MRI and Bladder Cancer Chemotherapy

Purpose:

Primary Endpoint:

1. To assess the feasibility of using pre-treatment ADC as a predictor of complete
pathologic response to neo-adjuvant chemotherapy at radical cystectomy

Secondary Endpoint:

1. To explore the association between pre-treatment ADC values and complete pathologic
response to neoadjuvant chemotherapy at radical cystectomy.

Background and Rationale

1. Management of Muscle-Invasive Bladder Cancer Bladder cancer is a common malignancy with
an estimated 15,210 deaths for 2013 in the United States.1 Although the majority of
patients present with non-invasive disease, approximately 20% to 40% of patients either
present with more advanced disease, or progress after treatment for superficial
disease. Muscle-invasive bladder cancer is characterized by a distinct biology which
includes the loss of tumor suppressor genes such as TP53, Rb, and PTEN resulting in
more than 50% of cases progressing to the lethal phenotype of metastatic disease. This
necessitates an aggressive approach to management as compared to non-invasive disease
which is typically managed with resection of the tumor with or without intravesical
therapy such as Bacillus Calmette-Guérin.

The standard treatment for muscle-invasive bladder cancer is a radical cystectomy with
bilateral pelvic lymphadenectomy This is a morbid surgery that includes the removal of
the prostate gland, seminal vesicles and proximal urethra in men and removal of the
urethra, uterus, fallopian tubes, anterior vaginal wall and surrounding fascia in women
with the creation of a urinary diversion. There is also level one evidence for
preoperative systemic chemotherapy (neoadjuvant) in patients with T2-T4a, node negative
disease. A US phase 3 intergroup trial randomized patients with invasive bladder
cancer to neoadjuvant M-VAC (methotrexate, vinblastine, adriamycin and cisplatin) plus
cystectomy or to cystectomy alone and demonstrated an 85% 5-year survival for patients
who experienced a complete pathologic response.2 In total, 2 prospective randomized
trials as well as 2 large meta-analyses have demonstrated a survival benefit with the
use of cisplatin-based combination neoadjuvant chemotherapy prior to chemotherapy.2-5
These data establish cisplatin-based neoadjuvant chemotherapy as standard of care for
patients with MIBC considered for radical cystectomy. Current standard regimens used
as neoadjuvant cisplatin-based chemotherapy include gemcitabine and cisplatin (GC),
M-VAC and cisplatin, methotrexate and vinblastine (CMV).

However, not all patients will respond to neoadjuvant chemotherapy. In the US
Intergroup study, the complete pathologic response rate to neoadjuvant chemotherapy was
38% which was significantly greater than the rate observed in the cystectomy alone arm
(15%; p<0.001).2 For patients who has residual invasive disease at the time of
cystectomy, the median survival for patients with residual invasive disease at the time
of cystectomy was 3.8 years establishing complete pathologic response to chemotherapy
as a reliable surrogate for long-term survival. To date, there are no effective means
to differentiate muscle-invasive bladder cancer patients who are more or less likely to
benefit from neoadjuvant chemotherapy, thus potentially leading to its relative
underutilization.6 Clearly, the ability to reliably predict which patients will respond
to neoadjuvant chemotherapy would be of tremendous clinical value. This ability would
facilitate selective application of neoadjuvant chemotherapy in those patients most
likely to respond, while allowing other patients unlikely to respond to proceed
directly to surgery. While various host and tumor markers have been explored for this
purpose, none have been validated prospectively and thus are not part of routine
clinical use.7,8

2. Standard Imaging in Bladder Cancer Current imaging modalities used for staging of
bladder cancer include contrast-enhanced multi-detector computed tomography (MDCT) and
magnetic resonance imaging (MRI) of the abdomen and pelvis. MRI is also limited in its
ability to detect pelvic lymph node metastases with a reported sensitivity of 50%.9,10
While both are considered standard of care, MRI may perform better than CT in the
determination of local disease extent with a reported accuracy for detection of deep
muscle invasion and extravesical tumor invasion of 94% and 97%, respectively.

