A Study of SHR-1210 in Combination With Pemetrexed and Carboplatin in Subjects With Non-squamous NSCLC

Phase 3

Completed

• Conditions: Lung Neoplasms; Carcinoma, Non-Small-Cell Lung; Respiratory Tract Neoplasms; Respiratory Tract Disease; Thoracic Neoplasms; Lung Diseases; Neoplasms by Site; Neoplasm, Bronchial; Carcinoma, Bronchogenic
• Interventions: Biological: SHR-1210; Drug: Carboplatin; Drug: Pemetrexed

• Registration Number: NCT03134872
• Lead Sponsor: Jiangsu HengRui Medicine Co., Ltd.

Brief Summary

SHR-1210 is a humanized anti-PD1 IgG4 monoclonal antibody. This is a randomized,Phase III, multicenter ,open-label study designed to evaluate the safety and efficacy of SHR-1210 with carboplatin and pemetrexed versus carboplatin-pemetrexed in subjects who are chemotherapy naive and have Stage IIIB/IV non-squamous NSCLC.

The primary hypothesis is that SHR-1210 combined with carboplatin and pemetrexed prolongs Progression Free Survival (PFS) in per RECIST 1.1 by blinded independent central review (ITT population and population was indicated by high PD-L1 expression) compared to carboplatin and pemetrexed treatment .

Detailed Description

In this study, subjects will be randomly assigned to receive either carboplatin and pemetrexed for 4-6 cycles followed by pemetrexed maintenance until progression or unacceptable toxicity, OR receive SHR-1210 combined with carboplatin and pemetrexed chemotherapy for 4-6 cycles followed by pemetrexed maintenance with SHR-1210 until progression or unacceptable toxicity (SHR-1210 for a maximum of 2 years).

Subjects assigned to the chemotherapy arm will have the opportunity to crossover to receive SHR-1210 monotherapy once they experience progression of disease (PD) defined by RECIST 1.1 and meet all the crossover criteria.

Study Timeline

• Study First Submitted: 2017-04-25
• Study First Submitted QC: 2017-04-25
• Study First Posted: 2017-05-01
• Study Start: 2017-05-12
• Primary Completion: 2019-07-27
• Study Completion: 2019-08-29
• Status Verified: 2020-06
• Last Update Submitted: 2020-06-07
• Last Update Posted: 2020-06-09

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 419

Inclusion Criteria

• 1. Subjects who are chemotherapy naive and have Stage IIIB-IV non-squamous NSCLC.
• 2. Subjects should not have a previously detected sensitizing EGFR mutation or ALK fusion oncogene.
• 3. Fresh cutting or ≤6 months preservation specimens must be provided.
• 4. No prior systemic treatment. Subjects who have received prior neo-adjuvant, adjuvant chemotherapy, or chemoradiotherapy with curative intent for non-metastatic disease must have experienced a treatment free interval of at least 12 months from randomization since the last chemotherapy cycle.
• 5. Subjects must have measurable disease by CT or MRI per RECIST 1.1 criteria;
• 6. Eastern Cooperative Oncology Group (ECOG) performance status of ≤ 1.
• 7. Have a life expectancy of at least 3 months.
• 8. All baseline laboratory requirements will be assessed and should be obtained within 14 days prior to the first administration of study treatment.
• 9. Female Subjects of childbearing potential must have a negative serum pregnancy test within 3 days before the first dose and must be willing to use very efficient barrier methods of contraception for the course of the study through 180 days after the last dose of study treatment.
• 10. Male Subjects with a female partner(s) of child-bearing potential must be willing to use very efficient barrier methods of contraception for the course of the study through 180 days after the last dose of study treatment.
• 11. Subjects has voluntarily agreed to participate by giving written informed consent/assent for the trial. The subject may also provide consent/assent for Future Biomedical Research.

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Exclusion Criteria

• 1. Target Disease Exceptions

  2. Subjects with predominantly squamous cell histology NSCLC, or SCLC.

  3. Subjects with epidermal growth factor receptor (EGFR)-sensitizing mutation and/or anaplastic lymphoma kinase (ALK) translocation.

  4. Subjects with no measurable disease by CT or MRI per RECIST 1.1 criteria.

  5. Subjects with carcinomatous meningitis, or symptoms of spinal cord compression.

  6. Subjects with active CNS metastases are excluded.

  7. Subjects who can receive surgical resection or radical radiotherapy.

  8. Prior therapy with anti-PD-1, anti-PD-L1, anti-PD-L2, or anti-CTLA-4 antibody (including any other antibody or drug specifically targeting T-cell co-stimulation or checkpoint pathways).

• 2. Medical History and Concurrent Diseases

  3. Subjects with active, known or suspected autoimmune disease. Subjects in conditions not expected to recur in the absence of an external trigger, or not requiring systemic treatment are permitted to enroll.

  4. Subjects with a condition requiring systemic treatment with either corticosteroids (>10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of first administration of study treatment. Inhaled or topical steroids, and adrenal replacement steroid doses > 10 mg daily prednisone equivalent, are permitted in the absence of active autoimmune disease.

  5. Prior therapy with systemic immunostimulatory agents within 1 months of the first dose of trial treatment.

  6. Subjects are currently participating and receiving study therapy or had participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks or 5 half-value period life of the agent, before the first dose of trial treatment.

  7. Subjects who expected to require any other form of antineoplastic therapy while on study (including maintenance therapy with another agent for NSCLC).

