Study of Regorafenib for Urothelial Cancer Following Chemotherapy (UAB 1477)

• Sponsor: University of Alabama at Birmingham (Other)
• Overall Status: Completed
• CT.gov ID: NCT02459119
• Collaborator: Bayer Healthcare Pharmaceuticals, Inc./Bayer Schering Pharma (Industry)
• Enrollment: 17
• Locations: 3
• Arm: 1
• Duration (Months): 59
• Patients Per Site: 5.7
• Patients Per Site Per Month: 0.1

Study Details

Study Description

Brief Summary

This study will test how well Regorafenib controls disease progression in urothelial cancer (cancer occurring in the urinary bladder, ureters, or renal pelvis) following previous therapy with chemotherapy.

Condition or Disease	Intervention/Treatment	Phase
Urothelial Cancer (Urinary Bladder, Ureters, or Renal Pelvis Cancer)	Drug: Regorafenib	Phase 2

Detailed Description

Advanced urothelial carcinoma (UC) has a poor long-term prognosis. The disease has not seen improved outcomes despite research efforts in over two decades. Novel therapeutic options are needed. Regorafenib is a novel oral multikinase inhibitor but is more potent than a similar multikinase inhibitor drug that treats advanced renal cell carcinoma and hepatocellular carcinoma. Regorafenib has been shown to have a broader capacity to inhibit blood supply to tumor sources.

This trial evaluates a proof-of-concept using Regorafenib in patients with metastatic progressive urothelial carcinoma following chemotherapy but still have a high level of activity performance in their daily living. The initial dose of Regorafenib will be 120 mg daily and then be escalated to 160 mg daily before gradually tapering.

Study Design

• Study Type: Interventional
• Actual Enrollment: 17 participants
• Allocation: N/A
• Intervention Model: Single Group Assignment
• Masking: None (Open Label)
• Primary Purpose: Treatment
• Official Title: A Multicenter, Non-Randomized, Phase II Study of Regorafenib for Advanced Urothelial Cancer Following Prior Chemotherapy
• Study Start Date: May 1, 2015
• Actual Primary Completion Date: Feb 1, 2019
• Actual Study Completion Date: Apr 1, 2020

Arms and Interventions

Arm

Intervention/Treatment

Experimental: Regorafenib Regorafenib will be administered orally to all patients on study. The drug will be taken once a day for 3 of every 4 week cycle (3 weeks on/1 week off). The dose is 120 mg once daily for the first cycle, then 160 mg once daily from the second cycle if no significant Regorafenib-associated toxicities occur during the first cycle. Drug dosage may be modified if toxicities occur. Patients will undergo up to 4 cycles of treatment and may continue on additional at the discretion of the investigator.

Drug: Regorafenib; Regorafenib will be packaged as 40 mg tablets in a bottle. Patients will be instructed to maintain a daily medication calendar.

Outcome Measures

Primary Outcome Measures

1. Number of Participants With Progression-free Survival at 6 Months [Baseline to 6 months following start of treatment]

   Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions. Death is also considered as progression in the analysis.

Secondary Outcome Measures

1. Disease Response Rate [Every 8 weeks until the time of disease progression upto 2 years]

   The number of participants showing response at first restaging scan after the start of study treatment. The response will be assessed using tumor measurements which will be documented through CT scans, magnetic resonance imaging (MRI), and x-rays using the Response Evaluation Criteria in Solid Tumors (RECIST). Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR."

2. Overall Survival [Baseline to 3 years]

   Length of subject survival after starting study treatment

3. Rate of Progression-free Survival [From start of treatment to time of progression or death, assessed up to 6 months]

   Duration of time from the start of treatment to time of progression or death, whichever comes first. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions

4. Number of Participants With Adverse Events [At the end of first treatment until 6 months following last treatment, an expected average of 10 months]

   The Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 4.0 will be used for assessment of toxicities.

Eligibility Criteria

Criteria

• Ages Eligible for Study: 19 Years and Older
• Sexes Eligible for Study: All
• Accepts Healthy Volunteers: No

Inclusion Criteria:

• Patients must have pathologically or cytologically proven transitional cell carcinoma of the urothelium.

