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Systemic Consolidation Therapy After Chemoradiation Therapy Following Operation for High Risk Early Stage Cervical Cancer

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Seoul National University

Status

Unknown

Conditions

Cervical Cancer

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

The purpose of this study is to determine the therapeutic efficacy and complications of systemic consolidation therapy with paclitaxel plus carboplatin following radical hysterectomy and adjuvant chemoradiation for high risk early stage cervical cancer.

Full description

Systemic consolidation therapy with paclitaxel plus carboplatin (3 cycles per 3 weeks) following radical hysterectomy and adjuvant chemoradiation (3 cycles per 3 weeks) for high risk early stage cervical cancer will elevate the therapeutic efficacy by removing the microscopic metastatic lesions which could not be identified by naked eye and diagnostic imaging tests.

Enrollment

77 estimated patients

Sex

Female

Ages

20 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • patients who underwent radical hysterectomy for cervical cancer stage IB-IIA
  • Patients who had at least one of the following risk factors in pathologic results; lymph node metastasis, positive residual resection margin, parametrial invasion
  • above 20 years
  • GOG performance status 0-2
  • Informed consent
  • Platelet>100K, Hb> 10.0 g/dl, ANC>1500/mm3, Cr <1.25*upper normal limit, bilirubin<1.5mg/dl, AST & ALT<*3 upper normal limit
  • Expected life > 6 months

Exclusion criteria

  • Peripheral neurotoxicity > NCI grade 2
  • Sever infection
  • Previous history with chemotherapy or radiation therapy
  • Pleural effusion, pericardial effusion, and ascites which could cause dyspnea > NCI grade 2
  • Paraaortic lymph node metastasis
  • Allergy with platinum
  • Previous history of atrial or ventricular arrhythmia or congestive heart failure
  • Uncontrolled infection, diabetes mellitus, hypertension, ischemic heart disease, myocardiac infarct within 6 months
  • Severe disease such as acute or chronic renal failure and acute cerebral infarct, cerebral hemorrhage, recurrent hepatitis, liver cirrhosis, unknown fever above 39 degrees centigrade

Trial contacts and locations

1

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Central trial contact

Seung Su Han, MD

Data sourced from clinicaltrials.gov

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