Adjuvant Chemotherapy Versus Radiotherapy For Postoperative Cervical Cancer (AFTER): A Phase 3 Trial
- Conditions
- Neoplasms
- Registration Number
- KCT0006893
- Lead Sponsor
- Konkuk University Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Female
- Target Recruitment
- 50
1) Preoperative clinical stage IB1, IB2, IIA1, IIA2, or IIB cervical cancer
2) In case of histological diagnosis as follows from the tumor tissue after surgery
- Squamous cell carcinoma (keratinizing type, nonkeratinizing type)
- Adenocarcinoma (usual type of endocervical adenocarcinoma, intestinal type of mucinous carcinoma, endometrioid carcinoma)
- Adenosquamous cell carcinoma
3) Pathologically confirmed pelvic lymph node metastasis or uterine chamber invasion from surgically resected tissue
4) In contrast-enhanced CT performed within 56 days before surgery, there should be no metastases other than pelvic lymph nodes (short diameter =10 mm) or distant metastases to the chest, upper abdomen, or pelvis, even when PET/CT was performed instead of contrast-enhanced CT Recognition. Simple CT is also permitted if it is difficult to use a contrast medium due to complications such as allergies or bronchial asthma.
5) There should be no lymph node metastasis other than the surgically resected pelvic lymph node. For invasive cancer, the incision should be negative. Intraepithelial lesions in the cut plane are acceptable.
6) Type III radical hysterectomy is performed by laparotomy or laparoscopy, and all of the following conditions must be met.
- There should be no gross residual tumor and negative amputation
- More than 20 pathologically confirmed pelvic lymph nodes
- Ligamentum cardinal amputation
- The vaginal incision (length from the vaginal fornix) measured before fixation is more than 2 cm
- The operating surgeon must meet the following requirements
? Gynecologic oncology expert recognized by the Korea Society of Gynecologic Oncology
? Gynecological oncologist or obstetrician-gynecologist recognized by the Korea Society of Obstetrics and Gynecology
7) At the time of registration, age 20 or older, 75 or younger
8) General condition ECOG score 0 or 1
9) Within 42 days after surgery
10) Primary treatment (previously radiotherapy or prior chemotherapy is not allowed)
11) Normal function of major organs (bone marrow, heart, liver, kidney, etc.)
In the inspection within 14 days before registration
- Neutrophil count: =1,500/mm3
- Platelet count: =100,000/mm3
- Hemoglobin level: =10.0 g/dL (values ??after blood transfusion will be acceptable)
- AST (GOT) and ALT (GPT): =100 IU/L
- Total bilirubin: =1.5 mg/dL
- Serum creatinine: =1.2 mg/dL
- Ccr (Modified Jelliffe equation): =50 mL/min
Modified Jlliffe equation
Ccr (mL/min) = [98 - {0.8 * (Age - 20)}] / Serum creatinine (mg/dL)
- ECG: Normal or minor changes not requiring treatment
12) When the consent form is signed
1) Pathologically not completely resected (including positive amputation)
2) Aortic lymph node metastasis (short diameter =10 mm on pathological diagnosis or CT)
3) adnexal metastasis
4) peritoneal metastasis
5) Surgical water infection requiring systemic treatment
6) Serious comorbidities (liver/kidney/heart disease, myelosuppression, infection, etc.)
7) Intestinal insufficiency or intestinal obstruction
8) Bladder or rectal fistula
9) Diabetes mellitus that is being treated or not controlled by continuous insulin administration
10) Interstitial pneumonia or pulmonary fibrosis suspected on plain chest radiography or CT
11) Other cancers within 5 years of active or disease-free period. Intra-epithelial cancer or mucosal tumors that have been cured with local treatment are permitted.
12) History of serious drug hypersensitivity reaction
13) Contraindication to PTX, CBDCA or CDDP
14) ascites or pleural effusion requiring treatment
15) HBs antigen or HCV antibody positive
16) HIV antibody positive
17) During oral or intravenous systemic steroid treatment
18) If you have ever had a hypersensitivity reaction to Polysorbate 80, polyoxyethylene castor oil (Cremophor EL) (such as ciclosporin), or hydrogenated castor oil (such as vitamins for injection)
19) In case the lead researcher is judged to be ineligible
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method overall survival (OS)
- Secondary Outcome Measures
Name Time Method Relapse-free Survival ;Incidence rate of adverse events;Quality of Life (QOL)