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Trastuzumab deruxtecan (T-DXd) is an approved therapy for non-small cell lung cancer (NSCLC) in China. Despite the clinical trial evidence, there is no real-world data of T-DXd used in Chinese lung cancer patients with HER2 mutations.
This real world, prospective study will assess the effectiveness and safety of T-DXd in patients with locally advanced or metastatic, HER2 mutation-positive NSCLC in real-world setting.
T-DXd is an approved therapy in China for locally advanced or metastatic NSCLC patients with human epidermal growth factor receptor 2 mutations (HER2m). In previous clinical trials, T-DXd demonstrated efficacy and manageable safety profiles in the ≥ second-line setting for NSCLC harboring HER2m. However, patient populations are more diverse in routine practice and no real-world data of T-DXd used in Chinese lung cancer patients with HER2 mutations exist.
This study will assess the effectiveness of ≥ second-line treatment of T-DXd in real-world setting as the primary objective. Secondary objectives will further assess the effectiveness and overall survival of ≥ second-line treatment of T-DXd in real-world setting as well as evaluate the safety and tolerability of any-line treatment of T-DXd in real-world setting. This is an non-interventional, observational study. No drug will be provided or administered as part of this protocol; however, participants on T-DXd will be enrolled in this study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| NSCLC patients with HER2 mutations | Patients with NSCLC with HER2 mutations who receive T-DXd based on physician's decisions will be enrolled. |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| No drug | Other | This is an non-interventional, observational study. No drug will be provided or administered as part of this protocol; however, participants on T-DXd will be enrolled in this study. |
| Measure | Description | Time Frame |
|---|---|---|
| Progression-free survival (PFS) by Investigator Assessment in Real-world Setting (rwPFS) | rwPFS is defined as the time from the initiated date of ≥ second-line treatment of T-DXd until disease progression or death by investigator report as recorded in the electronic case report forms (eCRF). | Baseline up to approximatley 2 years |
| Measure | Description | Time Frame |
|---|---|---|
| Time to Treatment Discontinuation or Death (TTD) | TTD is defined as the time from the initiated date of ≥ second-line treatment of T-DXd to the date of treatment discontinuation or death from any cause. | Baseline up to approximately 2 years |
| Best Overall Response Rate (BORR) |
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The key inclusion criteria for this study are:
The key exclusion criteria for this study are:
Previously treated with HER2-targeted/directed therapies, including:
Has spinal cord compression or clinically active CNS metastases, defined as untreated and symptomatic, or requiring therapy with corticosteroids or anticonvulsants to control associated symptoms.
Any evidence of severe or uncontrolled systemic diseases, including uncontrolled hypertension active bleeding diatheses, etc.
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NSCLC patients with HER2 mutations who receive T-DXd based on physicians' discretion will be enrolled from about 30 sites in China.
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Contact for Clinical Trial Information | Contact | 908-992-6400 | CTRinfo_us@daiichisankyo.com |
| Name | Affiliation | Role |
|---|---|---|
| Project Manager | Daiichi Sankyo Co., Ltd. | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Cancer Hospital Chinese Academy of Medical Sciences | Not yet recruiting | Beijing | 100021 | China |
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BORR is defined as the percentage of patients with complete response (CR) or partial response (PR) as assessed by investigator for ≥ second-line treatment of T-DXd. Based on RECIST guidelines, CR was defined as a disappearance of all target lesions and PR was defined as at least a 30% decrease in the sum of diameters of target lesions. |
| Baseline up to approximately 2 years |
| Overall Survival | Overall survival is defined as the time from the initiated date of ≥ second-line treatment of T-DXd until death due to any cause. | Baseline up to approximately 2 years |
| Number of Patients Reporting Treatment-related Adverse Events (TRAEs), Adverse Events of Special Interests (AESIs), and AEs Leading to Dose Interruption, Reduction, Discontinuation | TRAEs, AESIs and AEs leading to dose interruption, reduction, discontinuation will be graded by the investigators using National Cancer Institute (NCI) common terminology criteria for adverse events (CTCAE) version 5.0 and coded using the medical dictionary for regulatory activities (MedDRA). | Baseline up to approximately 2 years |
| Peking University International Hospital | Not yet recruiting | Beijing | 100125 | China |
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| Beijing Cancer Hospital | Not yet recruiting | Beijing | 100142 | China |
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| Hunan Second People's Hospital | Not yet recruiting | Changsha | 410007 | China |
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| Fujian Cancer Hospital | Not yet recruiting | Fuzhou | 350014 | China |
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| Affiliated Cancer Hospital and Institute of Guangzhou Medical University | Not yet recruiting | Guangzhou | 510060 | China |
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| The First Affiliated Hospital of Sun Yat-sen University | Not yet recruiting | Guangzhou | 510062 | China |
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| Zhejiang Cancer Hospital | Not yet recruiting | Hangzhou | 310022 | China |
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| Anhui Provincial Cancer Hospital | Not yet recruiting | Hefei | 230031 | China |
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| First Affiliated Hospital of Shandong First Medical University | Not yet recruiting | Jinan | 250014 | China |
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| Cancer Hospital of Shandong First Medical University | Not yet recruiting | Jinan | 250103 | China |
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| The First Affiliated Hospital of Jinzhou Medical University | Not yet recruiting | Jinzhou | 121001 | China |
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| The First Affiliated Hospital of Nanchang University | Not yet recruiting | Nanchang | 330000 | China |
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| Guangxi Medical University Cancer Hospital | Not yet recruiting | Nanning | 541000 | China |
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| Ruijin Hospital, Shanghai Jiaotong University School Of Medicine | Not yet recruiting | Shanghai | 200025 | China |
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| Zhongshan Hospital Fudan University | Not yet recruiting | Shanghai | 200032 | China |
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| The First Hospital of China Medical University | Not yet recruiting | Shenyang | 110001 | China |
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| Cancer Hospital Chinese Academy of Medical Sciences, Shenzhen Center | Not yet recruiting | Shenzhen | 518116 | China |
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| The Fourth Hospital of Hebei Medical University | Not yet recruiting | Shijiazhuang | 050011 | China |
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| Shangxi Provincial Cancer Hospital | Recruiting | Taiyuan | 030013 | China |
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| The First Affiliated Hospital of Xiamen University | Not yet recruiting | Xiamen | 361102 | China |
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| Henan Cancer Hospital | Not yet recruiting | Zhengzhou | 450052 | China |
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| The First Affiliated Hospital of Zhengzhou University | Not yet recruiting | Zhengzhou | 450052 | China |
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| ID | Term |
|---|---|
| D002289 | Carcinoma, Non-Small-Cell Lung |
| ID | Term |
|---|---|
| D002283 | Carcinoma, Bronchogenic |
| D001984 | Bronchial Neoplasms |
| D008175 | Lung Neoplasms |
| D012142 | Respiratory Tract Neoplasms |
| D013899 | Thoracic Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
| D008171 | Lung Diseases |
| D012140 | Respiratory Tract Diseases |
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