-
Je něco špatně v tomto záznamu ?
Stereotactic Radiotherapy Plus Nivolumab in Patients with Locally Advanced Pancreatic Cancer: Results from Phase 1/2 Clinical CA209-9KH Trial
M. Vošmik, S. John, J. Dvořák, B. Mohelníková-Duchoňová, B. Melichar, R. Lohynská, A. Ryška, AM. Banni, J. Krempová, I. Sirák
Status neindexováno Jazyk angličtina Země Nový Zéland
Typ dokumentu časopisecké články
Grantová podpora
UHHK
Ministerstvo Zdravotnictví Ceské Republiky
00179906
Ministerstvo Zdravotnictví Ceské Republiky
NLK
Directory of Open Access Journals
od 2015
PubMed Central
od 2018
ROAD: Directory of Open Access Scholarly Resources
od 2016
Springer Journals Complete - Open Access
od 2016
Springer Nature OA/Free Journals
od 2013-12-01
- Publikační typ
- časopisecké články MeSH
INTRODUCTION: The dismal prognosis of pancreatic ductal adenocarcinoma (PDAC) highlights the urgent need for novel therapeutic strategies. Immune checkpoint inhibitors (ICIs) seem to be ineffective in most PDAC studies. Therefore, we conducted an open-label, multicenter phase 1/2 study (CA209-9KH) to evaluate the safety of stereotactic radiotherapy (SRT) and sequential ICI therapy in PDAC, as well as to validate the efficacy of this regimen as a potential activator of antitumor immunity. METHODS: Patients aged ≥ 18 years with unresectable non-metastatic PDAC following four FOLFIRINOX induction cycles were included. Treatment comprised SRT (4 × 8 Gy) and sequential nivolumab administration until disease progression or unacceptable toxicity. The primary endpoints were safety and toxicity assessment. Secondary endpoints included progression-free survival (PFS), overall survival (OS), biomarker evaluation, and quality of life (QoL) analysis. RESULTS: Twenty-two patients were screened, with 15 enrolled. Eleven (median) nivolumab cycles were administered. SRT demonstrated low and clinically nonsignificant toxicity, whereas nivolumab toxicity aligned with prior safety profiles, without grade 4-5 events observed. Three patients discontinued therapy owing to toxicity. Median PFS and OS were 8.1 and 13.0 months, respectively, with 12-month PFS and OS rates of 0% and 66.7%, respectively, and a 24-month OS rate of 8.9%. Biomarker levels correlated with clinical or radiological disease control. Patient-reported QoL remained acceptable, deteriorating with disease progression. CONCLUSION: SRT and nivolumab therapy exhibited manageable toxicity profiles consistent with previous findings; however, long-term treatment responses were not achieved with this regimen in locally advanced PDAC. Another strategy to trigger antitumor immunity in PDAC needs to be sought. TRIAL REGISTRATION: EudraCT: 2017-003404-52; ClinicalTrials.gov: NCT04098432.
1st Faculty of Medicine Charles University Prague Czech Republic
Department of Oncology Thomayer University Hospital Prague Czech Republic
Department of Oncology University Hospital Olomouc Olomouc Czech Republic
Faculty of Medicine and Dentistry Palacký University Olomouc Czech Republic
Faculty of Medicine in Hradec Králové Charles University Prague Czech Republic
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc25002041
- 003
- CZ-PrNML
- 005
- 20250123102022.0
- 007
- ta
- 008
- 250117s2024 nz f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s40487-024-00309-z $2 doi
- 035 __
- $a (PubMed)39441483
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a nz
- 100 1_
- $a Vošmik, Milan $u Department of Oncology and Radiotherapy, University Hospital Hradec Králové, Sokolská 581, 50005, Hradec Králové, Czech Republic. milan.vosmik@fnhk.cz $u Faculty of Medicine in Hradec Králové, Charles University, Prague, Czech Republic. milan.vosmik@fnhk.cz $1 https://orcid.org/0000000164977505 $7 xx0135408
- 245 10
- $a Stereotactic Radiotherapy Plus Nivolumab in Patients with Locally Advanced Pancreatic Cancer: Results from Phase 1/2 Clinical CA209-9KH Trial / $c M. Vošmik, S. John, J. Dvořák, B. Mohelníková-Duchoňová, B. Melichar, R. Lohynská, A. Ryška, AM. Banni, J. Krempová, I. Sirák
- 520 9_
