Data extracts from the included studies.

Background
Cancer remains one of the leading causes of mortality and morbidity worldwide with colorectal, cervical, and breast cancers accounting for significant proportion of preventable deaths. Early screening, diagnosis, and treatment could prevent many of these deaths. However, migrants face persistent disparities in the screening, early diagnosis, and treatment of these cancers. This study synthesizes evidence on cancer screening uptake, implementation strategies, as well as their enablers and barriers among migrants in English-speaking high-income countries (Australia, the USA, the UK, Canada, and New Zealand).
Methods
We conducted a scoping review of studies published in any language between 1 January 2015 and 31 December 2024. Studies were retrieved from four databases: PubMed, Scopus, Embase, and Web of Science. Search terms were developed based on four domains: types of cancer (colorectal, cervical, and breast), migrant populations, screening coverage, and country of residence. The uptake of cancer screening among migrants in selected countries was determined. A thematic analysis was conducted to analyze the data and identify key themes related to the implementation of cancer screening strategies, as well as their enablers and barriers.
Results
A total of 80 studies were included in the review. Migrants exhibited varied levels of utilization of cancer screening such as cervical cancer (41% − 84%), breast cancer (24%−87%), and colorectal cancer (4%−55%). Four themes related to the implementation of cancer screening strategies were identified: i) culturally tailored health education and communication, ii) trust-building initiatives with providers and health systems, iii) family and community support for acculturation and engagement, iv) awareness and knowledge on increased risk perception. Several barriers to the implementation of cancer screening strategies were identified, including lack of insurance, transportation challenges, difficulty in speaking and understanding English, inflexible work hours of health services, cultural taboos, stigma, poverty, and undocumented (illegal) status of migrants. Enablers of the implementation of cancer screening strategies included faith-based messaging on cancer screening, community partnerships, home-based fecal immunochemical test kits, availability of after-hours services, gender-concordant care, social networks, acculturation, and trust-building.
Conclusions
The uptake of cancer screening (breast, cervical, colorectal) varied and had low among migrants (e.g., refugees, culturally and linguistically diverse populations). Targeted, culturally tailored approaches, expanding interpreter services, and fostering cross-sector collaborations (e.g., linking screenings to cultural events) are essential for addressing disparities in cancer screening among migrants. Culturally sensitive and adaptive, equity-focussed interventions on cancer screening should be prioritized by ensuring sustained funding, disaggregated data collection on the uptake of cancers screening and design and implementation of programs on targeting diverse population groups.