This trial is to assess the efficacy of pembrolizumab (MK3475) added to concurrent radiation and gemcitabine in the management of patients with muscle-invasive urothelial cancer who are not candidates for or decline radical cystectomy.
The investigators hypothesize that the addition of immune checkpoint inhibition with
pembrolizumab, an anti-PD-1 inhibitor, to chemo-radiation therapy to the bladder may work to
both increase eradication of local tumor as well as distant micrometastases through
heightened immune surveillance.
Due to the lack of a previous phase I trial establishing the safety of this combination
(pembrolizumab, gemcitabine, and radiation therapy (RT)), an initial safety lead-in cohort of
3 to 6 patients is enrolled for assessing dose-limiting toxicities. Similar to the Phase I
3+3 design, if there is no or only one patient in that cohort experiencing a dose-limiting
toxicity, the trial continues to the Phase II part to enroll additional 48 patients for
|Overal Status||Start Date||Phase||Study Type|
|Recruiting||Start Date: October 2014||Phase 2||Interventional|
Primary Outcome 1 - Measure: Two-year bladder-intact disease-free survival rate
Primary Outcome 1 - Time Frame: 2 years
- Histologically confirmed muscle-invasive urothelial cancer of the bladder within 60
days of study enrollment. Patients must be willing to provide a TURBT specimen during
screening and prior to enrollment if adequate specimen (FFPE tissue block or 20
unstained slides) from initial TURBT documenting muscle-invasive urothelial bladder
cancer is not available.
- Clinical stage T2-T4a, N0, M0 urothelial bladder cancer.
- Deemed to not be a candidate for radical cystectomy by attending urologic oncologist
or refuse radical cystectomy.
- Be willing and able to provide written informed consent/assent for the trial.
- Be ≥ 18 years of age on day of signing informed consent.
- Have a performance status of 0 or 1 on the Eastern Cooperative Oncology Group
- Demonstrate adequate organ function as defined below, all screening labs should be
performed within 10 days of protocol enrollment.
- Absolute neutrophil count >= 1,500 /mcL;
- Platelets >= 100,000 /mcL;
- Hemoglobin >= 9.0 g/dL;
- Serum creatinine <=1.5 x upper limit of normal (ULN) or calculated creatinine
clearance >= 30 mL/min as calculated by Cockcrof-Gault formaulae or by 24 hour
- Serum total bilirubin <=1.5 x ULN or direct bilirubin <= ULN for subjects with
total bilirubin levels > 1.5 x ULN;
- Aspartate aminotransferase and alanine aminotransferase <= 1.5 x ULN;
- Albumin >= 2.5 mg/dL;
- International normalized ratio or prothrombin time (PT) <= 1.5 x ULN unless
subject is receiving anticoagulant therapy as long as PT or partial prothrombin
time (PTT) is within therapeutic range of intended use of anticoagulants;
- Activated Partial Thromboplastin Time (aPTT) <= 1.5 x ULN unless subject is
receiving anticoagulant therapy as long as PT or PTT is within therapeutic range
of intended use of anticoagulants.
- Female subject of childbearing potential should have a negative urine or serum
pregnancy within 72 hours prior to receiving the first dose of study medication. If
the urine test is positive or cannot be confirmed as negative, a serum pregnancy test
will be required.
- Female subjects of childbearing potential should be willing to use 2 methods of birth
control or be surgically sterile, or abstain from heterosexual activity for the course
of the study through 120 days after the last dose of study medication. Subjects of
childbearing potential are those who have not been surgically sterilized or have not
been free from menses for > 1 year.
- Male subjects should agree to use an adequate method of contraception starting with
the first dose of study therapy through 120 days after the last dose of study therapy.
- Has received prior targeted small molecule therapy, radiation therapy or systemic
chemotherapy for urothelial bladder cancer including neoadjuvant chemotherapy. Prior
intravesical chemotherapy or intravesical immunotherapy is permissible, however, no
prior intravesical therapy is permitted within 4 weeks of study enrollment; adjuvant
therapy is not permitted.
- Has received prior pelvic radiation therapy.
- Has a history of inflammatory bowel disease or history of scleroderma.
- Is currently participating and receiving study therapy or has participated in a study
of an investigational agent and received study therapy or used an investigational
device within 4 weeks of the first dose of treatment.
- Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any
other form of immunosuppressive therapy within 7 days prior to the first dose of trial
- Has a known history of active TB (Bacillus Tuberculosis).
- Hypersensitivity to pembrolizumab or any of its excipients.
- Has had a prior anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study
Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events
due to agents administered more than 4 weeks earlier.
- If subject received major surgery, they must have recovered adequately from the
toxicity and/or complications from the intervention prior to starting therapy.
- Any prior history of invasive malignancy within the past 5 years except non-melanoma
skin cancer, carcinoma in-situ, localized prostate cancer without biochemical
recurrence following definitive treatment.
- Has any history of inflammatory bowel disease or scleroderma.
- Has other active autoimmune disease that has required systemic treatment in the past 2
years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive
drugs). Replacement therapy (eg., thyroxine, insulin, or physiologic corticosteroid
replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a
form of systemic treatment.
- History of Guillain-Barre Syndrome or Stevens-Johnson Syndrome
- Has known history of, or any evidence of active, non-infectious pneumonitis.
- Has an active infection requiring systemic therapy.
- Has a history or current evidence of any condition, therapy, or laboratory abnormality
that might confound the results of the trial, interfere with the subject's
participation for the full duration of the trial, or is not in the best interest of
the subject to participate, in the opinion of the treating investigator.
- Has known psychiatric or substance abuse disorders that would interfere with
cooperation with the requirements of the trial.
- Is pregnant or breastfeeding, or expecting to conceive or father children within the
projected duration of the trial, starting with the pre-screening or screening visit
through 120 days after the last dose of trial treatment.
- Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.
- Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
- Has known active Hepatitis B (e.g., HBsAg reactive) or Hepatitis C (e.g., HCV RNA
[qualitative] is detected).
- Has received a live vaccine within 30 days of planned start of study therapy. Seasonal
influenza vaccines for injection are generally inactivated flu vaccines and are
allowed; however intranasal influenza vaccines (e.g., Flu-Mist®) are live attenuated
vaccines, and are not allowed.
Minimum Age: 18 Years
Maximum Age: N/A
Healthy Volunteers: No
Name: Arjun Balar, MD
Role: Principal Investigator
Affiliation: NYU Perlmutter Cancer Center
Name: Arjun Balar, MD
|University of Chicago
Chicago, Illinois 60637
|University of Michigan Health System
Ann Arbor, Michigan 48109
|NYU Perlmutter Cancer Center
New York, New York 10016
Arjun Balar, MD
|University of North Carolina
Chapel Hill, North Carolina 27599-7305