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Efficacy and Safety of TQB2450 Injection Combined With Chemotherapy ± Anlotinib Hydrochloride Capsules for Advanced Endometrial Cancer or Sarcoma of Uterus.

Primary Purpose

Advanced Endometrial Cancer, Sarcoma of Uterus

Status
Recruiting
Phase
Phase 2
Locations
China
Study Type
Interventional
Intervention
TQB2450 injection
Anlotinib Hydrochloride Capsule
Carboplatin Injection
Paclitaxel Injection
Doxorubicin Hydrochloride Injection
Gemcitabine Hydrochloride Injection
Docetaxel injection
Sponsored by
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Advanced Endometrial Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • 1 The subjects voluntarily participated in this study, signed the informed consent, and had good compliance;
  • 2 Age: ≥18 years old (when signing the informed consent form); ECOG PS score: 0-1; expected survival period of more than 3 months; body mass index (BMI) > 18.5 and weight > 40kg;
  • 3 Stage III/IV epithelial endometrial cancer (including endometrioid carcinoma, non-endometrioid carcinoma, carcinosarcoma) confirmed by histopathology, who have not received first-line systemic anticancer therapy and are not suitable for receiving Treatment other than systemic treatment, and the subject also needs to meet one of the following categories:

    1. Newly diagnosed subjects: there are still residual lesions visible on imaging after non-radical surgery, and can start receiving trial drug treatment within 8 weeks;
    2. Subjects with initial recurrence: the recurrence time is more than 12 months from the end of the initial treatment (complete remission after surgery or surgery + adjuvant treatment).
  • 4 According to the RECIST 1.1 criteria, there is at least one measurable lesion. If the measurable lesion is located in the area of previous radiotherapy, it should be clearly defined as progressing state;
  • 5 Tumor tissue samples can be provided to detect MSI/MMR status or traceable test reports;
  • 6 The main organs function well and meet the following standards:

    1. Blood routine examination standards (no blood transfusion within 7 days before screening, no correction with hematopoietic stimulating factor drugs):

      1. Hemoglobin (HGB) ≥90 g/L;
      2. The absolute value of neutrophils (NEUT)≥1.5×109/L;
      3. Platelet count (PLT) ≥ 90 × 109/L;
    2. The biochemical examination shall meet the following standards:

      1. Total bilirubin (TBIL) ≤ 1.5 times the upper limit of normal (ULN);
      2. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5×ULN. If accompanied by liver metastasis, ALT and AST≤5×ULN;
      3. Serum creatinine (Cr) ≤ 1.5×ULN or creatinine clearance (Ccr) ≥ 60ml/min;
    3. Urine routine examination standard: urine routine indicates urine protein <++; if urine protein ≥++, it is necessary to confirm the 24-hour urine protein quantitative ≤1.0g;
    4. Coagulation function or thyroid function tests should meet the following criteria:

      1. Prothrombin time (PT), activated partial thromboplastin time (APTT), international normalized ratio (INR) ≤ 1.5×ULN (no anticoagulation therapy);
      2. Thyroid-stimulating hormone (TSH) ≤ ULN; T3 and T4 levels should be investigated if abnormal, and normal T3 and T4 levels can be selected.
    5. Echocardiography assessment: Left ventricular ejection fraction (LVEF) ≥50%.
  • 7 Female subjects should agree that contraceptive measures (such as intrauterine devices or condoms) must be used during the study period and within 6 months after the end of the study; the serum pregnancy test must be negative within 7 days before study enrollment, and must be Non-lactating subjects.

