Treatment with therapeutic anticoagulation is not associated with immunotherapy response in advanced cancer patients.


Journal

Journal of translational medicine
ISSN: 1479-5876
Titre abrégé: J Transl Med
Pays: England
ID NLM: 101190741

Informations de publication

Date de publication:
30 01 2021
Historique:
received: 10 12 2020
accepted: 22 01 2021
entrez: 31 1 2021
pubmed: 1 2 2021
medline: 15 5 2021
Statut: epublish

Résumé

Recent preclinical data suggest that there may be therapeutic synergy between immune checkpoint blockade and inhibition of the coagulation cascade. Here, we investigate whether patients who received immune checkpoint inhibitors (ICI) and were on concomitant anticoagulation (AC) experienced better treatment outcomes than individuals not on AC.Affiliation: Kindly confirm if corresponding authors affiliation is identified correctly.The corresponding author's affiliation is correct. We studied a cohort of 728 advanced cancer patients who received 948 lines of ICI at NYU (2010-2020). Patients were classified based on whether they did (n = 120) or did not (n = 828) receive therapeutic AC at any point during their treatment with ICI. We investigated the relationship between AC status and multiple clinical endpoints including best overall response (BOR), objective response rate (ORR), disease control rate (DCR), progression free survival (PFS), overall survival (OS), and the incidence of bleeding complications.Affiliations: Journal instruction requires a country for affiliations; however, this is missing in affiliations 1 to 5. Please verify if the provided country is correct and amend if necessary.The country is correct for all affiliations (1 - 5). Treatment with AC was not associated with significantly different BOR (P = 0.80), ORR (P =0.60), DCR (P =0.77), PFS (P = 0.59), or OS (P =0.64). Patients who received AC were significantly more likely to suffer a major or clinically relevant minor bleed (P = 0.05). AC does not appear to impact the activity or efficacy of ICI in advanced cancer patients. On the basis of our findings, we caution that there is insufficient evidence to support prospectively evaluating the combination of AC and immunotherapy.

Sections du résumé

BACKGROUND
Recent preclinical data suggest that there may be therapeutic synergy between immune checkpoint blockade and inhibition of the coagulation cascade. Here, we investigate whether patients who received immune checkpoint inhibitors (ICI) and were on concomitant anticoagulation (AC) experienced better treatment outcomes than individuals not on AC.Affiliation: Kindly confirm if corresponding authors affiliation is identified correctly.The corresponding author's affiliation is correct.
METHODS
We studied a cohort of 728 advanced cancer patients who received 948 lines of ICI at NYU (2010-2020). Patients were classified based on whether they did (n = 120) or did not (n = 828) receive therapeutic AC at any point during their treatment with ICI. We investigated the relationship between AC status and multiple clinical endpoints including best overall response (BOR), objective response rate (ORR), disease control rate (DCR), progression free survival (PFS), overall survival (OS), and the incidence of bleeding complications.Affiliations: Journal instruction requires a country for affiliations; however, this is missing in affiliations 1 to 5. Please verify if the provided country is correct and amend if necessary.The country is correct for all affiliations (1 - 5).
RESULTS
Treatment with AC was not associated with significantly different BOR (P = 0.80), ORR (P =0.60), DCR (P =0.77), PFS (P = 0.59), or OS (P =0.64). Patients who received AC were significantly more likely to suffer a major or clinically relevant minor bleed (P = 0.05).
CONCLUSION
AC does not appear to impact the activity or efficacy of ICI in advanced cancer patients. On the basis of our findings, we caution that there is insufficient evidence to support prospectively evaluating the combination of AC and immunotherapy.

Identifiants

pubmed: 33516263
doi: 10.1186/s12967-021-02712-w
pii: 10.1186/s12967-021-02712-w
pmc: PMC7847556
doi:

Substances chimiques

Anticoagulants 0

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

47

Subventions

Organisme : NCI NIH HHS
ID : R01 CA231295
Pays : United States
Organisme : NCI NIH HHS
ID : P30CA016087
Pays : United States
Organisme : NCI NIH HHS
ID : P50 CA225450
Pays : United States

Références

Cell. 2017 Feb 9;168(4):707-723
pubmed: 28187290
Ann Palliat Med. 2018 Apr;7(2):265-273
pubmed: 29307210
Blood. 2007 Jul 1;110(1):133-41
pubmed: 17371949
Cancers (Basel). 2019 Dec 25;12(1):
pubmed: 31881699
N Engl J Med. 2010 Aug 19;363(8):711-23
pubmed: 20525992
Sci Immunol. 2019 Sep 20;4(39):
pubmed: 31541031
N Engl J Med. 2016 Nov 10;375(19):1823-1833
pubmed: 27718847
N Engl J Med. 2018 Apr 05;378(14):1277-1290
pubmed: 29562145
N Engl J Med. 2018 Feb 15;378(7):615-624
pubmed: 29231094
N Engl J Med. 2020 Apr 23;382(17):1599-1607
pubmed: 32223112
Blood. 2005 Jan 1;105(1):178-85
pubmed: 15367435
J Thromb Haemost. 2015 Nov;13(11):2119-26
pubmed: 26764429
Sci Transl Med. 2020 Jan 8;12(525):
pubmed: 31915300
J Clin Oncol. 2015 Feb 20;33(6):654-6
pubmed: 25605844
J Thromb Haemost. 2005 Apr;3(4):692-4
pubmed: 15842354
Am J Hematol. 2019 Jul;94(7):780-785
pubmed: 31006890

Auteurs

Paul Johannet (P)

Department of Medicine, NYU Langone Health, New York, USA.

Amelia Sawyers (A)

Ronald O. Perelman Department of Dermatology, NYU Langone Health, New York, USA.

Nicholas Gulati (N)

Ronald O. Perelman Department of Dermatology, NYU Langone Health, New York, USA.

Douglas Donnelly (D)

Ronald O. Perelman Department of Dermatology, NYU Langone Health, New York, USA.

Samuel Kozloff (S)

Department of Medicine, NYU Langone Health, New York, USA.

Yingzhi Qian (Y)

Department of Population Health, NYU Langone Health, New York, USA.

Alfredo Floristan (A)

Department of Pathology, NYU Langone Health, New York, USA.

Eva Hernando (E)

Department of Pathology, NYU Langone Health, New York, USA.

Judy Zhong (J)

Department of Population Health, NYU Langone Health, New York, USA.

Iman Osman (I)

Ronald O. Perelman Department of Dermatology, NYU Langone Health, New York, USA. Iman.Osman@nyulangone.org.
Ronald O. Perelman Department of Dermatology, NYU Grossman School of Medicine, 550 First Ave, Smilow 403, New York, NY, 10016, USA. Iman.Osman@nyulangone.org.

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