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Skeletal muscle mass predicts the outcome of nivolumab treatment for non-small cell lung cancer
被引:34
|作者:
Tsukagoshi, Mariko
[1
,2
]
Yokobori, Takehiko
[1
]
Yajima, Toshiki
[1
,3
]
Maeno, Toshitaka
[4
]
Shimizu, Kimihiro
[3
]
Mogi, Akira
[3
]
Araki, Kenichiro
[2
]
Harimoto, Norifumi
[2
]
Shirabe, Ken
[2
]
Kaira, Kyoichi
[1
,5
]
机构:
[1] Gunma Univ, Grad Sch Med, Dept Innovat Canc Immunotherapy, Maebashi, Gunma, Japan
[2] Gunma Univ Hosp, Div Hepatobiliary & Pancreat Surg, Maebashi, Gunma, Japan
[3] Gunma Univ Hosp, Integrat Ctr Gen Surg, Div Gen Thorac Surg, Maebashi, Gunma, Japan
[4] Gunma Univ Hosp, Integrat Ctr Internal Med, Div Allergy & Resp Med, Maebashi, Gunma, Japan
[5] Saitama Med Univ, Int Med Ctr, Dept Resp Med, 1397-1 Yamane, Hidaka, Saitama 3501298, Japan
来源:
关键词:
lung cancer;
nivolumab;
programmed death 1;
sarcopenia;
skeletal muscle mass;
CLINICAL-RESPONSE;
PD-1;
BLOCKADE;
DOCETAXEL;
IMPACT;
TUMORS;
D O I:
10.1097/MD.0000000000019059
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Nivolumab, a monoclonal antibody targeting programmed cell death-1, significantly prolongs survival for patients with advanced non-small-cell lung cancer (NSCLC). However, little is known about the value of predictive biomarkers. Hence, we investigated the impact of skeletal muscle (SM) mass loss on clinical outcomes in NSCLC patients undergoing nivolumab treatment. Thirty patients with histologically confirmed NSCLC treated with nivolumab were included in this study. Computed tomography was used to determine SM loss based on the SM index (SMI). The SMI is the cross-sectional area of the bilateral psoas muscles at the third lumbar vertebra, divided by height squared. The cut-off values were defined as 6.36cm(2)/m(2) for men and 3.92cm(2)/m(2) for women. Among the 30 patients, 13 (43%) had SM loss. There was no significant association between SM loss and immune-related adverse events. The SM loss group had undergone significantly more prior chemotherapy cycles (P=.04). SM loss was significantly associated with fewer nivolumab cycles (P=.01). No patients in the SM loss group achieved a partial response. Patients with SM loss had a significantly shorter progression-free survival period (P=.008) and median overall survival than those with normal SM mass (10 vs 25 months, respectively, P=.03). SM loss was an independent prognostic factor of poor survival. In conclusion, SM loss may be a predictive factor of poor outcomes in NSCLS patients undergoing nivolumab therapy.
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