Further, functional MRI-based metrics may provide a simple and non-invasive method for
evaluating bladder tumors and predicting sensitivity to neoadjuvant chemotherapy. In
particular, diffusion-weighted imaging (DWI) is a functional technique that reflects tissue
cellularity and molecular motion of water molecules. Apparent diffusion coefficient (ADC)
values obtained from DWI have been shown in prior studies to be predict to tumor
aggressiveness. In other solid tumors, ADC values have shown to predict response to
neoadjuvant chemotherapy and chemoradiotherapy.11,12 In addition, one small retrospective
study has suggested a role for ADC values to predict response to chemoradiation
muscle-invasive bladder cancer.13 If substantiated in a prospective study, such utility has
potential to greatly impact the clinical management of bladder cancer.

Methods This prospective study will enroll 40 patients with clinical stage T2-T4aN0M0
urothelial cancer of the bladder who are candidates for cisplatin-based neoadjuvant
chemotherapy followed by radical cystectomy. All patients will undergo pre- and
post-neoadjuvant chemotherapy DW-MRI of the abdomen and pelvis and ADC values of the primary
tumor will be measured. The choice between standard options for neoadjuvant cisplatin-based
chemotherapy will be determined according to treating physicians' discretion. The primary
endpoint of this study is to explore the association between ADC values from pre-treatment
DW-MRI of the abdomen and pelvis and complete pathologic response rate to neoadjuvant
chemotherapy as assessed at radical cystectomy and pelvic lymph node dissection.

Patients will be undergoing gadolinium-enhanced MRI both before and after chemotherapy as
part of their standard treatment of bladder cancer, regardless of their participation in
this research. Both of these studies will be evaluated as part of this research. No
additional imaging or contrast administration will be performed for participation in this
research.

MRI Patients will undergo a standard clinical MRI within 4 weeks prior to starting
neoadjuvant chemotherapy and after completing chemotherapy.

The MRI will be done using a Siemens scanner and a pelvic phased-array coil. A
state-of-the-art protocol will be performed, including multi-planar high-resolution turbo
spin-echo T2-weighted imaging. In addition, all examinations will include
diffusion-weighted imaging of the pelvis performed using b-values of 0, 400, and 800 s/mm2.
DWI will be performed using an echo-planar imaging sequence and tri-directional
motion-probing gradients, and in-line reconstruction of ADC maps.

Neoadjuvant Chemotherapy Patients will receive standard neoadjuvant cisplatin-based
chemotherapy recommended in clinical practice guidelines (http://ww.nccn.org) and supported
by level 1 evidence.2,4,14,15 Radical Cystectomy Patients eligible for surgery after
completion of neoadjuvant chemotherapy will undergo a radical cystectomy with pelvic lymph
node dissection which includes a prostatectomy in men and an anterior exenteration
(hysterectomy and bilateral salpingo-oophorectomy) in women. The standard bilateral pelvic
lymphadenectomy consists of removal of all nodal tissue from the obturator, internal and
external iliac nodal packets. The standard borders of lymph node dissection are the bladder
medially, the node of Cloquet distally, the pelvic sidewall to the genitofemoral nerve
laterally, and proximally to the common iliac vessels.

If MRI following chemotherapy demonstrates evidence of intra-abdominal metastasis that is
amenable to resection, standard of care becomes radical cystectomy with pelvic lymph node
dissection, and surgical resection of the intra-abdominal metastasis.

Pathologic Tumor Response Criteria:

Complete pathologic response will be defined as complete eradication of urothelial cancer in
the radical cystectomy with pelvic lymph node dissection specimen (pT0N0). Residual cancer
will be staged according to AJCC 2007 TNM staging system for bladder cancer.