• Progressive disease after 1-3 prior chemotherapy regimens (perioperative chemotherapy within 12 months will be considered one regimen).

• Prior regimen must be within 6 months of registration

• Measurable disease by RECIST 1.1

• Eastern Cooperative Oncology Group (ECOG) Performance status 0-1

• Patients with metastatic (lymph node or distant metastasis, i.e. N+ or M1) or locally advanced unresectable (T4b) transitional cell carcinoma.

• Age ≥19 years

• Life expectancy of at least 12 weeks (3 months)

• Subjects must be able to understand and be willing to sign the written informed consent form.

• Adequate bone marrow, liver and renal function as assessed by the following laboratory requirements:

• Total bilirubin ≤ 1.5 x the upper limits of normal (ULN)

• Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) less than or equal to 2.5 x ULN (≤ 5 x ULN for subjects with liver involvement of their cancer)

• Alkaline phosphatase limit ≤ 2.5 x ULN (≤ 5 x ULN for subjects with liver involvement of their cancer)

• Serum creatinine ≤ 1.5 x the ULN

• International normalized ratio (INR) less than or equal to 1.5 x ULN. (Subjects who are prophylactically treated with an agent such as warfarin or heparin will be allowed to participate provided that no prior evidence of underlying abnormality in coagulation parameters exists.Close monitoring of at least weekly evaluations will be performed until INR/PTT is stable based on a measurement that is pre-dose as defined by the local standard of care.

• Platelet count >100,000/mm3, hemoglobin (Hb) >8 g/dL, absolute neutrophil count (ANC) 1500/mm3. The patient cannot be transfused in order to meet study entry criteria.

• Women of childbearing potential must have a negative serum pregnancy test performed within 7 days prior to the start of study drug. Post- menopausal women (defined as no menses for at least 1 year) and surgically sterilized women are not required to undergo a pregnancy test. The definition of adequate contraception will be based on the judgment of the investigator.

• Subjects (men and women) of childbearing potential must agree to use adequate contraception beginning at the signing of the informed consent form until at least 3 months after the last dose of study drug. The definition of adequate contraception will be based on the judgment of the principal investigator or a designated associate.

• Subject must be able to swallow and retain oral medication.

Exclusion Criteria:

• Component of small-cell cancer or sarcomatoid cancer

• Prior therapy with any systemic therapy (chemotherapy or biologic therapy) within twenty-eight days prior to study entry

• Patients must have recovered from toxicities from prior systemic anticancer treatment or local therapies.

• Patients who have undergone major surgery <4 weeks or minor surgery <2 weeks prior to registration. Wounds must be completely healed prior to study entry and patients recovered from all toxicities from surgery. Placement of a vascular access device is not considered major or minor surgery in this regard.

• Prior radiation therapy is allowed as long as the irradiated area was not the sole source of measurable disease and radiotherapy was completed with recovery from toxicity, at least three weeks prior to enrollment. If the irradiated area is the only site of disease, there must be evidence of progressive disease.

• Uncontrolled central nervous system (CNS) metastases (previously treated with radiation and off steroids is acceptable).

• Patient with active or uncontrolled infection.

• Recent or active bleeding diathesis or arterial vascular event within 4 weeks.

• Pregnant or nursing (Fertile patients must use effective contraception during and for up to 3 months after completion of study treatment.)

• Patients may not be receiving any other investigational agents.

• Previous assignment to treatment during this study. Subjects permanently withdrawn from study participation will not be allowed to re-enter study.

• Uncontrolled hypertension (systolic pressure >140 mm Hg or diastolic pressure >90 mm Hg on repeated measurement) despite optimal medical management.

• Active or clinically significant cardiac disease including:

• Congestive heart failure - New York Heart Association (NYHA) Class II.

• Active coronary artery disease.

• Cardiac arrhythmias requiring anti-arrhythmic therapy other than beta blockers or digoxin.

• Unstable angina (angina symptoms at rest), new-onset angina within 3 months before randomization, or myocardial infarction within 6 months before randomization.

• Evidence or history of bleeding diathesis or coagulopathy.

• Any hemorrhage or bleeding event ≥ NCI CTCAE Grade 3 within 4 weeks prior to start of study medication.