Exclusion Criteria:

  • 1 Tumor disease and medical history:

    1. Other malignant tumors that have occurred or are currently concurrently present within 3 years. The following conditions were eligible for enrollment: other malignancies treated with a single surgery, achieving 5 consecutive years of disease-free survival (DFS); cured cervical carcinoma in situ, non-melanoma skin cancer, and superficial bladder tumors [Ta ( non-invasive tumor), Tis (carcinoma in situ) and T1 (tumor-infiltrating basement membrane)];
    2. Pathologically suggested endometrial leiomyosarcoma, endometrial stromal sarcoma, undifferentiated uterine sarcoma or other high-grade sarcoma;
    3. The presence of tumor thrombus, spinal cord compression caused by bone metastases, brain metastases or cancerous meningitis;
    4. Imaging (CT or MRI) shows that the tumor has invaded around important blood vessels or the investigator judges that the tumor is very likely to invade important blood vessels and cause fatal bleeding during the follow-up study;
    5. Severe bone damage caused by tumor bone metastasis; including weight-bearing bone pathological fractures and spinal cord compression that occurred within 6 months or predicted by the investigator to be likely to occur in the near future;
    6. Uncontrolled pleural effusion, pericardial effusion or ascites judged by the investigator that still needs repeated drainage.
  • 2 Previous anti-tumor therapy or concomitant medication (the washout period is calculated from the end of the last treatment):

    1. Previously received anti-angiogenesis drugs, related immunotherapy drugs for PD-1, PD-L1, CTLA-4;
    2. Received drugs with immunomodulatory function, chemotherapy, radiotherapy, clinical trial drug treatment, traditional Chinese medicine or proprietary Chinese medicine with anti-tumor indications, or other anti-cancer therapy within 4 weeks before receiving the study drug for the first time;
    3. Received hormone therapy for endometrial cancer within 1 week before receiving the first study drug treatment;
    4. It is not satisfied that at least 5 half-lives have elapsed from the last use of the targeted drug to the first receiving of the study drug, if it is a combination drug, the drug with the longest half-life shall be calculated;
    5. Those who have undergone major surgery, major surgical treatment, incisional biopsy, obvious traumatic injury, or have not recovered sufficiently from previous surgery in the judgment of the investigator within 3 weeks before the first treatment with the study drug, or are expected to be required during the study period. Major surgery;
    6. The toxicity related to previous anti-tumor therapy has not recovered to CTCAE ≤ grade 1, except for alopecia and grade 2 peripheral neuropathy.
  • 3 Comorbid diseases and medical history:

    1. History of liver-related diseases: a. Decompensated cirrhosis; b. Active or chronic hepatitis; c. Bleeding disease secondary to hepatic insufficiency.
    2. Kidney related medical history: a. Renal failure requiring hemodialysis or peritoneal dialysis; b. Past or existing nephrotic syndrome, chronic nephritis.
    3. Cardiovascular and cerebrovascular related medical history: a. Suffering from epilepsy and requiring treatment; b. New York Heart Association class II-IV heart failure, second-degree or higher heart block, myocardial infarction within the past 6 months or Arterial thrombosis events, unstable arrhythmia or unstable angina; c. Cerebrovascular accident, cerebral infarction, etc. within 6 months; d. If the treatment can adequately control blood pressure, the group is allowed to enter the group; e. Past or current heart valve inflammation, endocarditis; f. Cardiovascular syncope, pathological ventricular arrhythmia.
    4. Gastrointestinal-related medical history: a. Inability to take oral medications; b. History of malabsorption syndrome or other diseases that interfere with gastrointestinal absorption; c. Active peptic ulcer or ulcerated lower gastrointestinal tract in the past 6 months Treated for inflammation; d. Persistent chronic diarrhea of grade 2 and above despite maximum medical treatment.
    5. Lung-related medical history: a. History of idiopathic pulmonary fibrosis, organized pneumonia, drug-induced pneumonia, idiopathic pneumonia, or evidence of active pneumonia found on chest CT scan during screening; b. Bronchodilator required Medically intervened bronchial asthma; c. The clinical manifestations are suspected to be tuberculosis, T-SPOT positive is judged by the investigator to have tuberculosis infection or active tuberculosis within 1 year before enrollment;
    6. Endocrine-related medical history: a. Poor control of type I or II diabetes; b. History of pituitary or adrenal dysfunction; c. Thyroid-stimulating hormone (TSH) > ULN, if T3 and T4 levels are normal, they can be enrolled.
    7. Immune-related medical history: a. A history of immunodeficiency, including HIV positive or other acquired and congenital immunodeficiency diseases; b. Organ transplantation planned or previously received, or hematopoietic stem cells received within 60 days before the first dose Transplant, or have obvious host transplant response; c. Active autoimmune disease; d. Systemic or topical immunosuppressive or hormonal therapy is required to achieve immunosuppression, and continue to be used within 7 days before the first dose Glucocorticoids, or patients who still need immunosuppressive drugs within 5 half-lives before the first dose.
    8. Bleeding risk: a. Suffering from bleeding (hemoptysis), coagulation disease or using warfarin, aspirin and other antiplatelet aggregation drugs (except aspirin ≤100 mg/d for prophylaxis); b. Regardless of severity, there are any signs or history of bleeding constitution; c. within 4 weeks before the first dose, any CTC AE ≥ grade 3 bleeding or bleeding events;
    9. The patient has an active systemic infection or an excessive viral load;
    10. Combining serious or not well-controlled diseases or diseases that the investigator determines may have a greater risk or affect the completion of the study, including but not limited to: a. History of clear neurological or mental disorders; b. Treponema pallidum specific antibody positive.
    11. Those who have a history of drug abuse and cannot quit or have a history of drug use.
  • 4 Research and treatment related:

