Body mass index and serum markers associated with progression-free survival in lung cancer patients treated with immune checkpoint inhibitors

被引:6
作者
Liu, Zhenzhen [1 ]
Diao, Yuzhu [1 ]
Li, Xiaoling [1 ]
机构
[1] China Med Univ, Liaoning Canc Hosp & Inst, Canc Hosp, Dept Thorac Canc 1, Xiaoheyan Rd, Shenyang 110042, Liaoning, Peoples R China
关键词
MUSCLE MASS; CELL; CHEMOTHERAPY; SARCOPENIA; DOCETAXEL; NIVOLUMAB; GLUTAMINE; THERAPY; RISK;
D O I
10.1186/s12885-022-09744-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: ICIs have remarkably affected the treatment strategies for numerous malignancies, including lung cancer. However, only a fraction of patients experience durable responses to ICIs; thus, there is an urgent need to identify the parameters related to ICI therapeutic effects. In this study, we investigated nutritional status surrogates and several serum markers to estimate the efficacy of ICIs. Materials and methods: The records of 66 patients with stage III/IV lung cancer who received ICIs were retrospectively analyzed. Features of patients' clinical pathology, including age, sex, histology, line of treatment, BMI, serum albumin, serum creatinine, and serum inflammatory markers such as LMR and PLR, were examined. Progression-free survival was the primary endpoint. Relationships among categorical variables were assessed by the chi-squared test. Survival analysis was performed using the Kaplan-Meier method followed by the log-rank test. Cox multivariate analysis was performed to analyze the association between each variable and the survival time of patients. Results: The patients with BMI >= 25 (kg/m2), serum ALB >= 37 (g/dL), serum creatinine >= 61.8 (mu mol/L), LMR >= 2.12 had a significantly prolonged PFS in comparison with BMI<25 (kg/m2), ALB<37 (g/dL), creatinine<61.8 (mu mol/L), LMR<2.12 (p < 0.05). No statistically significant difference was detected between patients with PLR < 135 and PLR >= 135 (p = 0.612). Multivariate analysis revealed that ALB >= 37 (g/dL) and creatinine >= 61.8 (mu mol/L) were associated with prolonged PFS, while statistical significance was not achieved in the BMI groups. Conclusions: The current results indicated that high BMI is related to longer PFS in lung cancer patients treated with ICIs, which may be correlated with high levels of serum albumin and creatinine.
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页数:10
相关论文
共 40 条
  • [21] Targeting monocyte-intrinsic enhancer reprogramming improves immunotherapy efficacy in hepatocellular carcinoma
    Liu, Man
    Zhou, Jingying
    Liu, Xiaoyu
    Feng, Yu
    Yang, Weiqin
    Wu, Feng
    Cheung, Otto Ka-Wing
    Sun, Hanyong
    Zeng, Xuezhen
    Tang, Wenshu
    Mok, Myth T. S.
    Wong, John
    Yeung, Philip Chun
    Lai, Paul Bo San
    Chen, Zhiwei
    Jin, Hongchuan
    Chen, Jie
    Chan, Stephen Lam
    Chan, Anthony W. H.
    To, Ka Fai
    Sung, Joseph J. Y.
    Chen, Minhu
    Cheng, Alfred Sze-Lok
    [J]. GUT, 2020, 69 (02) : 365 - 379
  • [22] Association of body-mass index and outcomes in patients with metastatic melanoma treated with targeted therapy, immunotherapy, or chemotherapy: a retrospective, multicohort analysis
    McQuade, Jennifer L.
    Daniel, Carrie R.
    Hess, Kenneth R.
    Mak, Carmen
    Wang, Daniel Y.
    Rai, Rajat R.
    Park, John J.
    Haydu, Lauren E.
    Spencer, Christine
    Wongchenko, Matthew
    Lane, Stephen
    Lee, Dung-Yang
    Kaper, Mathilde
    McKean, Meredith
    Beckermann, Kathryn E.
    Rubinstein, Samuel M.
    Rooney, Isabelle
    Musib, Luna
    Budha, Nageshwar
    Hsu, Jessie
    Nowicki, Theodore S.
    Avila, Alexandre
    Haas, Tomas
    Puligandla, Maneka
    Lee, Sandra
    Fang, Shenying
    Wargo, Jennifer A.
    Gershenwald, Jeffrey E.