• Subjects with thrombotic, embolic, venous, or arterial events, such as cerebrovascular accident (including transient ischemic attacks) deep vein thrombosis or pulmonary embolism within 6 months of start of study treatment within 6 months of informed consent.

• Subjects with any previously untreated or concurrent cancer that is distinct in primary site or histology from breast cancer except cervical cancer in-situ, treated localized basal cell carcinoma, Gleason score 6 prostate cancer or superficial bladder tumor. Subjects surviving a cancer that was curatively treated and without evidence of disease for more than 3 years before randomization are allowed. All cancer treatments for another malignancy must be completed at least 3 years prior to study entry (i.e., signature date of the informed consent form).

• Patients with pheochromocytoma.

• Known history of human immunodeficiency virus (HIV) infection or current chronic or active hepatitis B or C infection requiring treatment with antiviral therapy.

• Ongoing infection >Grade 2 NCI-CTCAE v4.0.

• Symptomatic metastatic brain or meningeal tumors.

• Presence of a non-healing wound, non-healing ulcer, or bone fracture.

• Renal failure requiring hemo-or peritoneal dialysis.

• Dehydration Grade >1 NCI-CTCAE v4.0.

• Patients with seizure disorder requiring medication.

• Persistent proteinuria greater than or equal to Grade 3 NCI-CTCAE v4.0 (> 3.5 g/24 hrs, measured by urine protein:creatinine ratio on a random urine sample).

• Interstitial lung disease with ongoing signs and symptoms at the time of informed consent.

• Pleural effusion or ascites that causes respiratory compromise (≥ NCI- CTCAE version 4.0 Grade 2 dyspnea).

• History of organ allograft (including corneal transplant).

• Known or suspected allergy or hypersensitivity to any of the study drugs, study drug classes, or excipients of the formulations given during the course of this trial.

• Any malabsorption condition.

• Women who are pregnant or breast-feeding.

• Any condition which, in the investigator's opinion, makes the subject unsuitable for trial participation.

• Substance abuse, medical, psychological or social conditions that may interfere with the subject's participation in the study or evaluation of the study results.

Contacts and Locations

Locations

	Site	City	State	Country	Postal Code
1	University of Alabama at Birmingham	Birmingham	Alabama	United States	35294
2	Wayne State University	Detroit	Michigan	United States	48201-2013
3	Cleveland Clinic	Cleveland	Ohio	United States	44195

Sponsors and Collaborators

• University of Alabama at Birmingham
• Bayer Healthcare Pharmaceuticals, Inc./Bayer Schering Pharma

Investigators

• Principal Investigator: Lisle Nabell, MD, University of Alabama at Birmingham

Study Documents (Full-Text)

• Study Protocol and Statistical Analysis Plan - Feb 19, 2020

More Information

Publications

None provided.

• Responsible Party: Lisle Nabell, Professor, University of Alabama at Birmingham
• ClinicalTrials.gov Identifier: NCT02459119
• Other Study ID Numbers: F150302002 (UAB 1477)
• First Posted: Jun 1, 2015
• Last Update Posted: Aug 6, 2020
• Last Verified: Jul 1, 2020

• Individual Participant Data (IPD) Sharing Statement: No
• Plan to Share IPD: No
• Studies a U.S. FDA-regulated Drug Product: Yes
• Studies a U.S. FDA-regulated Device Product: No
• Keywords provided by Lisle Nabell, Professor, University of Alabama at Birmingham: urothelial cancer; Regorafenib
• Additional relevant MeSH terms: Pelvic Neoplasms

Study Results

Participant Flow

Arm/Group Title	Regorafenib
Arm/Group Description	Regorafenib will be administered orally to all patients on study. The drug will be taken once a day for 3 of every 4 week cycle (3 weeks on/1 week off). The dose is 120 mg once daily for the first cycle, then 160 mg once daily from the second cycle if no significant Regorafenib-associated toxicities occur during the first cycle. Drug dosage may be modified if toxicities occur. Patients will undergo up to 4 cycles of treatment and may continue on additional at the discretion of the investigator. Regorafenib: Regorafenib will be packaged as 40 mg tablets in a bottle. Patients will be instructed to maintain a daily medication calendar.
Period Title: Overall Study
STARTED	17
COMPLETED	17
NOT COMPLETED	0

