| Eligibility |
Inclusion Criteria:
1. Signed and dated informed consent;
2. Male or female, age =18 years at time of informed consent signature;
3. Histological confirmed locally advanced (any T N2-3) or metastatic urothelial bladder
carcinoma, eligible to first-line treatment (previous neo adjuvant or adjuvant
treatment must have been given and stopped more than one year before);
4. Evidence of progressive disease in the previous 6 months, documented by chest and/or
abdominal CT-scan or MRI;
5. Measurable disease according to RECIST 1.1;
6. Karnofsky index = 70%;
7. Availability of a representative formalin-fixed, paraffin-embedded (FFPE) tumour
specimen (infiltrative urothelial bladder carcinoma or metastasis) collected within 12
months before Cycle 1 Day 1;
8. At least 3 weeks since the end of prior local intravesical treatment (BCG-therapy or
ametycine) with resolution of all treatment-related toxicity to grade =1 (NCI CTCAE
4.0);
9. Palliative local treatment is allowed if performed = 2 weeks prior study entry for
radiotherapy, cimentoplasty or minor surgery, and =4 weeks for major surgery;
10. Adequate organ function as defined by the following criteria:
1. Absolute White Blood Cells count (WBC) = 2000 cells/mm3
2. Absolute Neutrophils count (ANC) = 1500 cells/mm3
3. Platelets =100 000 cells/mm3
4. Hemoglobin = 9.0 g/dL
5. Total bilirubin level = 1.5 × the upper limit of normal (ULN) range and AST and
ALT levels = 2.5 × ULN or AST and ALT levels = 5 x ULN (for subjects with
documented metastatic disease to the liver).
6. Calculated creatinine clearance = 60 mL/min
11. Women of childbearing potential must have a negative serum ßHCG or urine pregnancy
test within 7 days prior to initiation of treatment; both sexually active females and
males (and their female partners) patients must agree to use two methods of effective
contraception one of them being a barrier method, or to abstain from sexual activity
during the study, for at least 3 months after the last administration of study
treatment;
12. Willingness and ability to comply with scheduled visits, treatment plans, laboratory
tests, and other study procedures;
13. Patient affiliated to a social security system or beneficiary of the same.
Exclusion Criteria:
1. Other prior first-line therapy;
2. Any concurrent chemotherapy, immunotherapy, biologic or hormonal therapy for cancer
treatment; focal radiation therapy less than 14 days prior to the first day of the
first cycle;
3. Other invasive malignancy within 3 years (except for locally curable cancers that have
been apparently cured, such as basal or squamous cell skin cancer, superficial bladder
cancer, or carcinoma in situ of the prostate, cervix or breast); Patient with low risk
prostate cancer (defined as Stage T1/T2a, Gleason score = 7 and PSA = 10ng/mL) who are
treatment-naïve and undergoing active surveillance are eligible;
4. Persisting toxicity related to prior therapy (NCI CTCAE v. 4.03 Grade > 1); however,
alopecia, sensory neuropathy Grade = 2, or other Grade = 2 not constituting a safety
risk based on investigator's judgment are acceptable;
5. Symptomatic central nervous system (CNS) metastases or untreated CNS metastases
requiring concurrent treatment;
6. Clinically significant (i.e. active) cardiovascular disease: cerebral vascular
accident/stroke (< 6 months prior to enrollment), myocardial infarction (< 6 months
prior to enrollment), unstable angina, congestive heart failure (= New York Heart
Association Classification Class II), or serious cardiac arrhythmia requiring
medication;
7. Uncontrolled adrenal insufficiency;
8. Active chronic liver disease;
9. Other severe acute or chronic medical conditions including colitis, inflammatory bowel
disease, pneumonitis, pulmonary fibrosis or psychiatric conditions including recent
(within the past year) or active suicidal ideation or behavior; or laboratory
abnormalities that may increase the risk associated with study participation or study
treatment administration or may interfere with the interpretation of study results
and, in the judgment of the investigator, would make the patient inappropriate for
entry into this study;
10. Active infection requiring systemic antibiotic;
11. Vaccination within 4 weeks of the first dose of avelumab and while on trials is
prohibited except for administration of inactivated vaccines;
12. Current use of immunosuppressive medication, EXCEPT for the following: a. intranasal,
inhaled, topical steroids, or local steroid injection (e.g., intra-articular
injection); b. Systemic corticosteroids at physiologic doses = 10 mg/day of prednisone
or equivalent; c. Steroids as premedication for hypersensitivity reactions (e.g., CT
scan premedication);
13. Major surgery less than 28 days prior to the first day of the first cycle. Minor
surgery less than 14 days prior to the first day of the first cycle;
14. Active autoimmune disease that might deteriorate when receiving an immuno-stimulatory
agent. Patients with diabetes type I, vitiligo, psoriasis, or hypo- or hyperthyroid
diseases not requiring immunosuppressive treatment are eligible;
15. History of primary immunodeficiency;
16. History of organ transplant including allogeneic stem-cell transplantation;
17. Known prior severe hypersensitivity to investigational product or any component in its
formulations, including known severe hypersensitivity reactions to monoclonal
antibodies (NCI CTCAE v4.03 Grade = 3);
18. Women who are pregnant or lactating;
19. Known history of testing positive for HIV or known acquired immunodeficiency syndrome;
20. Positive test for hepatitis B virus surface antigen (HBV sAg) or hepatitis C virus
ribonucleic acid (HCV RNA) indicating acute or chronic infection.
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