The Tumor Immune Microenvironment Is Associated With Recurrence in Early-Stage Lung Adenocarcinoma

被引:3
作者
Kanemura, Hiroaki [1 ]
Yokoyama, Toshihide [2 ]
Nakajima, Ryu [3 ]
Nakamura, Atsushi [4 ]
Kuroda, Hiroaki [5 ]
Kitamura, Yoshitaka [6 ]
Shoda, Hiroyasu [7 ]
Mamesaya, Nobuaki [8 ]
Miyata, Yoshihiro [9 ]
Okamoto, Tatsuro [10 ]
Okishio, Kyoichi [11 ]
Oki, Masahide [12 ]
Sakairi, Yuichi [13 ]
Chen-Yoshikawa, Toyofumi Fengshi [14 ]
Aoki, Tadashi [15 ]
Ohira, Tatsuo [16 ]
Matsumoto, Isao [17 ]
Ueno, Kiyonobu [18 ]
Miyazaki, Takuro [19 ]
Matsuguma, Haruhisa [20 ]
Yokouchi, Hideoki [21 ]
Otani, Tomoyuki [22 ]
Ito, Akihiko [22 ]
Sakai, Kazuko [23 ]
Chiba, Yasutaka [24 ]
Nishio, Kazuto [23 ]
Yamamoto, Nobuyuki [25 ]
Okamoto, Isamu [26 ]
Nakagawa, Kazuhiko [1 ]
Takeda, Masayuki [1 ,27 ]
机构
[1] Kindai Univ, Fac Med, Dept Med Oncol, 377-2 Ohno Higashi, Osakasayama, Osaka 5898511, Japan
[2] Kurashiki Cent Hosp, Dept Resp Med, Kurashiki, Japan
[3] Osaka City Gen Hosp, Dept Gen Thorac Surg, Osaka, Japan
[4] Sendai Kousei Hosp, Dept Pulm Med, Sendai, Japan
[5] Aichi Canc Ctr Hosp, Dept Thorac Surg, Nagoya, Japan
[6] Hyogo Canc Ctr, Div Chest Surg, Akashi, Japan
[7] Hiroshima City Hiroshima Citizen Hosp, Dept Resp Med, Hiroshima, Japan
[8] Shizuoka Canc Ctr, Div Thorac Oncol, Shizuoka, Japan
[9] Hiroshima Univ, Dept Surg Oncol, Hiroshima, Japan
[10] NHO Kyushu Canc Ctr, Dept Thorac Oncol, Fukuoka, Japan
[11] NHO Kinki Chuo Chest Med Ctr, Dept Clin Res Ctr, Osaka, Japan
[12] NHO Nagoya Med Ctr, Dept Resp Med, Nagoya, Japan
[13] Chiba Univ, Grad Sch Med, Dept Gen Thorac Surg, Chiba, Japan
[14] Nagoya Univ, Grad Sch Med, Dept Thorac Surg, Nagoya, Japan
[15] Niigata Canc Ctr Hosp, Dept Chest Surg, Niigata, Japan
[16] Tokyo Med Univ, Dept Surg, Tokyo, Japan
[17] Kanazawa Univ, Dept Thorac Surg, Kanazawa, Japan
[18] Osaka Gen Med Ctr, Dept Resp Med, Osaka, Japan
[19] Nagasaki Univ, Grad Sch Biomed Sci, Dept Surg Oncol, Nagasaki, Japan
[20] Tochigi Canc Ctr, Dept Thorac Surg, Utsunomiya, Japan
[21] Suita Municipal Hosp, Dept Surg, Osaka, Japan
[22] Kindai Univ, Dept Pathol, Fac Med, Osaka, Japan
[23] Kindai Univ, Fac Med, Dept Genome Biol, Osakasayama, Japan
[24] Kindai Univ Hosp, Clin Res Ctr, Osakasayama, Japan
[25] Wakayama Med Univ, Internal Med 3, Wakayama, Japan
[26] Kyushu Univ, Grad Sch Med Sci, Dept Resp Med, Fukuoka, Japan
[27] Nara Med Univ, Dept Canc Genom & Med Oncol, Nara, Japan
关键词
Non -small cell lung cancer; Adjuvant chemotherapy; Cancer stem cell; Tumor immune microenvironment; CANCER STEM-CELLS; POOLED ANALYSIS; TP53; MUTATIONS; EXPRESSION; INFILTRATION; CHEMOTHERAPY; THERAPY; TRIALS;
D O I
10.1016/j.jtocrr.2024.100658
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Immune checkpoint inhibitors have recently been approved for the treatment of early -stage NSCLC in the perioperative setting on the basis of phase 3 trials. However, the characteristics of such patients who are susceptible to recurrence after adjuvant chemotherapy or who are likely to benefit from postoperative immunotherapy have remained unclear. Methods: This biomarker study (WJOG12219LTR) was designed to evaluate cancer stem cell markers (CD44 and CD133), programmed death-ligand 1 (PD -L1) expression on tumor cells, CD8 expression on tumor -infiltrating lymphocytes, and tumor mutation burden in completely resected stage II to IIIA NSCLC with the use of archived DNA and tissue samples from the prospective WJOG4107 trial. Tumors were classified as inflamed or noninflamed on the basis of the PD -L1 tumor proportion score and CD8 & thorn; tumorinfiltrating lymphocyte density. The association between each potential biomarker and relapse -free survival (RFS) during adjuvant chemotherapy was assessed by KaplanMeier analysis. Results: A total of 117 patients were included in this study. The median RFS was not reached (95% confidence intervals [CI]: 22.4 mo -not reached; n = 39) and 23.7 months (95% CI: 14.5 -43.6; n = 41) in patients with inflamed or noninflamed adenocarcinoma, respectively (log -rank p = 0.02, hazard ratio of 0.52 [95% CI: 0.29 -0.93]). Analysis of the combination of tumor inflammation category and TP53 mutation status revealed that inflamed tumors without TP53 mutations were associated with the longest RFS. Conclusions: PD -L1 expression on tumor cells, CD8 & thorn; T cell infiltration, and TP53 mutation status may help identify patients with early -stage NSCLC susceptible to recurrence after adjuvant chemotherapy. (c) 2024 The Authors. Published by Elsevier Inc. on behalf of the International Association for the Study of Lung Cancer. This is an open access article under the CC BY -NC -ND license (http://creativecommons.org/licenses/by-nc-nd/ 4.0/).
