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 |
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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 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_11303639</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3089681542</sourcerecordid><originalsourceid>FETCH-LOGICAL-c356t-e6d96f8444efef59cc44ce97fb97ad8970bb5da0cf18ac8e5bd690e3972ad4443</originalsourceid><addsrcrecordid>eNp9ks1u1DAUhSMEoqXwAiyQJTYsCNix82M2CJWfjlSpSIDEzrqxb2ZcJXZqO0jT1-FFMTPtUFiw8tG93z32lU9RPGX0FaO0fR0prZqqpJUoKW-FKK_vFcdM8Fzqanb_jj4qHsV4SamoqJQPiyMuGa27jh4XP8-2sx8C6GS9g4SGBDDWpw0GmLdkHpdIPr8vGQGXbO_NNgtDvlx8J3qD04GDSCJq70w5WofktmwdmTBBTJCsJjM4HXAndZYY3hAg0br1iCWE6SWZNxCRrFZEZxerYSQpWBgfFw8GGCM-uTlPim8fP3w9PSvPLz6tTt-dl5rXTSqxMbIZOiEEDjjUUmshNMp26GULppMt7fvaANUD60B3WPemkRS5bCsweYqfFG_3vvPST2g0uhRgVHOwE4St8mDV3x1nN2rtfyjGOOUNl9nhxY1D8FcLxqQmGzWOIzj0S1ScdrJmnFc8o8__QS_9Elzeb0c1HatFlalqT-ngYww4HF7DqPodArUPgcohULsQqOs89OzuHoeR21_PAN8DMbfcGsOfu_9j-ws1I8GS</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3089681542</pqid></control><display><type>article</type><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><source>MEDLINE</source><source>SpringerLink Journals</source><source>Springer Nature OA Free Journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Wang, Qin ; Tong, Fan ; Qiao, Li ; Qi, Liang ; Sun, Yi ; Zhu, Yahui ; Ni, Jiayao ; Liu, Juan ; Kong, Weiwei ; Liu, Baorui ; Du, Juan</creator><creatorcontrib>Wang, Qin ; Tong, Fan ; Qiao, Li ; Qi, Liang ; Sun, Yi ; Zhu, Yahui ; Ni, Jiayao ; Liu, Juan ; Kong, Weiwei ; Liu, Baorui ; Du, Juan</creatorcontrib><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.</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 & 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</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.
Clinical trial registration
:
https://www.chictr.org.cn/showproj.html?proj=130211
, identifier: ChiCTR2100049799, date of registration: 2021–08-09.</description><subject>Adult</subject><subject>Aged</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Antitumor activity</subject><subject>Biomarkers</subject><subject>Cancer Research</subject><subject>Chemoradiotherapy - methods</subject><subject>Chemotherapy</subject><subject>Clinical trials</subject><subject>Disease control</subject><subject>Female</subject><subject>Gemcitabine</subject><subject>Humans</subject><subject>Immune checkpoint inhibitors</subject><subject>Immune Checkpoint Inhibitors - therapeutic use</subject><subject>Immunology</subject><subject>Inflammation</subject><subject>L-Lactate dehydrogenase</subject><subject>Lymphocytes</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Monocytes</subject><subject>Neoplasm Metastasis</subject><subject>Oncology</subject><subject>Oxonic Acid - administration & dosage</subject><subject>Oxonic Acid - therapeutic use</subject><subject>Pancreatic cancer</subject><subject>Pancreatic Neoplasms - drug therapy</subject><subject>Pancreatic Neoplasms - pathology</subject><subject>Pancreatic Neoplasms - radiotherapy</subject><subject>Pancreatic Neoplasms - therapy</subject><subject>Patients</subject><subject>PD-1 protein</subject><subject>Programmed Cell Death 1 Receptor - antagonists & inhibitors</subject><subject>Radiation Dose Hypofractionation</subject><subject>Radiation therapy</subject><subject>Tegafur - administration & dosage</subject><subject>Tegafur - therapeutic