    1. History of vaccination with live attenuated vaccine within 28 days before the start of study treatment, inactivated vaccine within 7 days, or planned vaccination during the study period;
    2. Those who have a history of severe allergic diseases, severe drug allergies, and are known to be allergic to macromolecular protein preparations or TQB2450 injection or any components in the prescription of Anlotinib capsules, their adjuvants and similar drugs;
  • 5 Subjects with insufficient compliance or other reasons are not suitable for enrollment after the investigator's assessment.

Sites / Locations

  • Sun Yat-sen Memorial HospitalRecruiting
  • Zhongnan Hospital of Wuhan UniversityRecruiting
  • Hunan Cancer HospitalRecruiting
  • Taizhou People's HospitalRecruiting
  • Liaoning Cancer Hospital & InstituteRecruiting
  • The First Affiliated Hospital of Xi'an Jiaotong UniversityRecruiting
  • Shandong Cancer HospitalRecruiting
  • Linyi Cancer HospitalRecruiting
  • Yantai Yuhuangding HospitalRecruiting
  • Obstetrics & Gynecology Hospital of Fudan UniversityRecruiting
  • TianJin Medical University Cancer Institute & HopspitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Group one

Group two

Group three

Arm Description

First-line treatment: TQB2450 injection 1200mg,d1/Q3W+Carboplatin Injection, AUC=5 mg/ml.min,d1/Q3W + Paclitaxel Injection 175mg/m2,d1/Q3W;6-8 cycles; Maintenance treatment: TQB2450 injection, 1200mg,d1/Q3W

First-line treatment: TQB2450 Injection 1200mg, d1/Q3W + Anlotinib Hydrochloride Capsules 8mg/qd, d8-21/Q3W + Carboplatin Injection AUC=5 mg/ml.min, d1/Q3W + Paclitaxel Injection 175mg/m2, d1/Q3W ; 6-8 cycles; Maintenance treatment: TQB2450 injection+ Anlotinib Hydrochloride Capsules 8mg/qd, d8-21/Q3W

First-line treatment stage: TQB2450 injection 1200mg, d1/Q3W + anlotinib hydrochloride capsules 8mg/qd, d8-21/Q3W+ chemotherapy(① Doxorubicin Hydrochloride Injection 60mg/㎡,d1/Q3W; or ② Gemcitabine Hydrochloride Injection 900mg/㎡, d1, d8/Q3W+ Docetaxel Injection 75mg/㎡, d8/Q3W); 6-8 cycles; Maintenance phase: TQB2450 injection 1200mg, d1/Q3W+ Anlotinib hydrochloride capsules 10mg/qd, d8-21/Q3W

Outcomes

Primary Outcome Measures

Investigator-assessed objective response rate (ORR)
The proportion of patients whose tumors have shrunk to a certain amount and maintained for a certain period of time, including cases with complete remission and partial remission

