Interleukin-12 in Treating Patients With Refractory Advanced-Stage Ovarian Cancer or Abdominal Cancer
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Purpose
Phase I trial to study the effectiveness of interleukin-12 in treating patients with refractory ovarian or abdominal cancers. Interleukin-12 may kill tumor cells by stopping blood flow to the tumor and by stimulating a persons's white blood cells to kill cancer cells.
| Condition | Intervention | Phase |
|---|---|---|
|
Cancer |
Biological: recombinant interleukin-12 |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Single Group Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | A Phase I Dose-Escalating Study of Recombinant Human Interleukin-12 (NSC # 672423) Administered by Intraperitoneal Infusion in Refractory Advanced Stage Ovarian Cancer and Other Abdominal Carcinomatosis |
| Enrollment: | 36 |
| Study Start Date: | August 1998 |
| Primary Completion Date: | May 2001 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: Arm I
Cohorts of 3-6 patients each receive escalating doses of intraperitoneal recombinant human interleukin-12 (rhIL-12) administered weekly for 9 weeks. If a patient tolerates rhIL-12 and shows evidence of objective response or stable disease, patient may receive up to 9 additional weeks of treatment. Treatment continues in the absence of unacceptable toxicity or disease progression. Dose escalation continues until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which no more than 1 of 6 patients experiences dose limiting toxicity.
|
Biological: recombinant interleukin-12 |
Detailed Description:
OBJECTIVES:
I. Assess the safety and maximum tolerated dose of recombinant human interleukin-12 (rhIL-12) administered by intraperitoneal infusion in patients with chemotherapy refractory advanced ovarian cancer and other diffuse abdominal carcinomatosis.
II. Determine the immunopharmacologic profile of rhIL-12 in this patient population.
III. Evaluate the biologic response in selected patients to rhIL-12 administered through intraperitoneal infusions.
OUTLINE: This is a dose escalation, multicenter study.
Cohorts of 3-6 patients each receive escalating doses of intraperitoneal recombinant human interleukin-12 (rhIL-12) administered weekly for 9 weeks. If a patient tolerates rhIL-12 and shows evidence of objective response or stable disease, patient may receive up to 9 additional weeks of treatment. Treatment continues in the absence of unacceptable toxicity or disease progression. Dose escalation continues until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which no more than 1 of 6 patients experiences dose limiting toxicity.
All patients are followed for survival.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
DISEASE CHARACTERISTICS:
- Histologically or cytologically confirmed intraabdominal cancer
- Diffuse abdominal carcinomatosis Chemotherapy refractory advanced stage ovarian cancer
- Measurable disease
- Residual, recurrent, or metastatic disease beyond the scope of standard curative therapy
- Extension of disease to sites distant to the peritoneal cavity allowed Retroperitoneal lymphadenopathy allowed as long as there is evaluable intraabdominal disease
- No history of progressive brain metastases
PATIENT CHARACTERISTICS:
- Age: 18 and over
- Performance status: Karnofsky 70-100%
- Hemoglobin greater than 9 g/dL
- WBC greater than 3,000/mm3
- Platelet count greater than 100,000/mm3
- Bilirubin less than 2.0 mg/dL
- ALT less than 100 U/L
- Creatinine clearance greater than 60 mL/min
- Normal electrocardiogram
- No recent history of cardiac ischemia
- Not pregnant or nursing
- Negative pregnancy test
- Fertile patients must use effective contraception
- Hepatitis B negative
- No evidence of clinical immunodeficiency syndromes or immunodeficiency associated diseases
- No history of autoimmune disease
- No concurrent major illness
- No serious infection requiring intravenous antibiotics
- No active peptic ulcer disease
- Must have free flow of fluid into the peritoneal space
- No leakage from the catheter exit site
PRIOR CONCURRENT THERAPY:
- At least 3 weeks since prior biologic therapy (6 weeks for interleukin-2)
- No prior recombinant human interleukin-12
- At least 3 weeks since prior chemotherapy (6 weeks for nitrosoureas)
- No concurrent systemic chemotherapy
- No concurrent systemic corticosteroids
- No prior radiation therapy to the whole abdomen
- No concurrent radiotherapy
- At least 3 weeks since prior exposure to any investigational drug
- No concurrent investigational drug
Contacts and Locations| United States, Pennsylvania | |
| University of Pittsburgh Cancer Institute | |
| Pittsburgh, Pennsylvania, United States, 15213 | |
| Study Chair: | Robert P. Edwards, MD | University of Pittsburgh |
More Information
Additional Information:
No publications provided
| Responsible Party: | National Cancer Institute (NCI) |
| ClinicalTrials.gov Identifier: | NCT00003439 History of Changes |
| Other Study ID Numbers: | NCI-2012-02272, PCI-98-031, PCI-MWH-97-039, NCI-T97-0031, CDR0000066467 |
| Study First Received: | November 1, 1999 |
| Last Updated: | February 6, 2013 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by National Cancer Institute (NCI):
|
stage IV colon cancer stage IV gastric cancer recurrent gastric cancer recurrent pancreatic cancer stage IV rectal cancer recurrent colon cancer recurrent rectal cancer stage IV anal cancer recurrent anal cancer stage IV ovarian epithelial cancer recurrent ovarian epithelial cancer metastatic gastrointestinal carcinoid tumor recurrent gastrointestinal carcinoid tumor advanced adult primary liver cancer |
recurrent adult primary liver cancer stage IV endometrial carcinoma recurrent endometrial carcinoma small intestine adenocarcinoma unresectable gallbladder cancer recurrent gallbladder cancer unresectable extrahepatic bile duct cancer recurrent extrahepatic bile duct cancer recurrent small intestine cancer stage IV prostate cancer recurrent prostate cancer fallopian tube cancer primary peritoneal cavity cancer stage IV pancreatic cancer |
Additional relevant MeSH terms:
|
Ovarian Neoplasms Endocrine Gland Neoplasms Neoplasms by Site Neoplasms Ovarian Diseases Adnexal Diseases Genital Diseases, Female Genital Neoplasms, Female Urogenital Neoplasms Endocrine System Diseases Gonadal Disorders |
Interleukin-12 Angiogenesis Inhibitors Angiogenesis Modulating Agents Growth Substances Physiological Effects of Drugs Pharmacologic Actions Growth Inhibitors Antineoplastic Agents Therapeutic Uses Adjuvants, Immunologic Immunologic Factors |
ClinicalTrials.gov processed this record on May 16, 2013