- $a INTRODUCTION: The dismal prognosis of pancreatic ductal adenocarcinoma (PDAC) highlights the urgent need for novel therapeutic strategies. Immune checkpoint inhibitors (ICIs) seem to be ineffective in most PDAC studies. Therefore, we conducted an open-label, multicenter phase 1/2 study (CA209-9KH) to evaluate the safety of stereotactic radiotherapy (SRT) and sequential ICI therapy in PDAC, as well as to validate the efficacy of this regimen as a potential activator of antitumor immunity. METHODS: Patients aged ≥ 18 years with unresectable non-metastatic PDAC following four FOLFIRINOX induction cycles were included. Treatment comprised SRT (4 × 8 Gy) and sequential nivolumab administration until disease progression or unacceptable toxicity. The primary endpoints were safety and toxicity assessment. Secondary endpoints included progression-free survival (PFS), overall survival (OS), biomarker evaluation, and quality of life (QoL) analysis. RESULTS: Twenty-two patients were screened, with 15 enrolled. Eleven (median) nivolumab cycles were administered. SRT demonstrated low and clinically nonsignificant toxicity, whereas nivolumab toxicity aligned with prior safety profiles, without grade 4-5 events observed. Three patients discontinued therapy owing to toxicity. Median PFS and OS were 8.1 and 13.0 months, respectively, with 12-month PFS and OS rates of 0% and 66.7%, respectively, and a 24-month OS rate of 8.9%. Biomarker levels correlated with clinical or radiological disease control. Patient-reported QoL remained acceptable, deteriorating with disease progression. CONCLUSION: SRT and nivolumab therapy exhibited manageable toxicity profiles consistent with previous findings; however, long-term treatment responses were not achieved with this regimen in locally advanced PDAC. Another strategy to trigger antitumor immunity in PDAC needs to be sought. TRIAL REGISTRATION: EudraCT: 2017-003404-52; ClinicalTrials.gov: NCT04098432.
- 590 __
- $a NEINDEXOVÁNO
- 655 _2
- $a časopisecké články $7 D016428
- 700 1_
- $a John, Stanislav $u Department of Oncology and Radiotherapy, University Hospital Hradec Králové, Sokolská 581, 50005, Hradec Králové, Czech Republic $u Faculty of Medicine in Hradec Králové, Charles University, Prague, Czech Republic
- 700 1_
- $a Dvořák, Josef $u Department of Oncology, Thomayer University Hospital, Prague, Czech Republic $u First Faculty of Medicine, Charles University, Prague, Czech Republic
- 700 1_
- $a Mohelníková-Duchoňová, Beatrice $u Department of Oncology, University Hospital Olomouc, Olomouc, Czech Republic $u Faculty of Medicine and Dentistry, Palacký University, Olomouc, Czech Republic
- 700 1_
- $a Melichar, Bohuslav $u Department of Oncology, University Hospital Olomouc, Olomouc, Czech Republic $u Faculty of Medicine and Dentistry, Palacký University, Olomouc, Czech Republic
- 700 1_
- $a Lohynská, Radka $u Department of Oncology, Thomayer University Hospital, Prague, Czech Republic $u First Faculty of Medicine, Charles University, Prague, Czech Republic
- 700 1_
- $a Ryška, Aleš $u Faculty of Medicine in Hradec Králové, Charles University, Prague, Czech Republic $u The Fingerland Department of Pathology, University Hospital Hradec Králové, Hradec Králové, Czech Republic
- 700 1_
- $a Banni, Aml Mustafa $u Department of Oncology and Radiotherapy, University Hospital Hradec Králové, Sokolská 581, 50005, Hradec Králové, Czech Republic $u Faculty of Medicine in Hradec Králové, Charles University, Prague, Czech Republic
- 700 1_
- $a Krempová, Johana $u Department of Oncology and Radiotherapy, University Hospital Hradec Králové, Sokolská 581, 50005, Hradec Králové, Czech Republic
- 700 1_
- $a Sirák, Igor $u Department of Oncology and Radiotherapy, University Hospital Hradec Králové, Sokolská 581, 50005, Hradec Králové, Czech Republic $u Faculty of Medicine in Hradec Králové, Charles University, Prague, Czech Republic
- 773 0_
- $w MED00205578 $t Oncology and therapy $x 2366-1089 $g Roč. 12, č. 4 (2024), s. 817-831
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/39441483 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y - $z 0
- 990 __
- $a 20250117 $b ABA008
- 991 __
- $a 20250123102016 $b ABA008
- 999 __
- $a ok $b bmc $g 2254458 $s 1238044
- BAS __
- $a 3
- BAS __
- $a PreBMC-PubMed-not-MEDLINE
- BMC __
- $a 2024 $b 12 $c 4 $d 817-831 $e 20241023 $i 2366-1089 $m Oncology and therapy $n Oncol Ther $x MED00205578
- GRA __
- $a UHHK $p Ministerstvo Zdravotnictví Ceské Republiky
- GRA __
- $a 00179906 $p Ministerstvo Zdravotnictví Ceské Republiky
- LZP __
- $a Pubmed-20250117