Breast CancerNCT04476485
Sj-subway, a Predictor for the Recurrence of High-risk Hormone Receptor-positive Breast That is Sensitive to Extended Endocrine Therapy
An observational study of Breast Cancer, run by Shengjing Hospital at 12 sites in China.
Trial summary
Hormone receptor-positive breast cancer accounts for about 70% of all breast cancers. Extended endocrine therapy with aromatase inhibitor is the current main treatment for hormone receptor-positive breast cancer. Read more about this study
- Who is it for?
- Ages 18 to 70 years, women only
- Conditions the study is for
- Breast Cancer
- What is being tested?
- endocrine therapy
- How many people
- 1,000 participants
- Where
- 12 sitesChina
- Study dates
- 19 Jul 2021to 31 Dec 2026
- How long will I take part?
- 10 Years
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 70 years
- Women only
- No healthy volunteers
- Adult, Older adult
Study population: The early-stage invasive breast cancer positive for estrogen receptor and / or progesterone receptor and have completed standard endocrine therapy for 5 years.
Who may be able to join
- early-stage invasive breast cancer positive for estrogen receptor and / or progesterone receptor is pathologically confirmed;
- patients who have completed standard endocrine therapy for 5 years without recurrence and metastasis;
- 18-70 years old;
- patients with one of the following six manifestations: KI67 ≥ 30%; tumor size > 2 cm; positive lymph nodes; histological grade III; vascular cancer thrombus; HER-2 gene overexpression or amplification.
Who cannot join
- with a history of other malignancies;
- patients who have severe abnormalities in important organs, such as the heart, liver, and kidney or who cannot be tolerant to extended treatment due to poor constitution;
- patients with severe osteoporosis or dyslipidemia, or those who cannot tolerate endocrine therapy ;
- patients who have participated in other clinical trials.
Trial locations and contacts
12 sites in 1 country. Contact the study team or a site near you to ask about taking part.
12 sites in 1 country
China12 sites, 12 recruiting
- Recruiting
The Second Hospital of Jilin University
Changchun, Jilin, 130041
Yingchao Zhang, zhang_yc@jlu.edu.cn
Yingchao Zhang
- Recruiting
Dalian Municipal Central Hospital
Dalian, Liaoning, 116033
Wenbin Guo, +8613079850586, drguowb@hotmail.com
Wenbin Guo
- Recruiting
Cancer Hospital Affiliated to Harbin Medical University
Harbin, Heilongjiang, 150081
Xuesong Chen, +8615804500816, cxs1978@163.com
Xuesong Chen
- Recruiting
Panjin Liaohe Oilfield Gem Flower Hospital
Panjin, Liaoning, 124010
Hongbin Han, +8613704236001, rose_030201@163.com
Hongbin Han
- Recruiting
Shengjing Hospital affiliated to China Medical University
Shenyang, Liaoning, 110004
Nan Niu, MD
Cai-Gang Liu, MD
- Recruiting
Shengjing Hospital of China Medical University
Shenyang, Liaoning, 110004
Xi Gu, +86 18940255116, jadegx@163.com
- Recruiting
Shengjing Hospital of China Medical University
Shenyang, Liaoning, 110004
Caigang Liu, +86 18940254967, liucg@sj-hospital.org
Rong Wu, +86 18940251156, wur@sj-hospital.com
- Recruiting
Shengjing Hospital of China Medical University
Shenyang, Liaoning, 110004
Nan Niu, MD, +8618940256668, niunannancy@163.com
Cai-Gang Liu, MD
- Recruiting
The Fourth Affiliated Hospital of China Medical University
Shenyang, Liaoning, 110032
Wei Tu, +8618900913000, cmu4htw@126.com
Wei Tu
- Recruiting
Liaoning Cancer Hospital & Institute
Shenyang, Liaoning, 110042
Hong Xu, +8618900917779, xh4015@163.com
Hong Xu
- Recruiting
Liaoning Tumor Hospital & Institute
Shenyang, Liaoning
Hong Xu, +86-18900917779, xh4015@163.com
- Recruiting
People's Hospital of Liaoning Province
Shenyang, Liaoning
Qingfeng Liu, +86-17702486789, drliuqf1970@126.com
About this study
Official title: A Newly Discovered Clinical Recurrence Predictor for High-risk Hormone Receptor-positive Breast Cancer: a Real Word Study
Hormone receptor-positive breast cancer accounts for about 70% of all breast cancers. Extended endocrine therapy with aromatase inhibitor is the current main treatment for hormone receptor-positive breast cancer. However, previous studies have shown a long-lasting risk of the recurrence of hormone receptor-positive breast cancer at early stage, and disease recurrence is considered inevitable only depending on a 5-year of adjuvant endocrine therapy. Therefore, extended endocrine therapy is considered as a possible measure to reduce the risk of recurrence.
