| Eligibility |
Inclusion Criteria:
- 1. Capable of giving signed informed consent which includes compliance with the
requirements and restrictions listed in the informed consent form (ICF) and in this
protocol.
2. Age > 18 years at time of study entry. 3. Evidence of muscle-invasive bladder
cancer in a pretreatment transurethral biopsy sample.
4. All histologic subtypes (with exception of small-cell carcinoma) will be eligible
if urothelial carcinoma was the predominant histopathologic feature.
5. Clinical stage T2-T4aN0M0 or T1-T4aN1M0 disease on imaging by American Joint
Commission on Cancer, eighth edition.
6. Available primary tumor tissue (formalin-fixed paraffin embedded FFPE or slides)
from transurethral biopsy/resection for biorepository.
7. Residual disease post transurethral resection prior to protocol inclusion and
initiation.
8. Patient must be planning to undergo a radical cystectomy at the time of
randomization.
9. Unfit for cisplatin-based neoadjuvant chemotherapy defined as the presence of at
least one of the characteristics below:
1. Creatinine clearance less than 60 mL/min;
2. Grade 2 or worse hearing loss;
3. Grade 2 or worse neuropathy;
4. New York Heart Association class III heart failure. 10. Eastern Cooperative
Oncology Group (ECOG) performance status of 0 to 1. 11. Body weight >30kg 12.
Adequate normal organ and marrow function as defined below:
- Haemoglobin =10.0 g/dL with no blood transfusion in the past 28 days
- Absolute neutrophil count (ANC) 1.5 x 109/L
- Platelet count =100 x 109/L
- Total bilirubin =1.5 x institutional upper limit of normal (ULN).
- AST (SGOT)/ALT (SGPT) =2.5 x institutional upper limit of normal unless liver
metastases are present, in which case it must be =5x ULN 13. Evidence of
post-menopausal status or negative urinary or serum pregnancy test prior to ICF
signature for female pre-menopausal patients. Women will be considered post-menopausal
if they have been amenorrheic for 12 months without an alternative medical cause. The
following age-specific requirements apply: Women <50 years of age would be considered
post-menopausal if they have been amenorrheic for 12 months or more following
cessation of exogenous hormonal treatments and if they have luteinizing hormone and
follicle-stimulating hormone levels in the post-menopausal range for the institution
or underwent surgical sterilization (bilateral oophorectomy or hysterectomy).
Women =50 years of age would be considered post-menopausal if they have been amenorrheic
for 12 months or more following cessation of all exogenous hormonal treatments, had
radiation-induced menopause with last menses >1 year ago, had chemotherapy-induced
menopause with last menses >1 year ago, or underwent surgical sterilization (bilateral
oophorectomy, bilateral salpingectomy or hysterectomy).
14. Female patients of childbearing potential who are not abstinent and intend to be
sexually active with a non sterilized male partner must be in use of at least 1 highly
effective method of contraception (see table in Section 7.1) before ICF signature/screening
throughout the total duration of the drug treatment and the drug washout period (90 days
after the last dose of durvalumab monotherapy). The study will not provide any method of
contraception; this is responsibility of the patient in case of intention to participate in
the study.
15. Male patients must use a condom during treatment and for 3 months after the last dose
of study drug when having sexual intercourse with a pregnant woman or with a woman of
childbearing potential. Female partners of male patients should also use a highly effective
form of contraception. The study will not provide any method of contraception; this is
responsibility of the patient in case of intention to participate in the study.
16. Patient is willing and able to comply with the protocol for the duration of the study,
including undergoing treatment, scheduled visits, examinations and follow up.
Exclusion Criteria:
1. Participation in another clinical study with an investigational product during the
last 3 weeks.
2. Concurrent enrolment in another clinical study, unless it is an observational
(non-interventional) clinical study or during the follow-up period of an
interventional study
3. Any concurrent or within 3 weeks prior to study treatment systemic chemotherapy, IP,
biologic, hormonal therapy or radiotherapy for cancer treatment. Concurrent use of
hormonal therapy for non-cancer-related conditions (e.g., hormone replacement therapy)
is acceptable.
4. Major surgical procedure (as defined by the Investigator) within 28 days prior to the
first dose of IP. Patients must have recovered from any effects of any major surgery.
5. History of allogenic organ transplantation or double umbilical cord blood
transplantation (dUCBT).
