Everolimus (RAD001) in Metastatic Transitional Cell Carcinoma of the Urothelium

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Brief Title

Everolimus (RAD001) in Metastatic Transitional Cell Carcinoma of the Urothelium

Official Title

Phase II Study of Everolimus (RAD001) in Metastatic Transitional Cell Carcinoma of the Urothelium

Brief Summary

      The purpose of this study is to learn what effects, good and/or bad, Everolimus has on
      advanced urothelial cancer.

      The goal of this clinical research study is to learn if the study drug Everolimus can shrink
      or slow the growth of urothelial cancer. The safety of this drug will also be studied. The
      patients physical state, changes in the size of the tumor, and laboratory findings taken
      while on-study will help us decide if Everolimus is safe and effective.
    


Study Phase

Phase 2

Study Type

Interventional


Primary Outcome

To measure the two-month PFS rate of Everolimus (RAD001) as determined by RECIST.

Secondary Outcome

 To determine the response rate of Everolimus in patients with progressive urothelial cancer who have received prior cytotoxic chemotherapy.

Condition

Bladder Cancer

Intervention

Everolimus

Study Arms / Comparison Groups

 Everolimus
Description:  Everolimus will be administered at a dose of 10 mg orally once daily continuously.

Publications

* Includes publications given by the data provider as well as publications identified by National Clinical Trials Identifier (NCT ID) in Medline.

Recruitment Information


Recruitment Status

Drug

Estimated Enrollment

46

Start Date

December 2008

Completion Date

December 2021

Primary Completion Date

December 2021

Eligibility Criteria

        Inclusion Criteria:

          -  Patients must have a diagnosis of urothelial carcinoma of the bladder, urethra,
             ureter, or renal pelvis, with histological confirmation at MSKCC.

          -  Patients must have progressive metastatic disease. Progressive disease will be defined
             as new or progressive lesions on cross-sectional imaging.

          -  Patients must have at least one measurable site of disease (according to RECIST
             criteria) that has not been previously irradiated.

          -  Patients must have been previously treated, as defined by the following:

        Treatment with at least one prior cytotoxic agent but not more than four prior cytotoxic
        agents. Up to four prior chemotherapy agents are allowed, since conventional chemotherapy
        ranges from just one drug (e.g., gemcitabine) to regimens that contain four agents (e.g.,
        M-VAC is a four-drug regimen containing methotrexate, vinblastine, doxorubicin, and
        cisplatin).

          -  The prior therapy must have included at least one of the following: cisplatin,
             carboplatin, paclitaxel, docetaxel, or gemcitabine.

          -  The prior cytotoxic agents may have been administered in the perioperative or
             metastatic setting and may have been administered sequentially (e.g., first-line
             treatment followed by second-line treatment at time of progression) or as part of a
             single regimen.

          -  Patients must have pre-treatment tumor tissue available for analysis of m-TOR pathway
             markers. One paraffin block or 10 freshly-prepared unstained slides (on positively
             charged slides for immunohistochemistry) from the most representative single
             paraffin-embedded tumor tissue block. Slides from the primary tumor are preferred. If
             both the primary and metastatic tumor blocks are available, 10 slides from each of the
             sites should be submitted. If tissue from the primary tumor is not available, a
             paraffin block or unstained slides from a metastatic site are acceptable. Fine needle
             aspirates (FNAs) have insufficient tumor tissue and are not permitted.

          -  Age ≥ 18 years

          -  Karnofsky Performance Status ≥ 60%

          -  Adequate bone marrow function as shown by: ANC ≥ 1.5 x 109/L, Platelets ≥ 100 x 109/L,
             Hb >9 g/dL

          -  Adequate liver function as shown by:

          -  serum bilirubin ≤ 1.5 x ULN

          -  INR < 1.3 (or < 3 on anticoagulants)

          -  ALT and AST ≤ 2.5x ULN (≤ 5x ULN in patients with liver metastases)

          -  Adequate renal function: serum creatinine ≤ 1.5 x ULN

          -  Fasting serum cholesterol ≤300 mg/dL OR ≤7.75 mmol/L AND fasting triglycerides ≤ 2.5 x
             ULN. NOTE: If a patient's lipid values exceed either one of these criteria upon
             screening, the patient can only become eligible after successful initiation of
             appropriate lipid-lowering medication. After lipid-lowering therapy, patients must
             meet the same criteria - i.e. a fasting serum cholesterol ≤300 mg/dL OR ≤7.75 mmol/L
             AND fasting triglycerides ≤ 2.5 x ULN - to be eligible for study treatment

          -  Signed informed consent.

