Patient Derived Organoid-guided Personalized Treatment Versus Treatment of Physician's Choice in Breast Cancer

NCT ID: NCT06268652

Last Updated: 2024-02-20

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE3
• Total Enrollment: 302 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-01-15
• Study Completion Date: 2028-01-15

Brief Summary

This multicenter, open-label, randomized phase III trial is designed to study the efficacy and safety of organoid-guided personalized treatment （OGPT）versus treatment of physician's choice (TPC) in previously treated refractory breast cancer.

Detailed Description

This multicenter, open-label, randomized phase III trial is designed to study the efficacy and safety of organoid-guided personalized treatment （OGPT）versus treatment of physician's choice (TPC) in previously treated refractory breast cancer. Molecular subtype, presence of visceral metastases, and number of prior chemotherapy treatments for advanced or metastatic disease will stratify randomization. subjects in the OGPT arm will receive the treatment predicted to be the most effective by PDO drug sensitivity screening, and subjects in the TPC arm will receive treatment of physician's choice. The primary population to be included in the study will be patients with refractory breast cancer who have received multiple lines of prior therapy and who have at least one measurable target lesion according to RECIST 1.1 criteria.

Conditions

Breast Cancer; Refractory Breast Carcinoma

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: NONE

Study Groups

Organoid-guided personalized treatment

Subjects randomly assigned to OGPT need to provide sufficient tissue for organoid culture. After successful organoid culture, drug screening will be performed, and they will be treated with drugs predicted to be sensitive by PDO drug susceptibility screening.

Group Type: EXPERIMENTAL

Organoid-guided personalized treatment

Intervention Type: OTHER

After the organoid culture is successful, the personalized drug library customized by our team will be used for screening. Sensitive drugs are selected based on the results of drug screening, and the most appropriate personalized treatment plan is selected based on NCCN guideline recommendations, drug safety, and conventional drugs used in the treatment of breast cancer. The personalized drug library customized by our team contains 55 drugs approved by the FDA. For specific usage, dosage and time intervals, please refer to the instructions of the corresponding drug.

Treatment of physician's choice

Subjects in the TPC arm will receive treatment with one of the following regimens selected by the physician following NCCN guidelines: capecitabine, gemcitabine, vinorelbine, and eribulin. If it is HER2-positive, anti-HER2 therapy can be combined with it, except for ADC drugs.

Group Type: ACTIVE_COMPARATOR

Gemcitabine

Intervention Type: DRUG

1000mg/m2，IV, days 1, 8, q3w

Capecitabine

Intervention Type: DRUG

1000mg/m² , PO, bid, days1-14, q3w

Vinorelbine

Intervention Type: DRUG

25mg/m2, IV or 60mg/m² (oral), days 1 and 8, q3w

Eribulin

Intervention Type: DRUG

1.4mg/m², IV, days 1 and 8, q3w

Interventions

Organoid-guided personalized treatment

After the organoid culture is successful, the personalized drug library customized by our team will be used for screening. Sensitive drugs are selected based on the results of drug screening, and the most appropriate personalized treatment plan is selected based on NCCN guideline recommendations, drug safety, and conventional drugs used in the treatment of breast cancer. The personalized drug library customized by our team contains 55 drugs approved by the FDA. For specific usage, dosage and time intervals, please refer to the instructions of the corresponding drug.

Intervention Type: OTHER

Gemcitabine

1000mg/m2，IV, days 1, 8, q3w

Intervention Type: DRUG

Capecitabine

1000mg/m² , PO, bid, days1-14, q3w

Intervention Type: DRUG

Vinorelbine

25mg/m2, IV or 60mg/m² (oral), days 1 and 8, q3w

Intervention Type: DRUG

Eribulin

1.4mg/m², IV, days 1 and 8, q3w

Intervention Type: DRUG

Other Intervention Names

OGPT; Gemzar; Xeloda; Navelbine; Halaven

Eligibility Criteria

Inclusion Criteria

1. Voluntarily participate and sign the informed consent form

2. Aged over 18 years old, regardless of gender;

3. Locally advanced or metastatic breast cancer confirmed by histopathology;

4. Received ≥2 previous lines of anti-tumor treatment and developed resistance to standard treatment;

5. Life expectancy ≥3 months;

6. ECOG performance status 0 to 2;

7. Have measurable or/and evaluable lesions (non-radiotherapy target areas) (lesion evaluation is based on Recist1.1 standards);

8. No serious organ (main organ: heart, lung, liver, kidney) functional abnormalities (refer to respective standards);

9. Routine blood test: white blood cells (WBC) ≥3 × 109/L; absolute neutrophil count (ANC) ≥1.5 × 109/L; platelets (PLT) ≥100 × 109/L; hemoglobin (Hgb) ≥8g /dL;

10. Blood biochemical indicators: AST (SGOT), ALT (SGPT) ≤ 2.5 × upper limit of normal value (ULN) (in the case of no liver invasion) or ≤ 5 × upper limit of normal value (ULN) (in the case of liver invasion) Bottom); total bilirubin (TBIL) ≤ ULN; serum creatinine clearance calculated according to the CG formula > 30 mL/min

11. Coagulation function: prothrombin time (PT), international normalized ratio (INR) ≤ 1.5 × ULN (unless warfarin is being used for anticoagulation);

12. Able to comply with the research visit plan and other program requirements;

13. All patients of childbearing age must agree to take effective contraceptive measures during the study and within 6 months of stopping treatment. Female patients of childbearing age must have a negative urine pregnancy test before treatment.

Subjects must meet all of the following additional criteria to be included in the OGPT group:

1. No absolute contraindications to tissue-invasive procedures required to obtain organoid cultures。

2. Sufficient tissue can be provided for organoid culture: biopsy samples (length >1cm, 3 strips), surgical resection samples (total volume >1cm3, weight >0.2g), thoracentesis, abdominal puncture, pericardiocentesis and other malignant effusion samples (pleural effusion >500mL, ascites >500m) and confirmed to contain malignant tumor cells.

Exclusion Criteria

1. The medical history and comorbidities are as follows:

1. The patient is participating in other interventional clinical studies or the end of treatment in the previous clinical study is less than 4 weeks;（2）Those who have been treated less than 4 weeks since the last anti-tumor treatment (radiotherapy, chemotherapy, targeted therapy, immunotherapy or local-regional treatment); the adverse reactions related to anti-tumor treatment (except alopecia) after previous systemic anti-tumor treatment have not returned to NCI- Patients with CTC AE ≤ grade 1;

2. Other active malignant tumors that require simultaneous treatment;

3. Known history of organ transplantation and allogeneic hematopoietic stem cell transplantation;

4. For subjects who have undergone major surgery or severe trauma, the effects of the surgery or trauma have been eliminated for less than 14 days before enrollment;

5. Patients with active pulmonary tuberculosis need to be excluded. Patients suspected of having active pulmonary tuberculosis should have chest X-rays, sputum, and clinical symptoms and signs to rule out the disease. Patients with a history of active pulmonary tuberculosis infection within the previous year must be excluded, even if they have been treated; patients with a history of active pulmonary tuberculosis infection more than 1 year ago must also be excluded, unless it is proven that the course and type of anti-tuberculosis treatment previously used are satisfactory. appropriate;

6. Severe acute or chronic infection requiring systemic treatment

7. Suffering from heart failure (New York Heart Association Class III or IV) and despite receiving appropriate medical treatment, poorly controlled coronary artery disease or arrhythmia, or a history of myocardial infarction within 6 months before screening patient.

2. Pregnant or lactating women.

3. No anti-tumor treatment is planned.

4. Known to have a positive history of human immunodeficiency virus (HIV) test or known to have acquired immunodeficiency syndrome (AIDS);

5. Untreated active hepatitis (hepatitis B: HBsAg positive and HBV DNA ≥ 500IU/mL; hepatitis C: HCV RNA positive and abnormal liver function); combined with hepatitis B and hepatitis C co-infection;

6. Hypersensitivity to any study drug;

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Sun Yat-sen University

OTHER

Sponsor Role: lead

Responsible Party

Shi Yanxia

Principal Investigator, Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Yanxia Shi

Role: PRINCIPAL_INVESTIGATOR

Sun Yat-sen University

Locations

Yanxia Shi

Guangzhou, None Selected, China

Site Status: RECRUITING

Countries

China

Central Contacts

Yanxia Shi

Role: CONTACT

shiyx@sysucc.org.cn

020-87343368

Facility Contacts

Yanxia Shi

Role: primary

shiyx@sysucc.org.cn

020-87343368

Provided Documents

Document Type: Study Protocol

View Document

Document Type: Informed Consent Form

View Document

Other Identifiers

B2023-686-01

Identifier Type: -

Identifier Source: org_study_id