Numerous clinical studies have focused on extended endocrine therapy in patients with specific types of breast cancer. In 2017, the National Comprehensive Cancer Network (NCCN) updated the recommends for extended endocrine therapy with aromatase inhibitor, where postmenopausal early-stage breast cancer patients wo have high risk factors may be considered to be given an extended 5-year endocrine treatment with aromatase inhibitor after the initial 5-year treatment. In 2019, the Chinese Society of Clinical Oncology also suggested that postmenopausal hormone receptor-positive patients who have been well tolerated to the initial 5 years of adjuvant endocrine therapy can be given the extended endocrine therapy under some restrictions.
Read more
However, extended endocrine therapy may also cause other risks in patients. Long-term tamoxifen treatment can significantly increase the incidence of adverse reactions such as endometrial cancer, thrombotic disease, and dyslipidemia, and long-term aromatase inhibitor treatment can also increase the incidence of osteoporosis, fractures, dyslipidemia, and hypertension. Although anti-cancer treatment can reduce cancer deaths, it may increase deaths due to cardiovascular diseases.
An attempt has been proposed to find out an indicator that can effectively determine the necessity of extended endocrine therapy in such patients, not only improving the prognosis of breast cancer patients, but also reducing treatment-related side effects. The author's team recently discovered sj-subway, a possible factor with a long tubular structure in breast cancer lesions. The authors found that the higher expression of sj-subway indicates the worse patient's prognosis. So the positive expression of sj-subway may be a predictor of recurrence and metastasis in high-risk hormone receptor-positive patients. However, whether this predictor can be used clinically remains to be studied.
This real-world study intends to analyze the difference in the clinical efficacy of extended endocrine therapy under different sj-subway expression in high-risk hormone receptor-positive breast cancer patients, and to explore whether sj-subway can screen out the patients who can benefit from extended endocrine therapy, thus providing a therapeutic help for hormone receptor-positive breast cancer patients.
Read the detailed description
Breast cancer has been one of the most common malignant tumors in women, accounting for 23% of all the malignancies. There are estimated 1,300,000 new cases of breast cancers and 400,000 deaths due to breast cancers every year in the world. Hormone receptor-positive breast cancer accounts for about 70% of all breast cancers.
Since ovarian resection was first used in the treatment of advanced breast cancer in the late 19th century, with more than a century of development, endocrine therapy has become the most important adjuvant therapy for hormone receptor-positive breast cancers, especially for advanced breast cancers. Increasing clinical trials of adjuvant endocrine therapy such as ATAC, BIG1-98, and IES, which have been implemented since 2002, have ascertained the effect of adjuvant endocrine therapy with aromatase inhibitor, and the guidelines for the diagnosis and treatment of breast cancer have been also changed accordingly.
Although early-stage hormone receptor-positive breast cancer patients have a better prognosis than HER-2 positive and triple-negative patients, there is still a long-lasting risk of postoperative recurrence, which has been confirmed in two large-scale meta-analyses reported by the Early Breast Cancer Trialists' Collaborative Group (EBCTCG). A meta-analysis released by the EBCTCG in 1998 indicated that early-stage hormone receptor-positive breast cancer patients, especially lymph node-positive patients, experienced the second recurrence peak at 2-3 years and 7-9 years after completion of endocrine therapy. In 2016, the EBCTCG released another relevant study at the annual meeting of the American Society of Clinical Oncology (ASCO), in which the long-term recurrence rate within 5-20 years was up to 14% in T1N0 breast cancer patients who had undergone 5 years of adjuvant endocrine therapy. Therefore, the 5 years of standard adjuvant endocrine therapy cannot eliminate the risk of recurrence. Most scholars have suggested that the duration of endocrine therapy should be extended to reduce the recurrence risk of breast cancer.
