Lactobacillus Vaginalis Capsules for the Management of Vulvovaginal Atrophy in Young Breast Cancer Patients

Sponsor
The First Affiliated Hospital with Nanjing Medical University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05974449
Collaborator
(none)
100
2
17

Study Details

Study Description

Brief Summary

This study is a prospective, randomized controlled, phase II clinical study with a planned enrolment of 60 patients. The study focuses on the efficacy and safety of Lactobacillus vaginalis capsules for the prevention and/or treatment of vulvovaginal symptoms in young breast cancer patients receiving ovarian protection during chemotherapy, in order to improve compliance and quality of life in breast cancer patients.

Condition or Disease Intervention/Treatment Phase
  • Drug: Vaginal Lactobacillus capsules
Phase 2

Detailed Description

Breast cancer is the most common malignancy in women, and its incidence is increasing year by year. While systemic combination therapy (e.g., Chemotherapy, endocrine therapy, targeted therapy, etc.) can increase the cure rate of patients, it can also bring about some adverse effects that can negatively affect the life of patients. The most common form of chemotherapy, for example, is chemotherapy drugs (especially cyclophosphamide-containing chemotherapy regimens), which can lead to impaired ovarian function. Inhibition of ovarian function with gonadotropin-releasing hormone agonists (GnRHa) can achieve protection of the ovaries during chemotherapy and help restore ovarian function. As the trend towards younger breast cancer has become more pronounced in recent years, ovarian protection has also received increasing attention. However, ovarian protection can also dramatically reduce serum estrogen levels in patients, leading to vulvovaginal symptoms such as vaginal dryness, difficulty with intercourse, genital skin irritation, itching, burning, and increased vaginal discharge. Moreover, patients are often too shy to express these symptoms, leading to underdiagnosis and under-treatment.

The North American Menopause Society states that topical estrogen therapy is the first-line option for moderate to severe vulvovaginal symptoms, but its safety in women with breast cancer is not known. Some studies have shown an increase in serum estradiol levels with the use of estradiol vaginal rings and creams, and there are no clinical studies to suggest a relationship between a mild increase and the risk of breast cancer recurrence. and short-term effects are limited. --The hierarchy is not out: hormonal therapy first, then non-hormonal therapy The onset of vulvovaginal symptoms is primarily due to a decrease in serum circulating estrogen in women, but many researchers are beginning to explore whether these changes can be attributed to changes in the dynamics of the vaginal microbiome. The vaginal microecology of healthy women is dominated by lactic acid bacteria, which proliferate in the anaerobic environment of the vagina, producing various antimicrobial compounds such as lactic acid, hydrogen peroxide (H2O2) and bacteriocins and maintaining vaginal health by enhancing epithelial barrier function, symbiotic colonization, blocking pathogenic bacterial adhesion, lowering pH, influencing antimicrobial peptide production/secretion and overall mucosal immunity. In patients presenting with vulvovaginal symptoms, vaginal microecology is no longer dominated by lactobacilli and it has been shown that the severity of vaginal dryness, dyspareunia, and vaginal pain symptoms are negatively correlated with the number of lactobacilli in the vagina. To address this issue, researchers have explored the fact that Donders et al. found that Lactobacillus combined with low-dose estrogen significantly improved vulvovaginal symptoms in women but caused a concomitant increase in serum estradiol, the risk of which is not yet known in breast cancer patients , whereas this study explored the use of Lactobacillus alone as an intervention to see if there was an increase in serum estradiol after the intervention, and prophylactic medication was administered to address patients who endure vulvovaginal symptoms due to shyness of expression. However, there is a lack of large randomized controlled clinical studies to determine the effectiveness of Lactobacillus in modulating or restoring a dysregulated vaginal microbiome and improving vaginal symptoms in different populations. The aim of this study was to explore, in the small sample size, whether prophylactic use of Lactobacillus vaginalis capsules during ovarian protection in breast cancer patients could prevent vulvovaginal symptoms in patients and to assess its safety in order to improve treatment adherence in breast cancer patients and improve the quality of life of breast cancer patients.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Phase II Clinical Study of Lactobacillus Vaginalis Capsules for the Management of Vulvovaginal Atrophy During Ovarian Protection in Young Breast Cancer Patients
Anticipated Study Start Date :
Aug 1, 2023
Anticipated Primary Completion Date :
Aug 1, 2024
Anticipated Study Completion Date :
Dec 30, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: T1, T2 dosing group

T1 and T2 dosing groups: The drug is administered on the day of the T1 and T2 chemotherapy cycles for 7 days, washing the vulva and placing the drug deep into the vagina, once a night, 2 capsules each time.

