Cadonilimab Plus Anlotinib for R/M/P Cervical Cancer

NCT05817214 | Recruiting Phase 2

• 1 other identifier: CC-01
• Study Type: interventional
• Target: 35
• Locations: 1 country
• Sites: 1

Brief Summary

The goal of this clinical trial is to test a new treatment combination including cadonilimab, anlotinib and granulocyte-macrophage colony-stimulating factor (GM-CSF) in recurrent, metastasis and persistent cervical cancer. The main questions it aims to answer are:

• The efficacy of this combination in R/M/P CC;
• The tolerance of this combination in R/M/P CC;
• Possible biomarker of treatment response for this combination. Participants will receive cadonilimab of 10mg/kg every three weeks at day 1, take anlotinib (12mg) orally in day 1 to day 14, then take a 7 days break and subcutaneously injection of GM-CSF (200ug) from day 1 to day 14, then also take a 7-days break. This treatment will continue until progression or intolerable toxicity or withdraw of participants and it will last for no longer than 2 years.

Conditions

Cervical Cancer

Keywords

Cervical Cancer; Cadonilimab; Anlotinib; Granulocyte-macrophage colony-stimulating factor; Immunotherapy

Outcome Measures

Primary Outcomes (1)

• Objective response rate

  Rate of participants with complete response plus partial response as best response in the intent to treatment group according to RECIST 1.1

  up to 2 years

Secondary Outcomes (5)

• Rate and grade of adverse events

  From enrollment to 90 days after last treatment of all subjects

• Disease control rate

  up to 2 years

• Duration of Response

  Up to 2 years

• Progression free survival rate

  Up to 2 years

• Overall survival rate

  Up to 2 years

Study Arms (1)

Treatment arm

EXPERIMENTAL

This trial has a single treatment arm. All participants will receive small treatment including cadonilimab, anlotinib and granulocyte-macrophage colony-stimulating factor in this arm

Drug: Cadonilimab; Drug: Anlotinib; Drug: Granulocyte-Macrophage Colony-Stimulating Factor

Interventions

Cadonilimab DRUG

All Participants will receive cadonilimab of 10mg/kg every three weeks at day 1

Also known as: AK104

Treatment arm

Anlotinib DRUG

All Participants will take anlotinib (12mg) orally in day 1 to day 14, then take a 7 days break.

Also known as: AL001

Treatment arm

Granulocyte-Macrophage Colony-Stimulating Factor DRUG

All Participants will have subcutaneously injection of granulocyte-macrophage colony-stimulating factor from day 1 to day 14, then take a 7 days break.

Treatment arm

Eligibility Criteria

• Age: 18 Years - 75 Years
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Obtain informed consent signed by the patient or their legal representative;
• Female patients aged ≥18 and ≤75 years old;
• ECOG PS score of 0-1;
• Expected survival period ≥6 months;
• Pathological types include squamous cell carcinoma, adenocarcinoma, or adenosquamous carcinoma originating from the cervix;
• Can provide tumor tissue specimens archived within 2 years or willing to undergo tumor tissue biopsy to provide fresh specimens for further testing;
• At least one evaluable lesion meeting the criteria of RECIST 1.1;
• Have only received standard first-line systemic treatment in the past: (1) If first-line treatment does not include immunotherapy, failure of first-line treatment is sufficient (for patients who have previously achieved cure, any number of neoadjuvant or adjuvant chemotherapy cycles do not count towards the line count, unless disease progression occurs within 3 months after ≥3 cycles of neoadjuvant/adjuvant chemotherapy; for persistent disease, ≥2 cycles of previous chemotherapy can be counted as one line, otherwise not counted); (2) If first-line treatment includes immunotherapy, clinical benefit must occur after first-line treatment, namely partial or complete tumor remission, with the duration of efficacy lasting more than 6 months.
• Sitting blood pressure in a resting state is below the normal high value (\<140/90 mmHg), or 24-hour dynamic blood pressure monitoring average blood pressure is below the normal high value (\<140/90 mmHg), regardless of whether antihypertensive drugs are being taken orally;
• Hematological indicators meet the following criteria (not transfused or administered hematopoietic growth factor drugs within the past 7 days): white blood cell count (WBC) ≥3.5×109/L, absolute neutrophil count (ANC) ≥1.5×109/L, platelets (PLT) ≥100×109/L, hemoglobin (Hb) ≥90g/L;
• Liver function indicators meet the following criteria: ALT and AST ≤2.5 times the upper limit of normal (ULN), bilirubin ≤1.5×ULN, albumin ≥35g/L;
• Coagulation function indicators meet the following criteria (not receiving anticoagulant or hemostatic drug therapy): PT and APTT ≤1.5×ULN, while INR ≤1.5 ULN;
• Renal function indicators meet the following criteria: blood urea nitrogen (BUN) and creatinine (Cr) ≤1.5×ULN, urinary protein \<2+ or 24-hour urinary protein quantification \<1g;
• Women of childbearing age must undergo serum pregnancy testing within 7 days before initial medication, with negative results, and not be lactating. Female subjects of childbearing age must agree to use effective contraception during the study period and within 180 days after the last dose of the study drug;
• Good compliance.

