Famitinib Plus Anti-PD1 Therapy for Advanced Urinary System Tumor, Advanced Gynecological Tumors

Cervical Cancer Clinical Trial

Official title:

Famitinib Malate Plus Anti-PD1 Therapy (SHR-1210) in Advanced Renal Cell Carcinoma, Urothelial Carcinoma, Advanced Cervical Cancer, Relapse Ovarian Cancer, Endometrial Cancer: Multi-institutional, Open-label, Phase 2 Trial

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03827837
• Other study ID #: SHR-1210-II-213
• Status: Recruiting
• Phase: Phase 2
• Start date: January 23, 2019
• Est. completion date: December 2022

Study information

• Verified date: June 2022
• Source: Jiangsu HengRui Medicine Co., Ltd.
• Contact: Quanren Wang, MD
• Phone: (+86) 021-50118402
• Email: wangquanren[@]hrglobe.cn
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Phase II multi-chort, adaptive two-stage, open label, nonrandomized study. The aim of our study is to evaluate the efficacy and safety of anti-PD-1 antibody SHR-1210(Camrelizumab) in combination with a small-molecule multikinase inhibitor Famitinib in subjects with advanced RCC/UC/CC/EC and recurrent OC.

chort1: Renal Cell Carcinoma (RCC) chort2: Urothelial Carcinoma(UC) chort3: Ovarian Cancer (OC) chort4: Cervical Cancer (CC) chort5: Endometrial Cancer (EC)

Description:

Stage 1: Approximately 110 participants will be recruited, 22 participants per chort; Stage 2: Approximately 55 participants will be recruited, 11 participants per chort, if more than 7（including 7） patients reached ORR in every chort ; Approximately 155 participants will be recruited, 21 participants per chort, if 3 ≤ patients <7 patients reached ORR in every chort.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 265
• Est. completion date: December 2022
• Est. primary completion date: December 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Be willing and able to provide written informed consent/ for the trial.

2. Be at least 18 years of age on day of signing informed consent, male or female.

3. Patients with one of the following tumors:

• Histologically or cytologically confirmed diagnosis of advanced renal cell carcinoma (defined as more than 50% clear cell component) after failure of IL-2 and/or anti-VEGF TKI treatment. If patients didn't want to use anti-VEGF TKI medicine or couldn't stand anti-VEGF TKI medicine costs, they will also be considered.

• Histologically or cytologically confirmed diagnosis of unresectable urothelial carcinoma of the renal pelvis, ureter, bladder, or urethra (defined as more than 50% transitional cell component) after failure of no more than two prior platinum-based chemotherapeutic regimen.

• Histologically or cytologically confirmed diagnosis of advanced squamous cell carcinoma of the cervix after failure of first-line system treatment.

• Histologically confirmed diagnosis of recurrent or refractory epithelial ovarian cancer, fallopian tube cancer or primary peritoneal cancer that are relapsed and resistant (recurred less than 6 months after chemotherapy) or refractory (progressed on chemotherapy) to prior platinum-based standard care systemic regimen.

• Histologically confirmed diagnosis of recurrent or refractory endometrial cancer that are relapsed and resistant or refractory (progressed on chemotherapy) to prior platinum-based standard care systemic regimen.

4. At least one measurable lesion according to RECIST 1.1.

5. The patients can swallow pills.

6. Eastern Cooperative Oncology Group (ECOG) performance status of = 1.

7. Life expectancy of at least 12 weeks.

8. The results of patients' blood tests are as follows:-Neutrophils=1.5E+9/L; - Plt=90E+9/L; -Hb=90g/L; -ALB=30g/L ;-TSH=1×ULN;-TBIL = 1 ×ULN;-ALT and AST = 3 ×ULN; AKP= 2.5×ULN; -Creatinine = 1.5×ULN.

9. Male or Female patient of childbearing potential (entering the study after a menstrual period and who have a negative pregnancy test), who agrees to use two methods (one for the patient and one for the partner) of medically acceptable forms of contraception during the study and for 3 months after the last treatment intake.

Exclusion Criteria:

1. Patients with any active autoimmune disease or history of autoimmune disease, including but not limited to the following: hepatitis, pneumonitis, uveitis, colitis (inflammatory bowel disease), hypophysitis, vasculitis, nephritis, hyperthyroidism, and hypothyroidism, except for subjects with vitiligo or resolved childhood asthma/atopy. Asthma that requires intermittent use of bronchodilators or other medical intervention should also be excluded.

2. Concurrent medical condition requiring the use of immunosuppressive medications, or immunosuppressive doses of systemic or absorbable topical corticosteroids. Doses > 10 mg/day prednisone or equivalent are prohibited within 2 weeks before study drug administration.

3. Known history of hypersensitivity to other antibody formulation.

4. Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis. Subjects with previously treated brain metastases may participate provided they are stable (without evidence of progression by imaging for at least four weeks prior to the first dose of trial treatment and any neurologic symptoms have returned to baseline), have no evidence of new or enlarging brain metastases, and are not using steroids for at least 2 weeks prior to trial treatment.