Secondary Outcome Measures

Progression Free Survival (PFS)
From randomization to the first occurrence of disease progression or death from any cause. Disease progression refers to tumor growth, or the metastasis of primary tumor lesions, or the discovery of new lesions, etc.
Overall survival (OS)
From randomization to the time of death of death from any cause
Duration of Remission (DOR)
The period from the first judgment of complete remission (CR) or partial remission (PR) to the discovery of disease progression (PD).
Disease Control Rate (DCR)
the proportion of patients whose tumors shrink or remain stable for a certain period of time, including complete remission (CR, Complete Response), partial remission (PR, Partial Response) and stable (SD, stable Disease) cases
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs)
The occurrence of all adverse events (AEs), serious adverse events (SAEs) and treatment-related adverse events (TEAEs).
Abnormal laboratory test indicators
The incidence of abnormal laboratory test indicators of participants by attachment 1 in the test protocol.
The surgical conversion rate
The proportion of subjects who meet the criteria and undergo radical resection surgery.

Full Information

First Posted
July 6, 2022
Last Updated
July 21, 2023
Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.
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1. Study Identification

Unique Protocol Identification Number
NCT05481645
Brief Title
Efficacy and Safety of TQB2450 Injection Combined With Chemotherapy ± Anlotinib Hydrochloride Capsules for Advanced Endometrial Cancer or Sarcoma of Uterus.
Official Title
Evaluating the Efficacy and Safety of TQB2450 Injection Combined With Chemotherapy ± Anlotinib Hydrochloride Capsules for First-line Treatment of Patient With Advanced Endometrial Cancer or Sarcoma of Uterus: a Multi-center, Open-label, Randomized Controlled, Phase II Clinical Trial.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 22, 2022 (Actual)
Primary Completion Date
June 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Chia Tai Tianqing Pharmaceutical Group Co., Ltd.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This study plans to enroll 69 subjects of endometrial cancer and 5-10 subjects of sarcoma of uterus. The experimental set is divided into lead-in trial and formal trial. The lead-in trial includes 9 subjects to observe the safety of the combination and determine the dosage of anlotinib dihydrochloride capsules before the formal phase. The formal trial includes 60 subjects of endometrial cancer and 5-10 subjects of sarcoma of uterus. The purpose is to evaluate efficacy and safety of TQB2450 injection combined with chemotherapy ± anlotinib hydrochloride capsules for first-line treatment and maintenance treatment of patient with advanced endometrial cancer or sarcoma of uterus, and explore biomarkers related to efficacy, mechanism of action, safety and/or pathological mechanisms, the surgical conversion rate. ORR is the primary endpoint.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Advanced Endometrial Cancer, Sarcoma of Uterus

