Official Title
Assessment of Reliability of Cystoscopic Evaluation Predicting pT0 Urothelial Carcinoma of the Bladder at the Time of Radical Cystectomy
Brief Title
Cystoscopic Evaluation Predicting pT0 Urothelial Carcinoma of the Bladder
Protocol ID
NCT02968732
Lead Sponsor
Fox Chase Cancer Center
Brief Summary
A prospective, investigational study to assess the accuracy of standardized cystoscopic
evaluation with tissue sampling performed immediately prior to definitive radical
cystectomy to predict pathologic tumor stage and identify patients who may benefit from
bladder preservation therapy.
Detailed Description
Archival specimen of prior diagnostic TUR will be prepared as 10-20 unstained 5-10 micron
slides to under-go next generation sequencing and be compared to final cystectomy
specimen to investigate potential pre-treatment signatures predictive of response to
chemotherapy and to understand genomic evolution of primary tumors after chemotherapy.
All patients will also have urine, PBMC, and serum/plasma collected at baseline, day of
procedure, 4-6 weeks post-procedure, and 6 months post-procedure. The baseline samples
will be collected prior to any chemotherapy administration and prior to the procedure.
On the day of the patient's radical cystectomy, standard rigid cystourethroscopy will be
performed. A urine sample will be collected from the bladder. A plasma sample will be
collected while the patient is under anesthesia or in pre-op holding area. Visible tumor
and prior tumor sites will be targeted for tissue sampling (no more than two sites will
be targeted). A standardized tumor quantification system will be employed to document
location and presence of tumor and previous biopsy sites. To this end, the investigators
have developed a novel scoring system that allows for objective quantification of
endoscopic findings at the time of cystoscopy and indexes presence and location of
papillary tumor, erythema, and scar. Two additional random biopsies will be obtained, one
from the posterior wall and one from the lateral wall for assessment of genomic
signatures within normal-appearing mucosa.
Tumor location and its relationship to the ureteral orifices will be noted in order to
assist the surgeon in performance of radical cystectomy. The patient will then undergo
radical cystectomy as per standard of care.
Study Period
-
Enrollment Count
65 participants
Eligibility Criteria
Inclusion Criteria:
1. Male or female patients age >18 years at the time of consent.
2. Patients with a diagnosis of urothelial carcinoma clinical stage T1-T4NanyM0.
3. Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status
of 0-3.
4. Patients must have a clinical decision to proceed with radical cystectomy by any
conventional approach (open, laparoscopic, robot-assisted laparoscopic). Time from
decision to surgery is usually 3-8 weeks for those who do not receive neoadjuvant
chemotherapy and 10-14 weeks for those who receive neo-adjuvant chemotherapy
treatment. During this time, eligibility for study participation will be verified.
5. Ability to understand and willingness to sign a written informed consent and HIPAA
authorization document or a legally authorized representative who has the ability to
understand and willingness to sign a written informed consent and HIPAA
authorization on behalf of the participant.
6. Women of reproductive potential must have agreed to use an effective contraceptive
measure.
Exclusion Criteria:
1. Patients who undergo cystectomy with non-curative intent will be excluded.
2. Patients who have undergone any prior pelvic irradiation.
3. Patients who are pregnant or nursing. Radical cystectomy and prolonged general
anesthesia would place the fetus at considerable risk of demise. The prolonged
recovery and debility of the patient would severely limit the patient's ability to
nurse and care for an infant.
Filters
Urothelial Carcinoma
NA
ACTIVE_NOT_RECRUITING
ADULT
OLDER_ADULT