Study of Neoadjuvant Endocrine Therapy in HR Positive and HER2 Negative Premenopausal Breast Cancer Patients

NCT ID: NCT06009627

Last Updated: 2023-08-24

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2/PHASE3
• Total Enrollment: 119 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-04-11
• Study Completion Date: 2026-09-11

Brief Summary

A multicenter, prospective, open, randomized cohort, non controlled phase II clinical study to evaluate the effectiveness and safety of Darxil combined with Exemestane+goserelin neoadjuvant endocrine therapy in HR positive and HER2 negative premenopausal breast cancer patients. The study object was to evaluate the HR positive and HER2 negative premenopausal breast cancer patients with SD after 2 cycles of neoadjuvant chemotherapy. The main endpoint was the objective response rate (ORR) of treatment

Detailed Description

A multicenter, prospective, open, randomized cohort, non controlled phase II clinical study to evaluate the effectiveness and safety of Darxil combined with Exemestane+goserelin neoadjuvant endocrine therapy in HR positive and HER2 negative premenopausal breast cancer patients. The study object was to evaluate the HR positive and HER2 negative premenopausal breast cancer patients with SD after 2 cycles of neoadjuvant chemotherapy. The main endpoint was the objective response rate (ORR) of treatment。Objective: To evaluate the efficacy and safety of darsilide combined with endocrine therapy in SD patients with HR positive and HER2 negative premenopausal breast cancer after 2 cycles of neoadjuvant chemotherapy. It is planned to recruit 119 HR positive and HER2 negative premenopausal breast cancer patients in Group A to conduct the trial with Simon's two-stage design. The null hypothesis is a true response rate of 0.2, while the alternative hypothesis is a true response rate of 0.4. The experiment was conducted in two stages. In the first stage, 13 patients were enrolled. If there are ≤ 3 responses in 13 patients, the study will be stopped Early stopping. Otherwise, continue30 patients were enrolled, with a total sample size of 43. If there are ≥ 13 patients responding, the treatment is effective. Group B was randomly assigned in a 1:1 ratio, with the same number of participants as Group A, resulting in 43 final participants. Calculated based on the proportion of SD patients in 2 cycles of neoadjuvant chemotherapy accounting for 80%, and considering a 10% dropout rate, the final enrollment was made The sample size is 119 cases. The actual samples for molecular testing can be randomly selected based on clinical efficacy, with a statistically significant number.

Conditions

Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Dalcelli+Goserelin+Exemestane

SD patients undergoing 2 cycles of preoperative treatment were randomly assigned to Group A and received darcelli, Exemestane, and Goserelin

Group Type: EXPERIMENTAL

Dalcelli、Exemestane、Gosserine

Intervention Type: DRUG

Dalcelli: once a day, 125 mg each time, taken for 3 weeks, stopped for 1 week, 1 for 4 weeks

Period. It is recommended to take the medication at approximately the same time every day, delivered in warm water, on an empty stomach, at least before taking the medication

Fasting for 1 hour before and after.

Exemestane: 25mg, oral, once a day, continuous administration.

Gosserine: 3.6mg, subcutaneous injection, once every four weeks, continuous administration

Docetaxel, epirubicin hydrochloride, Cyclophosphamide

SD patients undergoing 2 cycles of preoperative treatment were randomly assigned to Group B and received TAC chemotherapy

Group Type: ACTIVE_COMPARATOR

Docetaxel for injection、Epirubicin hydrochloride for injection、Cyclophosphamide for injection

Intervention Type: DRUG

Docetaxel for injection: 75mg/m2, intravenous drip, approximately 30 minutes. Dose reduction and delayed administration are allowed every three weeks, with a maximum of three weeks of delayed administration allowed since the last administration time

Calculate, otherwise terminate treatment.

5. Epirubicin hydrochloride for injection: 75mg/m2, intravenous drip. Once every three weeks, allowing for dose reduction

And delayed administration, with a maximum allowable delay of 3 weeks, calculated from the last administration time. Otherwise

Stop treatment.

