Hypofractionated radiotherapy plus PD-1 antibody and SOX chemotherapy as second-line therapy in metastatic pancreatic cancer: a single-arm, phase II clinical trial

Purpose To assess the efficacy and safety of concurrent hypofractionated radiotherapy plus anti-PD-1 antibody and SOX chemotherapy in the treatment of metastatic pancreatic cancer (mPC) after failure of first-line chemotherapy. Methods Patients with pathologically confirmed mPC who failed standard f...

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Veröffentlicht in:Cancer Immunology, Immunotherapy : CII Immunotherapy : CII, 2024-08, Vol.73 (10), p.201, Article 201
Hauptverfasser: Wang, Qin, Tong, Fan, Qiao, Li, Qi, Liang, Sun, Yi, Zhu, Yahui, Ni, Jiayao, Liu, Juan, Kong, Weiwei, Liu, Baorui, Du, Juan
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container_issue 10
container_start_page 201
container_title Cancer Immunology, Immunotherapy : CII
container_volume 73
creator Wang, Qin
Tong, Fan
Qiao, Li
Qi, Liang
Sun, Yi
Zhu, Yahui
Ni, Jiayao
Liu, Juan
Kong, Weiwei
Liu, Baorui
Du, Juan
description Purpose To assess the efficacy and safety of concurrent hypofractionated radiotherapy plus anti-PD-1 antibody and SOX chemotherapy in the treatment of metastatic pancreatic cancer (mPC) after failure of first-line chemotherapy. Methods Patients with pathologically confirmed mPC who failed standard first-line chemotherapy were enrolled. The patients were treated with a regimen of hypofractionated radiotherapy, SOX chemotherapy, and immune checkpoint inhibitors at our institution. We collected the patients’ clinical information and outcome measurements. The median progression-free survival (mPFS) was the primary endpoint of the study, followed by disease control rate (DCR), objective response rate (ORR), median overall survival (mOS) and safety. Exploratory analyses included biomarkers related to the benefits. Results Between February 24, 2021, and August 30, 2023, twenty-five patients were enrolled in the study, and twenty-three patients who received at least one dose of the study agent had objective efficacy evaluation. The mPFS was 5.48 months, the mOS was 6.57 months, and the DCR and ORR were 69.5% and 30.4%, respectively. Among the seven patients who achieved a PR, the median duration of the response was 7.41 months. On-treatment decreased serum CA19-9 levels were associated with better overall survival. Besides, pretreatment inflammatory markers were associated with tumor response and survival. Conclusions Clinically meaningful antitumor activity and favorable safety profiles were demonstrated after treatment with these combination therapies in patients with refractory mPC. On-treatment decreased serum CA19-9 levels and pretreatment inflammatory markers platelet-to-lymphocyte ratio (PLR), lymphocyte-to-monocyte ratio (LMR), lactate dehydrogenase (LDH) might be biomarkers related to clinical benefits. Clinical trial registration : https://www.chictr.org.cn/showproj.html?proj=130211 , identifier: ChiCTR2100049799, date of registration: 2021–08-09.
doi_str_mv 10.1007/s00262-024-03744-z
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Methods Patients with pathologically confirmed mPC who failed standard first-line chemotherapy were enrolled. The patients were treated with a regimen of hypofractionated radiotherapy, SOX chemotherapy, and immune checkpoint inhibitors at our institution. We collected the patients’ clinical information and outcome measurements. The median progression-free survival (mPFS) was the primary endpoint of the study, followed by disease control rate (DCR), objective response rate (ORR), median overall survival (mOS) and safety. Exploratory analyses included biomarkers related to the benefits. Results Between February 24, 2021, and August 30, 2023, twenty-five patients were enrolled in the study, and twenty-three patients who received at least one dose of the study agent had objective efficacy evaluation. The mPFS was 5.48 months, the mOS was 6.57 months, and the DCR and ORR were 69.5% and 30.4%, respectively. Among the seven patients who achieved a PR, the median duration of the response was 7.41 months. On-treatment decreased serum CA19-9 levels were associated with better overall survival. Besides, pretreatment inflammatory markers were associated with tumor response and survival. Conclusions Clinically meaningful antitumor activity and favorable safety profiles were demonstrated after treatment with these combination therapies in patients with refractory mPC. On-treatment decreased serum CA19-9 levels and pretreatment inflammatory markers platelet-to-lymphocyte ratio (PLR), lymphocyte-to-monocyte ratio (LMR), lactate dehydrogenase (LDH) might be biomarkers related to clinical benefits. Clinical trial registration : https://www.chictr.org.cn/showproj.html?proj=130211 , identifier: ChiCTR2100049799, date of registration: 2021–08-09.