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Study on Bisphosphonates Targeting Triple-negative Breast Cancer

A Multicenter Prospective Real-world Study on Bisphosphonates Targeting Triple-negative Breast Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04045522
Enrollment
120
Registered
2019-08-05
Start date
2019-09-01
Completion date
2022-08-31
Last updated
2021-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Breast Cancer

Keywords

triple-negative breast cancer, zoledronic acid, real-world study

Brief summary

Triple-negative breast cancer has a poor prognosis and lacks effective adjuvant treatment. A number of preclinical and clinical trials have shown that bisphosphonates have direct or indirect anti-tumor activity, and early use of bisphosphonate adjuvant therapy can prevent cancer recurrence and metastasis including bone metastasis and greatly improve the prognosis of cancer patients. Bisphosphonates have the advantages of low cost, low toxicity, and strong tolerance and can be used as an auxiliary treatment for triple-negative breast cancer. The preliminary study found that bisphosphonates can be chimeric with erlotinib, an epidermal growth factor receptor tyrosine kinase inhibitor, which can synergistically inhibit the in vitro tumor formation of cancer (such as non-small-cell lung cancer and breast cancer) cells and the growth of transplanted tumors. Therefore, the purpose of this multi-center prospective real-world study was to further investigate the effects of bisphosphonate adjuvant therapy on breast cancer.

Detailed description

Triple-negative breast cancer lacks expression of estrogen receptor, progesterone receptor, and proto-oncogene HER2 as shown by immunohistochemical examination. Its incidence accounts for 15-25% of that of all breast cancer types. This type of breast cancer lacks the opportunity of endocrine therapy and anti-human epidermal growth factor receptor 2 (HER2) therapy. The main currently available treatment is still chemotherapy. Some patients may choose anti-angiogenic therapy. The prognosis of triple-negative breast cancer is worse than that of other types of breast cancer due to fewer treatment options. Bisphosphonates used to treat bone metastasis of breast cancer have been shown to have anti-tumor effects and can be used as an adjuvant treatment for triple-negative breast cancer. The preliminary study found that bisphosphonates can be chimeric with erlotinib, an epidermal growth factor receptor tyrosine kinase inhibitor, which can synergistically inhibit the in vitro tumor formation of cancer (such as non-small-cell lung cancer and breast cancer) cells and the growth of transplanted tumors. The persistence of tumor stem cells is reportedly the root cause of malignant biological behavior of triple-negative breast cancer. Bisphosphonates may synergistically inhibit triple-negative breast cancer (stem) cells with existing molecular targeted drugs. Although randomized controlled trials can provide highest-level clinical evidence, the test conditions should be strictly controlled, resulting in a small sample size and short follow-up time. However, real-world studies can include patients with multiple diseases and treatment strategies can be adjusted according to patient's needs and clinical conditions. In addition, a variety of interventions can be simultaneously used to accurately meet patient's needs, so that the research evidence is more clinically useful. Therefore, the purpose of this multi-center prospective real-world study was to investigate the significance of use of bisphosphonates as an adjuvant therapy against breast cancer.

Interventions

DRUGZoledronic Acid

Based on routine treatment, 4 mg zoledronic acid (Novartis Pharma Stein AG, Switzerland, registration No. H20140218) was intravenously administered, once every 3-4 weeks, for 1-2 years.

Sponsors

Liaoning Cancer Hospital & Institute
CollaboratorOTHER
The People's Hospital of Liaoning Province
CollaboratorOTHER
Shengjing Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
55 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* developing breast cancer as confirmed by X-ray examination, and cancer tissue was negative for estrogen receptor, progesterone receptor and HER2 * presence of metastatic axillary lymph nodes * standardized adjuvant therapy * age over 55 years

Exclusion criteria

* pregnant or lactating women * those allergic to bisphosphonates * those who are participating in other trials

Design outcomes

Primary

MeasureTime frameDescription
Pathologic complete response time5 yearsPathologic complete response is defined as no residual invasive tumor cells in the breast and axillary lymph nodes

Secondary

MeasureTime frameDescription
Disease-free survival5 yearsIt refers to the time from the start of the enrollment to the recurrence of the disease or the death of the patient due to disease progression.
Overall survival5 yearsThe length of time from either the date of diagnosis or the start of treatment for cancer, that patients diagnosed with the disease are still alive.
Incidence of osteoporosis5 yearsOsteoporosis is considered to be present when a patient's bone density or bone mineral content is more than 2.5 standard deviations below the mean value of normal adult bone density.
Incidence of bone-related events5 yearsIncidence of bone pain, fracture and other bone related events.
Incidence of other distant organ metastasis-related events5 yearsIncidence of metastasis to other distant organs such as the lung, liver, bone marrow, brain and ovary.

Countries

China

Contacts

Primary ContactXi Gu
jadegx@163.com86-18940255116

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026