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Postoperative intensity-modulated radiation therapy with concurrent chemotherapy in cervical cancer trial

Not Applicable
Recruiting
Conditions
Diseases of The genitoruinary system
Registration Number
KCT0004702
Lead Sponsor
Samsung Medical Center
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
84
Inclusion Criteria

) histologicall confirmed cervical cancer
2) radical hysterectomy and pelvic lymph node dissection was done
3) indicated as below in pathology (more than one)
- pelvic lymph node metastasis
- parametrial involvement
- resection margin positive
4) age 20-70
5) ECOG 0-1
6) granulocyte =1.0 x 103/µl, platelet =30 x 103/µl, hemoglobin =10 g/dl
7) creatinine <2.0 mg/dL, bilirubin 1.5 mg/dl
8) If the patient voluntarily completes the consent form

Exclusion Criteria

1) distant metastiss (retroperitoneal lymph node metastasis)
2) previous pelvic radiohterapy
3) more than 3 months after radical hysterectomy
4) serious acute illness
5) neoadjuvant chemotherapy
6) radiotherapy alone patient
7) other cancer history except for thyroid cancer, skin cancer, cervix is situ

Study & Design

Study Type
Interventional Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
more than acute grade 3 toxicities
Secondary Outcome Measures
NameTimeMethod
more than chronic grade 3 toxicities
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