</description><identifier>ISSN: 1432-0851</identifier><identifier>ISSN: 0340-7004</identifier><identifier>EISSN: 1432-0851</identifier><identifier>DOI: 10.1007/s00262-024-03744-z</identifier><identifier>PMID: 39105880</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adult ; Aged ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Antitumor activity ; Biomarkers ; Cancer Research ; Chemoradiotherapy - methods ; Chemotherapy ; Clinical trials ; Disease control ; Female ; Gemcitabine ; Humans ; Immune checkpoint inhibitors ; Immune Checkpoint Inhibitors - therapeutic use ; Immunology ; Inflammation ; L-Lactate dehydrogenase ; Lymphocytes ; Male ; Medicine ; Medicine &amp; Public Health ; Metastases ; Metastasis ; Middle Aged ; Monocytes ; Neoplasm Metastasis ; Oncology ; Oxonic Acid - administration &amp; dosage ; Oxonic Acid - therapeutic use ; Pancreatic cancer ; Pancreatic Neoplasms - drug therapy ; Pancreatic Neoplasms - pathology ; Pancreatic Neoplasms - radiotherapy ; Pancreatic Neoplasms - therapy ; Patients ; PD-1 protein ; Programmed Cell Death 1 Receptor - antagonists &amp; inhibitors ; Radiation Dose Hypofractionation ; Radiation therapy ; Tegafur - administration &amp; dosage ; Tegafur - therapeutic use</subject><ispartof>Cancer Immunology, Immunotherapy : CII, 2024-08, Vol.73 (10), p.201, Article 201</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2024 2024</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c356t-e6d96f8444efef59cc44ce97fb97ad8970bb5da0cf18ac8e5bd690e3972ad4443</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11303639/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC11303639/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,27905,27906,41101,41469,42170,42538,51300,51557,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39105880$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Qin</creatorcontrib><creatorcontrib>Tong, Fan</creatorcontrib><creatorcontrib>Qiao, Li</creatorcontrib><creatorcontrib>Qi, Liang</creatorcontrib><creatorcontrib>Sun, Yi</creatorcontrib><creatorcontrib>Zhu, Yahui</creatorcontrib><creatorcontrib>Ni, Jiayao</creatorcontrib><creatorcontrib>Liu, Juan</creatorcontrib><creatorcontrib>Kong, Weiwei</creatorcontrib><creatorcontrib>Liu, Baorui</creatorcontrib><creatorcontrib>Du, Juan</creatorcontrib><title>Hypofractionated radiotherapy plus PD-1 antibody and SOX chemotherapy as second-line therapy in metastatic pancreatic cancer: a single-arm, phase II clinical trial</title><title>Cancer Immunology, Immunotherapy : CII</title><addtitle>Cancer Immunol Immunother</addtitle><addtitle>Cancer Immunol Immunother</addtitle><description>Purpose To assess the efficacy and safety of concurrent hypofractionated radiotherapy plus anti-PD-1 antibody and SOX chemotherapy in the treatment of metastatic pancreatic cancer (mPC) after failure of first-line chemotherapy. Methods Patients with pathologically confirmed mPC who failed standard first-line chemotherapy were enrolled. The patients were treated with a regimen of hypofractionated radiotherapy, SOX chemotherapy, and immune checkpoint inhibitors at our institution. We collected the patients’ clinical information and outcome measurements. The median progression-free survival (mPFS) was the primary endpoint of the study, followed by disease control rate (DCR), objective response rate (ORR), median overall survival (mOS) and safety. Exploratory analyses included biomarkers related to the benefits. Results Between February 24, 2021, and August 30, 2023, twenty-five patients were enrolled in the study, and twenty-three patients who received at least one dose of the study agent had objective efficacy evaluation. The mPFS was 5.48 months, the mOS was 6.57 months, and the DCR and ORR were 69.5% and 30.4%, respectively. Among the seven patients who achieved a PR, the median duration of the response was 7.41 months. On-treatment decreased serum CA19-9 levels were associated with better overall survival. Besides, pretreatment inflammatory markers were associated with tumor response and survival. Conclusions Clinically meaningful antitumor activity and favorable safety profiles were demonstrated after treatment with these combination therapies in patients with refractory mPC. On-treatment decreased serum CA19-9 levels and pretreatment inflammatory markers platelet-to-lymphocyte ratio (PLR), lymphocyte-to-monocyte ratio (LMR), lactate dehydrogenase (LDH) might be biomarkers related to clinical benefits. 