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Concurrent Chemoradiation With Cisplatin Every 3 Week in Advanced Cervical Cancer

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Sang-Young Ryu, Korea Cancer Center Hospital
ClinicalTrials.gov Identifier:
NCT00916500
First received: June 7, 2009
Last updated: April 29, 2014
Last verified: April 2014

June 7, 2009
April 29, 2014
March 2006
December 2013   (final data collection date for primary outcome measure)
DISEASE-FREE SURVIVAL [ Time Frame: 5 YEAR AFTER THERAPY ] [ Designated as safety issue: No ]
Same as current
Complete list of historical versions of study NCT00916500 on ClinicalTrials.gov Archive Site
  • DISEASE-FREE SURVIVAL [ Time Frame: 2 YEAR AFTER THERAPY ] [ Designated as safety issue: No ]
  • OVERALL SURVIVAL [ Time Frame: FROM THERAPY TO DEATH ] [ Designated as safety issue: No ]
  • RECURRENCE RATE [ Time Frame: 2 YEAR AFTER THERAPY ] [ Designated as safety issue: No ]
  • RECURRENCE RATE [ Time Frame: 5 YEAR AFTER THERAPY ] [ Designated as safety issue: No ]
Same as current
Not Provided
Not Provided
 
Concurrent Chemoradiation With Cisplatin Every 3 Week in Advanced Cervical Cancer
A Phase II Trial of Concurrent Chemoradiation With Cisplatin Every 3 Week in Advanced Cervical Cancer Patients

Concurrent chemoradiation (CCRT) is the standard therapy for locally advanced cervical cancer.

However, the most effective chemotherapy regimen is controversial. Weekly cisplatin, hydroxyurea + cisplatin, 5-FU + cisplatin are tested in clinical trials.

Weekly cisplatin needs frequent hospital visits and had a poor compliance profile in korea.

Combination chemotherapy regimens had more adverse effects than weekly cisplatin without improving outcomes.

We conducted a retrospective analysis comparing weekly cisplatin with cisplatin every 3 weeks and observed favorable outcome for cisplatin every 3 weeks regimen (still not published).

Therefore, we designed a phase 2 trial evaluating the efficacy and feasibility of CCRT with cisplatin every 3 weeks.

Cervical carcinoma is one of the most common gynecologic cancers worldwide. The prognosis of cervical cancer is favorable, with an approximately 80-90% 5-year survival rate in early-stage disease. However, advanced disease carries a poor prognosis.

Current standard treatment for locally advanced cervical cancer, which is not eligible for surgical treatment, is cisplatin-based concurrent chemoradiation. On the basis of the results of five randomized clinical trials, which consistently showed improved survival in patients treated with cisplatin-based chemoradiation, the U.S. National Cancer Institute (NCI) announced in 1992 that "Strong consideration should be given to the incorporation of concurrent cisplatin-based chemotherapy with radiotherapy in women who require radiotherapy for treatment of cervical cancer".

Although recently reported meta-analyses also demonstrated improved local control rates and survival with cisplatin-based chemotherapy concurrent with radiation, the optimal cisplatin dose and dosing schedule are still undetermined.

Among the previous five randomized clinical trials, two trials performed by the Gynecologic Oncology Group (GOG) used weekly cisplatin 40 mg/m2 while the other three trials used tri-weekly cisplatin at a dosage range of 50 mg/m2 to 75 mg/m2 combined with 5-fluorouracil (5-FU). Despite the diversity in cisplatin dose and dosing schedules, weekly cisplatin at a dose of 40 mg/m2 concurrent to RT is widely accepted as the standard regimen of CRT because of its convenience, equal effectiveness, and favorable toxicity in comparison to other 5-FU combined regimens.

However weekly cisplatin regimen needs frequent hospital visits and had a poor compliance profile in korea. With weekly cisplatin regimen, planned treatment was not completed in 58% patients adn treatment delayed in 29% patient. among these patients, 9% patients were not related associated toxicities.

To overcome toxicities and poor compliance of weekly regimen, the investigators tried to evaluate the efficacy and feasibility of CCRT with cisplatin 75mg/m2 every 3 weeks.

Interventional
Phase 2
Endpoint Classification: Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
CERVICAL NEOPLASMS
Drug: CONCURRENT CHEMORADIATION (CISPLATIN)
Cisplatin IV 75mg/m2 Every 3 Week For 3 Cycles; External Pelvic Radiation 40Gy; Brachytherapy Up To 85-90 Gy To Point A
Other Name: Cisplatin
Experimental: CISPLATIN
Patients With Locally Advanced Cervical Cancer Who Underwent Concurrent Chemoradiation; Cisplatin 75mg/m2 IV Every 3 Week For 3 Cycles; External Pelvic Radiation 40 Gy; Brachytherapy Up to 85-90 Gy To Point A
Intervention: Drug: CONCURRENT CHEMORADIATION (CISPLATIN)
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
71
December 2013
December 2013   (final data collection date for primary outcome measure)

Inclusion criteria:

  1. Histologically confirmed cervical cancer
  2. Clinical stage from 2b to 4a
  3. Equal to or younger than 75
  4. Gog performance status 0 - 2
  5. Anc > 1500/mm3 and platelet > 100000/mm3 and hemoglobin > 10 g/dl
  6. Serum creatinine < 2.0
  7. AST, ALT < 3 * upper normal level and serum bilirubin < 1.5 mg/dl
  8. Expected survival equal to or longer than 6 months
  9. Who agreed to participate in this study

Exclusion criteria:

  1. History of chemotherapy or radiation to abdomen or pelvis
  2. History of other cancers
  3. Pleural or pericardial effusion, ascites causing respiratory difficulties equal to or worse than NCI CTCAE grade 2
  4. History of allergy or hypersensitivity reaction to platinum
  5. History of atrial or ventricular arrhythmia, or congestive heart failure
  6. Uncontrolled diabetes, hypertension, or ischemic heart disease
  7. Myocardial infarction within 6 months
  8. Sepsis or severe infection
  9. Pregnant women
  10. An unapproved therapy within 30 days before enrollment
  11. Other serious diseases which can threat the safety of participants or impair the ability of participants to participate this trial
Female
20 Years to 75 Years
No
Contact information is only displayed when the study is recruiting subjects
Korea, Republic of
 
NCT00916500
KCCH GY 1001
No
Sang-Young Ryu, Korea Cancer Center Hospital
Korea Cancer Center Hospital
Not Provided
Principal Investigator: SANG YOUNG RYU, M.D. STAFF
Korea Cancer Center Hospital
April 2014

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP