Impact of chemoradiotherapy on the immune-related tumour microenvironment and efficacy of anti-PD-(L)1 therapy for recurrences after chemoradiotherapy in patients with unresectable locally advanced non-small cell lung cancer

A history of radiotherapy and chemoradiotherapy (CRT) reportedly increases the efficacy of the PD-1 blockade in patients with advanced non-small cell lung cancer (NSCLC). We investigated the efficacy of anti-PD-(L)1 therapy after CRT failure and how CRT changes the status of PD-L1 expression on tumo...

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Veröffentlicht in:European journal of cancer (1990) 2020-11, Vol.140, p.28-36
Hauptverfasser: Shirasawa, Masayuki, Yoshida, Tatsuya, Matsumoto, Yuji, Shinno, Yuki, Okuma, Yusuke, Goto, Yasushi, Horinouchi, Hidehito, Yamamoto, Noboru, Watanabe, Shun-ichi, Ohe, Yuichiro, Motoi, Noriko
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container_title European journal of cancer (1990)
container_volume 140
creator Shirasawa, Masayuki
Yoshida, Tatsuya
Matsumoto, Yuji
Shinno, Yuki
Okuma, Yusuke
Goto, Yasushi
Horinouchi, Hidehito
Yamamoto, Noboru
Watanabe, Shun-ichi
Ohe, Yuichiro
Motoi, Noriko
description A history of radiotherapy and chemoradiotherapy (CRT) reportedly increases the efficacy of the PD-1 blockade in patients with advanced non-small cell lung cancer (NSCLC). We investigated the efficacy of anti-PD-(L)1 therapy after CRT failure and how CRT changes the status of PD-L1 expression on tumours and on tumour-infiltrated lymphocytes (TILs). We retrospectively reviewed patients with unresectable locally advanced NSCLC (LA-NSCLC) who were treated with CRT between 2007 and 2018 and evaluated the efficacy of the PD-(L)1 blockade after CRT failure. We also compared the PD-L1 (clone: 22C3) expression levels and the tumoral and stromal distributions of CD8-positive TILs using paired formalin-fixed, paraffin-embedded specimens obtained before and after CRT. We identified 422 patients and 65 patients who had relapsed after CRT received anti-PD-(L)1 therapy. The objective response rate (ORR) and the progression-free survival (PFS) after anti-PD-(L)1 therapy were 48% and 8.7 months (95% CI, 4.5–13), respectively. The RR and PFS did not differ according to the pre-CRT PD-L1 expression levels. PD-L1 expression changed in 16 of the 18 patients between before and after CRT, but a specific trend was not seen (increased, 9 patients; decreased, 7 patients; no change, 2 patients). In contrast, the density of tumoral CD8-positive TILs increased after CRT treatment (pre-CRT median, 110/mm2 versus post-CRT median, 470/mm2; p = 0.025). Anti-PD-(L)1 therapy was effective in patients with LA-NSCLC who had progressed after CRT regardless of their pre-CRT PD-L1 expression. The efficacy of anti-PD-(L)1 therapy for patients with NSCLC with CRT failure was superior to that of standard second-line treatment for patients with advanced NSCLC. •We evaluated the efficacy of anti–PD-(L)1 therapy after chemoradiotherapy (CRT) failure in locally advanced non-small cell carcinoma (LA-NSCLC).•Anti-PD-(L)1 therapy after CRT failure in LA-NSCLC was effective.•The density of tumoral CD8-positive tumour-infiltrated lymphocytes increased after CRT treatment.•The efficacy did not differ in accordance with PD-L1 expression at baseline.•The efficacy was compared favourably with that of second-line therapy in advanced NSCLC.
