- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT04769388
오시머티닙 플러스 화학요법 대 지속성이 있는 EGFR 변이 비소세포폐암에서 오시머티닙 1L 오시머티닙 투여 후 3주차 ctDNA EGFRm (FLAME)
The Efficacy and Safety of Osimertinib Plus Carboplatin and Pemetrexed Versus Osimertinib Monotherapy in Locally Advanced or Metastatic EGFRm NSCLC Patients With EGFRm Persistence in ctDNA at 3 Weeks After 1L Osimertinib: A Multicenter, Randomized Controlled Study
This is a prospective, randomised, open-label, positive-controlled study to investigate the efficacy and safety of Osimertinib plus Carboplatin/Pemetrexed versus Osimertinib monotherapy in locally advanced or metastatic EGFRm NSCLC patients with EGFRm persistence in ctDNA at 3 weeks after first-line therapy with Osimertinib.
연구 개요
연구 유형
등록 (실제)
단계
- 2 단계
연락처 및 위치
연구 장소
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Beijing, 중국
- Cancer Hospital Chinese Academy of Medical Sciences
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참여기준
자격 기준
공부할 수 있는 나이
건강한 자원 봉사자를 받아들입니다
연구 대상 성별
설명
Inclusion Criteria:
- Provision and signed of informed consent prior to any study specific procedures;
- Male or female, aged at least 18 years;
- Eastern Cooperative Oncology Group (ECOG) performance-status score of 0 or 1;
- Newly diagnosed, and histologically documented locally advanced or metastatic non-squamous NSCLC with sensitizing EGFR mutations positive (either Exon 19 deletion or 21 L858R, confirmed by histology or cytology ), and classified as stage IIIB, IIIC, IV or recurrent NSCLC which are not amenable to curative surgery or radiotherapy;
- Life expectancy of at least 3 months at recruitment;
- Only the patients receiving osimertinib as 1L treatment and meeting the following criteria will be considered:
A. Prior to 1L osimertinib:
- History of EGFRm (exon 19 deletion or exon 21 L858R) in the plasma ctDNA by the local testing methods.
- No previous systemic treatment. Adjuvant therapies, or definitive radiation/chemoradiation are permitted as long as treatment was completed at least 6 months prior to receiving 1L treatment.
- Patients with asymptomatic and stable CNS metastases for at least 2 weeks will be allowed, including leptomeningeal metastases.
B. Prior to randomization: Patients after 3 weeks of 1L osimertinib treatment who have persistence ctDNA EGFRm by SuperARMS at 3 weeks will be considered to be enrolled. They will need to further meet the criteria below before randomization:
- Patients without disease progression by RECIST 1.1 evaluation;
- At least 1 measurable extracranial lesion according to RECIST 1.1 .
- Female subjects should be using highly effective contraceptive measures, and must have a negative pregnancy test and not be breast-feeding prior to start of dosing if of child-bearing potential, or must have evidence of non-child-bearing potential.
- Male subjects should be willing to agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures and agreement to refrain from donating sperm.
Exclusion Criteria:
- Involvement in the planning and/or conduct of the study;
- History of hypersensitivity to active or inactive excipients of Osimertinib and/or Pemetrexed and/or Carboplatin or drugs with a similar chemical structure or class to Osimertinib and/or Pemetrexed and/or Carboplatin;
- For patients, inability to collect plasma samples at baseline and disease progression;
- QT prolongation or any clinically important abnormalities in rhythm;
- Any evidence of severe or uncontrolled systemic diseases;
- Currently receiving medications or herbal supplements known to be strong inducers of CYP3A4;
- Any unresolved toxicities from prior therapy greater than CTCAE 5.0 grade 1 at the time of starting study treatment.
- Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the formulated product or previous significant bowel resection that would preclude adequate absorption of osimertinib.
- Inadequate bone marrow reserve or organ function;
- Past medical history of interstitial lung disease, drug-induced interstitial lung disease, radiation pneumonitis which required steroid treatment, or any evidence of clinically active interstitial lung disease.
- Judgment by the investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions and requirements.
- Contraindication for osimertinib, pemetrexed and carboplatin according to China approved label.
- Women who are pregnant or breast-feeding.
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 없음(오픈 라벨)
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
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실험적: Osimertinib 80 mg QD and platinum-based chemotherapy
Osimertinib 80 mg in combination with pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks. |
Pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks.
다른 이름들:
Pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks. |
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활성 비교기: Osimertinib 80mg QD
All patients randomized into this will only receive Osimertinib 80mg. |
Pemetrexed (500 mg/m2) plus carboplatin (AUC5) on Day 1 of 21day cycles (every 3 weeks) for up to 6 cycles, followed by Osimertinib daily with pemetrexed maintenance (500 mg/m2) every 3 weeks.
다른 이름들:
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연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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Progression free survival
기간: The analysis of PFS based on Investigator assessment (according to RECIST 1.1) will occur when approximately 54 progression events have been observed in the 80 randomized patients (approximately 67.5% PFS maturity).
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Progression-free survival (PFS) using Investigator assessment as defined by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1). |
The analysis of PFS based on Investigator assessment (according to RECIST 1.1) will occur when approximately 54 progression events have been observed in the 80 randomized patients (approximately 67.5% PFS maturity).
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2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
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OS rate at 18 months
기간: The OS rate at 18 months will be defined as the Kaplan-Meier estimate of OS at 18 months.
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Proportion of patients alive at 18 months |
The OS rate at 18 months will be defined as the Kaplan-Meier estimate of OS at 18 months.
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Objective Response Rate (ORR)
기간: Objective Response Rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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ORR (per RECIST 1.1 using Investigator assessments) is defined as the number (percent) of patients with at least 1 visit response of CR or PR. |
Objective Response Rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Disease Control Rate (DCR)
기간: Disease control rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Disease control rate (DCR) is defined as the percentage of subjects who have a best overall response of CR or PR or SD by RECIST 1.1 as assessed by the Investigator. |
Disease control rate analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Duration of Response (DoR)
기간: Duration of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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DoR is defined as the time from the date of first documented response until the date of documented progression or death in the absence of disease progression. |
Duration of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Depth of Response
기간: Depth of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Depth of response by Investigator is defined as the relative change in the sum of the longest diameters of RECIST target lesions at the nadir in the absence of NLs or progression of NTLs when compared to baseline. |
Depth of Response analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Safety and tolerability: Adverse event
기간: Safety and tolerability analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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All Adverse events/≥grade 3 AE/SAE incidence rate (AE/SAE graded by CTCAE v5); All ADR incidence rate; AESI: ILD/pneumonitis-like event, Cardiac failure |
Safety and tolerability analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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Molecular resistance mechanism
기간: Molecular resistance mechanism analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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To evaluate potential molecular resistance mechanism by biomarker analysis of plasma at baseline and disease progression and tissue samples (if applicable) by next-generation sequencing (NGS). |
Molecular resistance mechanism analysis will occur when Progression-free survival (PFS) maturity is observed at approximately 31 months from the first patient being randomized.
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공동 작업자 및 조사자
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
추가 관련 MeSH 약관
기타 연구 ID 번호
- ESR-19-20439
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
약물 및 장치 정보, 연구 문서
미국 FDA 규제 의약품 연구
미국 FDA 규제 기기 제품 연구
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