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Travel burden associated with rare cancers: The example of Merkel cell carcinoma

BACKGROUND: There are limited data on the travel burden for cancer patients with rare tumor types, such as Merkel cell carcinoma (MCC). OBJECTIVE: The objective of this study was to understand the travel burden of MCC patients. METHODS: This study used data from an MCC registry at the Seattle Cancer...

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Autores principales: Jain, Rahul, Menzin, Joseph, Lachance, Kristina, McBee, Patrick, Phatak, Hemant, Nghiem, Paul T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536956/
https://www.ncbi.nlm.nih.gov/pubmed/30950224
http://dx.doi.org/10.1002/cam4.2085
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author Jain, Rahul
Menzin, Joseph
Lachance, Kristina
McBee, Patrick
Phatak, Hemant
Nghiem, Paul T.
author_facet Jain, Rahul
Menzin, Joseph
Lachance, Kristina
McBee, Patrick
Phatak, Hemant
Nghiem, Paul T.
author_sort Jain, Rahul
collection PubMed
description BACKGROUND: There are limited data on the travel burden for cancer patients with rare tumor types, such as Merkel cell carcinoma (MCC). OBJECTIVE: The objective of this study was to understand the travel burden of MCC patients. METHODS: This study used data from an MCC registry at the Seattle Cancer Care Alliance (SCCA). All MCC patients enrolled at SCCA with a valid 3‐digit ZIP code were included. Patients were followed up from January 1, 2012 until their last follow‐up, death, or end of data (January 1, 2017). Travel burden was measured by one‐way travel distance to SCCA from each patient's 3‐digit ZIP code. Patient demographics, tumor characteristics, and follow‐up visit were evaluated and stratified by one‐way driving distance of ≤300 and >300 miles. RESULTS: A total of 391 MCC patients were included (68% men, mean age = 67 years [±SD = ±11 years], 67% residing in the West, and 70% white). At diagnosis, 53% of the patients had Stage III or IV MCC. Mean one‐way distance traveled by patients was 1,137 (median: 813) miles, and 57% of patients traveled >300 miles. Compared to patients who traveled ≤300 miles, those who traveled >300 miles were more likely to be <70 years old (46% vs 65%; P < 0.001), were diagnosed with advanced stage (III or IV) MCC (46% vs 59%; P = 0.01), had shorter follow‐up in the cancer registry (mean: 509 vs 212 days; P < 0.001), and had fewer visits during follow‐up (mean: 5.2 vs 2.5; P < 0.001). CONCLUSIONS: In this single cancer center study, the majority of MCC patients trav‐eled long distances to receive expert care. Longer travel distances appeared to be associated with younger age, a more advanced stage of cancer at study entry and fewer in‐clinic visits, suggesting that travel burden may impact timely and adequate patient care for this rare cancer.
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spelling pubmed-65369562019-06-03 Travel burden associated with rare cancers: The example of Merkel cell carcinoma Jain, Rahul Menzin, Joseph Lachance, Kristina McBee, Patrick Phatak, Hemant Nghiem, Paul T. Cancer Med Cancer Prevention BACKGROUND: There are limited data on the travel burden for cancer patients with rare tumor types, such as Merkel cell carcinoma (MCC). OBJECTIVE: The objective of this study was to understand the travel burden of MCC patients. METHODS: This study used data from an MCC registry at the Seattle Cancer Care Alliance (SCCA). All MCC patients enrolled at SCCA with a valid 3‐digit ZIP code were included. Patients were followed up from January 1, 2012 until their last follow‐up, death, or end of data (January 1, 2017). Travel burden was measured by one‐way travel distance to SCCA from each patient's 3‐digit ZIP code. Patient demographics, tumor characteristics, and follow‐up visit were evaluated and stratified by one‐way driving distance of ≤300 and >300 miles. RESULTS: A total of 391 MCC patients were included (68% men, mean age = 67 years [±SD = ±11 years], 67% residing in the West, and 70% white). At diagnosis, 53% of the patients had Stage III or IV MCC. Mean one‐way distance traveled by patients was 1,137 (median: 813) miles, and 57% of patients traveled >300 miles. Compared to patients who traveled ≤300 miles, those who traveled >300 miles were more likely to be <70 years old (46% vs 65%; P < 0.001), were diagnosed with advanced stage (III or IV) MCC (46% vs 59%; P = 0.01), had shorter follow‐up in the cancer registry (mean: 509 vs 212 days; P < 0.001), and had fewer visits during follow‐up (mean: 5.2 vs 2.5; P < 0.001). CONCLUSIONS: In this single cancer center study, the majority of MCC patients trav‐eled long distances to receive expert care. Longer travel distances appeared to be associated with younger age, a more advanced stage of cancer at study entry and fewer in‐clinic visits, suggesting that travel burden may impact timely and adequate patient care for this rare cancer. John Wiley and Sons Inc. 2019-04-05 /pmc/articles/PMC6536956/ /pubmed/30950224 http://dx.doi.org/10.1002/cam4.2085 Text en © 2019 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Prevention
Jain, Rahul
Menzin, Joseph
Lachance, Kristina
McBee, Patrick
Phatak, Hemant
Nghiem, Paul T.
Travel burden associated with rare cancers: The example of Merkel cell carcinoma
title Travel burden associated with rare cancers: The example of Merkel cell carcinoma
title_full Travel burden associated with rare cancers: The example of Merkel cell carcinoma
title_fullStr Travel burden associated with rare cancers: The example of Merkel cell carcinoma
title_full_unstemmed Travel burden associated with rare cancers: The example of Merkel cell carcinoma
title_short Travel burden associated with rare cancers: The example of Merkel cell carcinoma
title_sort travel burden associated with rare cancers: the example of merkel cell carcinoma
topic Cancer Prevention
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536956/
https://www.ncbi.nlm.nih.gov/pubmed/30950224
http://dx.doi.org/10.1002/cam4.2085
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