TROP2 NMR Concordance Study (ALINEAR)
A Two-stage, Multi-center Concordance Study of Trophoblast Cell Surface Antigen 2 (TROP2) Normalized Membrane Ratio (NMR) in Non-Small Cell Lung Cancer Without Systemic Therapy
연구 개요
상태
상태
정황
정황
개입 / 치료
개입 / 치료
상세 설명
연구 유형
연구 유형
등록 (추정된)
등록
연락처 및 위치
연구 연락처
연구 연락처
- 이름: AstraZeneca Clinical Study Information Center
- 전화번호: 1-877-240-9479
- 이메일: information.center@astrazeneca.com
연구 장소
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Beijing Municipality
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Beijing, Beijing Municipality, 중국, 100730
- 아직 모집하지 않음
- Research Site
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Guangdong
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Guangzhou, Guangdong, 중국, 510000
- 아직 모집하지 않음
- Research Site
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Shanghai Municipality
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Shanghai, Shanghai Municipality, 중국, 200000
- 아직 모집하지 않음
- Research Site
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Shanghai, Shanghai Municipality, 중국, 200000
- 모병
- Research Site
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참여기준
자격 기준
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
Inclusion Criteria:
- Age ≥18 years at sampling.
Histologically or cytologically documented non squamous NSCLC including:
- Stage IIIB or IIIC disease not amenable for surgical resection or definitive chemoradiation, or Stage IV metastatic NSCLC disease at the time of sampling who have not received any systemic therapy for first-line Stage IIIB, IIIC or IV NSCLC.
Participants who provide surgical samples for early-stage disease (Stage I to IIIA) are eligible. The capping for surgical samples is 70% and biopsy samples 30%.
2. (b) Lacks sensitising EGFR tumour tissue mutation (eg, exon 19 deletion or exon 21 L858R, exon 21 L861Q, exon 18 G719X, or exon 20 S768I mutation), as well as ALK and ROS1 rearrangements.
(c) Has no documented tumour genomic alteration results in NTRK, BRAF, RET, MET or HER2, KRAS oncogenes for which there are locally approved and available targeted first-line therapies.
(d) Participants have documented PD-L1 status with TPS (or TC).
- Willing to provide and have adequate tissue samples for biomarker testing, at least ≥5 FFPE slides for Stage 1, and at least ≥7 FFPE slides for Stage 2. Archival surgical samples less than 2 years before enrollment are eligible.
- Informed Consent: Signed inform consent form or waived inform consent per EC requirements.
- -1.Age ≥18 years at sampling.
- 2.Histologically or cytologically documented non squamous NSCLC including:
- (a)Stage IIIB or IIIC disease not amenable for surgical resection or definitive chemoradiation, or Stage IV metastatic NSCLC disease at the time of sampling who have not received any systemic therapy for first-line Stage IIIB, IIIC or IV NSCLC.
- Participants who provide surgical samples for early-stage disease (Stage I to IIIA) are eligible. The capping for surgical samples is 70% and biopsy samples 30%.
- (b)Lacks sensitising EGFR tumour tissue mutation (eg, exon 19 deletion or exon 21 L858R, exon 21 L861Q, exon 18 G719X, or exon 20 S768I mutation), as well as ALK and ROS1 rearrangements.
- (c)Has no documented tumour genomic alteration results in NTRK, BRAF, RET, MET or HER2, KRAS oncogenes for which there are locally approved and available targeted first-line therapies.
- (d) Participants have documented PD-L1 status with TPS (or TC).
- 3. Willing to provide and have adequate tissue samples for biomarker testing, at least ≥5 FFPE slides for Stage 1, and at least ≥7 FFPE slides for Stage 2. Archival surgical samples less than 2 years before enrollment are eligible.
- 4. Informed Consent: Signed inform consent form or waived inform consent per EC requirements.
Exclusion Criteria:
- Mixed small-cell lung cancer and NSCLC histology; sarcomatoid variant of NSCLC.