5. Hypertension and unable to be controlled within normal level following treatment of anti-hypertension agents: systolic blood pressure =140 mmHg, diastolic blood pressure = 90 mmHg.

6. Clinically significant cardiovascular and cerebrovascular diseases, including but not limited to(1)Congestive heart failure (New York heart association (NYHA) class > 2);(2)unstable or severe angina; (3)myocardial infarction within 12 months before enrollment;(4) ventricular arrhythmia which need medical intervention.(5)QTc>450ms(male)/QTc>470ms (female);

7. Coagulation abnormalities (INR>2.0?PT>16s), with bleeding tendency or are receiving thrombolytic or anticoagulant therapy.

8. Bleeding history, having bleeding event(=3 Grade according CTCAE 4.0 )within 4 weeks before screening.

9. Tumor invasion around major vessels shown by imaging, high risk of major vascular invasion leading to massive hemorrhage judged by investigators.

10. Previous Arterial/venous thrombosis events within 6 months.

11. Known hereditary or acquired bleeding and thrombosis tendency.

12. Proteinuria = (++) and 24 hours total urine protein > 1.0 g.

13. Prior chemotherapy, radiotherapy, surgery therapy within 4 weeks or palliative radiotherapy within 2 weeks or target therapy within 5 half-life of the drug before the study drug administration, or any unresolved AEs > Common Terminology Criteria for Adverse Events (CTCAE) Grade 1.

14. Active infection or an unexplained fever > 38.5°C within 7 days before the study drug administration, or baseline WBC>15×E+9/L .

15. Has known history of Interstitial lung disease, or using steroids evidence of active, non-infectious pneumonitis, or would interfere with the detection and handling of suspicious drug-related pulmonary toxicity.

16. History of immunodeficiency or human immunodeficiency virus (HIV) infection.

17. HBV DNA>500 IU/ml,HCV RNA>1000copies/ml,HBsAg+ and anti-HCV+;

18. Has a known additional malignancy within the last 5 years, or that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer or patients with recurrent ovarian cancer has a known additional breast cancer that has been radical mastectomy and doesn't relapse within 3 years.

19. Patients with treatment history of SHR-1210 or any other PD-L1 or PD-1 antagonists or famitinib.

20. Patients who may receive live vaccine during the study, or previous had vaccination within 4 weeks.

21. Any other medical, psychiatric, or social condition deemed by the investigator to be likely to interfere with a subject's safety and participate in the study or would interfere with the interpretation of the results or lead to the trial being terminated early.

Related Conditions & MeSH terms

• Carcinoma
• Carcinoma, Ovarian Epithelial
• Carcinoma, Renal Cell
• Carcinoma, Transitional Cell
• Cervical Cancer
• Endometrial Cancer
• Endometrial Neoplasms
• Ovarian Cancer Recurrent
• Ovarian Neoplasms
• Renal Cell Carcinoma
• Urothelial Carcinoma
• Uterine Cervical Neoplasms

Intervention

Biological:
• SHR-1210
SHR-1210 is a humanized anti-PD1 IgG4 monoclonal antibody

Drug:
• Famitinib
a small-molecule multikinase inhibitor

Locations

Country	Name	City	State
China	Huadong Hospital Affiliated to Fudan University	Shanghai	Shanghai

Sponsors (1)

Lead Sponsor	Collaborator
Jiangsu HengRui Medicine Co., Ltd.

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Overall response rate (ORR)	Defined as complete or partial response per RECIST 1.1 criteria with assessment every 9 weeks	Up to 2 years
Secondary	Duration of Response (DoR)	Duration of Response (DoR) per RECIST 1.1	Up to 2 years
Secondary	Disease Control Rate (DCR)	Disease Control Rate per RECIST 1.1	Up to 2 years
Secondary	Time to objective response(TTR)	Time to objective response per RECIST 1.1	Up to 2 years
Secondary	Progression-free survival(PFS)	Progression-free survival(PFS) per RECIST 1.1	Up to 2 years
Secondary	Overall survival(OS)	Overal Survial will be calculated based on Kaplan-Meier estimates	Up to 2 years
Secondary	12-month survival rate	12-month survival rate will be calculated based on Kaplan-Meier estimates of Overall survival at 12 months	Up to 1 year
Secondary	number of participants who experience an adverse event (AE)	number of participants who experience an adverse event (AE) per CTCAE 4.03	From the first assignment of informed consent form up to 90 days after the last dose
Secondary	serum SHR-1210 concentrations	serum SHR-1210 concentrations	From the first dose up to 30 days after the last dose
Secondary	Positive rate of ADA	Positive rate of anti-SHR1210 antibody	From the first dose up to 30 days after the last dose
Secondary	Maximum Observed Plasma Concentration (Cmax)	Cmax, based PK parameters	Day 1 of cycle 3 (each cycle is 21 days)
Secondary	Time to Reach Maximum Observed Plasma Concentration (Tmax)	Summarized by dose, cycle, day and time	Day 1 of cycle 3 (each cycle is 21 days)
Secondary	Apparent Oral Clearance (CL/F)	Clearance of a drug is a measure of the rate at which a drug is metabolized or eliminated by normal biological processes.	Day 1 of cycle 3 (each cycle is 21 days)