Numerous clinical trials have focused on the use of extended endocrine therapy in patients with specific types of breast cancer. In the MA17R trial, patients received 3-5 years of tamoxifen or 5 years of aromatase inhibitor treatment, followed by another 5 years of aromatase inhibitor treatment. The extended aromatase inhibitor treatment was found to significantly improve the disease-free survival time of hormone receptor-positive early breast cancer patients, while also reducing the risk of contralateral breast cancer and distant relapse. In the NSABP B42 trial, patients who had received initial 5 years of aromatase inhibitor treatment or initial 5 years of tamoxifen + aromatase inhibitor treatment were all treated with extended aromatase inhibitor. Although the primary endpoint (P = 0.048) did not reach the expected value, extended treatment with aromatase inhibitors significantly reduced the secondary endpoints - breast cancer-free interval and distant relapse, confirming the conclusion of the MA17R study. In the DATA trial, although extended treatment with aromatase inhibitor did not benefit in general, subgroup analysis showed that some high-risk patients, such as patients with positive lymph nodes, tumors larger than 2 cm in diameter, or receiving chemotherapy, could benefit from 6 years of anastrozole treatment. The IDEAL trial showed that there is a trend of benefit in patients with positive lymph nodes. With the support of many large-scale clinical studies published in succession, the NCCN practice guidelines for breast cancer released in 2017 recommends an additional 5 years of aromatase inhibitor treatment following the initial 5-year treatment in postmenopausal patients with early-stage breast cancer at high risk for relapse. As per the Chinese Society of Clinical Oncology guidelines published in 2019, the extended endocrine therapy is also recommended for postmenopausal hormone receptor-positive patients who have been well tolerated to the initial 5-year adjuvant treatment. However, there are some restrictions, such as positive lymph nodes, G3 or other risk factors that require adjuvant chemotherapy. For premenopausal hormone receptor-positive patients who have been well tolerated to the initial 5 years of endocrine treatment, extended endocrine therapy is also recommended in some situations, such as the presence of positive lymph nodes, G3, less than 35 years old at diagnosis, high-level Ki-67 or pT2 and above.
However, the extended endocrine therapy also has some adverse events. Multiple studies have shown that long-term use of tamoxifen can significantly increase the incidence of adverse reactions such as endometrial cancer, thrombotic disease, and dyslipidemia. Similarly, long-term treatment with aromatase inhibitors can also increase the incidence of adverse reactions such as osteoporosis, fractures, dyslipidemia, and hypertension. In the ATLAS trial, the incidence of endometrial cancer in patients treated with 10 years of tamoxifen was higher than that in patients treated with 5 years of tamoxifen. Similar results are discovered in the aTTom trial. In the IDEAL trial, the incidence rates of osteoarthritis and osteoporosis in patients treated with 5 years of letrozole was increased by 14% and 10% of that in patients undergoing 2.5 years of treatment. A study involving nearly 100,000 breast cancer patients showed that only 49.9% of breast cancer patients died of breast cancer, 16.3% died of cardiovascular disease, and 33.8% died of other causes. Among them, breast cancer and cardiovascular disease were the main causes of death in well- and poor-tolerated patients, respectively. This suggests that although anti-cancer treatment can reduce cancer deaths, it may increase the death due to cardiovascular disease. Such deaths are often offset, which often improves the BCFI, but does not benefit the overall survival.
Therefore, an effective predictor for relapse risks that can accurately determine the necessity of extended endocrine therapy is expected to be discovered. The use of this predictor will both improve patient's prognosis and reduce treatment-related side effects. The author's team recently discovered a possible factor with a long tubular structure in breast cancer lesions using immunofluorescence staining, which was named as sj-subway. The authors conducted a retrospective analysis based on the specimen library and case follow-up library of the Breast Center of Shengjing Hospital Affiliated to China Medical University. They found that sj-subway was positively expressed in various subtypes of breast cancer tissues, and mostly expressed in the hormone receptor-positive subtype. The group with more sj-subway expression had a higher positive expression of hormone receptor/ progesterone receptor. Further survival analysis also revealed the worse prognosis of patients with the existence of higher sj-subway expression. Therefore, the authors speculate that positively expressed sj-subway may become a predictor of recurrence and metastasis in high-risk patients with hormone receptor positive. However, the clinical use of this factor to screen the population benefiting from extended endocrine therapy remains to be studied.