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
79 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Group one
Arm Type
Experimental
Arm Description
First-line treatment: TQB2450 injection 1200mg,d1/Q3W+Carboplatin Injection, AUC=5 mg/ml.min,d1/Q3W + Paclitaxel Injection 175mg/m2,d1/Q3W;6-8 cycles; Maintenance treatment: TQB2450 injection, 1200mg,d1/Q3W
Arm Title
Group two
Arm Type
Experimental
Arm Description
First-line treatment: TQB2450 Injection 1200mg, d1/Q3W + Anlotinib Hydrochloride Capsules 8mg/qd, d8-21/Q3W + Carboplatin Injection AUC=5 mg/ml.min, d1/Q3W + Paclitaxel Injection 175mg/m2, d1/Q3W ; 6-8 cycles; Maintenance treatment: TQB2450 injection+ Anlotinib Hydrochloride Capsules 8mg/qd, d8-21/Q3W
Arm Title
Group three
Arm Type
Experimental
Arm Description
First-line treatment stage: TQB2450 injection 1200mg, d1/Q3W + anlotinib hydrochloride capsules 8mg/qd, d8-21/Q3W+ chemotherapy(① Doxorubicin Hydrochloride Injection 60mg/㎡,d1/Q3W; or ② Gemcitabine Hydrochloride Injection 900mg/㎡, d1, d8/Q3W+ Docetaxel Injection 75mg/㎡, d8/Q3W); 6-8 cycles; Maintenance phase: TQB2450 injection 1200mg, d1/Q3W+ Anlotinib hydrochloride capsules 10mg/qd, d8-21/Q3W
Intervention Type
Drug
Intervention Name(s)
TQB2450 injection
Intervention Description
TQB2450 is a humanized monoclonal antibody targeting programmed death ligand-1 (PD-L1), which prevents the binding of PD-L1 to PD-1 and B7.1 receptors on the surface of T cells, thereby reactivating T cells and enhancing the immune response.
Intervention Type
Drug
Intervention Name(s)
Anlotinib Hydrochloride Capsule
Intervention Description
Anlotinib hydrochloride is a muti-target tyrosine kinase inhibitor.
Intervention Type
Drug
Intervention Name(s)
Carboplatin Injection
Intervention Description
Carboplatin which s similar to alkylating agent, is a second-generation platinum anti-tumor drug, which mainly causes cross-linking of DNA within and between chains, destroys DNA molecules, and disintegrates the helix.
Intervention Type
Drug
Intervention Name(s)
Paclitaxel Injection
Intervention Description
Paclitaxel is a diterpene alkaloid with anticancer activity
Intervention Type
Drug
Intervention Name(s)
Doxorubicin Hydrochloride Injection
Intervention Description
Doxorubicin hydrochloride is a cycle non-specific anticancer chemotherapy drug, which directly acts on DNA, changes the nature of DNA template, and inhibits DNA polymerase.
Intervention Type
Drug
Intervention Name(s)
Gemcitabine Hydrochloride Injection
Intervention Description
Gemcitabine is a cell cycle specific antimetabolic drug, which mainly acts on tumor cells at the DNA synthesis stage.
Intervention Type
Drug
Intervention Name(s)
Docetaxel injection
Intervention Description
Docetaxel is an anti-tumor drug of paclitaxel, which plays an anti-tumor role by interfering with the microtubule network necessary for cell Mitosis and interphase cell function.
Primary Outcome Measure Information:
Title
Investigator-assessed objective response rate (ORR)
Description
The proportion of patients whose tumors have shrunk to a certain amount and maintained for a certain period of time, including cases with complete remission and partial remission
Time Frame
Through study completion, an average of 24 months
Secondary Outcome Measure Information:
Title
Progression Free Survival (PFS)
Description
From randomization to the first occurrence of disease progression or death from any cause. Disease progression refers to tumor growth, or the metastasis of primary tumor lesions, or the discovery of new lesions, etc.
Time Frame
From data of randomization until the date of first documented progression or date death from any cause, whichever came first, assessed up to 24 months
Title
Overall survival (OS)
Description
From randomization to the time of death of death from any cause
Time Frame
From date of randomization until the date of death from any cause, assessed up to 60 months
Title
Duration of Remission (DOR)
Description
The period from the first judgment of complete remission (CR) or partial remission (PR) to the discovery of disease progression (PD).
Time Frame
The length of time the patient received this regimen to keep the tumor shrinking, through study completion, an average of 24 months
Title
Disease Control Rate (DCR)
Description
the proportion of patients whose tumors shrink or remain stable for a certain period of time, including complete remission (CR, Complete Response), partial remission (PR, Partial Response) and stable (SD, stable Disease) cases
Time Frame
Through study completion, an average of 24 months
Title
Incidence and severity of adverse events (AEs) and serious adverse events (SAEs)
Description