          -  Testing for hepatitis B viral load and serological markers (HBV-DNA, HBsAg, HBsAb, and
             HBcAb) for the following patients:

               -  All patients who currently live in (or have lived in) Asia, Africa, Central and
                  South America, Eastern Europe, Spain, Portugal, or Greece

               -  Patients with any of the following risk factors:

               -  Known or suspected past hepatitis B infection Blood transfusion(s) prior to 1990

          -  Current or prior IV drug users

          -  Current or prior dialysis

          -  Household contact with hepatitis B infected person(s)

          -  Current or prior high-risk sexual activity

          -  Body piercing or tattoos

          -  Mother known to have hepatitis B History suggestive of hepatitis B infection, e.g dark
             urine, jaundice, or right upper quadrant pain

          -  Additional patients at the discretion of the investigator

          -  Testing for hepatitis C infection (using quantitative RNA-PCR) for patients with any
             of the following risk factors:

          -  Known or suspected past hepatitis C infection (including patients with past interferon
             "curative" treatment)

          -  Blood transfusion(s) prior to 1990

          -  Current or prior IV drug users

          -  Household contact of hepatitis C infected person(s)

          -  Current or prior high-risk sexual activity

          -  Body piercing or tattoos

          -  Additional patients at the discretion of the investigator

        Exclusion Criteria:

          -  Patients currently receiving anticancer therapies or who have received anticancer
             therapies within 4 weeks of the start of study drug (including chemotherapy, radiation
             therapy, antibody based therapy, etc.)

          -  Patients who have had a major surgery or significant traumatic injury within 4 weeks
             of start of study drug, patients who have not recovered from the side effects of any
             major surgery (defined as requiring general anesthesia), or patients who may require
             major surgery during the course of the study.

          -  Prior treatment with any investigational drug within the preceding 4 weeks.

          -  Patients receiving chronic, systemic treatment with corticosteroids or another
             immunosuppressive agent, except corticosteroids with a daily dosage equivalent to
             prednisone ≤ 20 mg. Patients receiving these corticosteroids must have been on a
             stable dosage regimen for a minimum of 4 weeks prior to the first treatment with
             Everolimus. Topical or inhaled corticosteroids are allowed.

          -  Patients should not receive immunization with attenuated live vaccines within one week
             of study entry or during study period.

          -  Uncontrolled brain or leptomeningeal metastases, including patients who continue to
             require glucocorticoids for brain or leptomeningeal metastases.

          -  Evidence of another active cancer, except for non-melanoma skin carcinoma, in-situ
             carcinoma of the cervix curatively treated, and adenocarcinoma of the prostate that
             has been surgically treated with a post-treatment PSA that is non-detectable

          -  Patients who have any severe and/or uncontrolled medical conditions or other
             conditions that could affect their participation in the study such as:

          -  Symptomatic congestive heart failure of New York Heart Association Class III or IV.

          -  Unstable angina pectoris, symptomatic congestive heart failure, myocardial infarction
             within 6 months of start of study drug, serious uncontrolled cardiac arrhythmia, or
             any other clinically significant cardiac disease.

          -  Severely impaired lung function as evidenced by:

        (TLC) <50% predicted, OR (FVC) <50% predicted OR, (DLCO) <40% predicted

          -  Uncontrolled diabetes as defined by fasting serum glucose >1.5 x ULN.

          -  Active (acute or chronic) or uncontrolled severe infections.

          -  Liver disease such as cirrhosis, chronic active hepatitis, or chronic persistent
             hepatitis.

          -  A known history of HIV seropositivity.

          -  Impairment of gastrointestinal function or gastrointestinal disease that may
             significantly alter the absorption of Everolimus (e.g. ulcerative disease,
             uncontrolled nausea, vomiting, diarrhea, malabsorption syndrome, or small bowel
             resection).

          -  Patients with an active, bleeding diathesis.

          -  Female patients who are pregnant or breast-feeding, Women of childbearing potential
             must have a negative urine or serum pregnancy test within 7 days prior to
             administration of Everolimus.

          -  Adults of reproductive potential who are not using effective birth control methods.
             Men and women of childbearing potential must be willing to use effective barrier
             method contraception during the trial and for at least three months thereafter.
             Patients are encouraged to continue barrier -method contraception for two years or
             longer after treatment. Hormonal contraceptives are not acceptable as a sole method of
             contraception

          -  Patients who have received prior treatment with an mTOR inhibitor (sirolimus,
             temsirolimus, everolimus).

          -  Patients with a known hypersensitivity to Everolimus (RAD001) or other rapamycins
             (sirolimus, temsirolimus) or to its excipients.

          -  History of noncompliance to medical regimens.

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

Gender

All

Ages

18 Years - N/A

Accepts Healthy Volunteers

No

Contacts

Dean Bajorin, MD, , 

Location Countries

United States

Location Countries

United States

Administrative Informations


NCT ID

NCT00805129

Organization ID

08-123


Responsible Party

Sponsor

Study Sponsor

Memorial Sloan Kettering Cancer Center

Collaborators

 Novartis Pharmaceuticals

Study Sponsor

Dean Bajorin, MD, Principal Investigator, Memorial Sloan Kettering Cancer Center


Verification Date

October 2020