This real-world study intends to observe the difference in the clinical efficacy of extended endocrine therapy under different sj-subway expression in high-risk hormone receptor-positive breast cancer patients, and to analyze whether the use of sj-subway can further screen out the population with benefit from extended endocrine therapy, thus further improving the survival of such patients without additional adverse events.
- Conditions
- Breast Cancer
- Being tested
- endocrine therapy
- Keywords
- receptor, estrogen, endocrine therapy, aromatase inhibitor
- Medical subject headings
- Breast Neoplasms
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
endocrine therapyOther
If the expression of sj-subway in the surgical wax block is eligible, it is recommended but not mandatory that patients follow the guidelines to choose the appropriate extended endocrine therapy. 1. For postmenopausal patients: Extend treatment with aromatase inhibitors 10 years: letrozole or anastrozole or exemestane. 2. For premenopausal patients: An initial 5 years tamoxifen treatment followed by additional 5 years extended tamoxifen treatment. Postmenopausals are treated with aromatase inhibitors 5 years. 3. For patients have completed ovarian function suppression plus initial 5-year aromatase inhibitor treatment: Menopausals: Aromatase inhibitors; Non-menopausals: 5 years of tamoxifen treatment or ovarian function suppression plus 5 years of aromatase inhibitor treatment. 4. For patients have completed ovarian function suppression plus initial 5-year tamoxifen treatment: Menopausals: Aromatase inhibitors for additional 5 years; Non-menopausals: Tamoxifen for additional 5 years.
| Study group | Role | What they receive |
|---|---|---|
| experimental group | If the expression of sj-subway in the surgical wax block is eligible, it is recommended but not mandatory that patients follow the guidelines to choose the appropriate extended endocrine therapy. Receives: Other: endocrine therapy |
What is being measured
The primary outcome is the main question the study is designed to answer.
disease-free survival
the time from enrollment to relapse or death due to any reason.
Measured: 5 years after enrollment
Secondary outcomes (3)
Overall survival
the time from enrollment to death due to any reason
Measured: 5 years after enrollment
Incidence of contralateral breast cancer
the proportion of contralateral breast cancer. Evaluations will be made at 1, 2, 3, 4, and 5 years after enrollment
Measured: 1, 2, 3, 4, and 5 years after enrollment
Incidence of adverse events
the proportion of adverse events, including osteoporosis, bone pain, fractures, dyslipidemia, endometrial lesions. Evaluations will be made 1, 2, 3, 4, and 5 years after enrollment
Measured: 1, 2, 3, 4, and 5 years after enrollment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted20 Jul 2020
- Study start19 Jul 2021 (estimated)
- Primary completion31 Dec 2021 (estimated)
- Study completion31 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Breast CancerStudies of the same condition, open and under way.
- More trials run by Shengjing HospitalThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Prospective
- Enrolment
- 1,000 participants (estimated)
- Target duration
- 10 Years
Sponsor and investigators
- Lead sponsor
- Shengjing Hospital
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Caigang Liu, Shengjing Hospital
- Investigators
- Jin-Qi Xue, Principal investigator, Shengjing HospitalXi Gu, Principal investigator, Shengjing HospitalNan Niu, Principal investigator, Shengjing HospitalTian-Hui Xia, Principal investigator, Shengjing HospitalWei Tu, Principal investigator, Fourth Affiliated Hospital of China Medical UniversityHong Xu, Principal investigator, Liaoning Cancer Hospital & InstituteHao Zhang, Principal investigator, Liaoning Cancer Hospital & InstituteYuan-Xi Huang, Principal investigator, Heilongjiang Provicial Hospital
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04476485
- Sponsor's protocol ID
- ShengjingH 3
- Status last verified
- Jul 2021
- First submitted
- 15 Jul 2020
- Last updated
- 20 Jul 2021
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- Undecided
Study at a glance
From the registry record, last updated by the sponsor on 20 Jul 2021. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A Newly Discovered Clinical Recurrence Predictor for High-risk Hormone Receptor-positive Breast Cancer: a Real Word Study
- ClinicalTrials.gov ID
- NCT04476485
- Acronym / sponsor ID
- ShengjingH 3
- Conditions
- Breast Cancer
- Keywords
- receptor, estrogen, endocrine therapy, aromatase inhibitor
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 1,000 participants (estimated)
- Lead sponsor
- Shengjing HospitalUniversity, hospital or other
- Study start
- 19 Jul 2021 (estimated)
- Primary completion
- 31 Dec 2021 (estimated)
- Study completion
- 31 Dec 2026 (estimated)
- First posted
- 20 Jul 2020 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Hormone receptor-positive breast cancer accounts for about 70% of all breast cancers. Extended endocrine therapy with aromatase inhibitor is the current main treatment for hormone receptor-positive breast cancer. However, previous studies have shown a long-lasting risk of the recurrence of hormone receptor-positive breast cancer at early stage, and disease recurrence is considered inevitable only depending on a 5-year of adjuvant endocrine therapy. Therefore, extended endocrine therapy is considered as a possible measure to reduce the risk of recurrence.