You may not qualify if:

• Translation:
• Any unstable systemic diseases, including but not limited to active infections within 4 weeks (defined as fever exceeding 38.5°C, evidence of bacteremia, or evidence of infectious changes in the heart, brain, kidneys, lungs, liver, and intestines), circulatory accidents within 6 months (malignant hypertensive crisis, myocardial infarction, severe/unstable angina, heart failure above NYHA class 2, clinically significant supraventricular or ventricular arrhythmias, or cerebral vascular accidents not yet recovered from or resulting in severe sequelae), uncontrolled type 2 diabetes (fasting blood glucose \>11.1 mmol/L or glycated hemoglobin \>8%), and pulmonary insufficiency (any cause leading to decreased lung function, defined as FEV1/FVC \<70%, FEV1 \<80% of predicted value).
• History of autoimmune diseases, including but not limited to systemic lupus erythematosus, rheumatoid arthritis, autoimmune liver diseases, systemic vasculitis, scleroderma, dermatomyositis, autoimmune hemolytic anemia;
• Human immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome (AIDS); active hepatitis (hepatitis B, defined as HBV-DNA ≥ 500 IU/ml; hepatitis C, defined as HCV-RNA higher than the detection limit of the assay) or combined hepatitis B and hepatitis C infection;
• History of attenuated live vaccine administration within 28 days before the first dose of the study drug or expected attenuated live vaccine administration during the study period;
• Tumor invasion of major blood vessels on imaging or investigator judgment indicating a high risk of tumor invasion of important vessels causing fatal bleeding or other diseases with a high risk of severe bleeding;
• Previous treatment with anlotinib or cadonilimab;
• Evidence of active tuberculosis infection within the past year before screening;
• Diagnosis of any other malignant tumors, adequately treated basal cell carcinoma or squamous cell skin carcinoma, or cervical carcinoma in situ within 5 years before entering the study;
• Major surgery within 28 days before randomization (tissue biopsy for diagnostic purposes and insertion of a central venous catheter via percutaneous puncture are allowed);
• Active venous or arterial thromboembolic events within 6 months before randomization, such as cerebrovascular accidents (including transient ischemic attacks), deep vein thrombosis, and pulmonary embolism;
• Previous or planned allogeneic bone marrow or solid organ transplantation;
• Clinically significant intestinal obstruction, occurrence of intestinal repair, intestinal anastomosis, intestinal diversion, or enterocutaneous fistula for any reason at any time;
• Participants who experienced symptoms of hemoptysis within 2 months before entering the study and had a maximum daily hemoptysis volume of approximately ≥2.5 mL. Participants who experienced significant bleeding symptoms or had a clear bleeding tendency, such as gastrointestinal bleeding, bleeding gastric ulcers, baseline fecal occult blood test ++ and above, or vasculitis, within 3 months before entering the study; known hereditary or acquired bleeding and thrombotic tendencies, such as hemophilia, coagulation disorders, thrombocytopenia, splenic hyperfunction, etc.;
• Visible hematuria or other evidence of active urinary system bleeding;

Sponsors & Collaborators

• Zhongnan Hospital: lead
• Akeso Biopharma Co., Ltd.: collaborator

Study Sites (1)

Zhongnan Hospital of Wuhan University

Wuhan, Hubei, 430071, China

RECRUITING

MeSH Terms

Conditions

Uterine Cervical Neoplasms

Interventions

anlotinib; Granulocyte-Macrophage Colony-Stimulating Factor

Condition Hierarchy (Ancestors)

Uterine Neoplasms; Genital Neoplasms, Female; Urogenital Neoplasms; Neoplasms by Site; Neoplasms; Uterine Cervical Diseases; Uterine Diseases; Genital Diseases, Female; Female Urogenital Diseases; Female Urogenital Diseases and Pregnancy Complications; Urogenital Diseases; Genital Diseases

Intervention Hierarchy (Ancestors)

Colony-Stimulating Factors; Glycoproteins; Glycoconjugates; Carbohydrates; Hematopoietic Cell Growth Factors; Cytokines; Intercellular Signaling Peptides and Proteins; Peptides; Amino Acids, Peptides, and Proteins; Proteins; Biological Factors

Study Officials

• Hui Qiu, Ph.D.

  Wuhan University

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Shaoxing Sun, M.D.

CONTACT

+08613871286154; sunshaoxing@whu.edu.cn

Study Design

• Study Type: interventional
• Phase: phase 2
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Chief of Department of Radiation and Medical Gynecologic Oncology

Study Record Dates

• First Submitted: April 5, 2023
• First Posted: April 18, 2023
• Study Start: February 16, 2023
• Primary Completion: November 30, 2025
• Study Completion (Estimated): February 28, 2027
• Last Updated: April 19, 2024

Record last verified: 2024-04

Data Sharing

• IPD Sharing: Will not share

Locations

CN (1)