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页数:11
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共 35 条
[1]   The prognostic significance of aldehyde dehydrogenase 1A1 (ALDH1A1) and CD133 expression in early stage non-small cell lung cancer [J].
Alamgeer, Muhammad ;
Ganju, Vinod ;
Szczepny, Anette ;
Russell, Prudence A. ;
Prodanovic, Zdenka ;
Kumar, Beena ;
Wainer, Zoe ;
Brown, Tracey ;
Schneider-Kolsky, Michal ;
Conron, Matthew ;
Wright, Gavin ;
Watkins, D. Neil .
THORAX, 2013, 68 (12) :1095-1104
[2]   Association of PD-L1 overexpression with activating EGFR mutations in surgically resected nonsmall- cell lung cancer [J].
Azuma, K. ;
Ota, K. ;
Kawahara, A. ;
Hattori, S. ;
Iwama, E. ;
Harada, T. ;
Matsumoto, K. ;
Takayama, K. ;
Takamori, S. ;
Kage, M. ;
Hoshino, T. ;
Nakanishi, Y. ;
Okamoto, I. .
ANNALS OF ONCOLOGY, 2014, 25 (10) :1935-1940
[3]   Cancer stem cells revisited [J].
Batlle, Eduard ;
Clevers, Hans .
NATURE MEDICINE, 2017, 23 (10) :1124-1134
[4]   Cancer stem cell-immune cell crosstalk in tumour progression [J].
Bayik, Defne ;
Lathia, Justin D. .
NATURE REVIEWS CANCER, 2021, 21 (08) :526-536
[5]   Nivolumab versus Docetaxel in Advanced Nonsquamous Non-Small-Cell Lung Cancer [J].
Borghaei, H. ;
Paz-Ares, L. ;
Horn, L. ;
Spigel, D. R. ;
Steins, M. ;
Ready, N. E. ;
Chow, L. Q. ;
Vokes, E. E. ;
Felip, E. ;
Holgado, E. ;
Barlesi, F. ;
Kohlhaeufl, M. ;
Arrieta, O. ;
Burgio, M. A. ;
Fayette, J. ;
Lena, H. ;
Poddubskaya, E. ;
Gerber, D. E. ;
Gettinger, S. N. ;
Rudin, C. M. ;
Rizvi, N. ;
Crino, L. ;
Blumenschein, G. R. ;
Antonia, S. J. ;
Dorange, C. ;
Harbison, C. T. ;
Finckenstein, F. Graf ;
Brahmer, J. R. .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 373 (17) :1627-1639
[6]   Prognostic Effect of Tumor Lymphocytic Infiltration in Resectable Non-Small-Cell Lung Cancer [J].
Brambilla, Elisabeth ;
Le Teuff, Gwenael ;
Marguet, Sophie ;
Lantuejoul, Sylvie ;
Dunant, Ariane ;
Graziano, Stephen ;
Pirker, Robert ;
Douillard, Jean-Yves ;
Le Chevalier, Thierry ;
Filipits, Martin ;
Rosell, Rafael ;
Kratzke, Robert ;
Popper, Helmut ;
Soria, Jean-Charles ;
Shepherd, Frances A. ;
Seymour, Lesley ;
Tsao, Ming Sound .
JOURNAL OF CLINICAL ONCOLOGY, 2016, 34 (11) :1223-+
[7]   Evolution of systemic therapy for stages I-III non-metastatic non-small-cell lung cancer [J].
Chaft, Jamie E. ;
Rimner, Andreas ;
Weder, Walter ;
Azzoli, Christopher G. ;
Kris, Mark G. ;
Cascone, Tina .
NATURE REVIEWS CLINICAL ONCOLOGY, 2021, 18 (09) :547-557
[8]   Targeting signalling pathways and the immune microenvironment of cancer stem cells - a clinical update [J].
Clara, Joseph A. ;
Monge, Cecilia ;
Yang, Yingzi ;
Takebe, Naoko .
NATURE REVIEWS CLINICAL ONCOLOGY, 2020, 17 (04) :204-232
[9]   The cancer stem cell: premises, promises and challenges [J].
Clevers, Hans .
NATURE MEDICINE, 2011, 17 (03) :313-319
[10]   Tumor Mutation Burden as a Biomarker in Resected Non-Small-Cell Lung Cancer [J].
Devarakonda, Siddhartha ;
Rotolo, Federico ;
Tsao, Ming-Sound ;
Lanc, Irena ;
Brambilla, Elisabeth ;
Masood, Ashiq ;
Olaussen, Ken A. ;
Fulton, Robert ;
Sakashita, Shingo ;
McLeer-Florin, Anne ;
Ding, Keyue ;
Le Teuff, Gwenael ;
Shepherd, Frances A. ;
Pignon, Jean-Pierre ;
Graziano, Stephen L. ;
Kratzke, Robert ;
Soria, Jean-Charles ;
Seymour, Lesley ;
Govindan, Ramaswamy ;
Michiels, Stefan .
JOURNAL OF CLINICAL ONCOLOGY, 2018, 36 (30) :2995-+