ClinicalTrials.gg
Status unknownNCT02313051MIRACLEUpdated Dec 9, 2014

Everolimus trIal for Advanced prememopausaL Breast Cancer Patients

A Phase 2 interventional study of Everolimus and Goserelin in Metastatic Breast Cancer, sponsored by Chinese Academy of Medical Sciences. Status unknown at 1 site in China. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2014-12-09.

Sponsored by Chinese Academy of Medical Sciences · Phase 2, Interventional, and Treatment

The sponsor has not verified this record recently (last verified Nov 2014), so the status shown — last known as Not yet recruiting — may be out of date.
Phase
Phase 2
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
18 Years and older
Sex
Female
01

Study summary

Everolimus has been approved to be effective when used with exemestane after progression on non-steroidal aromatase inhibitors in postmenopausal women based on the BOLERO-2 clinical trial. However, the superiority of addition of everolimus to endocrine therapy hasn't been established in the premenopausal women. This is a phase 2, multicentre clinical trial to evaluate the role of everolimus in the first-line endocrine treatment of premenopausal MBC patients after progression on tamoxifen.

Read the detailed description

Endocrine therapy is the cornerstone of treatment for patients with hormone receptor (HR)-positive advanced breast cancer. The selection of endocrine agents takes account of the menopausal status, the type of previous adjuvant endocrine treatment, the disease free interval and past medical history.

In premenopausal women with HR-positive advanced breast cancer, ovarian function suppression combined with aromatase inhibitors is a standard first-line choice of hormone treatment, especially patients progressed after tamoxifen. Unfortunately, not all patients have a response to first-line endocrine therapy, and even patients who have a response will eventually become resistant.

An emerging mechanism of endocrine resistance in aberrant signaling through the phosphatidylinositol 3-kinase (PI3K)-Akt-mammalian target of rapamycin (mTOR) signaling pathway7-9. Growing evidence supports a close interaction between the mTOR pathway and ER signaling. Everolimus is a sirolimus derivative that inhibits mTORactivation11. In preclinical models, the use of everolimus in combination with aromatase inhibitors results in synergistic inhibition of the proliferation and induction of apoptosis12. In a randomized, phase 2 study comparing neoadjuvant everolimus plus letrozole with letrozole alone in patients with newly diagnosed ER-positive breast cancer, the response rate for the combination was higher than that for letrozole alone. Recently, the Breast Cancer Trials of Oral Everolimus-2 (BOLERO-2) study showed that the addition of everolimus to exemestane significantly improved progression-free survival, with observed medians of 11 and 4 months, corresponding to a 62% reduction in the hazard ratio14 which is impressive and practice changing.

However, different from western countries, the majority (50-55%) of patients are premenopausal women in Asia including China.The benefit of everolimus plus endocrine therapy in premenopausal women have not yet been well delineated. Although there was a report that efficacy was comparable between premenopausal metastatic breast cancer patients treated with letrozole plus goserelin and postmenopausal patients treated with letrozole alone as first line hormone therapy, it is generally accepted that endocrine treatment outcome in premenopausal women, especially in younger age is known to be poor. So the addition of everolimusin this population would be a potential viable treatment option to overcome resistance to endocrine therapies that needs to be evaluated.

In addition, the feasibility of patients progressed on the endocrine continue to receive the same endocrine agent plus everolimus is unclear. At the same time, the difference between concurrent and sequential medication of endocrine agent and everolimus is not yet addressed.

Based on this rationale, the investigators introduced randomized trial to evaluate the efficacy of addition of everolimus to letrozole with LHRH agonist in premenopausal metastatic breast cancer patients who failed to tamoxifen treatment and also explore the best schedule of endocrine therapy together with everolimus.

02

Conditions studied

  • Metastatic Breast Cancer

Browse trials for

Keywords

  • metastatic breast cancer, everolimus
03

In context

Breast Neoplasms

12,815 studies on the registry are indexed under Breast Neoplasms; 2,920 are open to participants now.

This study's planned enrollment of 200 is above the median of 72 across 9,494 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Chinese Academy of Medical Sciences is the lead sponsor of 237 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Adult women (≥ 18 years of age) with metastatic or locally advanced breast cancer not amenable to curative surgery.
  • Histological confirmation of estrogen and/or progesterone-receptor positive (ER+), human epidermal growth factor receptor 2 negative (HER2 -) breast cancer.