Drug: Vaginal Lactobacillus capsules
This product is a micro-ecological preparation made from live enteric streptococci and is used for the treatment of vaginosis caused by disorders of the flora.
Other Names:
  • blank
  • Experimental: T3, T4 dosing group

    T3 and T4 dosing groups: The drug is given on the day of the T3 and T4 chemotherapy cycles and is administered for 7 days. The drug is placed deep into the vagina after washing the vulva, once a night, 2 capsules each time.

    Drug: Vaginal Lactobacillus capsules
    This product is a micro-ecological preparation made from live enteric streptococci and is used for the treatment of vaginosis caused by disorders of the flora.
    Other Names:
  • blank
  • Outcome Measures

    Primary Outcome Measures

    1. Vaginal PH [1 year]

      Reactive vaginal pH

    2. Functional Assessment of Breast Cancer Therapy Scale (FACT-B) [1year]

      For assessing quality of life and vulvovaginal symptoms in women

    3. Functional Assessment of Endocrine Therapy Scale (FACT-ES) [1year]

      For assessing quality of life and vulvovaginal symptoms in women

    Secondary Outcome Measures

    1. The detection rate of vaginal secretions of Gardnerella vaginalis, Lactobacillus janus, Lactobacillus garciae; Lactobacillus curvatus, Lactobacillus inertus, Lactobacillus chimaerae, Prevotella spp. and Streptococcus spp; [1year]

      Detection of target flora in vaginal secretions using qPCR. Reflecting changes in vaginal microecology

    2. Serum concentrations of estrone, estradiol and oestrogen binding protein [1 year]

      Testing serum hormone levels

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    1. Pathologically confirmed invasive breast cancer (regardless of pathology type)

    2. Receiving ≥ 4 cycles of a chemotherapy regimen containing paclitaxel and/or anthracyclines

    3. Not yet menopausal prior to injection of ovarian protective drugs

    4. Female patients aged 18-40 years or 41-45 years with pathologically confirmed breast cancer and negative HR;

    5. Good compliance, normal comprehension, and ability to receive treatment as required;

    6. ECOG score : 0-1;

    7. Patients volunteered to participate in this study and signed an informed consent form.-

    Exclusion Criteria:
    1. Use of any other vaginal medication in the 3 months prior to the study;

    2. Use of any anti-infective medication in the 3 months prior to the study;

    3. Active genital tract infection;

    4. Previous development of other malignancies

    5. Any reason why they are unable to complete the full course of follow-up treatment as prescribed by their doctor;

    6. AST and ALT ≥ 1.5 times the upper limit of normal, alkaline phosphatase ≥ 2.5 times the upper limit of normal, total bilirubin ≥ 1.5 times the upper limit of normal, serum creatinine ≥ 1.5 times the upper limit of normal; LEVF < 50% on cardiac ultrasound;

    7. Severe coagulation disorder, severe systemic disease, or uncontrollable infection;

    8. Persons without personal freedom and independent civil capacity; the presence of mental disorders, addictions, etc., which in the judgment of the investigator do not qualify for enrolment.-

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • The First Affiliated Hospital with Nanjing Medical University

    Investigators

    • Study Director: wang jue, MD, The First Affiliated Hospital with Nanjing Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Jue Wang, Prof., The First Affiliated Hospital with Nanjing Medical University
    ClinicalTrials.gov Identifier:
    NCT05974449
    Other Study ID Numbers:
    • BC-OFSAE-Lactobacillus
    First Posted:
    Aug 3, 2023
    Last Update Posted:
    Aug 3, 2023
    Last Verified:
    Jul 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Jue Wang, Prof., The First Affiliated Hospital with Nanjing Medical University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Aug 3, 2023