Evaluation of Treatment Outcomes Using dNLR and GNRI in Combination Therapy With Atezolizumab and Bevacizumab for Hepatocellular Carcinoma

被引:0
作者
Naganuma, Atsushi [1 ]
Kakizaki, Satoru [2 ,3 ]
Hiraoka, Atsushi [4 ]
Tada, Toshifumi [5 ]
Hatanaka, Takeshi [6 ]
Kariyama, Kazuya [7 ]
Tani, Joji [8 ]
Atsukawa, Masanori [9 ]
Takaguchi, Koichi [10 ]
Itobayashi, Ei [11 ]
Fukunishi, Shinya [12 ]
Tsuji, Kunihiko [13 ]
Ishikawa, Toru [14 ]
Tajiri, Kazuto [15 ]
Toyoda, Hidenori [16 ]
Ogawa, Chikara [17 ]
Nishikawa, Hiroki [18 ]
Nishimura, Takashi [12 ]
Kawata, Kazuhito [19 ]
Kosaka, Hisashi [20 ]
Hirooka, Masashi [21 ]
Yata, Yutaka [22 ]
Ohama, Hideko [23 ]
Kuroda, Hidekatsu [24 ]
Matono, Tomomitsu [25 ]
Aoki, Tomoko [26 ]
Kanayama, Yuki [6 ]
Tanaka, Kazunari [13 ]
Tada, Fujimasa [4 ]
Nouso, Kazuhiro [7 ]
Morishita, Asahiro [8 ]
Tsutsui, Akemi [10 ]
Nagano, Takuya [10 ]
Itokawa, Norio [9 ]
Okubo, Tomomi [9 ]
Arai, Taeang [9 ]
Imai, Michitaka [14 ]
Nakamura, Shinichiro [5 ]
Enomoto, Hirayuki [12 ]
Kaibori, Masaki [20 ]
Hiasa, Yoichi [21 ]
Kudo, Masatoshi [26 ]
Kumada, Takashi [27 ]
机构
[1] NHO Takasaki Gen Med Ctr, Dept Gastroenterol, Takasaki, Japan
[2] NHO Takasaki Gen Med Ctr, Dept Clin Res, Takasaki, Japan
[3] Gunma Univ, Grad Sch Med, Dept Gastroenterol & Hepatol, Maebashi, Japan
[4] Ehime Prefectural Cent Hosp, Gastroenterol Ctr, Matsuyama, Ehime, Japan
[5] Japanese Red Cross Himeji Hosp, Dept Internal Med, Himeji, Japan
[6] Gunma Saiseikai Maebashi Hosp, Dept Gastroenterol, Maebashi, Japan
[7] Okayama City Hosp, Dept Gastroenterol, Okayama, Japan
[8] Kagawa Univ, Dept Gastroenterol & Neurol, Takamatsu, Kagawa, Japan
[9] Nippon Med Sch, Dept Internal Med, Div Gastroenterol & Hepatol, Tokyo, Japan
[10] Kagawa Prefectural Cent Hosp, Dept Hepatol, Takamatsu, Japan
[11] Asahi Gen Hosp, Dept Gastroenterol, Asahi 2892511, Japan
[12] Hyogo Med Univ, Dept Gastroenterol, Div Hepatobiliary & Pancreat Dis, Nishinomiya, Japan
[13] Teine Keijinkai Hosp, Ctr Gastroenterol, Sapporo, Japan
[14] Saiseikai Niigata Hosp, Dept Gastroenterol, Niigata, Japan
[15] Toyama Univ Hosp, Dept Gastroenterol, Toyama, Japan
[16] Ogaki Municipal Hosp, Dept Gastroenterol & Hepatol, Ogaki, Japan
[17] Takamatsu Red Cross Hosp, Dept Gastroenterol & Hepatol, Takamatsu, Japan
[18] Osaka Med & Pharmaceut Univ, Dept Gastroenterol, Osaka, Japan
[19] Hamamatsu Univ Sch Med, Dept Internal Med 2, Hepatol Div, Hamamatsu, Shizuoka, Japan
[20] Kansai Med Univ, Dept Gastroenterol, Hirakata, Japan
[21] Ehime Univ, Grad Sch Med, Dept Gastroenterol & Metabol, Matsuyama, Japan
[22] Hanwa Mem Hosp, Dept Gastroenterol, Osaka, Japan
[23] Takarazuka City Hosp, Dept Urol, Takarazuka, Japan
[24] Iwate Med Univ, Dept Internal Med, Div Gastroenterol & Hepatol, Yahaba, Iwate, Japan
[25] Hyogo prefectural Harima Himeji Gen Med Ctr, Dept Gastroenterol, Himeji, Japan
[26] Kindai Univ, Dept Gastroenterol & Hepatol, Fac Med, Osaka, Japan
[27] Gifu Kyoritsu Univ, Ogaki, Japan
来源
CANCER MEDICINE | 2025年 / 14卷 / 02期
关键词
dNLR; GNRI; hepatocellular carcinoma; immune checkpoint inhibitor; prognosis; LYMPHOCYTE RATIO; PLUS BEVACIZUMAB; NEUTROPHIL; CANCER;
D O I
10.1002/cam4.70618
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aim: This study aims to investigate the clinical utility of the derived neutrophil-to-lymphocyte ratio (dNLR) and the Geriatric Nutritional Risk Index (GNRI) in predicting treatment outcomes for patients with unresectable hepatocellular carcinoma (HCC) undergoing combination therapy with atezolizumab and bevacizumab (Atez/Bev). Methods: A retrospective analysis was conducted on 310 patients. The dNLR, NLR, and GNRI were calculated, and their impact on progression-free survival (PFS) and overall survival (OS) was assessed. The formula for calculating dNLR is: (neutrophil count divided by [white blood cell count-neutrophil count]), which means it does not require lymphocyte count. Furthermore, GNRI-dNLR and GNRI-NLR scores were defined, and their prognostic values were also analyzed. Results: The median PFS of this cohort was 7.2 months (95% CI: 5.9-8.5), and the median OS was 24.9 months (95% CI: 19.6-30.2). The dNLR, NLR, and GNRI were significant predictors of both PFS and OS. The dNLR showed a significant correlation with the NLR (Pearson correlation coefficient, p < 0.0001). Patients with high GNRI-dNLR scores demonstrated significantly worse PFS and OS compared to those with low scores (p = 0.001, p < 0.001, respectively). Compared to stratification by GNRI alone, the GNRI-dNLR or GNRI-NLR provided better stratification for both PFS and OS. Conclusion: The dNLR could be a valuable substitute for NLR as a prognostic marker in patients with unresectable HCC undergoing Atez/Bev therapy. It offers a feasible alternative for databases lacking lymphocyte count information, ensuring comprehensive patient stratification and outcome prediction. The GNRI-NLR or GNRI-dNLR score provided better stratification compared to GNRI alone.
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页数:10
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