  8. Subjects received major surgery or radiation therapy of > 30 Gy not to chest within 4 weeks of the first dose of study treatment, or radiation therapy of > 30 Gy to chest within 24 weeks of the first dose of study treatment, or radiation therapy of < 30 Gy to chest within 2 weeks of the first dose of study treatment, and had not recovered from the toxicity and/or complications of the most recent prior chemotherapy to Grade 1 or less (except alopecia or fatigue).

  9. Subjects with a history of interstitial lung disease, or other disease may interfere with the detection or treatment of suspected drug-related lung toxicity.

  10. Other active malignancy requiring concurrent intervention.

  11. Subjects with previous malignancies (except non-melanoma skin cancers, and thefollowing in situ cancers: bladder, endometrial, cervical/dysplasia) are excluded unless a complete remission was achieved at least 5 years prior to study entry.

  12. Subjects with clinically significant cardiovascular and cerebrovascular diseases.

  13. Subjects with active pulmonary tuberculosis.

  14. Subjects have severe infections within 4 weeks of the first dose of study treatment.

  15. Subjects had or plan to have allogeneic bone marrow transplantation or solid organ transplant.

  16. Subjects had administration of a live, attenuated vaccine within 30 days of the first dose of study treatment or anticipation that such a live attenuated vaccine will be required during the study.

  17. Subjects with contraindications to platinum therapy.

• 3. Physical and Laboratory Test Findings

  4. Known history of testing positive for human immunodeficiency virus (HIV) or

  5. known acquired immunodeficiency syndrome (AIDS).

  6. Known history of active Hepatitis B or C.

  7. Subjects with severe pleural effusion, pericardial effusion, or ascites need repeated drainage.

• 4. History of severe hypersensitivity reactions to other monoclonal antibodies, or intravenous infusion, or carboplatin, or pemetrexed.
• 5. Subjects have known psychiatric or substance abuse disorder (including alcohol\smoking), or be regular user (including "recreational use") of any illicit drugs that would interfere with cooperation with the requirements of the trial.
• 6. Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the study, interfere with the subject's participation for the full duration of the study, or is not in the best interest of the subject to participate, in the opinion of the treating Investigator.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
SHR-1210+Chemotherapy	SHR-1210	Subjects receive SHR-1210 200mg and pemetrexed 500 mg/m\^2 and carboplatin AUC 5, administered as IV infusion on Day 1 of each 21-day cycle for 4-6 cycles followed by optional SHR-1210 200mg and pemetrexed 500 mg/m\^2 every three weeks (Q3W) maintenance for the remainder of the study or until documented PD.
SHR-1210+Chemotherapy	Carboplatin	Subjects receive SHR-1210 200mg and pemetrexed 500 mg/m\^2 and carboplatin AUC 5, administered as IV infusion on Day 1 of each 21-day cycle for 4-6 cycles followed by optional SHR-1210 200mg and pemetrexed 500 mg/m\^2 every three weeks (Q3W) maintenance for the remainder of the study or until documented PD.
SHR-1210+Chemotherapy	Pemetrexed	Subjects receive SHR-1210 200mg and pemetrexed 500 mg/m\^2 and carboplatin AUC 5, administered as IV infusion on Day 1 of each 21-day cycle for 4-6 cycles followed by optional SHR-1210 200mg and pemetrexed 500 mg/m\^2 every three weeks (Q3W) maintenance for the remainder of the study or until documented PD.
Chemotherapy	Carboplatin	Subjects receive pemetrexed 500 mg/m\^2 and carboplatin Area Under the Curve (AUC) 5, administered as IV infusion on Day 1 of each 21-day cycle for 4-6 cycles followed by optional pemetrexed 500 mg/m\^2 every three weeks (Q3W) maintenance for the remainder of the study or until documented PD. If PD occurs, Subjects may be able to receive SHR-1210 Q3W for the remainder of the study or until documented PD.
Chemotherapy	Pemetrexed	Subjects receive pemetrexed 500 mg/m\^2 and carboplatin Area Under the Curve (AUC) 5, administered as IV infusion on Day 1 of each 21-day cycle for 4-6 cycles followed by optional pemetrexed 500 mg/m\^2 every three weeks (Q3W) maintenance for the remainder of the study or until documented PD. If PD occurs, Subjects may be able to receive SHR-1210 Q3W for the remainder of the study or until documented PD.

Primary Outcome Measures

Name	Time	Method
Progression-Free Survival in the intent-to-treat (ITT) population	up to 24 months	PFS, defined as the time from randomization to the first occurrence of disease progression as determined by the investigator with use of RECIST v1.1 or death from any cause, whichever occurs first. Patients who have not experienced disease progression or death at the time of analysis will be censored at the time of last tumor assessment.
Progression-Free Survival in the PD-L1-selected population	up to 24 months	PFS, defined as the time from randomization to the first occurrence of disease progression as determined by the investigator with use of RECIST v1.1 or death from any cause, whichever occurs first. Patients who have not experienced disease progression or death at the time of analysis will be censored at the time of last tumor assessment.

Secondary Outcome Measures

Name	Time	Method
Overall Response Rate (ORR)	up to 24 months	Determined using RECIST v1.1 criteria
Duration of Response Rate(DoR)	up to 24 months	Determined using RECIST v1.1 criteria
Time To Progression (TTP)	up to 24 months	Determined using RECIST v1.1 criteria
Disease Control Rate (DCR)	up to 24 months	Determined using RECIST v1.1 criteria
Overall Survival	up to 24 months	Defined as the time from randomization to death from any cause.
Number of Subjects with treatment-related adverse events (AEs)	up to 24 months	Incidence, nature, and severity of adverse events graded according to the NCI CTCAE v4.03.

Trial Locations

Locations (1)

Tongji University, Shanghai Pulmonary Hospital; 🇨🇳 Shanghai, Shanghai, China