Baseline Characteristics

Arm/Group Title	Regorafenib
Arm/Group Description	Regorafenib will be administered orally to all patients on study. The drug will be taken once a day for 3 of every 4 week cycle (3 weeks on/1 week off). The dose is 120 mg once daily for the first cycle, then 160 mg once daily from the second cycle if no significant Regorafenib-associated toxicities occur during the first cycle. Drug dosage may be modified if toxicities occur. Patients will undergo up to 4 cycles of treatment and may continue on additional at the discretion of the investigator. Regorafenib: Regorafenib will be packaged as 40 mg tablets in a bottle. Patients will be instructed to maintain a daily medication calendar.
Overall Participants	17
Age (years) [Median (Full Range) ]
Median (Full Range) [years]	67.5
Sex: Female, Male (Count of Participants)
Female	3 17.6%
Male	14 82.4%
Race (NIH/OMB) (Count of Participants)
American Indian or Alaska Native	0 0%
Asian	0 0%
Native Hawaiian or Other Pacific Islander	0 0%
Black or African American	1 5.9%
White	16 94.1%
More than one race	0 0%
Unknown or Not Reported	0 0%
Region of Enrollment (participants) [Number]
United States	17 100%

Outcome Measures

1. Primary Outcome

Title	Number of Participants With Progression-free Survival at 6 Months
Description	Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions. Death is also considered as progression in the analysis.
Time Frame	Baseline to 6 months following start of treatment

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Regorafenib
Arm/Group Description	Regorafenib will be administered orally to all patients on study. The drug will be taken once a day for 3 of every 4 week cycle (3 weeks on/1 week off). The dose is 120 mg once daily for the first cycle, then 160 mg once daily from the second cycle if no significant Regorafenib-associated toxicities occur during the first cycle. Drug dosage may be modified if toxicities occur. Patients will undergo up to 4 cycles of treatment and may continue on additional at the discretion of the investigator. Regorafenib: Regorafenib will be packaged as 40 mg tablets in a bottle. Patients will be instructed to maintain a daily medication calendar.
Measure Participants	17
Count of Participants [Participants]	3 17.6%

2. Secondary Outcome

Title	Disease Response Rate
Description	The number of participants showing response at first restaging scan after the start of study treatment. The response will be assessed using tumor measurements which will be documented through CT scans, magnetic resonance imaging (MRI), and x-rays using the Response Evaluation Criteria in Solid Tumors (RECIST). Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR."
Time Frame	Every 8 weeks until the time of disease progression upto 2 years

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Regorafenib
Arm/Group Description	Regorafenib will be administered orally to all patients on study. The drug will be taken once a day for 3 of every 4 week cycle (3 weeks on/1 week off). The dose is 120 mg once daily for the first cycle, then 160 mg once daily from the second cycle if no significant Regorafenib-associated toxicities occur during the first cycle. Drug dosage may be modified if toxicities occur. Patients will undergo up to 4 cycles of treatment and may continue on additional at the discretion of the investigator. Regorafenib: Regorafenib will be packaged as 40 mg tablets in a bottle. Patients will be instructed to maintain a daily medication calendar.
Measure Participants	17
Count of Participants [Participants]	9 52.9%

3. Secondary Outcome

Title	Overall Survival
Description	Length of subject survival after starting study treatment
Time Frame	Baseline to 3 years

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Regorafenib
Arm/Group Description	Regorafenib will be administered orally to all patients on study. The drug will be taken once a day for 3 of every 4 week cycle (3 weeks on/1 week off). The dose is 120 mg once daily for the first cycle, then 160 mg once daily from the second cycle if no significant Regorafenib-associated toxicities occur during the first cycle. Drug dosage may be modified if toxicities occur. Patients will undergo up to 4 cycles of treatment and may continue on additional at the discretion of the investigator. Regorafenib: Regorafenib will be packaged as 40 mg tablets in a bottle. Patients will be instructed to maintain a daily medication calendar.
Measure Participants	17
Mean (Standard Error) [days]	100 (10.33)

4. Secondary Outcome

Title	Rate of Progression-free Survival
Description	Duration of time from the start of treatment to time of progression or death, whichever comes first. Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions
Time Frame	From start of treatment to time of progression or death, assessed up to 6 months