Inclusion Criteria

- Histologically confirmed muscle invasive urothelial carcinoma of the bladder

- Clinical stage T2-T4a N0/X M0 disease

- Age ≥ 18 years of age

- Medically appropriate candidate for radical cystectomy, as per NYU Attending Urologic
Oncologist

- Medically appropriate candidate for cisplatin-based neoadjuvant chemotherapy as per NYU
Attending Medical Oncologist

- If female of childbearing potential, pregnancy test is negative Exclusion Criteria

- Prior systemic chemotherapy (prior intravesical therapy is allowed)

- Prior radiation therapy to the bladder

- Medical contraindication to cisplatin-based neoadjuvant chemotherapy as determined by
NYU Attending Medical Oncologist

- Concomitant use of any other investigational drugs

- Inability to tolerate MRI including conditions such as claustrophobia or inability to
lay flat for > 45 minutes.

- Presence of pacemaker/ICD or perfusion pumps

- Ferromagnetic implants such as aneurysm clips, surgical clips, prostheses, artificial
heart, valves with steel parts, metal fragments, shrapnel, bullets, tattoos near the
eye, or steel implants.

- Substance abuse, medical, psychological, or social conditions that may interfere with
the patient's participation in the study Statistical Analysis The primary objective of
the study is to assess the feasibility of using pre-treatment ADC values as a predictor
of complete pathologic response (CPR) to neo-adjuvant chemotherapy at radical
cystectomy. Specifically, the objective is test whether pre-treatment ADC demonstrates
sufficient accuracy as a predictor of CPR to warrant a larger scale clinical trial to
formally assess the prognostic utility of pre-treatment ADC. Formally, we will consider
pre-treatment ADC to warrant further study if it is reasonable to conclude that it will
correctly predict the presence versus absence of CPR for at least 80% of patients
undergoing neo-adjuvant chemotherapy and will declare further investigation unwarranted
if the data suggest it will accurately predict the response of fewer than 60% of such
patients. Therefore, the study was designed to test the null hypothesis H0: P < 60%
against the alternative hypothesis HA: P ≥ 80%, where P is the true percentage of times
pre-treatment ADC will correctly predict whether or not a patient with manifest CPR. A
jackknife procedure will be used to derive a valid assessment of prediction accuracy.
It is anticipated that 36 patients will have a reference standard evaluation of
treatment response. If pre-treatment ADC is observed to correctly predict the treatment
response of at least 27 of these 36 patients (i.e. TC ≥ 27), the null hypothesis will
be rejected and it will be concluded that further study is warranted. It is noted that
The sample size was determined so that the study will have 80% power at the 5%
significance level to test the null hypothesis H0: P < 60% against the alternative
hypothesis HA: P ≥ 80%. A statistical power assessment indicated that the study would
need data from at least 36 patients with a reference standard evaluation of treatment
response. Since prior experience indicates that 90% of patients will be evaluable for
treatment response, the study will accrue 40 patients in order to achieve the target
sample size.

We will also perform unpaired t-tests to assess differences in the ADC values between
patients who achieve pT0N0 versus those who do not. An exact 95% confidence interval will be
derived for the true percentage of times pre-treatment ADC can be expected to correctly
predict whether or not a patient with manifest CPR.

Inclusion Criteria:

- Histologically confirmed muscle invasive urothelial carcinoma of the bladder

- Clinical stage T2-T4a N0/X M0 disease

- Age ≥ 18 years of age

- Medically appropriate candidate for radical cystectomy, as per NYU Attending Urologic
Oncologist

- Medically appropriate candidate for cisplatin-based neoadjuvant chemotherapy as per
NYU Attending Medical Oncologist

- If female of childbearing potential, pregnancy test is negative

Exclusion Criteria:

- Prior systemic chemotherapy (prior intravesical therapy is allowed)

- Prior radiation therapy to the bladder

- Medical contraindication to cisplatin-based neoadjuvant chemotherapy as determined by
NYU Attending Medical Oncologist

- Concomitant use of any other investigational drugs

- Inability to tolerate MRI including conditions such as claustrophobia or inability to
lay flat for > 45 minutes.

- Presence of pacemaker/ICD or perfusion pumps

- Ferromagnetic implants such as aneurysm clips, surgical clips, prostheses, artificial
heart, valves with steel parts, metal fragments, shrapnel, bullets, tattoos near the
eye, or steel implants.

- Substance abuse, medical, psychological, or social conditions that may interfere with
the patient's participation in the study