Ph II Study of Perifosine for Patients With Carcinoma of the Kidney

Kidney Cancer Clinical Trial

Official title:

Phase II Study of Perifosine for Patients With Metastatic Carcinoma of the Kidney Who Have Progressed on a VEGF Receptor Inhibitor

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00498966
• Other study ID #: Perifosine 231
• Status: Completed
• Phase: Phase 2
• First received: July 9, 2007
• Last updated: February 2, 2018
• Start date: July 2007
• Est. completion date: October 2011

Study information

• Verified date: February 2018
• Source: AEterna Zentaris
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This is a Phase II study. Patients with kidney carcinoma will be considered in two groups. The goals of this study are:

• To measure clinical benefit defined as tumor response or progression-free survival for more than 12 weeks in patients with metastatic carcinoma of the kidney who have failed or have progressed on a VEGF receptor inhibitor

• To evaluate the safety of perifosine in patients with metastatic carcinoma of the kidney who have failed or have progressed on a VEGF receptor inhibitor

Description:

This is a Phase II study. Patients with kidney carcinoma will be considered in two groups. Patients in group A will have previously failed a VEGF receptor inhibitor but not an mTOR inhibitor, while patients in group B will have failed both a VEGF receptor inhibitor and an mTOR inhibitor. Evaluation of each group will be performed separately. The goals of this study are:

1. To measure clinical benefit defined as an objective tumor response using RESIST or progression-free survival for more than 12 weeks in patients with metastatic carcinoma of the kidney who have failed or have progressed on a VEGF receptor inhibitor

2. To evaluate the safety of perifosine in patients with metastatic carcinoma of the kidney who have failed or have progressed on a VEGF receptor inhibitor.

Treatment Phase/duration of treatment: All patients will be treated with daily perifosine at 100 mg PO daily until tumor progression (by the RECIST criteria) or unacceptable toxicity. Once radiological disease progression has been documented by the treating physician, the patient will go off study. Patients are encouraged to have two measurements for confirmation of progression.

Follow-Up Phase: All patients will be followed-up for SAEs until at least 30 days after discontinuation of perifosine. All patients who are discontinued from perifosine for any reason other than disease progression will continue to have tumor assessments until the patient has documented disease progression or has begun other therapies.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 50
• Est. completion date: October 2011
• Est. primary completion date: July 2011
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patients with confirmed metastatic RCC

• Patients must have documented progression on treatment with sunitinib or sorafenib. Prior therapy with bevacizumab and/or cytokines (i.e., IL-2, interferon) is permitted. Prior vaccine therapy in the adjuvant setting is also permitted. Patients can have failed therapy with ONE prior mTOR inhibitor.

• Patients must have at least one measurable lesion on computer tomography (CT) Scan or magnetic resonance imaging (MRI) using Modified RECIST criteria.

• Patients must have normal organ and marrow function, unless in the opinion of the treating investigator, the abnormality is related to tumor, and the study chairman agree the abnormality is unlikely to affect the safety of perifosine use. Normal organ and marrow function is described below:

• ANC >= 1.5 x 109/L

• Platelets >= 75,000/ mm3

• HCT >= 28% (with or without growth factor support)

• Creatinine <= 3.0 mg/dl

• Total bilirubin <= 1.5 x upper limit of normal

• Transaminase <= 2.5 x upper limit of normal

• ECOG performance status of 0 or 1

• Patients with CNS metastases must be clinically stable for at least 2 months following treatment with radiation therapy, surgery, or both; and be off corticosteroids and anti-seizure medication.

• Patients with a life expectancy =6 months

• Age =18 years old

• Patients who give a written informed consent obtained according to local guidelines

• Women of childbearing potential must have had a negative serum or urine pregnancy test 72 hours prior to the administration of the first study treatment.

Exclusion Criteria:

• Patients who have not recovered (<= grade 1) from adverse events from prior therapy (excluding alopecia).

• Patients currently receiving sorafenib or sunitinib who have received either of these within 2 weeks prior to study entry.

• Patients may have had prior sorafenib OR sunitinib BUT cannot have been treated with both VEGF receptor inhibitors.

• Patients with a known hypersensitivity to perifosine or its excipients.

• Female patients who are pregnant or breast feeding, or adults of reproductive potential who are not using effective birth control methods.

• Patients who are using other investigational agents or who had received investigational drugs <= 4 weeks prior to study entry.

• Patients unwilling to or unable to comply with the protocol.

• Patients who have a history of another primary malignancy <= 5 years with the exceptions of non melanomatous skin cancer and carcinoma in situ of the cervix.

Related Conditions & MeSH terms

• Carcinoma, Renal Cell
• Kidney Cancer
• Kidney Neoplasms

Intervention

Drug:
• Perifosine
Perifosine 100 mg PO Perifosine is supplied as a film-coated tablet containing 50 mg of active ingredient. Treatment will be administered on an outpatient basis in 28-day cycles. The patient dose for daily administration will be 100 mg qhs daily with food.

Locations

Country	Name	City	State
United States	Investigative Site	Armonk	New York
United States	Investigative Site	Louisville	Kentucky
United States	Investigative Site	Morristown	New Jersey

Sponsors (1)

Lead Sponsor	Collaborator
AEterna Zentaris

Country where clinical trial is conducted

United States, 

References & Publications (1)

Journal of Clinical Oncology, 2009 ASCO Annual Meeting Proceedings (Post-Meeting Edition). Vol 27, No 15S (May 20 Supplement), 2009: 5101

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Objective tumor response using RESIST OR progression-free survival	Clinical benefit, defined as either an objective response by RECIST or PFS >12 weeks, is a primary endpoint of the study. The clinical benefit rate together with its two-sided exact binomial 95% confidence interval will be reported.	12 weeks
Secondary	Evaluate the safety of perifosine in patients with metastatic carcinoma of the kidney	Safety endpoints include: incidence of adverse events, serious adverse events, change in vital signs and change in laboratory results (hematology, blood chemistry, urinalysis).	12 weeks