The views of cancer patients of Turkish, Moroccan, Surinamese, and Dutch-Caribbean descent on diagnosis, treatment and prognosis: A systematic literature review.

J Cancer Policy

Department of Medical Oncology, Erasmus MC Cancer Institute, Erasmus University Medical Center, 3015 GD Rotterdam, the Netherlands; Department of Medical Oncology, Netherlands Cancer Institute, 1006 BE Amsterdam, the Netherlands. Electronic address:

Published: March 2024

AI Article Synopsis

  • The study reviews the perspectives of Turkish, Moroccan, Surinamese, and Dutch-Caribbean cancer patients in the Netherlands regarding diagnosis, treatment, and prognosis.
  • A systematic literature review highlighted four main themes: diagnosis disclosure, communication practices, information provision, and decision-making, revealing significant differences between Turkey and the Netherlands.
  • There is a notable lack of research on the views of Surinamese and Dutch-Caribbean patients, emphasizing the need for further studies to improve communication and care for all ethnic groups.

Article Abstract

Background: The number of international migrants is increasing worldwide. The four major non-western ethnic groups in the Netherlands are Turkish, Moroccan, Surinamese, and Dutch-Caribbean. This review examined the scientific literature on the views of cancer patients from these four ethnic groups on cancer diagnosis, treatment, and prognosis.

Methods: A systematic literature review was conducted using the databases EMBASE, Medline Web of Science, and Cochrane Central Register. Studies with patients who were of Turkish, Moroccan, Surinamese, and Dutch-Caribbean descent were included. Both qualitative and quantitative studies were included, and thematic analysis was performed. The methodological quality was assessed using the Mixed Methods Appraisal Tool.

Results: Thirteen studies were conducted in Turkey on Turkish cancer patients, while three were conducted in the Netherlands on Turkish and Moroccan cancer patients. Four themes emerged from the included studies: disclosure of diagnosis, communication, information provision, and decision-making. The majority of cancer patients in Turkey wanted information regarding their diagnosis and treatment. However, disclosure of a cancer diagnosis was rarely discussed with cancer patients in Turkey, whereas in the Netherlands it was provided directly. Family members in both the host and native countries had a strong influence on communication and decision-making. No literature on this topic for Surinamese or Dutch-Caribbean cancer patients was found.

Conclusion: Although major ethnic groups live in host countries, there is a lack of knowledge on optimal communication and information disclosure on cancer to patients and their families.

Policy Summary: Further research into the views of ethnic groups on how to communicate about cancer is essential to ensuring that every patient receives optimal care and treatment.

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Source
http://dx.doi.org/10.1016/j.jcpo.2023.100455DOI Listing

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