A Prospective non-interventional study (NIS) of trastuzumab deRuxtecan (T-DXd) for adult patients with advanced HER2-pOsitive gaStric or gastroesoPhageal junction (GEJ) adEnocarcinoma who have Received a prIor Trastuzumab-based regimen, accompanied by a disease registrY of patients treated with conventional therapies in a real-world setting in Europe (PROSPERITY).

09/12/2024
09/12/2024
EU PAS number:
EUPAS1000000340
Study
Planned
Study type

Study type

Non-interventional study

Data collection methods

Primary data collection
Non-interventional study

Non-interventional study design

Cohort
Study drug and medical condition

Medicinal product name

Study drug International non-proprietary name (INN) or common name

TRASTUZUMAB DERUXTECAN

Medical condition to be studied

Gastric cancer
Population studied

Short description of the study population

Adult patients planned to be treated with T-DXd or conventional therapies for advanced HER2-positive gastric or gastroesophageal junction (GEJ) adenocarcinoma who have received a prior trastuzumab-based regimen
Study design details

Study design

Multinational, multicenter, prospective observational, non-interventional study with trastuzumab deruxtecan in adult patients with advanced HER2-positive gastric or GEJ adenocarcinoma who have received a prior trastuzumab-based regimen in a real-world setting in Europe

Main study objective

The primary objective is to describe the effectiveness of T-DXd based on real-world Time to Next Treatment (rwTTNT1) in adult patients with advanced HER2-positive gastric or GEJ adenocarcinoma who have received a prior trastuzumab-based regimen in a real-world setting.