6. Patients with myelodysplastic syndrome/acute myeloid leukaemia or with features
suggestive of MDS/AML
7. Active or prior documented autoimmune or inflammatory disorders (including
inflammatory bowel disease [e.g., colitis or Crohn's disease], diverticulitis [with
the exception of diverticulosis], systemic lupus erythematosus, Sarcoidosis syndrome,
or Wegener syndrome [granulomatosis with polyangiitis, Graves' disease, rheumatoid
arthritis, hypophysitis, uveitis, etc]). The following are exceptions to this
criterion:
1. Patients with vitiligo or alopecia
2. Patients with hypothyroidism (e.g., following Hashimoto syndrome) stable on
hormone replacement
3. Any chronic skin condition that does not require systemic therapy
4. Patients without active disease in the last 5 years may be included but only
after consultation with the study physician
5. Patients with celiac disease controlled by diet alone
8. Uncontrolled intercurrent illness, including but not limited to, ongoing or active
infection, symptomatic congestive heart failure, uncontrolled hypertension, unstable
angina pectoris, uncontrolled cardiac arrhythmia, recent (within 3 months) myocardial
infarction, uncontrolled major seizure disorder, unstable spinal cord compression,
superior vena cava syndrome, interstitial lung disease, serious chronic
gastrointestinal conditions associated with diarrhea, or psychiatric illness/social
situations that would limit compliance with study requirement, substantially increase
risk of incurring AEs or compromise the ability of the patient to give written
informed consent
9. Patients unable to swallow orally administered medication and patients with
gastrointestinal disorders likely to interfere with absorption of the study
medication.
10. History of another primary malignancy except for
1. Malignancy treated with curative intent and with no known active disease =5 years
before the first dose of IP and of low potential risk for recurrence
2. Adequately treated non-melanoma skin cancer or lentigo maligna without evidence
of disease
3. Curatively treated in situ cancer of the cervix
4. Ductal carcinoma in situ (DCIS) of the breast
5. Stage 1, grade 1 endometrial carcinoma
11. Persistent toxicities (>Common Terminology Criteria for Adverse Event (CTCAE) grade 2)
caused by previous cancer therapy, excluding alopecia
12. History of active primary immunodeficiency
13. Active infection including tuberculosis (clinical evaluation that includes clinical
history, physical examination and radiographic findings, and TB testing in line with
local practice), hepatitis B (known positive HBV surface antigen (HBsAg) result),
hepatitis C (known positive HCV antibody) or human immunodeficiency virus (positive
HIV 1/2 antibodies). Patients with a past or resolved HBV infection (defined as the
presence of hepatitis B core antibody [anti-HBc] and absence of HBsAg) are eligible.
Patients positive for hepatitis C (HCV) antibody are eligible only if polymerase chain
reaction is negative for HCV RNA. Screening for tuberculosis, hepatitis B, hepatitis
C, and/or HIV infections is not required, unless there is clinical suspicion of these
infections.
14. Current or prior use of immunosuppressive medication within 14 days before the first
dose of durvalumab. The following are exceptions to this criterion:
1. Intranasal, inhaled, topical steroids, or local steroid injections (e.g., intra
articular injection)
2. Systemic corticosteroids at physiologic doses not to exceed <<10 mg/day>> of
prednisone or its equivalent
3. Steroids as premedication for hypersensitivity reactions (e.g., CT scan
premedication)
15. Receipt of live attenuated vaccine within 30 days prior to the first dose of IP. Note:
Patients, if enrolled, should not receive live vaccine whilst receiving IP and up to
30 days after the last dose of IP.
16. Concomitant use of known strong CYP3A inhibitors (eg. itraconazole, telithromycin,
clarithromycin, protease inhibitors boosted with ritonavir or cobicistat, indinavir,
saquinavir, nelfinavir, boceprevir, telaprevir) or moderate CYP3A inhibitors (eg.
ciprofloxacin, erythromycin, diltiazem, fluconazole, verapamil). The required washout
period prior to starting study treatment is 2 weeks.
17. Concomitant use of known strong (eg. phenobarbital, enzalutamide, phenytoin,
rifampicin, rifabutin, rifapentine, carbamazepine, nevirapine and St John's Wort ) or
moderate CYP3A inducers (eg. bosentan, efavirenz, modafinil). The required washout
period prior to starting study treatment is 5 weeks for enzalutamide or phenobarbital
and 3 weeks for other agents
18. Female patients who are pregnant or breastfeeding or male or female patients of
reproductive potential who are not willing to employ effective birth control from
screening to 90 days after the last dose of durvalumab monotherapy.
19. Known allergy or hypersensitivity to any of the study drugs or any of the study drug
excipients.
20. Prior randomisation or treatment in a previous durvalumab clinical study regardless of
treatment arm assignment.
21. Patients who have received prior anti-PD-1, anti PD-L1, including durvalumab, or anti
CTLA-4 antibodies.
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