Numerous clinical studies have focused on extended endocrine therapy in patients with specific types of breast cancer. In 2017, the National Comprehensive Cancer Network (NCCN) updated the recommends for extended endocrine therapy with aromatase inhibitor, where postmenopausal early-stage breast cancer patients wo have high risk factors may be considered to be given an extended 5-year endocrine treatment with aromatase inhibitor after the initial 5-year treatment. In 2019, the Chinese Society of Clinical Oncology also suggested that postmenopausal hormone receptor-positive patients who have been well tolerated to the initial 5 years of adjuvant endocrine therapy can be given the extended endocrine therapy under some restrictions.
However, extended endocrine therapy may also cause other risks in patients. Long-term tamoxifen treatment can significantly increase the incidence of adverse reactions such as endometrial cancer, thrombotic disease, and dyslipidemia, and long-term aromatase inhibitor treatment can also increase the incidence of osteoporosis, fractures, dyslipidemia, and hypertension. Although anti-cancer treatment can reduce cancer deaths, it may increase deaths due to cardiovascular diseases.
An attempt has been proposed to find out an indicator that can effectively determine the necessity of extended endocrine therapy in such patients, not only improving the prognosis of breast cancer patients, but also reducing treatment-related side effects. The author's team recently discovered sj-subway, a possible factor with a long tubular structure in breast cancer lesions. The authors found that the higher expression of sj-subway indicates the worse patient's prognosis. So the positive expression of sj-subway may be a predictor of recurrence and metastasis in high-risk hormone receptor-positive patients. However, whether this predictor can be used clinically remains to be studied.
This real-world study intends to analyze the difference in the clinical efficacy of extended endocrine therapy under different sj-subway expression in high-risk hormone receptor-positive breast cancer patients, and to explore whether sj-subway can screen out the patients who can benefit from extended endocrine therapy, thus providing a therapeutic help for hormone receptor-positive breast cancer patients.
Detailed description
Breast cancer has been one of the most common malignant tumors in women, accounting for 23% of all the malignancies. There are estimated 1,300,000 new cases of breast cancers and 400,000 deaths due to breast cancers every year in the world. Hormone receptor-positive breast cancer accounts for about 70% of all breast cancers.
Since ovarian resection was first used in the treatment of advanced breast cancer in the late 19th century, with more than a century of development, endocrine therapy has become the most important adjuvant therapy for hormone receptor-positive breast cancers, especially for advanced breast cancers. Increasing clinical trials of adjuvant endocrine therapy such as ATAC, BIG1-98, and IES, which have been implemented since 2002, have ascertained the effect of adjuvant endocrine therapy with aromatase inhibitor, and the guidelines for the diagnosis and treatment of breast cancer have been also changed accordingly.
