瘤外科杂志,2024,16(6):521-525.
[30] 林兵,阳静,朱翠凤.益生菌联合低血糖生成指数高优质蛋白饮食调控肥胖患者肌肉脂肪代谢的临床应用[J/CD].肿瘤代谢与营养电子杂志,2025,12(6):814-819.
[31] MAZZIOTTA C, TOGNCN M, MARTINI F, et al. Probiotics mechanism of action on immune cells and beneficial effects on human health[J]. Cells,2023,12(1):184.
[32] LI X, GENG J, ZHAO J, et al. Trimethylamine N-Oxide exacerbates cardiac fibrosis via activating the NLRP3 Inflammasome[J]. Front Physiol,2019;10:866.
[33] ALGILALl M, DABANIYASTI E T, SENGUL E, et al. Probiotics containing lactobacillus are promising candidates for cisplatin-induced cardiotoxicity[J]. Sci Rep,2025,15(1):42064.
[34] 刘鹏林,逄承健,邸爱婷,等.短链脂肪酸影响肠道动力的机制研究进展[J].结直肠肛门外科,2021,27(2):179-182.
[35] NEJATI-KOSHKI K, FATHI F, ARABZADEH A, et al. Biomarkers and optical based biosensors in cardiac disease detection: early and accurate diagnosis[J]. Anal Methods, 2023 Oct 26, 15(41): 5441-5458.
[36] PONGPROT Y, SITTIWANGKUL R, CHAROENKWAN P, et al. Use of cardiac markers for monitoring of doxorubicin-induced cardiotoxicity in children with cancer[J]. J Pediat Hematol Onc,2012,34(8):589-595.
PDF(1309 KB)

Accesses

Citation

Detail

Sections
Recommended

/