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Regorafenib
Arm/Group Description	Regorafenib will be administered orally to all patients on study. The drug will be taken once a day for 3 of every 4 week cycle (3 weeks on/1 week off). The dose is 120 mg once daily for the first cycle, then 160 mg once daily from the second cycle if no significant Regorafenib-associated toxicities occur during the first cycle. Drug dosage may be modified if toxicities occur. Patients will undergo up to 4 cycles of treatment and may continue on additional at the discretion of the investigator. Regorafenib: Regorafenib will be packaged as 40 mg tablets in a bottle. Patients will be instructed to maintain a daily medication calendar.
Measure Participants	17
Mean (Standard Error) [days]	47.6 (3.6)

5. Secondary Outcome

Title	Number of Participants With Adverse Events
Description	The Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 4.0 will be used for assessment of toxicities.
Time Frame	At the end of first treatment until 6 months following last treatment, an expected average of 10 months

Outcome Measure Data

Analysis Population Description

[Not Specified]

Arm/Group Title	Regorafenib
Arm/Group Description	Regorafenib will be administered orally to all patients on study. The drug will be taken once a day for 3 of every 4 week cycle (3 weeks on/1 week off). The dose is 120 mg once daily for the first cycle, then 160 mg once daily from the second cycle if no significant Regorafenib-associated toxicities occur during the first cycle. Drug dosage may be modified if toxicities occur. Patients will undergo up to 4 cycles of treatment and may continue on additional at the discretion of the investigator. Regorafenib: Regorafenib will be packaged as 40 mg tablets in a bottle. Patients will be instructed to maintain a daily medication calendar.
Measure Participants	17
Count of Participants [Participants]	13 76.5%

Adverse Events

Time Frame	From the date of signing consent form until 6 months after stopping study treatment.
Arm/Group Title	Regorafenib
Arm/Group Description	Regorafenib will be administered orally to all patients on study. The drug will be taken once a day for 3 of every 4 week cycle (3 weeks on/1 week off). The dose is 120 mg once daily for the first cycle, then 160 mg once daily from the second cycle if no significant Regorafenib-associated toxicities occur during the first cycle. Drug dosage may be modified if toxicities occur. Patients will undergo up to 4 cycles of treatment and may continue on additional at the discretion of the investigator. Regorafenib: Regorafenib will be packaged as 40 mg tablets in a bottle. Patients will be instructed to maintain a daily medication calendar.
All Cause Mortality
	Regorafenib
	Affected / at Risk (%)	# Events
Total	8/17 (47.1%)
Serious Adverse Events
	Regorafenib
	Affected / at Risk (%)	# Events
Total	7/17 (41.2%)
Gastrointestinal disorders
Diarrhea	1/17 (5.9%)	1
General disorders
Fatigue	1/17 (5.9%)	1
Musculoskeletal and connective tissue disorders
Low Phospohorus	2/17 (11.8%)	2
Renal and urinary disorders
Urinary Tract Infection	1/17 (5.9%)	1
Vascular disorders
Anemia	1/17 (5.9%)	1
Thrombocytopenia	1/17 (5.9%)	1
Other (Not Including Serious) Adverse Events
	Regorafenib
	Affected / at Risk (%)	# Events
Total	13/17 (76.5%)
Cardiac disorders
intermittent tachycardia	1/17 (5.9%)	1
Ear and labyrinth disorders
Voice hoarseness	1/17 (5.9%)	1
Eye disorders
Dry eyes	1/17 (5.9%)	1
Gastrointestinal disorders
Diarrhea	2/17 (11.8%)	2
Vomitting	1/17 (5.9%)	1
Musculoskeletal and connective tissue disorders
Hand foot syndrome	3/17 (17.6%)	11
Hypomagnesemia	1/17 (5.9%)	1
Vascular disorders
Hyponatremia	1/17 (5.9%)	1
Hematuria	1/17 (5.9%)	1
Epistaxis	1/17 (5.9%)	1

Limitations/Caveats

[Not Specified]

More Information

Certain Agreements

All Principal Investigators ARE employed by the organization sponsoring the study.

There is NOT an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.