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Intraoperative Hyperthermic Intraperitoneal Chemotherapy With Ovarian Cancer

Randomized Trial of Intraoperative Hyperthermic Intraperitoneal Chemotherapy Followed by Intravenous Chemotherapy in Patients With Ovarian Cancer

Status
Completed
Phases
Phase 2Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01091636
Enrollment
184
Registered
2010-03-24
Start date
2010-03-31
Completion date
2020-01-10
Last updated
2020-02-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Epithelial Ovarian Cancer

Brief summary

The current standard treatment for ovarian cancer, tubal cancer, and primary peritoneal cancer is maximal cytoreductive surgery followed by chemotherapy. Recent randomized trials of Gynecologic Oncology Group (GOG) revealed the survival gain in intraperitoneal chemotherapy compared to the intravenous chemotherapy after the optimal cytoreduction in ovarian cancer (GOG#104, GOG#114, GOG#172). Experts attributed such survival gain to the earlier cycles of intraperitoneal chemotherapy when adhesion was minimal from extensive cytoreductive procedures. Hyperthermia has an anti-cancer activity itself. Especially, hyperthermia promotes chemotherapy to penetrate deeper into the cancer tissue. Therefore, the combination of intraperitoneal chemotherapy with hyperthermia theoretically could lead to higher response rate and better survival outcomes. \*HIPEC: hyperthermic intraperitoneal chemotherapy There will be an interim analysis when 50% of patients are enrolled. At the interim analysis, a statistical test will be performed. The nominal significance levels will be determined later. The exact nominal significance level will be determined based on the exact number of events at the time of the interim analysis. The Stopping boundaries will be calculated using an O'Brien-Fleming error spending function

Detailed description

If a patient is allocated to operation to remove ovarian cancer and metastatic disease in the abdomen, this trial could be considered. Before operation, laboratory test results, image result, patient's medical history, and baseline quality of life will be checked and reviewed. When optimal cytoreduction (residual tumor\<1cm) is attained, this HIPEC (hyperthermic intraperitoneal chemotherapy) could be considered. For the primary advanced epithelial ovarian cancer, HIPEC will be performed at random. For the recurrent ovarian cancer, HIPEC will be performed after completion of cytoreductive procedures. Usually, HIPEC takes one and half hours after cytoreductive surgery. After cytoreductive surgery followed by HIPEC, adjuvant chemotherapy will be added. The cycle of chemotherapy will be determined according to the patients' clinical outcomes. The laboratory test results, image result, patient's medical history, and baseline quality of life will be checked after the operation, during chemotherapy, and after chemotherapy. Cytoreduction: an operation to remove ovarian cancer and its metastatic disease There will be an interim analysis when 50% of patients are enrolled. At the interim analysis, a statistical test will be performed. The nominal significance levels will be determined later. The exact nominal significance level will be determined based on the exact number of events at the time of the interim analysis. The Stopping boundaries will be calculated using an O'Brien-Fleming error spending function

Interventions

PROCEDUREHyperthermic Intraperitoneal Chemotherapy

41.5 oC injected into the perfusion cisplatin (75 mg/m2)during 90min

Sponsors

Ajou University
CollaboratorOTHER
National Cancer Center, Korea
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Blinded to the participants

Intervention model description

HIPEC vs. no HIPEC after primary cytoreductive surgery or interval cytoreductive surgery

Eligibility

Sex/Gender
FEMALE
Age
No minimum to 75 Years
Healthy volunteers
No

Inclusion criteria

1. Disease status Primary ovarian cancer, tubal cancer, and primary peritoneal cancer (Stage III or more) 2. Residual tumor \< 1cm after completion of cytoreductive surgery 3. Age \< 75 year 4. Expected survival \> 3 months 5. Performance status: ECOG 0-1 6. Adequate bone marrow function Hb ≥8 g/dl (After correction in case of iron deficient anemia) WBC ≥ 3,000/mm3, Platelet ≥ 100,000/mm3 7. Adequate renal function Creatinine ≤ 1.5 mg/dl 8. Adequate hepatic function Bilirubin ≤ 1.5 mg/dl and AST and ALT ≤ 80 IU/L 9. Optimal cardiopulmonary function for surgery 10. Voluntary participation after getting written informed consent.

Exclusion criteria

1. Unresectable extraperitoneal metastasis (brain, bone, lung parenchyme, and supraclavicular lymph node) 2. Suboptimal debulking (residual tumor \> 1cm) 3. Previous History of other malignancies (except excision of skin cancer, thyroid cancer) 4. Serious heart disease or renal failure 5. Serious cardiopulmonary insufficiency 6. Uncontrolled infection 7. Uncontrolled intercurrent disease 8. Psychogenic disorder 9. Patients who are suitable candidates by legally 10. Pregnant or breast-feeding patients 11. Patients who are unsuitable candidates by doctor's decision 12. MMMT 13. Cancer tissue is not confirmed during surgery after neo-adjuvant chemotherapy

Design outcomes

Primary

MeasureTime frameDescription
Progression free survival2 yearsTo assess progression free survival rate during 2 years after Intraoperative Hyperthermic Intraperitoneal Chemotherapy followed by Intravenous Chemotherapy in Patients with Ovarian Cancer.

Secondary

MeasureTime frameDescription
Overall survival, quality of life3 yearsOvarian cancer patients after HIPEC are observed complication and 3-year survival rate. Ovarian cancer patients after HIPEC are analyzed quality of life.

Countries

South Korea

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026