The occurrence of all adverse events (AEs), serious adverse events (SAEs) and treatment-related adverse events (TEAEs).
Time Frame
Baseline to other antitumor therapy, through study completion, an average of 24 months
Title
Abnormal laboratory test indicators
Description
The incidence of abnormal laboratory test indicators of participants by attachment 1 in the test protocol.
Time Frame
Baseline to other antitumor therapy, through study completion, an average of 24 months
Title
The surgical conversion rate
Description
The proportion of subjects who meet the criteria and undergo radical resection surgery.
Time Frame
Baseline to other antitumor therapy, through study completion, an average of 24 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The subjects voluntarily participated in this study, signed the informed consent, and had good compliance; Age: ≥18 years old (when signing the informed consent form); ECOG PS score: 0-1; expected survival period of more than 3 months; body mass index (BMI) > 18.5 and weight > 40kg; Who have not received first-line systemic anticancer therapy and are not suitable for receiving treatment other than systemic treatment: Group 1 and 2: Stage III/IV epithelial endometrial cancer (including endometrioid carcinoma, non-endometrioid carcinoma, carcinosarcoma) confirmed by histopathology, and the subject also needs to meet one of the following categories: Newly diagnosed subjects: there are still residual lesions visible on imaging after non-radical surgery; Subjects with initial recurrence: if the subject received systemic platinum-based adjuvant and/or neoadjuvant chemotherapy,and the recurrence time is more than 6 months from the end of the last chemotherapy,then the previous chemotherapy is allowed. Group 3: Stage I-IV sarcoma of uterus, and the subject also needs to meet one of the following categories: Newly diagnosed/initial recurrence subject of high grade endometrial stromal sarcoma (ESS)、undifferentiated Uterine sarcoma (UUS) , uterine Leiomyosarcoma and adenosarcoma(uLMS) with sarcoma overgrowth (OS). The definition of new diagnosis and initial recurrence is the same as above. Low grade ESS, adenosarcoma without SO and other Uterine sarcoma with ER+/PR+,the subjects who failed in antiestrogen treatment. According to the RECIST 1.1 criteria, there is at least one measurable lesion. If the measurable lesion is located in the area of previous radiotherapy, it should be clearly defined as progressing state; Tumor tissue samples can be provided to detect MSI/MMR status or traceable test reports; The main organs function well and meet the following standards: Blood routine examination standards (no blood transfusion within 7 days before screening, no correction with hematopoietic stimulating factor drugs): Hemoglobin (HGB) ≥90 g/L; The absolute value of neutrophils (NEUT)≥1.5×109/L; Platelet count (PLT) ≥ 90 × 109/L; The biochemical examination shall meet the following standards: Total bilirubin (TBIL) ≤ 1.5 times the upper limit of normal (ULN); Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤ 2.5×ULN. If accompanied by liver metastasis, ALT and AST≤5×ULN; Serum creatinine (Cr) ≤ 1.5×ULN or creatinine clearance (Ccr) ≥ 60ml/min; Serum albumin (ALB)>30g/L; Urine routine examination standard: urine routine indicates urine protein <++; if urine protein ≥++, it is necessary to confirm the 24-hour urine protein quantitative ≤1.0g; Coagulation function or thyroid function tests should meet the following criteria: Prothrombin time (PT), activated partial thromboplastin time (APTT), international normalized ratio (INR) ≤ 1.5×ULN (no anticoagulation therapy); Thyroid-stimulating hormone (TSH) ≤ ULN; T3 and T4 levels should be investigated if abnormal, and normal T3 and T4 levels can be selected. Echocardiography assessment: Left ventricular ejection fraction (LVEF) ≥50%. 12-lead electrocardiogram evaluation: QTc<470ms. Female subjects should agree that contraceptive measures (such as intrauterine devices or condoms) must be used during the study period and within 6 months after the end of the study; the serum pregnancy test must be negative within 7 days before study enrollment, and must be Non-lactating subjects. Exclusion Criteria: Tumor disease and medical history: Other malignant tumors that have occurred or are currently concurrently present within 3 years. The following conditions were eligible for enrollment: other malignancies treated with a single surgery, achieving 5 consecutive years of disease-free survival (DFS); cured cervical carcinoma in situ, non-melanoma skin cancer, and superficial bladder tumors [Ta ( non-invasive tumor), Tis (carcinoma