Surgery and Oxaliplatin or Mitomycin C in Treating Patients With Tumors of the Appendix

Primary Peritoneal Cavity Cancer Clinical Trial

Official title:

A Multi-Center, Open-Label, Randomized Phase II Trial to Evaluate Hematologic Toxicities After HIPEC With Oxaliplatin or Mitomycin C in Patients With Appendiceal Tumors

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01580410
• Other study ID #: IRB00009326
• Secondary ID: NCI-2009-00947CC
• Status: Completed
• Phase: Phase 2
• Start date: May 2009
• Est. completion date: November 2016

Study information

• Verified date: June 2018
• Source: Wake Forest University Health Sciences
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This randomized phase II trial is studying the side effects and how well giving oxaliplatin or mitomycin C directly into the abdomen after surgery works in treating patients with tumors of the appendix. Drugs used in chemotherapy, such as oxaliplatin and mitomycin C, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Heating a chemotherapy solution and infusing it directly into the abdomen may kill more tumor cells. Giving these treatments after surgery may kill any tumor cells that remain after surgery.

Description:

PRIMARY OBJECTIVES:

I. To compare the toxicity profiles within 4 weeks of surgery of oxaliplatin and mitomycin C delivered via Hyperthermic Intraperitoneal Chemotherapy in patients with peritoneal surface malignancies from primary appendiceal tumors.

SECONDARY OBJECTIVES:

I. To compare the time to progression in patients treated with oxaliplatin vs. mitomycin C delivered via Hyperthermic Intraperitoneal Chemotherapy for surface malignancies from primary appendiceal tumors.

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

Arm I: Patients undergo surgical cytoreduction and receive mitomycin C by hyperthermic intraperitoneal chemotherapy (HIPEC).

Arm II: Patients undergo surgical cytoreduction and receive oxaliplatin by HIPEC.

After completion of study treatment, patients are followed up at 6, 12, 18, 24, 30, and 36 months.

Other known NCT identifiers

• NCT00904267

Recruitment information / eligibility

• Status: Completed
• Enrollment: 136
• Est. completion date: November 2016
• Est. primary completion date: October 2015
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients must have histologically or cytologically confirmed peritoneal surface malignancies from primary appendiceal tumors

• Eastern Cooperative Oncology Group (ECOG) performance status =< 2

• Absolute neutrophil count >= 1,500/mcL

• Platelets >=100,000/mcL

• Total bilirubin =< 1.5 mg/dL

• Creatinine =< 2.0 mg/dL

• Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase [SGOT])/alanine aminotransferase (ALT) (serum glutamic pyruvic transaminase [SGPT]) =< 3 X institutional upper limit of normal

• Alkaline phosphatase =< 3 X institutional upper limit of normal

• Patients must be recovered from both the acute and late effects of any prior surgery, radiotherapy, or other antineoplastic therapy

• Women of child-bearing potential and men must agree to use adequate contraception (hormonal or double-barrier method of birth control; abstinence) for the duration of study participation and for 90 days following HIPEC

• Ability to understand and the willingness to sign a written informed consent document (either directly or via a legally authorized representative)

• Participants who have received oxaliplatin during prior systemic chemotherapy regimens are eligible for enrollment in this protocol

Exclusion Criteria:

• Patients with an active infection or with a fever >= 101.3 degrees Fahrenheit (F) within 3 days of the first scheduled day of protocol treatment

• Patients who are receiving concurrent investigational therapy or who have received investigational therapy within 30 days of HIPEC (investigational therapy is defined as treatment for which there is currently no regulatory authority approved indication)

• Patients with carcinoid tumors

• Patients with active central nervous system (CNS) metastases

• Patients with known hypersensitivity to any of the components of oxaliplatin or mitomycin C

• History of prior malignancy within the past 5 years, except for curatively treated basal cell carcinoma of the skin, cervical intra-epithelial neoplasia, or localized prostate cancer with a current prostate-specific antigen (PSA) of < 1.0 mg/dL on 2 successive evaluations, at least 3 months apart, with the most recent evaluation no more than 4 weeks prior to entry

• Patients who received radiotherapy to more than 25% of their bone marrow

• Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements

• Pregnant/nursing women are excluded from this study because oxaliplatin is an agent with the potential for teratogenic or abortifacient effects; because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with oxaliplatin, breastfeeding should be discontinued if the mother is treated with oxaliplatin or mitomycin C

• Known human immunodeficiency virus (HIV), hepatitis B or C-positive patients (active, previously treated or both)

• Peripheral neuropathy >= grade 2

• History of allogenic transplant

• History of prior HIPEC

• Evidence of metastatic disease outside of the abdomen

Related Conditions & MeSH terms

• Appendiceal Neoplasms
• Carcinoma of the Appendix
• Primary Peritoneal Cavity Cancer

Intervention

Drug:
• mitomycin C
Given by HIPEC
• oxaliplatin
Given by HIPEC

Procedure:
• therapeutic conventional surgery
Undergo surgery

Other:
• quality-of-life assessment
Ancillary studies

Drug:
• hyperthermic intraperitoneal chemotherapy
Undergo HIPEC

Locations

Country	Name	City	State
United States	M D Anderson Cancer Center	Houston	Texas
United States	UPMC Hillman Cancer Center	Pittsburgh	Pennsylvania
United States	Wake Forest University Health Sciences	Winston-Salem	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
Wake Forest University Health Sciences	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The Difference in the Number of Grade 3 or 4 Hematologic Toxicities (Leukopenia, Thrombocytopenia, and Neutropenia) Between the Mitomycin C and Oxaliplatin Treatments	If a patient has a grade 3 or 4 standard hematologic toxicity (leukopenia, thrombocytopenia, and neutropenia), the patient will be considered to be an event. The observed rates of the 2 treatments will be the primary outcome, and the rates will be analyzed using a 2-sided chi-square test.	Within 4 weeks of surgery
Secondary	The Difference in Percentage of Disease-free Survival Between the Two Treatment Arms up to 3 Years		Time to first progression unless the patient's resection status is R2b or 2c, regardless of toxicity or response to study drug, assessed up to 3 years
Secondary	The Difference in Percentage of Overall Survival Between the Two Treatment Arms up to 3 Years		Interval between surgery and death or date of last contact, assessed up to 3 years
Secondary	Quality of Life as Assessed by Functional Assessment of Cancer Therapy: General (FACT-G)	The FACT-G (Functional Assessment of Cancer Therapy - General) consists of 27 core items assessing patient well-being in four components: Physical (7 items), Social/Family (7 items), Emotional (6 items), and Functional (7 items). Items are rated on a five-point scale: 0-"not at all", 1- "a little bit", 2-"somewhat", 3- "quite a bit" and 4-"very much". The score of each component is the mean times the number of items in the component. The range of the physical, social/family, and functional components I 0-28 and the range of the emotional component is 0-24. The sum of the component scores creates the overall score which has a range of 0-108. For all component scores and overall score, the higher the score the better the QOL.	Throughout study completion, up to 3 years