    Lee, Jeffrey E.
    Hwu, Patrick
    Chapman, Paul B.
    Sosman, Jeffrey A.
    Schadendorf, Dirk
    Grob, Jean-Jacques
    Flaherty, Keith T.
    Walker, Dana
    Yan, Yibing
    McKenna, Edward
    Legos, Jeffrey J.
    Carlino, Matteo S.
    Ribas, Antoni
    Kirkwood, John M.
    Long, Georgina V.
    Johnson, Douglas B.
    Menzies, Alexander M.
    Davies, Michael A.
    [J]. LANCET ONCOLOGY, 2018, 19 (03) : 310 - 322
  • [23] Parkin D. M., 1999, CA Cancer J. Clin, V49, P33, DOI [DOI 10.3322/CANJCLIN.49.1.33, 10.3322/canjclin.49.1.33, DOI 10.3322/CAAC.21492]
  • [24] Serum creatinine as a marker of muscle mass in chronic kidney disease: results of a cross-sectional study and review of literature
    Patel, Sapna S.
    Molnar, Miklos Z.
    Tayek, John A.
    Ix, Joachim H.
    Noori, Nazanin
    Benner, Deborah
    Heymsfield, Steven
    Kopple, Joel D.
    Kovesdy, Csaba P.
    Kalantar-Zadeh, Kamyar
    [J]. JOURNAL OF CACHEXIA SARCOPENIA AND MUSCLE, 2013, 4 (01) : 19 - 29
  • [25] Peripheral Blood Markers Identify Risk of Immune-Related Toxicity in Advanced Non-Small Cell Lung Cancer Treated with Immune-Checkpoint Inhibitors
    Pavana, Alberto
    Calvettid, Lorenzo
    Dal Masoa, Alessandro
    Attilia, Ilaria
    Del Biancob, Paola
    Paselloa, Giulia
    Guarneria, Valentina
    Apriled, Giuseppe
    Conte, PierFranco
    Bonanno, Laura
    [J]. ONCOLOGIST, 2019, 24 (08) : 1128 - 1136
  • [26] Understanding cachexia as a cancer metabolism syndrome
    Porporato, P. E.
    [J]. ONCOGENESIS, 2016, 5 : e200 - e200
  • [27] Lean Tissue Imaging: A New Era for Nutritional Assessment and Intervention
    Prado, Carla M. M.
    Heymsfield, Steven B.
    [J]. JOURNAL OF PARENTERAL AND ENTERAL NUTRITION, 2014, 38 (08) : 940 - 953
  • [28] Chronic inflammation: key player and biomarker-set to predict and prevent cancer development and progression based on individualized patient profiles
    Qian, Shehua
    Golubnitschaja, Olga
    Zhan, Xianquan
    [J]. EPMA JOURNAL, 2019, 10 (04) : 365 - 381
  • [29] Subpopulations of myeloid-derived suppressor cells impair T cell responses through independent nitric oxide-related pathways
    Raber, Patrick L.
    Thevenot, Paul
    Sierra, Rosa
    Wyczechowska, Dorota
    Halle, Daniel
    Ramirez, Maria E.
    Ochoa, Augusto C.
    Fletcher, Matthew
    Velasco, Cruz
    Wilk, Anna
    Reiss, Krzysztof
    Rodriguez, Paulo C.
    [J]. INTERNATIONAL JOURNAL OF CANCER, 2014, 134 (12) : 2853 - 2864
  • [30] Tumor and Microenvironment Evolution during Immunotherapy with Nivolumab
    Riaz, Nadeem
    Havel, Jonathan J.
    Makarov, Vladimir
    Desrichard, Alexis
    Urba, Walter J.
    Sims, Jennifer S.
    Hodi, F. Stephen
    Martin-Algarra, Salvador
    Mandal, Rajarsi
    Sharfman, William H.
    Bhatia, Shailender
    Hwu, Wen-Jen
    Gajewski, Thomas F.
    Slingluff, Craig L., Jr.
    Chowell, Diego
    Kendall, Sviatoslav M.
    Chang, Han
    Shah, Rachna
    Kuo, Fengshen
    Morris, Luc G. T.
    Sidhom, John-William
    Schneck, Jonathan P.
    Horak, Christine E.
    Weinhold, Nils
    Chan, Timothy A.
    [J]. CELL, 2017, 171 (04) : 934 - +