Although early-stage hormone receptor-positive breast cancer patients have a better prognosis than HER-2 positive and triple-negative patients, there is still a long-lasting risk of postoperative recurrence, which has been confirmed in two large-scale meta-analyses reported by the Early Breast Cancer Trialists' Collaborative Group (EBCTCG). A meta-analysis released by the EBCTCG in 1998 indicated that early-stage hormone receptor-positive breast cancer patients, especially lymph node-positive patients, experienced the second recurrence peak at 2-3 years and 7-9 years after completion of endocrine therapy. In 2016, the EBCTCG released another relevant study at the annual meeting of the American Society of Clinical Oncology (ASCO), in which the long-term recurrence rate within 5-20 years was up to 14% in T1N0 breast cancer patients who had undergone 5 years of adjuvant endocrine therapy. Therefore, the 5 years of standard adjuvant endocrine therapy cannot eliminate the risk of recurrence. Most scholars have suggested that the duration of endocrine therapy should be extended to reduce the recurrence risk of breast cancer.
Numerous clinical trials have focused on the use of extended endocrine therapy in patients with specific types of breast cancer. In the MA17R trial, patients received 3-5 years of tamoxifen or 5 years of aromatase inhibitor treatment, followed by another 5 years of aromatase inhibitor treatment. The extended aromatase inhibitor treatment was found to significantly improve the disease-free survival time of hormone receptor-positive early breast cancer patients, while also reducing the risk of contralateral breast cancer and distant relapse. In the NSABP B42 trial, patients who had received initial 5 years of aromatase inhibitor treatment or initial 5 years of tamoxifen + aromatase inhibitor treatment were all treated with extended aromatase inhibitor. Although the primary endpoint (P = 0.048) did not reach the expected value, extended treatment with aromatase inhibitors significantly reduced the secondary endpoints - breast cancer-free interval and distant relapse, confirming the conclusion of the MA17R study. In the DATA trial, although extended treatment with aromatase inhibitor did not benefit in general, subgroup analysis showed that some high-risk patients, such as patients with positive lymph nodes, tumors larger than 2 cm in diameter, or receiving chemotherapy, could benefit from 6 years of anastrozole treatment. The IDEAL trial showed that there is a trend of benefit in patients with positive lymph nodes. With the support of many large-scale clinical studies published in succession, the NCCN practice guidelines for breast cancer released in 2017 recommends an additional 5 years of aromatase inhibitor treatment following the initial 5-year treatment in postmenopausal patients with early-stage breast cancer at high risk for relapse. As per the Chinese Society of Clinical Oncology guidelines published in 2019, the extended endocrine therapy is also recommended for postmenopausal hormone receptor-positive patients who have been well tolerated to the initial 5-year adjuvant treatment. However, there are some restrictions, such as positive lymph nodes, G3 or other risk factors that require adjuvant chemotherapy. For premenopausal hormone receptor-positive patients who have been well tolerated to the initial 5 years of endocrine treatment, extended endocrine therapy is also recommended in some situations, such as the presence of positive lymph nodes, G3, less than 35 years old at diagnosis, high-level Ki-67 or pT2 and above.
However, the extended endocrine therapy also has some adverse events. Multiple studies have shown that long-term use of tamoxifen can significantly increase the incidence of adverse reactions such as endometrial cancer, thrombotic disease, and dyslipidemia. Similarly, long-term treatment with aromatase inhibitors can also increase the incidence of adverse reactions such as osteoporosis, fractures, dyslipidemia, and hypertension. In the ATLAS trial, the incidence of endometrial cancer in patients treated with 10 years of tamoxifen was higher than that in patients treated with 5 years of tamoxifen. Similar results are discovered in the aTTom trial. In the IDEAL trial, the incidence rates of osteoarthritis and osteoporosis in patients treated with 5 years of letrozole was increased by 14% and 10% of that in patients undergoing 2.5 years of treatment. A study involving nearly 100,000 breast cancer patients showed that only 49.9% of breast cancer patients died of breast cancer, 16.3% died of cardiovascular disease, and 33.8% died of other causes. Among them, breast cancer and cardiovascular disease were the main causes of death in well- and poor-tolerated patients, respectively. This suggests that although anti-cancer treatment can reduce cancer deaths, it may increase the death due to cardiovascular disease. Such deaths are often offset, which often improves the BCFI, but does not benefit the overall survival.