6. Cyclophosphamide for injection: 500mg/m2, intravenous drip. Once every three weeks, allowing for dose reduction and

Delayed administration, allowed up to 3 weeks, calculated from the last administration time, otherwise terminated treat

Interventions

Dalcelli、Exemestane、Gosserine

Dalcelli: once a day, 125 mg each time, taken for 3 weeks, stopped for 1 week, 1 for 4 weeks

Period. It is recommended to take the medication at approximately the same time every day, delivered in warm water, on an empty stomach, at least before taking the medication

Fasting for 1 hour before and after.

Exemestane: 25mg, oral, once a day, continuous administration.

Gosserine: 3.6mg, subcutaneous injection, once every four weeks, continuous administration

Intervention Type: DRUG

Docetaxel for injection、Epirubicin hydrochloride for injection、Cyclophosphamide for injection

Docetaxel for injection: 75mg/m2, intravenous drip, approximately 30 minutes. Dose reduction and delayed administration are allowed every three weeks, with a maximum of three weeks of delayed administration allowed since the last administration time

Calculate, otherwise terminate treatment.

5. Epirubicin hydrochloride for injection: 75mg/m2, intravenous drip. Once every three weeks, allowing for dose reduction

And delayed administration, with a maximum allowable delay of 3 weeks, calculated from the last administration time. Otherwise

Stop treatment.

6. Cyclophosphamide for injection: 500mg/m2, intravenous drip. Once every three weeks, allowing for dose reduction and

Delayed administration, allowed up to 3 weeks, calculated from the last administration time, otherwise terminated treat

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

• All patients were operable estrogen receptor (ER) positive (>1%), regardless of PR expression level, HER2 receptor negative invasive breast cancer. Follow the 2018 ASCO-CAP HER2 negative interpretation guideline standard. Confirmed by the pathological laboratory that the immunohistochemical (IHC) score is 0 or 1-2+and the in situ hybridization (ISH) test is negative (ISH amplification rate<2.0);
• Stage II-III initial treatment patients whose tumor staging meets the AJCC 8th edition standards;
• At least one measurable breast and/or axillary disease;
• ECOG 0-1, with an estimated lifespan of at least 12 months;
• The functional level of the main organs must meet the following requirements:

Blood routine: ANC ≥ 1.5 × ten9/L; PLT ≥ 90 × ten9/L; Hb ≥ 90 g/L;Blood biochemistry: TBIL ≤ 2.5 × ULN; ALT and AST ≤ 2.5 × ULN; BUN and Cr≤ 1.5 × ULN;

• Lead ECG: QT interval (QTcF) corrected by Fridericia method<470 ms for women;
• Able to accept all puncture biopsies required by the protocol;
• Volunteer to join this study, sign informed consent, have good compliance, and be willing to cooperate with follow-up;
• Women with fertility potential must have a negative Pregnancy test (urine or serum) within 7 days after administration,

And agree to use acceptable birth control methods during the study period to avoid pregnancy.

Exclusion Criteria

• Received any form of anti-tumor treatment within 28 days prior to the start of the study;
• Simultaneously receiving any anti-tumor treatment beyond the provisions of other protocols;
• Bilateral breast cancer, inflammatory breast cancer or occult breast;
• Stage IV breast cancer;
• Severe dysfunction of important organs such as heart, liver, and kidney;
• Unable to swallow, chronic diarrhea and Bowel obstruction, there are many factors that affect drug taking and absorption;
• Participated in other drug clinical trials within 4 weeks prior to enrollment;
• Those with a known history of allergies to the drug components of this protocol; Have a history of immunodeficiency, including positive Diagnosis of HIV/AIDS test Sex, HCV, active hepatitis B, or other acquired or congenital immunodeficiency diseases Illness or a history of organ transplantation;
• Have ever suffered from any heart disease, including: (1) arrhythmia that requires medication or has clinical significance

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 100 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Tianjin Medical University Cancer Institute and Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

jie 1 ge, 1

Role: STUDY_DIRECTOR

yes

Locations

Jie Ge

Tianjin, Tianjin Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

xuejing 1 liu, 1

Role: CONTACT

lxj8109@126.com

19502151516

Facility Contacts

xuejing 1 liu, 1

Role: primary

lxj8109@126.com

19502151516

Other Identifiers

Tianjin Hospital Cancer

Identifier Type: -

Identifier Source: org_study_id