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Nivolumab and Ipilimumab in T1aN0M0 Renal Cell Carcinoma Patients Ineligible for Surgical Treatment.

Primary Purpose

Renal Cell Carcinoma

Status
Unknown status
Phase
Phase 2
Locations
Russian Federation
Study Type
Interventional
Intervention
Nivolumab
Ipilimumab
Sponsored by
Kidney Cancer Research Bureau
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Renal Cell Carcinoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Cytologically proven clear-cell RCC
  2. CT-confirmed measurable primary tumor less than 4 cm and no evidence of extranodal metastatic disease (T1aN0M0)
  3. Inability to perform surgery for any reason (functional single kidney with a central, high-complexity RCC, high risk of nephrectomy and dialysis, patients with complex coagulation disorders, etc.) or preference of patient is to have no surgery for any reason
  4. No contradictions to nivolumab and ipilimumab
  5. Age 18 or older
  6. Written informed consent

Exclusion Criteria:

  1. prior treatment for RCC
  2. pregnant or nursing
  3. history of serious hypertension, cardiac arrhythmia, congestive heart failure, angina pectoris, or another severe cardiovascular disease (i.e., New York Heart Association class III or IV)
  4. evidence of metastatic disease
  5. local and/or systemic infections requiring antibiotics within 28 days prior to study entry
  6. other malignancy

Sites / Locations

  • N.N. Blokhin Russian Cancer Research CenterRecruiting
  • Russian Scientific Center of RoentgenoradiologyRecruiting

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Nivolumab + Ipilimumab

Arm Description

Patients will receive a combination of ipilimumab, followed by nivolumab for 16 weeks.

Outcomes

Primary Outcome Measures

Complete Response Rate
percentage of patients with localized RCC who have no tumor in kidney

Secondary Outcome Measures

Objective response rate
percentage of patients with localized RCC who have no tumor in kidney or tumor shrinkage more than 30%
3-year disease-free survival rate
percentage of patients who are disease free at 3 years after treatment start
5-year survival rate
percentage of patients who are alive at 5 years after treatment start
Rate of adverse events
percentage of patients who have adverse events

Full Information

First Posted
October 18, 2019
Last Updated
December 22, 2020
Sponsor
Kidney Cancer Research Bureau
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1. Study Identification

Unique Protocol Identification Number
NCT04134182
Brief Title
Nivolumab and Ipilimumab in T1aN0M0 Renal Cell Carcinoma Patients Ineligible for Surgical Treatment.
Official Title
A Phase 2 Pilot Study of the Efficacy and Safety of Nivolumab and Ipilimumab in T1aN0M0 Renal Cell Carcinoma Patients Ineligible for Surgical Treatment.
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 16, 2019 (Actual)
Primary Completion Date
September 2021 (Anticipated)
Study Completion Date
December 2021 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kidney Cancer Research Bureau

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The aim of this Phase 2 study is to evaluate the efficacy and safety of nivolumab, an anti-PD-1 antibody, and ipilimumab, an anti-CTLA-4 antibody, in T1aN0M0 clear-cell RCC patients ineligible for surgical treatment.
Detailed Description
Surgery remains the standard curative-intent therapy for localized renal cell carcinoma (RCC). Thus, systemic therapy for RCC should still be considered only in patients who have contraindications to surgery. Results of Phase 3 CheckMate 214 study showed that a combination of nivolumab and ipilimumab has a significant impact on tumor burden in intermediate- and poor-risk metastatic RCC patients with a complete response rate of 11% (Motzer et al. Lancet Oncology 2019). Median time to objective response was 2.8 months. Among all complete responders to nivolumab plus ipilimumab in the intention-to-treat population, 5% achieved a complete response at the first scan, whereas most converted from the partial response at a median of 6.9 months or from the stable disease at a median of 11.3 months. We hypothesize that this combination could completely eliminate primary tumors in patients with small primary (less than 4 cm) ineligible for surgical treatment. There are no studies evaluating checkpoint inhibitors in this setting in RCC patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Renal Cell Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
8 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Nivolumab + Ipilimumab
Arm Type
Experimental
Arm Description
Patients will receive a combination of ipilimumab, followed by nivolumab for 16 weeks.
Intervention Type
Drug
Intervention Name(s)
Nivolumab
Other Intervention Name(s)
Opdivo
Intervention Description
3 mg/kg intravenously every 2 weeks during 16 weeks
Intervention Type
Drug
Intervention Name(s)
Ipilimumab
Other Intervention Name(s)
Yervoy
Intervention Description
1 mg/kg intravenously every 3 weeks for four doses
Primary Outcome Measure Information:
Title
Complete Response Rate
Description
percentage of patients with localized RCC who have no tumor in kidney
Time Frame
16 weeks
Secondary Outcome Measure Information:
Title
Objective response rate
Description
percentage of patients with localized RCC who have no tumor in kidney or tumor shrinkage more than 30%
Time Frame
16 weeks
Title
3-year disease-free survival rate
Description
percentage of patients who are disease free at 3 years after treatment start
Time Frame
3 years
Title
5-year survival rate
Description
percentage of patients who are alive at 5 years after treatment start
Time Frame
5 years
Title
Rate of adverse events
Description
percentage of patients who have adverse events
Time Frame
16 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Cytologically proven clear-cell RCC CT-confirmed measurable primary tumor less than 4 cm and no evidence of extranodal metastatic disease (T1aN0M0) Inability to perform surgery for any reason (functional single kidney with a central, high-complexity RCC, high risk of nephrectomy and dialysis, patients with complex coagulation disorders, etc.) or preference of patient is to have no surgery for any reason No contradictions to nivolumab and ipilimumab Age 18 or older Written informed consent Exclusion Criteria: prior treatment for RCC pregnant or nursing history of serious hypertension, cardiac arrhythmia, congestive heart failure, angina pectoris, or another severe cardiovascular disease (i.e., New York Heart Association class III or IV) evidence of metastatic disease local and/or systemic infections requiring antibiotics within 28 days prior to study entry other malignancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ilya Tsimafeyeu, MD
Phone
+79265646581
Email
kidneycancer@yandex.ru
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ilya Tsimafeyeu, MD
Organizational Affiliation
Kidney Cancer Research Bureau
Official's Role
Study Director
Facility Information:
Facility Name
N.N. Blokhin Russian Cancer Research Center
City
Moscow
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Maria Volkova, MD
Facility Name
Russian Scientific Center of Roentgenoradiology
City
Moscow
Country
Russian Federation
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rustem Gafanov, MD

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Nivolumab and Ipilimumab in T1aN0M0 Renal Cell Carcinoma Patients Ineligible for Surgical Treatment.

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