Skip to content

Surgery Plus Intraoperative Peritoneal Hyperthermic Chemotherapy (IPHC) to Treat Peritoneal Carcinomatosis

Cytoreductive Surgery Plus Intraoperative Peritoneal Hyperthermic Chemotherapy for the Treatment of Peritoneal Carcinomatosis From Gastrointestinal Cancer: an Open Label, Randomized, Prospective, Phase 2 Clinical Trial

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00454519
Acronym
IPHC
Enrollment
60
Registered
2007-03-30
Start date
2007-03-31
Completion date
Unknown
Last updated
2009-02-13

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

Conditions

Colorectal Neoplasms, Mesothelioma, Neoplasm Metastasis, Stomach Neoplasms

Keywords

peritoneal carcinomatosis, cisplatin, mitomycin, gastric cancer, colorectal cancer

Brief summary

OBJECTIVES: * Determine response and survival of patients with peritoneal carcinomatosis treated with cytoreductive surgery plus intraoperative peritoneal hyperthermic chemotherapy with cisplatin and mitomycin * Assess the quality of life of patients treated with this regimen. OUTLINE: Patients are randomized into IPHC group and control group. In the former group, the patients undergo cytoreductive surgery plus intraoperative hyperthermic peritoneal perfusion with cisplatin and mitomycin over 60 minutes. Patients in the control group just underwent routine cytoreductive surgery. All patients in both groups receive the standard conventional chemotherapy after surgery. Quality of life is assessed at study initiation, at 1, 3, 6 months. Patients are followed at 4 weeks, every 3 months for 1 year, and then every 6 months for up to 3 years.

Detailed description

DISEASE CHARACTERISTICS: * Histologically confirmed peritoneal carcinomatosis with the following histologies: * Primary peritoneal mesothelioma * Adenocarcinoma of gastrointestinal tract origin * Confined to peritoneal cavity * Tumor mass could be debulked to less than 2.5 cm in diameter per tumor deposit * Must not have failed prior intraperitoneal platinum therapy * Treatment failure is defined as radiographic evidence of disease progression on 2 consecutive CT scans within 3 months after therapy PATIENT CHARACTERISTICS: Age: \- 20 to 70 years old Performance status: \- KPS\>50 Life expectancy: \- More than 8 weeks Hematopoietic: * WBC at least 3,500/mm\^3 * Platelet count at least 80,000/mm\^3 Hepatic: * Bilirubin no greater than 2 times upper limit of normal (ULN) * AST and ALT no greater than 2 times ULN * Liver enzymes no greater than 2 times ULN Renal: \- Creatinine no greater than 1.5 mg/dL Cardiovascular: * No significant irreversible cardiac ischemia * No significant changes in ECG recording Pulmonary: * FEV\_1 at least 1.2 liters * Maximum voluntary ventilation at least 50% expected Other: * Not pregnant or nursing * Negative pregnancy test * No concurrent medical problems that would preclude surgery

Interventions

PROCEDUREcytoreductive surgery

the whole abdominal-pelvic cavity is explored and maximal cytoreductive surgery is performed to remove visible tumor burden as much as possible.

PROCEDUREintraoperative peritoneal hyperthermic chemotherapy with cisplatin and mitomycin

Immediately after the cytoreductive surgery, cisplatin and mitomycin C dissolved in 12,000 ml of normal saline heated to 42 degrees celsius is infused into the abdominal cavity for a sustained hyperthermic intraperitoneal chemotherapy for 60 to 90 minutes.

Sponsors

NPO Organization to Support Peritoneal Dissemination Treatment
CollaboratorUNKNOWN
Kishiwada Tokushukai Hospital
CollaboratorOTHER
Kusatsu General Hopital
CollaboratorUNKNOWN
Ikeda Hospital
CollaboratorUNKNOWN
Wuhan University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Gastric cancer or colorectal cancer with peritoneal carcinomatosis * Gastric cancer or colorectal cancer with malignant ascites * Karnofsky Performance Scale(KPS)\>50

Exclusion criteria

* Age less than 20 years old, or beyond 70 years old * Any lung metastasis, liver metastasis, or prominent retroperitoneal lymph node metastasis * Bilirubin greater than 3 times upper limit of normal (ULN) * AST and ALT greater than 5 times ULN * Liver enzymes greater than 3 times ULN

Design outcomes

Primary

MeasureTime frame
overall survival timefrom operation to death due to cancer recurrence

Secondary

MeasureTime frame
perioperative morbidity and mortalityWithin 30 days postoperation

Countries

China

Contacts

Primary ContactYan Li, M.D., Ph.D
liyansd2@163.com+86-27-62337478

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 12, 2026