use</subject><issn>1432-0851</issn><issn>0340-7004</issn><issn>1432-0851</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>C6C</sourceid><sourceid>EIF</sourceid><recordid>eNp9ks1u1DAUhSMEoqXwAiyQJTYsCNix82M2CJWfjlSpSIDEzrqxb2ZcJXZqO0jT1-FFMTPtUFiw8tG93z32lU9RPGX0FaO0fR0prZqqpJUoKW-FKK_vFcdM8Fzqanb_jj4qHsV4SamoqJQPiyMuGa27jh4XP8-2sx8C6GS9g4SGBDDWpw0GmLdkHpdIPr8vGQGXbO_NNgtDvlx8J3qD04GDSCJq70w5WofktmwdmTBBTJCsJjM4HXAndZYY3hAg0br1iCWE6SWZNxCRrFZEZxerYSQpWBgfFw8GGCM-uTlPim8fP3w9PSvPLz6tTt-dl5rXTSqxMbIZOiEEDjjUUmshNMp26GULppMt7fvaANUD60B3WPemkRS5bCsweYqfFG_3vvPST2g0uhRgVHOwE4St8mDV3x1nN2rtfyjGOOUNl9nhxY1D8FcLxqQmGzWOIzj0S1ScdrJmnFc8o8__QS_9Elzeb0c1HatFlalqT-ngYww4HF7DqPodArUPgcohULsQqOs89OzuHoeR21_PAN8DMbfcGsOfu_9j-ws1I8GS</recordid><startdate>20240806</startdate><enddate>20240806</enddate><creator>Wang, Qin</creator><creator>Tong, Fan</creator><creator>Qiao, Li</creator><creator>Qi, Liang</creator><creator>Sun, Yi</creator><creator>Zhu, Yahui</creator><creator>Ni, Jiayao</creator><creator>Liu, Juan</creator><creator>Kong, Weiwei</creator><creator>Liu, Baorui</creator><creator>Du, Juan</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</scope><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>7T5</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20240806</creationdate><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><author>Wang, Qin ; Tong, Fan ; Qiao, Li ; Qi, Liang ; Sun, Yi ; Zhu, Yahui ; Ni, Jiayao ; Liu, Juan ; Kong, Weiwei ; Liu, Baorui ; Du, Juan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-e6d96f8444efef59cc44ce97fb97ad8970bb5da0cf18ac8e5bd690e3972ad4443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Antitumor activity</topic><topic>Biomarkers</topic><topic>Cancer Research</topic><topic>Chemoradiotherapy - methods</topic><topic>Chemotherapy</topic><topic>Clinical trials</topic><topic>Disease control</topic><topic>Female</topic><topic>Gemcitabine</topic><topic>Humans</topic><topic>Immune checkpoint inhibitors</topic><topic>Immune Checkpoint Inhibitors - therapeutic use</topic><topic>Immunology</topic><topic>Inflammation</topic><topic>L-Lactate dehydrogenase</topic><topic>Lymphocytes</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & 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 & 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 & inhibitors</topic><topic>Radiation Dose Hypofractionation</topic><topic>Radiation therapy</topic><topic>Tegafur - administration & 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 & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Cancer Immunology, Immunotherapy : CII</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Qin</au><au>Tong, Fan</au><au>Qiao, Li</au><au>Qi, Liang</au><au>Sun, Yi</au><au>Zhu, Yahui</au><au>Ni, Jiayao</au><au>Liu, Juan</au><au>Kong, Weiwei</au><au>Liu, Baorui</au><au>Du, Juan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hypofractionated radiotherapy plus PD-1 antibody and SOX chemotherapy as second-line therapy in metastatic pancreatic cancer: a single-arm, phase II clinical trial</atitle><jtitle>Cancer Immunology, Immunotherapy : CII</jtitle><stitle>Cancer Immunol Immunother</stitle><addtitle>Cancer Immunol Immunother</addtitle><date>2024-08-06</date><risdate>2024</risdate><volume>73</volume><issue>10</issue><spage>201</spage><pages>201-</pages><artnum>201</artnum><issn>1432-0851</issn><issn>0340-7004</issn><eissn>1432-0851</eissn><abstract>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.</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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source | MEDLINE; SpringerLink Journals; Springer Nature OA Free Journals; PubMed Central; Alma/SFX Local Collection |
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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