doi_str_mv 10.1016/j.ejca.2020.08.028
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PD-L1 expression changed in 16 of the 18 patients between before and after CRT, but a specific trend was not seen (increased, 9 patients; decreased, 7 patients; no change, 2 patients). In contrast, the density of tumoral CD8-positive TILs increased after CRT treatment (pre-CRT median, 110/mm2 versus post-CRT median, 470/mm2; p = 0.025). Anti-PD-(L)1 therapy was effective in patients with LA-NSCLC who had progressed after CRT regardless of their pre-CRT PD-L1 expression. 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All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. 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The efficacy of anti-PD-(L)1 therapy for patients with NSCLC with CRT failure was superior to that of standard second-line treatment for patients with advanced NSCLC. •We evaluated the efficacy of anti–PD-(L)1 therapy after chemoradiotherapy (CRT) failure in locally advanced non-small cell carcinoma (LA-NSCLC).•Anti-PD-(L)1 therapy after CRT failure in LA-NSCLC was effective.•The density of tumoral CD8-positive tumour-infiltrated lymphocytes increased after CRT treatment.•The efficacy did not differ in accordance with PD-L1 expression at baseline.•The efficacy was compared favourably with that of second-line therapy in advanced NSCLC.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Anti-PD-(L)1 therapy</subject><subject>Antineoplastic Agents - therapeutic use</subject><subject>B7-H1 Antigen - metabolism</subject><subject>Carcinoma, Non-Small-Cell Lung - metabolism</subject><subject>Carcinoma, Non-Small-Cell Lung - therapy</subject><subject>CD8</subject><subject>CD8 antigen</subject><subject>CD8-Positive T-Lymphocytes - drug effects</subject><subject>CD8-Positive T-Lymphocytes - metabolism</subject><subject>CD8-Positive T-Lymphocytes - radiation effects</subject><subject>Chemoradiotherapy</subject><subject>Chemoradiotherapy - methods</subject><subject>Chemotherapy</subject><subject>Failure</subject><subject>Female</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Locally advanced non-small cell lung cancer</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - therapy</subject><subject>Lymphocytes</subject><subject>Lymphocytes, Tumor-Infiltrating - drug effects</subject><subject>Lymphocytes, Tumor-Infiltrating - metabolism</subject><subject>Lymphocytes, Tumor-Infiltrating - radiation effects</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasm Recurrence, Local - metabolism</subject><subject>Neoplasm Recurrence, Local - therapy</subject><subject>Non-small cell lung carcinoma</subject><subject>Paraffin</subject><subject>Paraffins</subject><subject>PD-1 protein</subject><subject>PD-L1 expression</subject><subject>PD-L1 protein</subject><subject>Progression-Free Survival</subject><subject>Radiation therapy</subject><subject>Retrospective Studies</subject><subject>Small cell lung carcinoma</subject><subject>Tumor microenvironment</subject><subject>Tumor Microenvironment - drug effects</subject><subject>Tumor Microenvironment - radiation effects</subject><subject>Tumors</subject><subject>Tumour-infiltrated lymphocytes</subject><issn>0959-8049</issn><issn>1879-0852</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kc-OFCEQxonRuLOjL-DBkHjRQ49F_6UTL2Z1dZNJ9KBnwkDh0OmGFugx87Y-inRm15PxQhHqq1-F7yPkBYMdA9a-HXY4KLkroYQd8B2U_BHZMN71BfCmfEw20Dd9waHur8h1jAMAdLyGp-SqqqDqOWMb8vtumqVK1Buqjjj5ILX16YhBzmfqHc1XaqdpcVgEHGVCTdMy-SXQyarg0Z1s8G5Cl6h0mqIxVkl1XnnSJVt8_VC83r9h9AFpfKAB1RICOoWRSpMw_GO1dXSWyWZupL9sOtLFBYyokjyMSEev5DieqdQnmTGaOu-KOOU3qjAf4-J-ULW2wjPyxMgx4vP7uiXfbz9-u_lc7L98urt5vy9UXfJUYGOkQY0N48wwNG1Tq75kUDZgeAcMgTFT9brGpmua5qBlfUBWdbqFqm5ZX23Jqwt3Dv7ngjGJIbvk8kpR1i2vemizdEvKiyp7F2NAI-ZgJxnOgoFYQxWDWEMVa6gCuMih5qGX9-jlMKH-O_KQYha8uwgwf_BkMYio7OqvttnrJLS3_-P_ASjRuIo</recordid><startdate>202011</startdate><enddate>202011</enddate><creator>Shirasawa, Masayuki</creator><creator>Yoshida, Tatsuya</creator><creator>Matsumoto, Yuji</creator><creator>Shinno, Yuki</creator><creator>Okuma, Yusuke</creator><creator>Goto, Yasushi</creator><creator>Horinouchi, Hidehito</creator><creator>Yamamoto, Noboru</creator><creator>Watanabe, Shun-ichi</creator><creator>Ohe, Yuichiro</creator><creator>Motoi, Noriko</creator><general>Elsevier