in situ) and T1 (tumor-infiltrating basement membrane)]; Pathologically suggested endometrial leiomyosarcoma, endometrial stromal sarcoma, undifferentiated uterine sarcoma or other high-grade sarcoma (Applicable to group 1 and 2), Pathologically suggested epithelial endometrial cancer or Carcinosarcoma (Applicable to group 3); The presence of tumor thrombus, spinal cord compression caused by bone metastases, brain metastases or cancerous meningitis; Imaging (CT or MRI) shows that the tumor has invaded around important blood vessels or the investigator judges that the tumor is very likely to invade important blood vessels and cause fatal bleeding during the follow-up study; Severe bone damage caused by tumor bone metastasis; including weight-bearing bone pathological fractures and spinal cord compression that occurred within 6 months or predicted by the investigator to be likely to occur in the near future; Uncontrolled pleural effusion, pericardial effusion or ascites judged by the investigator that still needs repeated drainage. Previous anti-tumor therapy or concomitant medication (the washout period is calculated from the end of the last treatment): Previously received anti-angiogenesis drugs, related immunotherapy drugs for PD-1, PD-L1, CTLA-4; Received drugs with immunomodulatory function, chemotherapy, radiotherapy, clinical trial drug treatment, traditional Chinese medicine or proprietary Chinese medicine with anti-tumor indications, or other anti-cancer therapy within 4 weeks before receiving the study drug for the first time; Received hormone therapy for endometrial cancer within 1 week before receiving the first study drug treatment; It is not satisfied that at least 5 half-lives have elapsed from the last use of the targeted drug to the first receiving of the study drug, if it is a combination drug, the drug with the longest half-life shall be calculated; Those who have undergone major surgery, major surgical treatment, incisional biopsy, obvious traumatic injury, or have not recovered sufficiently from previous surgery in the judgment of the investigator within 3 weeks before the first treatment with the study drug, or are expected to be required during the study period. Major surgery; The toxicity related to previous anti-tumor therapy has not recovered to CTCAE ≤ grade 1, except for alopecia and grade 2 peripheral neuropathy. Comorbid diseases and medical history: History of liver-related diseases: a. Decompensated cirrhosis; b. Active or chronic hepatitis; c. Bleeding disease secondary to hepatic insufficiency. Kidney related medical history: a. Renal failure requiring hemodialysis or peritoneal dialysis; b. Past or existing nephrotic syndrome, chronic nephritis. Cardiovascular and cerebrovascular related medical history: a. Suffering from epilepsy and requiring treatment; b. New York Heart Association class II-IV heart failure, second-degree or higher heart block, myocardial infarction within the past 6 months or Arterial thrombosis events, unstable arrhythmia or unstable angina; c. Cerebrovascular accident, cerebral infarction, etc. within 6 months; d. If the treatment can adequately control blood pressure, the group is allowed to enter the group; e. Past or current heart valve inflammation, endocarditis; f. Cardiovascular syncope, pathological ventricular arrhythmia. Gastrointestinal-related medical history: a. Inability to take oral medications; b. History of malabsorption syndrome or other diseases that interfere with gastrointestinal absorption; c. Active peptic ulcer or ulcerated lower gastrointestinal tract in the past 6 months Treated for inflammation; d. Persistent chronic diarrhea of grade 2 and above despite maximum medical treatment. Lung-related medical history: a. History of idiopathic pulmonary fibrosis, organized pneumonia, drug-induced pneumonia, idiopathic pneumonia, or evidence of active pneumonia found on chest CT scan during screening; b. Bronchodilator required Medically intervened bronchial asthma; c. The clinical manifestations are suspected to be tuberculosis, T-SPOT positive is judged by the investigator to have tuberculosis infection or active tuberculosis within 1 year before enrollment; Endocrine-related medical history: a. Poor control of type I or II diabetes; b. History of pituitary or adrenal dysfunction; c. Thyroid-stimulating hormone (TSH) > ULN, if T3 and T4 levels are normal, they can be enrolled. Immune-related medical history: a. A history of immunodeficiency, including HIV positive or other acquired and congenital immunodeficiency diseases; b. Organ transplantation planned or previously received, or hematopoietic stem cells received within 