Locally Advanced Cervical Cancer
Conditions
Brief summary
The standard treatment for locally advanced cervical cancer is cisplatin-based concurrent chemoradiotherapy with external beam radiotherapy (EBRT) and Brachytherapy (BT). overall treatment time (OTT) has been found to be an important predictor of treatment response. Some studies have shown that the acceleration of tumor cell regeneration during the extension of radiotherapy leads to poor local control. Prolonging the overall treatment time of cervical cancer radiotherapy for more than 8 weeks leads to an increase in pelvic local control failure. Therefore, shortening OTT has great potential benefits from both clinical efficacy and social benefits. Shortening OTT in radical cervical cancer radiotherapy includes hypofractionated EBRT and shortening the interval between BT and EBRT. However, further shortening OTT may lead to an increase in acute and late toxicity. Adaptive radiotherapy (ART) strategies systematically monitor variations in target and neighbouring structures to inform treatment-plan modification during radiotherapy. The application of image-guided adaptive brachytherapy (IGABT) has clearly demonstrated the advantages of this approach in the treatment of cervical cancer. Previous studies have shown that the implementation of IGABT can achieve personalized treatment, dose increase, improve clinical efficacy, reduce normal tissue toxicity and side effects, and strengthen international standardized quality control. In this study, online adaptive pelvic EBRT combined with IGABT based on uRT-linac was performed under online CT guidance. The aim of this study is to evaluate the safety and efficacy of pelvic concurrent chemoradiotherapy combined with CT-guided intracavitary brachytherapy with adaptive simultaneous dose escalation in locally advanced cervical cancer.
Interventions
OTHERBrachytherapy and CT-guided online adaptive external beam pelvic radiotherapy are delivered on the same day
Brachytherapy and CT-guided online adaptive external beam pelvic radiotherapy are delivered on the same day.
Sponsors
Peking University Third Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 75 Years
Healthy volunteers
No
Inclusion criteria
1. Sign the informed consent; 2. Age :18 to 75 years old; 3. Histologically or cytologically confirmed cervical cancer; 4. According to the International Federation of Gynecology and Obstetrics (FIGO 2018) stage IB3, IIA2, IIB, III, IV (local advanced), and had not received treatment before enrollment; 5. Measurable lesions according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1; 6. ECOG physical performance score 0-2; 7. Expected survival time \>= 3 months; 8. LVEF \>= 55%; 9. Bone marrow function: neutrophil \>= 1.5×109/L, platelet ≥ 100×109/L, white blood cell 4.0-10.0×109/L, hemoglobin \>= 90 g/L; 10. Liver and kidney function: serum creatinine \<= 1.5 times upper limit of normal; AST and ALT≤2.5 times upper limit of normal (ULN) or \<= 5 times ULN in the presence of liver metastasis; Total bilirubin \<=1.5 times upper limit of normal, or \<= 2.5 times upper limit of normal if the patient has Gilbert's syndrome; 11. Subjects of childbearing age must agree to use effective contraception during the trial, and women of childbearing age must have a negative serum or urine pregnancy test; 12. Non-lactating patients;
Exclusion criteria
1. Patients with prior abdominal or pelvic radiotherapy; 2. being mentally ill and unable to cooperate with treatment; 3. Serious uncontrolled medical diseases, such as serious internal medical diseases, including severe heart disease, cerebrovascular disease, uncontrolled diabetes, uncontrolled hypertension, uncontrolled infection, active peptic ulcer, etc.; 4. Unable to tolerate cisplatin chemotherapy; 5. receiving other experimental drugs or participating in clinical trials for other anticancer treatment purposes within 30 days before the first radiotherapy; 6. Severe infection within 4 weeks before study treatment, including but not limited to infectious complications requiring hospitalization, bacteremia, or severe pneumonia; 7. Human immunodeficiency virus (HIV) -positive persons; 8. HBsAg positive and HBV-DNA titer \>= 1×10\^3 IU/mL; Participants were eligible for inclusion if they were HBsAg positive and had a peripheral blood HBV-DNA level of \< 1×10\^3 IU/mL, and if the investigator considered the participant to be in a stable phase of chronic hepatitis B without increasing the risk to the participant. 9. Hepatitis C virus (HCV) antibody positive or human immunodeficiency virus (HIV) antibody positive and HCV RNA test positive; 10. Patients judged by the investigator to be ineligible for the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| the nature of adverse events | The time frame extends from the initiation of radiotherapy to 24 months after the completion of radiotherapy | the nature of adverse events is assessd by RTOG/EORTC radiation toxicity grading |
| the frequency of adverse events | The time frame extends from the initiation of radiotherapy to 24 months after the completion of radiotherapy | — |
Secondary
| Measure | Time frame |
|---|---|
| objective response rate | The time frame extends from the initiation of radiotherapy to 12 months after the completion of radiotherapy |
| tumor control rate | The time frame extends from the initiation of radiotherapy to 24 months after the completion of radiotherapy |
| local progression-free survival time | The time frame extends from the initiation of radiotherapy until the first recorded local recurrence, with an initial assessment period of 24 months. |
Countries
China
Contacts
Primary ContactJunjie Wang professor
Outcome results
None listed