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Public Health</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Middle Aged</topic><topic>Monocytes</topic><topic>Neoplasm Metastasis</topic><topic>Oncology</topic><topic>Oxonic Acid - administration &amp; dosage</topic><topic>Oxonic Acid - therapeutic use</topic><topic>Pancreatic cancer</topic><topic>Pancreatic Neoplasms - drug therapy</topic><topic>Pancreatic Neoplasms - pathology</topic><topic>Pancreatic Neoplasms - radiotherapy</topic><topic>Pancreatic Neoplasms - therapy</topic><topic>Patients</topic><topic>PD-1 protein</topic><topic>Programmed Cell Death 1 Receptor - antagonists &amp; inhibitors</topic><topic>Radiation Dose Hypofractionation</topic><topic>Radiation therapy</topic><topic>Tegafur - administration &amp; dosage</topic><topic>Tegafur - therapeutic use</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Qin</creatorcontrib><creatorcontrib>Tong, Fan</creatorcontrib><creatorcontrib>Qiao, Li</creatorcontrib><creatorcontrib>Qi, Liang</creatorcontrib><creatorcontrib>Sun, Yi</creatorcontrib><creatorcontrib>Zhu, Yahui</creatorcontrib><creatorcontrib>Ni, Jiayao</creatorcontrib><creatorcontrib>Liu, Juan</creatorcontrib><creatorcontrib>Kong, Weiwei</creatorcontrib><creatorcontrib>Liu, Baorui</creatorcontrib><creatorcontrib>Du, Juan</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; 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Methods Patients with pathologically confirmed mPC who failed standard first-line chemotherapy were enrolled. The patients were treated with a regimen of hypofractionated radiotherapy, SOX chemotherapy, and immune checkpoint inhibitors at our institution. We collected the patients’ clinical information and outcome measurements. The median progression-free survival (mPFS) was the primary endpoint of the study, followed by disease control rate (DCR), objective response rate (ORR), median overall survival (mOS) and safety. Exploratory analyses included biomarkers related to the benefits. Results Between February 24, 2021, and August 30, 2023, twenty-five patients were enrolled in the study, and twenty-three patients who received at least one dose of the study agent had objective efficacy evaluation. The mPFS was 5.48 months, the mOS was 6.57 months, and the DCR and ORR were 69.5% and 30.4%, respectively. Among the seven patients who achieved a PR, the median duration of the response was 7.41 months. On-treatment decreased serum CA19-9 levels were associated with better overall survival. Besides, pretreatment inflammatory markers were associated with tumor response and survival. Conclusions Clinically meaningful antitumor activity and favorable safety profiles were demonstrated after treatment with these combination therapies in patients with refractory mPC. On-treatment decreased serum CA19-9 levels and pretreatment inflammatory markers platelet-to-lymphocyte ratio (PLR), lymphocyte-to-monocyte ratio (LMR), lactate dehydrogenase (LDH) might be biomarkers related to clinical benefits. Clinical trial registration : https://www.chictr.org.cn/showproj.html?proj=130211 , identifier: ChiCTR2100049799, date of registration: 2021–08-09.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>39105880</pmid><doi>10.1007/s00262-024-03744-z</doi><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Antitumor activity
Biomarkers
Cancer Research
Chemoradiotherapy - methods
Chemotherapy
Clinical trials
Disease control
Female
Gemcitabine
Humans
Immune checkpoint inhibitors
Immune Checkpoint Inhibitors - therapeutic use
Immunology
Inflammation
L-Lactate dehydrogenase
Lymphocytes
Male
Medicine
Medicine & Public Health
Metastases
Metastasis
Middle Aged
Monocytes
Neoplasm Metastasis
Oncology
Oxonic Acid - administration & dosage
Oxonic Acid - therapeutic use
Pancreatic cancer
Pancreatic Neoplasms - drug therapy
Pancreatic Neoplasms - pathology
Pancreatic Neoplasms - radiotherapy
Pancreatic Neoplasms - therapy
Patients
PD-1 protein
Programmed Cell Death 1 Receptor - antagonists & inhibitors
Radiation Dose Hypofractionation
Radiation therapy
Tegafur - administration & dosage
Tegafur - therapeutic use
title Hypofractionated radiotherapy plus PD-1 antibody and SOX chemotherapy as second-line therapy in metastatic pancreatic cancer: a single-arm, phase II clinical trial
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