Ltd</general><general>Elsevier Science Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TO</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>NAPCQ</scope><orcidid>https://orcid.org/0000-0001-7098-3311</orcidid><orcidid>https://orcid.org/0000-0002-6137-073X</orcidid></search><sort><creationdate>202011</creationdate><title>Impact of chemoradiotherapy on the immune-related tumour microenvironment and efficacy of anti-PD-(L)1 therapy for recurrences after chemoradiotherapy in patients with unresectable locally advanced non-small cell lung cancer</title><author>Shirasawa, Masayuki ; 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We investigated the efficacy of anti-PD-(L)1 therapy after CRT failure and how CRT changes the status of PD-L1 expression on tumours and on tumour-infiltrated lymphocytes (TILs). We retrospectively reviewed patients with unresectable locally advanced NSCLC (LA-NSCLC) who were treated with CRT between 2007 and 2018 and evaluated the efficacy of the PD-(L)1 blockade after CRT failure. We also compared the PD-L1 (clone: 22C3) expression levels and the tumoral and stromal distributions of CD8-positive TILs using paired formalin-fixed, paraffin-embedded specimens obtained before and after CRT. We identified 422 patients and 65 patients who had relapsed after CRT received anti-PD-(L)1 therapy. The objective response rate (ORR) and the progression-free survival (PFS) after anti-PD-(L)1 therapy were 48% and 8.7 months (95% CI, 4.5–13), respectively. The RR and PFS did not differ according to the pre-CRT PD-L1 expression levels. PD-L1 expression changed in 16 of the 18 patients between before and after CRT, but a specific trend was not seen (increased, 9 patients; decreased, 7 patients; no change, 2 patients). In contrast, the density of tumoral CD8-positive TILs increased after CRT treatment (pre-CRT median, 110/mm2 versus post-CRT median, 470/mm2; p = 0.025). Anti-PD-(L)1 therapy was effective in patients with LA-NSCLC who had progressed after CRT regardless of their pre-CRT PD-L1 expression. 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identifier ISSN: 0959-8049
ispartof European journal of cancer (1990), 2020-11, Vol.140, p.28-36
issn 0959-8049
1879-0852
language eng
recordid cdi_proquest_journals_2468390660
source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Adult
Aged
Aged, 80 and over
Anti-PD-(L)1 therapy
Antineoplastic Agents - therapeutic use
B7-H1 Antigen - metabolism
Carcinoma, Non-Small-Cell Lung - metabolism
Carcinoma, Non-Small-Cell Lung - therapy
CD8
CD8 antigen
CD8-Positive T-Lymphocytes - drug effects
CD8-Positive T-Lymphocytes - metabolism
CD8-Positive T-Lymphocytes - radiation effects
Chemoradiotherapy
Chemoradiotherapy - methods
Chemotherapy
Failure
Female
Humans
Immunotherapy
Locally advanced non-small cell lung cancer
Lung cancer
Lung Neoplasms - metabolism
Lung Neoplasms - therapy
Lymphocytes
Lymphocytes, Tumor-Infiltrating - drug effects
Lymphocytes, Tumor-Infiltrating - metabolism
Lymphocytes, Tumor-Infiltrating - radiation effects
Male
Middle Aged
Neoplasm Recurrence, Local - metabolism
Neoplasm Recurrence, Local - therapy
Non-small cell lung carcinoma
Paraffin
Paraffins
PD-1 protein
PD-L1 expression
PD-L1 protein
Progression-Free Survival
Radiation therapy
Retrospective Studies
Small cell lung carcinoma
Tumor microenvironment
Tumor Microenvironment - drug effects
Tumor Microenvironment - radiation effects
Tumors
Tumour-infiltrated lymphocytes
title Impact of chemoradiotherapy on the immune-related tumour microenvironment and efficacy of anti-PD-(L)1 therapy for recurrences after chemoradiotherapy in patients with unresectable locally advanced non-small cell lung cancer
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