- At the time of tissue acquisition, the subject has the following known conditions: active tuberculosis infection, or clinically severe pulmonary function compromise resulting from intercurrent pulmonary illnesses including, but not limited to, any underlying pulmonary disorder (eg, pulmonary emboli within 3 months of the study enrollment, severe asthma, severe COPD, restrictive lung disease, pleural effusion, etc.).
- 1. Mixed small-cell lung cancer and NSCLC histology; sarcomatoid variant of NSCLC.
- 2. At the time of tissue acquisition, the subject has the following known conditions: active tuberculosis infection, or clinically severe pulmonary function compromise resulting from intercurrent pulmonary illnesses including, but not limited to, any underlying pulmonary disorder (eg, pulmonary emboli within 3 months of the study enrollment, severe asthma, severe COPD, restrictive lung disease, pleural effusion, etc.).
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
그룹/코호트 수
코호트 및 개입
그룹/코호트그룹/코호트 |
개입 / 치료개입 / 치료 |
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The study is a cross-sectional study with no cohort design
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Reference solution incorporates a TROP2 IHC assay, scanner and image analysis RUO algorithm into a solution for TROP2 NMR testing that has been well-established and validated.
Pathologists may interpret the results; they may also perform quality control steps and negative selection of nontumor areas, if needed.
Mixed solution for TROP2 NMR testing is defined as TROP2 IHC staining using identical clone with Reference, and stained slides will be transformed into digital images using KFBIO scanner (KF-PRO series).
Images will be analysed by QCS algorithm RUO and the pathologist role is same as Reference solution.
Local solution for TROP2 NMR testing is defined as TROP2 IHC staining using the identical assay with Reference, and stained slides will be transformed into digital images using KFBIO scanner (KF-PRO series).
Images will be analysed by QCS algorithm RUO and the pathologist role is same as Reference solution.
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연구는 무엇을 측정합니까?
주요 결과 측정
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Stage 1 - Solution concordance in central lab: To evaluate TROP2 NMR concordance between Local solution and Reference solution in the central lab
기간: Approximately 6 months after collection of the first slide.
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The primary endpoint will be analysed in the ACS1 with evaluable Local solution result.
The concordance between Local solution and Reference solution will be descriptive through calculation of Positive Percentage Agreement (PPA), Negative Percentage Agreement (NPA), and Overall Percentage Agreement (OPA).
These metrics will be computed using two-by-two contingency tables and reported with corresponding 95% Clopper-Pearson confidence intervals.
Cohen's kappa coefficient and 95% CI will also be used to assess the degree of agreement by chance.PPA = (number of patients with TROP2 NMR+ based on both solutions)/(total number of patients with TROP2 NMR+ based on Reference solution) × 100%;NPA = (number of patients with TROP2 NMR- based on both solutions)/(total number of patients with TROP2 NMR- based on Reference solution) × 100% ;OPA = (number of patients with concordant results based on both solutions)/(total number of patients) × 100%
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Approximately 6 months after collection of the first slide.
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Stage2 - TROP2 NMR testing concordance among labs:To evaluate TROP2 NMR concordance of Reference solution between sites and central lab
기간: Approximately 10 months after collection of the first slide.
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This primary endpoint will be analysed in the ACS2 with evaluable TROP2 NMR testing results by Reference solution from sites.
The concordance will be summarized using PPA, NPA, and OPA, with corresponding 95% confidence intervals.
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Approximately 10 months after collection of the first slide.
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Stage2 - TROP2 NMR testing concordance among labs:To evaluate TROP2 NMR concordance of Local solution in sites with Reference solution in central lab
기간: Approximately 10 months after collection of the first slide.
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This primary endpoint will be analysed in the ACS2 with evaluable TROP2 NMR testing results from Local solution.
The concordance will be summarized using the same statistical metrics as the primary endpoint in stage 1, including PPA, NPA, and OPA, with corresponding 95% confidence intervals.
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Approximately 10 months after collection of the first slide.
