Status:
RECRUITING
Camrelizumab Plus Famitinib as Treatment in Patient With Advanced or Metastatic Pulmonary Sarcomatoid Carcinoma
Lead Sponsor:
Qian Chu
Collaborating Sponsors:
Jiangsu HengRui Medicine Co., Ltd.
Conditions:
Sarcomatoid Carcinoma of Lung
Eligibility:
All Genders
18-75 years
Phase:
PHASE2
Brief Summary
This is a single arm, multi-center clinical trial. Target population is patients with Advanced or Metastatic Pulmonary Sarcomatoid Carcinoma，aiming to evaluate the efficacy and safety of the combinati...
Detailed Description
This trial enrolled patients with advanced or metastatic pulmonary sarcomatoid carcinoma. Patients will receive camrelizumab 200 mg every 3 weeks and famitinib 20 mg once per day. The primary endpoint...
Eligibility Criteria
Inclusion
- Patients with histologically stage IIIB, IIIC, IV Pulmonary Sarcomatoid Carcinoma according to WHO criteria or diagnosed with non-small cell lung cancer with sarcomatoid carcinoma component (sarcomatoid component tumour cells can be spindle cells, and/or giant cells and/or heterogenous sarcomatous differentiation including rhabdomyosarcoma, chondrosarcoma, etc.) ；
- Has no prior systemic therapy; (chemotherapy and/or radiotherapy is allowed as part of neoadjuvant/adjuvant therapy. Patients who have had recurrence or metastasis for more than 6 months from the end of neoadjuvant/adjuvant treatment would be enrolled ) ；
- Patients must have at least one measurable lesion according to RECIST 1.1 ；
- ECOG score 0-1 ；
- Agree to provide tumour tissue samples for biomarker exploration (including but not limited to PD-L1 IHC or NGS testing) ；
- Life expectancy more than 3 months;
- Has adequate organ function；
Exclusion
- Imaging (CT or MRI) showed tumor invasion of major vessels. hemoptysis ≥ 2.5 mL within 1 month before the first dose;
- Patients with EGFR-sensitive mutation (19Exondel/L858R), ALK, ROS1 gene rearrangement or fusion, BRAFV600E mutation, MET gene exon 14 skipping mutation;
- Patients with active bleeding or bleeding tendency ；
- With hypertension that cannot be reduced to the normal range after antihypertensive drug treatment (systolic blood pressure ≤ 140 mmHg/diastolic blood pressure ≤ 90 mmHg)；
- Urine protein ≥ (+ +), and 24-hour urine protein ≥ 1.0g;
- Presence of thrombotic disorder requiring anticoagulant therapy with warfarin or heparin, or requiring antiplatelet therapy (aspirin ≥ 300 mg/day or clopidogrel ≥ 75 mg/day) ；
- Has multiple factors affecting the absorption of oral drugs, such as inability to swallow, nausea and vomiting, chronic diarrhea and intestinal obstruction
- Has active central nervous system (CNS) metastases confirmed by CT or MRI
- Subjects diagnosed immunodeficiency or receiving systemic glucocorticoid therapy or any other form of immunosuppressive therapy of non-related tumor within 7 days before the first dose; allowed physiological dose of glucocorticoid (≤10 mg/day Prednisone or equivalent);
- Has active hepatitis B ;
- Has severe infections within 4 weeks of the first dose of study treatment ;
- Women who are pregnant or lactating ;
- With grade II or above myocardial ischemia or myocardial infarction and poorly controlled arrhythmias (QTc interval ≥ 450 ms for males and QTc interval ≥ 470 ms for females). Subjects with grade III-IV cardiac insufficiency or with left ventricular ejection fraction (LVEF) less than 50% according to NYHA criteria;
- Has known history of Human Immunodeficiency Virus (HIV)；
- Has known allergy to Camrelizumab, or famitinib or any of accessories ;
Key Trial Info
Start Date :
July 19 2021
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 30 2025
Estimated Enrollment :
28 Patients enrolled
Trial Details
Trial ID
NCT04888429
Start Date
July 19 2021
End Date
June 30 2025
Last Update
October 1 2024
Active Locations (8)
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1
The first Affiliated Hospital of Xiamen University
Xiamen, Fujian, China
2
Henan Cancer Hospital Affiliated Cancer Hospital of Zhengzhou University
Zhengzhou, Henan, China
3
Henan Provincial People's Hospital
Zhengzhou, Henan, China
4
Qian Chu
Wuhan, Hubei, China, 430000