Overview

Concurrent Radiochemotherapy Plus Anlotinib for Locally Advanced Cervical Cancer

Status:
Recruiting
Trial end date:
2026-01-01
Target enrollment:
0
Participant gender:
Female
Summary
To observe the efficacy and safety of hydrochloride anlotinib combined with concurrent radiochemotherapy for patients with FIGO stage IB3 and IIA2-IVA cervical cancer. Patient characteristics, image and genetic information of tumor, microbial sample of tumor microenvironment and biomarker in the blood sample will be collected and analysis by multi-omics and bioinformatic technology. Aim to provide a new treatment module for cervical cancer.
Phase:
N/A
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Zhongnan Hospital
Treatments:
Carboplatin
Cisplatin
Criteria
Inclusion Criteria:

1. Age ≥18 years old and ≤75 years old;

2. ECOG PS score 0-2 points;

3. After pathological examination, it is clear that it is cervical cancer, the
pathological types include squamous cell carcinoma, adenocarcinoma and adenosquamous
carcinoma;

4. The staging conforms to the definitions of IB3 and IIA2-IVA in FIGO2018;

5. The expected survival period is ≥6 months;

6. The lesion meets the requirements of RECIST 1.1 for evaluable lesions;

7. Have not received any form of anti-tumor treatment before joining the group (except
for partial cervical biopsy resection);

8. Expect to tolerate radiotherapy;

9. It is expected to tolerate concurrent chemotherapy with platinum drugs;

10. It is expected to tolerate oral Anlotinib treatment;

11. The sitting blood pressure at rest is less than the normal high value (<140/90mmHg),
or the average blood pressure of the 24-hour ambulatory blood pressure monitoring is
less than the normal high value (<140/90mmHg), regardless of whether you are taking
antihypertensive drugs or not;

12. Hematology indicators meet (no blood transfusion and no correction with hematopoietic
stimulating factor drugs within 7 days before screening): white blood cell count (WBC)
≥3.5×109/L and ≤10×109/L, neutrophil count ( ANC) ≥1.5×109/L, platelet (PLT)
≥125×109/L, hemoglobin (Hb) ≥90g/L;

13. The liver function index meets: ALT and AST≤2.5 times high normal value (ULN),
bilirubin≤1.5×ULN, albumin≥35g/L;

14. The coagulation function index meets (not receiving anticoagulation or drug hemostasis
treatment): PT and APTT ≤ 1.5×ULN, and INR ≤ 1.5 ULN;

15. Renal function indicators meet: urea nitrogen (BUN) and creatinine (Cr) ≤1.5×ULN and
creatinine clearance ≥60 mL/min (Cockcroft-Gault formula), urine protein <2+ or
24-hour urine protein quantitative <1g

16. Women of childbearing age must undergo a serum pregnancy study within 7 days before
the first medication, and the result is negative, and they are not breastfeeding.
Female subjects of childbearing age must agree to use effective methods of
contraception during the study period and within 180 days after the last
administration of the study drug;

17. Obtain informed consent signed by the patient or his legal representative;

18. Have good compliance.

Exclusion Criteria:

1. Any unstable systemic disease, including but not limited to active infection within 4
weeks (defined as fever with a body temperature exceeding 38.5℃ or clear evidence of
bacteremia or evidence of heart, brain, kidney, lung, etc.) Infectious changes in the
liver and intestines), circulatory accidents within 6 months (malignant hypertension,
myocardial infarction, severe/unstable angina pectoris, heart insufficiency above NYHA
level 2, clinically significant supraventricular or Ventricular arrhythmia,
cerebrovascular accident that has not recovered or caused serious sequelae),
uncontrolled type 2 diabetes (fasting blood glucose> 11.1mmol/L or glycosylated
hemoglobin> 8%), lung insufficiency (pulmonary function caused by any reason Decrease,
defined as lung function test FEV1/FVC<70%, FEV1<80% predicted value).

2. Past autoimmune diseases, including but not limited to systemic lupus erythematosus,
rheumatoid arthritis, autoimmune liver disease, autoimmune thyroiditis, systemic
vasculitis, scleroderma, dermatomyositis, self Immune hemolytic anemia;

3. 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 is higher than the detection limit of the analysis
method) or combined with hepatitis B and C infection;

4. The history of live attenuated vaccine vaccination within 28 days before the first
study medication or the expected live attenuated vaccine vaccination during the study
period;

5. Imaging shows that the tumor invades large 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 or other diseases with serious bleeding risk (the
bleeding caused by simple cervical tumor rupture is not included)

6. Previously received anti-angiogenesis targeted drug therapy, or other treatments for
VEGFR inhibitors;

7. There is evidence of active tuberculosis infection within 1 year before screening;

8. Any other malignant tumor has been diagnosed within 5 years before entering the study,
except for fully treated basal cell carcinoma or squamous cell skin cancer or cervical
carcinoma in situ;

9. Major surgery has been performed within 28 days before randomization (tissue biopsy
required for diagnosis and central venous catheter insertion via peripheral
venipuncture [PICC] are allowed);

10. Arteriovenous thrombosis events that occurred within 6 months before randomization,
such as cerebrovascular accidents (including temporary ischemic attacks), deep vein
thrombosis (venous thrombosis caused by intravenous catheterization due to
pre-chemotherapy, which has been cured by the investigator Except) and pulmonary
embolism;

11. Subjects who have previously received or plan to receive allogeneic bone marrow
transplantation or solid organ transplantation;

12. There is intestinal obstruction with significant clinical significance, intestinal
repair, intestinal anastomosis or intestinal fistula occurs at any time for any
reason;

13. Subjects with symptoms of hemoptysis and the maximum daily volume of hemoptysis ≥2.5
mL within 2 months before entering the study. Have had significant clinically
significant bleeding symptoms or have a clear bleeding tendency within 3 months before
entering the study, such as gastrointestinal bleeding, hemorrhagic gastric ulcer,
baseline stool occult blood++ or above, or suffering from vasculitis, etc.; Known to
have inherited or acquired bleeding and thrombotic tendency, such as: hemophilia,
blood coagulation disorder, thrombocytopenia, hypersplenism, etc.;

14. Macroscopic hematuria or urinary bleeding indicated by other evidence;

15. Are receiving thrombolysis or need long-term anticoagulation therapy with warfarin or
heparin, or need long-term antiplatelet therapy (aspirin ≥300 mg/day or clopidogrel
≥75 mg/day)

16. Peripheral neuropathy ≥ Grade 2;

17. Intolerance to platinum chemotherapy drugs (including intolerance caused by allergies
or other physical symptoms);

18. Kidney stones at risk of seizure, one kidney has no function or anatomically single
kidney;

19. Long-term bed rest for any reason;

20. Cachexia state;

21. Known allergy to Anlotinib or any of its excipients;

22. Those who have other anti-tumor treatment plan during treatment;

23. Participated in any other drug clinical research within 4 weeks before randomization,
or no more than 5 half-lives from the last study drug;

24. The subject is known to have a history of psychotropic drug abuse, alcohol abuse or
drug abuse;

25. Those who have a mental illness that seriously affects cognition and cannot achieve a
stable mental state;

26. According to the judgment of the investigator, the patient may have other factors that
may cause the study to be terminated halfway, such as other serious diseases or severe
laboratory abnormalities or other factors that will affect the safety of the subjects,
or test data And the family or society where the sample was collected