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Clinical features and KRAS mutation in colorectal cancer with bone metastasis

Bone metastasis is known as a poor prognostic factor in colorectal cancer (CRC), but its clinical manifestations and outcomes are uncertain. CRC with bone metastasis was searched from January 2006 to April 2016. Of 11,551 CRC patients, 321 (2.7%) patients had bone metastasis. Bone-only metastasis wa...

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Autores principales: Park, Hyung Soon, Chun, You Jin, Kim, Han Sang, Kim, Jee Hung, Lee, Choong-kun, Beom, Seung-Hoon, Shin, Sang Joon, Ahn, Joong Bae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713114/
https://www.ncbi.nlm.nih.gov/pubmed/33273596
http://dx.doi.org/10.1038/s41598-020-78253-x
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author Park, Hyung Soon
Chun, You Jin
Kim, Han Sang
Kim, Jee Hung
Lee, Choong-kun
Beom, Seung-Hoon
Shin, Sang Joon
Ahn, Joong Bae
author_facet Park, Hyung Soon
Chun, You Jin
Kim, Han Sang
Kim, Jee Hung
Lee, Choong-kun
Beom, Seung-Hoon
Shin, Sang Joon
Ahn, Joong Bae
author_sort Park, Hyung Soon
collection PubMed
description Bone metastasis is known as a poor prognostic factor in colorectal cancer (CRC), but its clinical manifestations and outcomes are uncertain. CRC with bone metastasis was searched from January 2006 to April 2016. Of 11,551 CRC patients, 321 (2.7%) patients had bone metastasis. Bone-only metastasis was found in only 8.7% of patients. Synchronous bone metastasis was present in 147 (45.8%) patients. In patients with metachronous bone metastasis, the median time from CRC diagnosis to bone metastasis (TTB) was 27.2 months. KRAS mutation status was a marginally significant factor affecting TTB (median TTB, KRAS wild-type or mutation: 29 or 25.8 months, respectively, P = 0.068). Skeletal-related events (SREs) were noted in 200 (62.3%) patients. Median overall survival (OS) from diagnosis of bone metastasis was 8.0 months. On multivariate analysis, multi-organ metastasis, peritoneal metastasis, neutrophil-to-lymphocyte ratio (NLR) ≥ 2.7, and alkaline phosphatase (ALP) ≥ 123 were independent factors for OS. Palliative chemotherapy prolonged survival in CRC patients with bone metastasis (HR 0.25, 95% CI 0.2–0.33). In conclusion, bone metastasis of CRC is rare, but it is related to SREs. Most patients have other organ metastasis and survival is 8.0 months. Attention should be paid to bone metastasis in CRC patients.
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spelling pubmed-77131142020-12-03 Clinical features and KRAS mutation in colorectal cancer with bone metastasis Park, Hyung Soon Chun, You Jin Kim, Han Sang Kim, Jee Hung Lee, Choong-kun Beom, Seung-Hoon Shin, Sang Joon Ahn, Joong Bae Sci Rep Article Bone metastasis is known as a poor prognostic factor in colorectal cancer (CRC), but its clinical manifestations and outcomes are uncertain. CRC with bone metastasis was searched from January 2006 to April 2016. Of 11,551 CRC patients, 321 (2.7%) patients had bone metastasis. Bone-only metastasis was found in only 8.7% of patients. Synchronous bone metastasis was present in 147 (45.8%) patients. In patients with metachronous bone metastasis, the median time from CRC diagnosis to bone metastasis (TTB) was 27.2 months. KRAS mutation status was a marginally significant factor affecting TTB (median TTB, KRAS wild-type or mutation: 29 or 25.8 months, respectively, P = 0.068). Skeletal-related events (SREs) were noted in 200 (62.3%) patients. Median overall survival (OS) from diagnosis of bone metastasis was 8.0 months. On multivariate analysis, multi-organ metastasis, peritoneal metastasis, neutrophil-to-lymphocyte ratio (NLR) ≥ 2.7, and alkaline phosphatase (ALP) ≥ 123 were independent factors for OS. Palliative chemotherapy prolonged survival in CRC patients with bone metastasis (HR 0.25, 95% CI 0.2–0.33). In conclusion, bone metastasis of CRC is rare, but it is related to SREs. Most patients have other organ metastasis and survival is 8.0 months. Attention should be paid to bone metastasis in CRC patients. Nature Publishing Group UK 2020-12-03 /pmc/articles/PMC7713114/ /pubmed/33273596 http://dx.doi.org/10.1038/s41598-020-78253-x Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Park, Hyung Soon
Chun, You Jin
Kim, Han Sang
Kim, Jee Hung
Lee, Choong-kun
Beom, Seung-Hoon
Shin, Sang Joon
Ahn, Joong Bae
Clinical features and KRAS mutation in colorectal cancer with bone metastasis
title Clinical features and KRAS mutation in colorectal cancer with bone metastasis
title_full Clinical features and KRAS mutation in colorectal cancer with bone metastasis
title_fullStr Clinical features and KRAS mutation in colorectal cancer with bone metastasis
title_full_unstemmed Clinical features and KRAS mutation in colorectal cancer with bone metastasis
title_short Clinical features and KRAS mutation in colorectal cancer with bone metastasis
title_sort clinical features and kras mutation in colorectal cancer with bone metastasis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7713114/
https://www.ncbi.nlm.nih.gov/pubmed/33273596
http://dx.doi.org/10.1038/s41598-020-78253-x
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