Yu Jin Lim1, Jaemoon Koh2, Kyubo Kim3, Eui Kyu Chie4, BoKyong Kim5, Kyoung Bun Lee6, Jin-Young Jang7, Sun-Whe Kim8, Do-Youn Oh9, Yung-Jue Bang10, Sung W Ha11. 1. Department of Radiation Oncology, Seoul National University College of Medicine, Republic of Korea. Electronic address: yujindw@gmail.com. 2. Department of Pathology, Seoul National University College of Medicine, Republic of Korea. Electronic address: tarda@naver.com. 3. Department of Radiation Oncology, Seoul National University College of Medicine, Republic of Korea. Electronic address: kyubokim@snu.ac.kr. 4. Department of Radiation Oncology, Seoul National University College of Medicine, Republic of Korea; Institute of Radiation Medicine, Medical Research Center, Seoul National University, Republic of Korea. Electronic address: ekchie93@snu.ac.kr. 5. Department of Radiation Oncology, Seoul National University College of Medicine, Republic of Korea. Electronic address: merdeglas@hanmail.net. 6. Department of Pathology, Seoul National University College of Medicine, Republic of Korea. Electronic address: kblee@snuh.org. 7. Department of Surgery, Seoul National University College of Medicine, Republic of Korea. Electronic address: jangjy4@gmail.com. 8. Department of Surgery, Seoul National University College of Medicine, Republic of Korea. Electronic address: sunkim@snu.ac.kr. 9. Department of Internal Medicine, Seoul National University College of Medicine, Republic of Korea. Electronic address: ohdoyoun@snu.ac.kr. 10. Department of Internal Medicine, Seoul National University College of Medicine, Republic of Korea. Electronic address: bangyj@snu.ac.kr. 11. Department of Radiation Oncology, Seoul National University College of Medicine, Republic of Korea; Institute of Radiation Medicine, Medical Research Center, Seoul National University, Republic of Korea. Electronic address: swha@snu.ac.kr.
Abstract
BACKGROUND AND PURPOSE: This study investigated the prognostic role of PD-L1 expression, PD-1(+) tumor-infiltrating lymphocytes (TILs), and the ratio of PD-1(+)/CD8(+) TILs in extrahepatic bile duct (EHBD) cancer. MATERIALS AND METHODS: We analyzed 83 patients with EHBD cancer who underwent curative surgery plus fluoropyrimidine-based chemoradiotherapy (CRT). Expressions of PD-L1, PD-1, and CD8 were assessed by immunohistochemistry. RESULTS: Fifty-six (68%) patients were PD-L1-positive, and its lower expression level was associated with hilar tumor location (P=0.044). A higher ratio of PD-1(+)/CD8(+) TILs was associated with poorer overall survival (OS) (P=0.032), relapse-free survival (RFS) (P=0.024), and distant metastasis-free survival (DMFS) (P=0.039) in Kaplan-Meier analyses, but survival differences were not observed according to the PD-L1 expression level. With Cox proportional hazards models, the ratio of PD-1(+)/CD8(+) TILs was the independent prognostic factor in OS (HR 2.47, 95% CI 1.04-5.86), RFS (HR 2.41, 95% CI 1.08-5.41), and DMFS (HR 2.67, 95% CI 1.00-7.11) after adjusting for other significant clinicopathologic variables. CONCLUSION: A strong survival impact of the ratio of PD-1(+)/CD8(+) TILs was observed in EHBD cancer. In the poor prognostic subgroup, the blockade of the immune checkpoint in combination with conventional multimodality treatment needs to be considered.
BACKGROUND AND PURPOSE: This study investigated the prognostic role of PD-L1 expression, PD-1(+) tumor-infiltrating lymphocytes (TILs), and the ratio of PD-1(+)/CD8(+) TILs in extrahepatic bile duct (EHBD) cancer. MATERIALS AND METHODS: We analyzed 83 patients with EHBD cancer who underwent curative surgery plus fluoropyrimidine-based chemoradiotherapy (CRT). Expressions of PD-L1, PD-1, and CD8 were assessed by immunohistochemistry. RESULTS: Fifty-six (68%) patients were PD-L1-positive, and its lower expression level was associated with hilar tumor location (P=0.044). A higher ratio of PD-1(+)/CD8(+) TILs was associated with poorer overall survival (OS) (P=0.032), relapse-free survival (RFS) (P=0.024), and distant metastasis-free survival (DMFS) (P=0.039) in Kaplan-Meier analyses, but survival differences were not observed according to the PD-L1 expression level. With Cox proportional hazards models, the ratio of PD-1(+)/CD8(+) TILs was the independent prognostic factor in OS (HR 2.47, 95% CI 1.04-5.86), RFS (HR 2.41, 95% CI 1.08-5.41), and DMFS (HR 2.67, 95% CI 1.00-7.11) after adjusting for other significant clinicopathologic variables. CONCLUSION: A strong survival impact of the ratio of PD-1(+)/CD8(+) TILs was observed in EHBD cancer. In the poor prognostic subgroup, the blockade of the immune checkpoint in combination with conventional multimodality treatment needs to be considered.
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