Therefore, an effective predictor for relapse risks that can accurately determine the necessity of extended endocrine therapy is expected to be discovered. The use of this predictor will both improve patient's prognosis and reduce treatment-related side effects. The author's team recently discovered a possible factor with a long tubular structure in breast cancer lesions using immunofluorescence staining, which was named as sj-subway. The authors conducted a retrospective analysis based on the specimen library and case follow-up library of the Breast Center of Shengjing Hospital Affiliated to China Medical University. They found that sj-subway was positively expressed in various subtypes of breast cancer tissues, and mostly expressed in the hormone receptor-positive subtype. The group with more sj-subway expression had a higher positive expression of hormone receptor/ progesterone receptor. Further survival analysis also revealed the worse prognosis of patients with the existence of higher sj-subway expression. Therefore, the authors speculate that positively expressed sj-subway may become a predictor of recurrence and metastasis in high-risk patients with hormone receptor positive. However, the clinical use of this factor to screen the population benefiting from extended endocrine therapy remains to be studied.
This real-world study intends to observe the difference in the clinical efficacy of extended endocrine therapy under different sj-subway expression in high-risk hormone receptor-positive breast cancer patients, and to analyze whether the use of sj-subway can further screen out the population with benefit from extended endocrine therapy, thus further improving the survival of such patients without additional adverse events.
Study design
- Observational model
- Cohort
- Time perspective
- Prospective
- Target follow-up
- 10 Years
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| experimental group | – | Other: endocrine therapyIf the expression of sj-subway in the surgical wax block is eligible, it is recommended but not mandatory that patients follow the guidelines to choose the appropriate extended endocrine therapy. |
Who may qualify
- Ages
- 18 to 70 years
- Sex
- Female only
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
- Study population
- The early-stage invasive breast cancer positive for estrogen receptor and / or progesterone receptor and have completed standard endocrine therapy for 5 years.
Key inclusion criteria (4 listed)
- early-stage invasive breast cancer positive for estrogen receptor and / or progesterone receptor is pathologically confirmed;
- patients who have completed standard endocrine therapy for 5 years without recurrence and metastasis;
- 18-70 years old;
- patients with one of the following six manifestations: KI67 ≥ 30%; tumor size > 2 cm; positive lymph nodes; histological grade III; vascular cancer thrombus; HER-2 gene overexpression or amplification.
Key exclusion criteria (4 listed)
- with a history of other malignancies;
- patients who have severe abnormalities in important organs, such as the heart, liver, and kidney or who cannot be tolerant to extended treatment due to poor constitution;
- patients with severe osteoporosis or dyslipidemia, or those who cannot tolerate endocrine therapy ;
- patients who have participated in other clinical trials.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| endocrine therapyIf the expression of sj-subway in the surgical wax block is eligible, it is recommended but not mandatory that patients follow the guidelines to choose the appropriate extended endocrine therapy. 1. For postmenopausal patients: Extend treatment with aromatase inhibitors 10 years: letrozole or anastrozole or exemestane. 2. For premenopausal patients: An initial 5 years tamoxifen treatment followed by additional 5 years extended tamoxifen treatment. Postmenopausals are treated with aromatase inhibitors 5 years. 3. For patients have completed ovarian function suppression plus initial 5-year aromatase inhibitor treatment: Menopausals: Aromatase inhibitors; Non-menopausals: 5 years of tamoxifen treatment or ovarian function suppression plus 5 years of aromatase inhibitor treatment. 4. For patients have completed ovarian function suppression plus initial 5-year tamoxifen treatment: Menopausals: Aromatase inhibitors for additional 5 years; Non-menopausals: Tamoxifen for additional 5 years. | Other | experimental group |
Primary outcome
disease-free survival
Time frame: 5 years after enrollment
the time from enrollment to relapse or death due to any reason.
3 secondary outcomes
Overall survival
Time frame: 5 years after enrollment
Incidence of contralateral breast cancer
Time frame: 1, 2, 3, 4, and 5 years after enrollment
Incidence of adverse events
Time frame: 1, 2, 3, 4, and 5 years after enrollment
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 20 Jul 2021.
- Individual participant dataSharing planned: Undecided
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Jin-Qi Xue principal investigator
Shengjing Hospital
Xi Gu principal investigator
Shengjing Hospital
Nan Niu principal investigator
Shengjing Hospital
12 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Breast Cancer, run by Shengjing Hospital at 12 sites in China.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 20 Jul 2021. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 12 sites in China. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Cai-Gang Liu, MD (18940254967, angel-s205@163.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
disease-free survival (time frame: 5 years after enrollment). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 20 Jul 2021.