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2차 결과 측정
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
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Stage1:To evaluate TROP2 NMR concordance between Mixed solution and Reference solution in the central lab
기간: Approximately 6 months after collection of the first slide.
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For the secondary endpoint of concordance between Mixed solution and Reference solution, the analysis will be performed in the ACS1 with evaluable Mixed solution results.
The component concordance will be analysed in the CCS, from which a subset of data will be extracted for each component-specific concordance.
The concordance will be summarized using the same statistical metrics as the primary endpoint, including PPA, NPA, and OPA, with corresponding 95% confidence intervals.
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Approximately 6 months after collection of the first slide.
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Stage1:To evaluate IHC assay concordance using Reference scanner and QCS
기간: Approximately 6 months after collection of the first slide.
|
For the secondary endpoint of concordance between Mixed solution and Reference solution, the analysis will be performed in the ACS1 with evaluable Mixed solution results.
The component concordance will be analysed in the CCS, from which a subset of data will be extracted for each component-specific concordance.
The concordance will be summarized using the same statistical metrics as the primary endpoint, including PPA, NPA, and OPA, with corresponding 95% confidence intervals.
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Approximately 6 months after collection of the first slide.
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Stage1:To evaluate scanner concordance using Reference IHC and QCS
기간: Approximately 6 months after collection of the first slide.
|
For the secondary endpoint of concordance between Mixed solution and Reference solution, the analysis will be performed in the ACS1 with evaluable Mixed solution results.
The component concordance will be analysed in the CCS, from which a subset of data will be extracted for each component-specific concordance.
The concordance will be summarized using the same statistical metrics as the primary endpoint, including PPA, NPA, and OPA, with corresponding 95% confidence intervals.
|
Approximately 6 months after collection of the first slide.
|
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Stage1:To evaluate QCS algorithm concordance using Reference IHC and scanner
기간: Approximately 6 months after collection of the first slide.
|
For the secondary endpoint of concordance between Mixed solution and Reference solution, the analysis will be performed in the ACS1 with evaluable Mixed solution results.
The component concordance will be analysed in the CCS, from which a subset of data will be extracted for each component-specific concordance.
The concordance will be summarized using the same statistical metrics as the primary endpoint, including PPA, NPA, and OPA, with corresponding 95% confidence intervals.
|
Approximately 6 months after collection of the first slide.
|
|
Stage2:To evaluate TROP2 NMR concordance of Mixed solution in sites with Reference solution in the central lab
기간: Approximately 10 months after collection of the first slide.
|
The secondary endpoint will be analysed in the ACS2 with evaluable TROP2 NMR testing results from Mixed solution in sites.
The concordance will be summarized using the same statistical metrics as above.
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Approximately 10 months after collection of the first slide.
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공동 작업자 및 조사자
수사관
수사관
- 수석 연구원: zhiyong Liang, Peking Union Medical College Hospital
- 수석 연구원: shun Lu, Shanghai Chest Hospital, Shanghai Jiaotong University
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
연구 시작
기본 완료 (추정된)
기본 완료
연구 완료 (추정된)
연구 완료
연구 등록 날짜
최초 제출
최초 제출
QC 기준을 충족하는 최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
처음 게시됨
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
마지막 업데이트 게시됨
QC 기준을 충족하는 마지막 업데이트 제출
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
마지막으로 확인됨
추가 정보
이 연구와 관련된 용어
기타 연구 ID 번호
기타 연구 ID 번호
- D9260R00030
개별 참가자 데이터(IPD) 계획
개별 참가자 데이터(IPD)를 공유할 계획입니까?
IPD 계획 설명
Qualified researchers can request access to anonymized individual patient-level data from AstraZeneca group of companies sponsored clinical trials via the request portal Vivli.org. All requests will be evaluated as per the AZ disclosure commitment: https://astrazenecagrouptrials.pharmacm.com/ST/Submission/Disclosure.
Yes, indicates that AZ are accepting requests for IPD, but this does not mean all requests will be shared.
IPD 공유 기간
IPD 공유 액세스 기준
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미국 FDA 규제 기기 제품 연구
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