Literature DB >> 31062115

Skeletal muscle loss during systemic chemotherapy for colorectal cancer indicates treatment response: a pooled analysis of a multicenter clinical trial (KSCC 1605-A).

Shun Sasaki1, Eiji Oki2, Hiroshi Saeki1, Takayuki Shimose3, Sanae Sakamoto3, Qingjiang Hu1, Kensuke Kudo1,4, Yasuo Tsuda1, Yuichiro Nakashima1, Koji Ando1, Yoshito Akagi5, Yoshihiro Kakeji6, Hideo Baba7, Yoshihiko Maehara1,8.   

Abstract

BACKGROUND: Sarcopenia or degenerative loss of skeletal muscle mass is related to poor prognosis in patients with cancer. This study aimed to clarify the clinical significance of skeletal muscle loss (SML) during chemotherapy for metastatic colorectal cancer (mCRC).
METHODS: A total of 249 patients who were secondarily registered in a pooled database of mCRC patients with the first-line systemic chemotherapy and prospectively enrolled in six clinical trials of Kyushu Study Group of Clinical Cancer were included in this study. Skeletal muscle area was calculated from computed tomography images before and 3 and 6 months after treatment. Baseline sarcopenia and SML (cut-off value = 9%) were evaluated.
RESULTS: Baseline sarcopenia was observed in 135 of 219 patients who were evaluated before treatment. They tended to be male; older; and have lower body mass index, lower visceral and subcutaneous fat contents, and a lower waist circumference (P < 0.01); however, baseline sarcopenia was not associated with prognosis. SML at 3 months was associated with an incidence of adverse events (P = 0.01), poor objective response rate (ORR) (P < 0.01), and poor progression-free survival (PFS) (P = 0.03), and it was an independent predictive factor for poor ORR (P < 0.01) and PFS (P = 0.04).
CONCLUSION: SML at 3 months after systemic chemotherapy for mCRC was associated with poor treatment response. Thus, clarifying the importance of SML prevention guarantees a more effective chemotherapy.

Entities:  

Keywords:  Cachexia; Chemotherapy response; Metastatic colorectal cancer; Sarcopenia; Skeletal muscle loss

Mesh:

Year:  2019        PMID: 31062115     DOI: 10.1007/s10147-019-01460-8

Source DB:  PubMed          Journal:  Int J Clin Oncol        ISSN: 1341-9625            Impact factor:   3.402


  45 in total

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5.  Prevalence and clinical implications of sarcopenic obesity in patients with solid tumours of the respiratory and gastrointestinal tracts: a population-based study.

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7.  Reassessment of the cutoff values of waist circumference and visceral fat area for identifying Japanese subjects at risk for the metabolic syndrome.

Authors:  Rie Oka; Junji Kobayashi; Kunimasa Yagi; Hideji Tanii; Susumu Miyamoto; Akimichi Asano; Tomomi Hagishita; Mika Mori; Tadashi Moriuchi; Makoto Kobayashi; Shouji Katsuda; Masa-aki Kawashiri; Atsushi Nohara; Yoshiyu Takeda; Hiroshi Mabuchi; Masakazu Yamagishi
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Authors:  Marina Mourtzakis; Carla M M Prado; Jessica R Lieffers; Tony Reiman; Linda J McCargar; Vickie E Baracos
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Review 10.  Pathophysiology of cancer cachexia: much more than host-tumour interaction?

Authors:  Richard J E Skipworth; Grant D Stewart; Cornelis H C Dejong; Tom Preston; Kenneth C H Fearon
Journal:  Clin Nutr       Date:  2007-05-15       Impact factor: 7.324

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9.  Effect of home-based prehabilitation in an enhanced recovery after surgery program for patients undergoing colorectal cancer surgery during the COVID-19 pandemic.

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10.  Multiplatform Urinary Metabolomics Profiling to Discriminate Cachectic from Non-Cachectic Colorectal Cancer Patients: Pilot Results from the ColoCare Study.

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