60 days before the first dose Transplant, or have obvious host transplant response; c. Active autoimmune disease; d. Systemic or topical immunosuppressive or hormonal therapy is required to achieve immunosuppression, and continue to be used within 7 days before the first dose Glucocorticoids, or patients who still need immunosuppressive drugs within 5 half-lives before the first dose. Bleeding risk: a. Suffering from bleeding (hemoptysis), coagulation disease or using warfarin, aspirin and other antiplatelet aggregation drugs (except aspirin ≤100 mg/d for prophylaxis); b. Regardless of severity, there are any signs or history of bleeding constitution; c. within 4 weeks before the first dose, any CTC AE ≥ grade 3 bleeding or bleeding events; The patient has an active systemic infection or an excessive viral load; Combining serious or not well-controlled diseases or diseases that the investigator determines may have a greater risk or affect the completion of the study, including but not limited to: a. History of clear neurological or mental disorders; b. Treponema pallidum specific antibody positive. Those who have a history of drug abuse and cannot quit or have a history of drug use. Research and treatment related: History of vaccination with live attenuated vaccine within 28 days before the start of study treatment, inactivated vaccine within 7 days, or planned vaccination during the study period; Those who have a history of severe allergic diseases, severe drug allergies, and are known to be allergic to macromolecular protein preparations or TQB2450 injection or any components in the prescription of Anlotinib capsules, their adjuvants and similar drugs; Subjects with insufficient compliance or other reasons are not suitable for enrollment after the investigator's assessment.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaojun Chen, Doctor
Phone
021-33189900
Email
cxjlhjj@163.com
Facility Information:
Facility Name
Sun Yat-sen Memorial Hospital
City
Guangzhou
State/Province
Guangdong
ZIP/Postal Code
510120
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ke Wang, Doctor
Phone
18622221098
Email
18622080116@163.com
Facility Name
Zhongnan Hospital of Wuhan University
City
Wuhan
State/Province
Hubei
ZIP/Postal Code
430062
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dapeng Li
Phone
+86 15553115531
Email
drldp@126.com
Facility Name
Hunan Cancer Hospital
City
Changsha
State/Province
Hunan
ZIP/Postal Code
410013
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ruifang An
Phone
+86 18991232090
Email
anruifang@163.com
Facility Name
Taizhou People's Hospital
City
Taizhou
State/Province
Jiangsu
ZIP/Postal Code
225399
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hui Qiu, Doctor
Phone
+86 18986255160
Email
qiuhuiznyy@whu.edu.cn
Facility Name
Liaoning Cancer Hospital & Institute
City
Shenyang
State/Province
Liaoning
ZIP/Postal Code
110801
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Keqiang Zhang, Doctor
Phone
+86 13054196067
Email
zhangkeqiang@hnca.org.cn
Facility Name
The First Affiliated Hospital of Xi'an Jiaotong University
City
Xi'an
State/Province
Shaanxi
ZIP/Postal Code
710061
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hua Qian, Doctor
Phone
+86 13515155623
Email
qhtzry@163.com
Facility Name
Shandong Cancer Hospital
City
Jinan
State/Province
Shandong
ZIP/Postal Code
250117
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yongjie Zhang, Doctor
Phone
+86 18762096966
Email
zhangyj0818@126.com
Facility Name
Linyi Cancer Hospital
City
Linyi
State/Province
Shandong
ZIP/Postal Code
276002
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ying Yang, Doctor
Phone
15966506506
Email
hxdany2004@126.com
Facility Name
Yantai Yuhuangding Hospital
City
Yantai
State/Province
Shandong
ZIP/Postal Code
264099
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bingzhong Zhang, Doctor
Phone
13925063030
Email
13925063030@163.com
Facility Name
Obstetrics & Gynecology Hospital of Fudan University
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200090
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiumin Li, Doctor
Phone
13583991399
Email
Lyzlyylxm@163.com
Facility Name
TianJin Medical University Cancer Institute & Hopspital
City
Tianjin
State/Province
Tianjin
ZIP/Postal Code
300181
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Chunyan Wang, Doctor
Phone
18900918586
Email
lnzlgyn@163.com

12. IPD Sharing Statement

Learn more about this trial

Efficacy and Safety of TQB2450 Injection Combined With Chemotherapy ± Anlotinib Hydrochloride Capsules for Advanced Endometrial Cancer or Sarcoma of Uterus.

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