ER/PR positive: nuclear reaction > 1%, HER2 negative: HER2; IHC 0,1+ or FISH/CISH (-) in case of IHC 2+

  • Patients who:

    • received Tamoxifen for at least 6 months during adjuvant treatment and recurred during or within 24 months after the end of adjuvant treatment completion,
    • progressed during tamoxifen treatment for advanced disease.
  • Pre-menopausal status was defined as either :
  • The patient has a history of regular menstrual periods within 12 weeks prior to study enrollment
  • The patient has FSH and E2 levels with in pre-menopausal range based on local laboratory assessments measured (i.e, FSH ≤ 40 mIU/mL and E2 ≥10 pg/mL)within 12 weeks prior to study enrollment.
  • ECOG performance status of 0,1, or 2
  • At least one measurable lesion or mainly lytic bone lesions in the absence of measurable disease(RECIST1.1)
  • Adequate bone marrow, hepatic, and renal function
  • Adequate bone marrow and coagulation function as shown by:
  • Absolute neutrophil count (ANC) ≥ 1.5 109/L;Platelets>100 x109/L;Hemoglobin (Hgb) > 9.0g/dLINR \< 2
  • Adequate liver function as shown by:
  • Serum aspartate aminotransferase (AST) and alanine aminotransferase (ALT) \< 2.5x ULN (or \<5 if hepatic metastases are present)
  • Total serum bilirubin \< 1.5 x ULN (\<3 x ULN for patients known to have Gilberts Syndrome)
  • Adequate renal function as shown by:
  • Serum creatinine\< 1.5 x ULN
  • Fasting serum cholesterol \<300 mg/dL or 7.75 mmol/L and fasting triglycerides \<2.5 x ULN. In case one or both of these thresholds are exceeded, the patient can only be included after initiation of statin therapy and when the above mentioned values have been achieved.
  • Written informed consent

Exclusion criteria

Exclusion Criteria:

  • Patients who have received endocrine treatment other than Tamoxifen for adjuvant or metastatic/locally advanced breast cancer.
  • Patients who have received goserelin at adjuvant setting
  • Patients who received more than one line of chemotherapy for metastatic or locally advanced breast cancer
  • Previous treatment with mTOR inhibitors.
  • Another malignancy within 5 years prior to enrollment with the exception of adequately treated in-situ carcinoma of the cervix, uteri, basal or squamous cell carcinoma or non-melanomatous skin cancer.
  • Symptomatic brain or other CNS metastases
  • Patients receiving chronic treatment with immunosuppressive agents.
  • Any severe and/or uncontrolled medical conditions, eg. currently active infection
  • Pregnant or lactating
  • Patients unwilling to or unable to comply with the protocol.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    Everolimus arm

    Everolimus+letrozole

    Drug: Everolimus · Drug: Goserelin · Drug: Letrozole

  • Active comparator
    Controll arm

    letrozole alone, and when progress, followed by everolimus

    Drug: Goserelin · Drug: Letrozole

Interventions

06

What researchers measure

Primary outcomes

  1. Progression free survival

    the time from randomization to the time of disease progression or relapse or death

    Time frame: 6 months after last patient was evaluated

Secondary outcomes

  1. Overall survival

    time from randomization to death

    Time frame: 1 year after the last patient was followed-up

  2. Number of Participants with Adverse Events as a Measure of Safety and Tolerability

    Time frame: during screening and treatment, withing 28 days after last medication

  3. Clinical benefit rate

    Time frame: at the time of tumor assessment of last patient

  4. Duration of clinical benefit

    from the date of confirmed response to the confirmed progression

    Time frame: 6 months after last patient was evaluated

07

Study locations

1 site
  • Cancer Institute and Hospital, Chinese Academy of Medical Sciences
    Beijing, 100021, China
08

References and documents

Publications

  • Fan Y, Sun T, Shao Z, Zhang Q, Ouyang Q, Tong Z, Wang S, Luo Y, Teng Y, Wang X, Wang S, Liu Q, Feng J, Shen K, Song Y, Wang J, Ma F, Li Q, Zhang P, Xu B. Effectiveness of Adding Everolimus to the First-line Treatment of Advanced Breast Cancer in Premenopausal Women Who Experienced Disease Progression While Receiving Selective Estrogen Receptor Modulators: A Phase 2 Randomized Clinical Trial. JAMA Oncol. 2021 Oct 1;7(10):e213428. doi: 10.1001/jamaoncol.2021.3428. Epub 2021 Oct 21. PubMed 34436536 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Dec 9, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02313051
Responsible party
Binghe Xu (Director of department of medical oncology, Chinese Academy of Medical Sciences) — Principal investigator
First posted
Dec 9, 2014
Start date
Dec 2014
Primary completion
Dec 2016 (estimated)
Completion
Dec 2017 (estimated)
Last update
Dec 9, 2014

Study contacts

Ying Fan, MD
Contact
fanyingfy@medmail.com.cn
861087788114
Bing he Xu, MD
principal investigator · Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Nov 2014. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Studies of the drug tested here: Everolimus

Start the discussion