Venous and Arterial Thromboembolism in Lung Cancer Patients : A Retrospective Analysis

GND
1340525887
ORCID
0009-0008-9292-162X
Affiliation
Klinik für Innere Medizin II, Hämatologie und Internistische Onkologie, Universitätsklinikum Jena, Am Klinikum 1, 07747 Jena, Germany;(K.S.);(A.H.)
Morath, Olga;
GND
1180621875
Affiliation
Klinik für Innere Medizin V, Pneumologie, Universitätsklinikum Jena, Am Klinikum 1, 07747 Jena, Germany;(J.H.);(S.M.L.)
Hoffmann, Julia;
Affiliation
Klinik für Innere Medizin II, Hämatologie und Internistische Onkologie, Universitätsklinikum Jena, Am Klinikum 1, 07747 Jena, Germany;(K.S.);(A.H.)
Schilling, Kristina;
GND
1107039339
ORCID
0000-0003-0626-0834
Affiliation
Klinik für Innere Medizin II, Hämatologie und Internistische Onkologie, Universitätsklinikum Jena, Am Klinikum 1, 07747 Jena, Germany;(K.S.);(A.H.)
Hochhaus, Andreas;
Affiliation
Internistisch-Onkologische Gemeinschaftspraxis, Wiesestrasse 22, 07548 Gera, Germany;
Rachow, Tobias;
GND
172217016
ORCID
0000-0003-1332-9879
Affiliation
Klinik für Innere Medizin V, Pneumologie, Universitätsklinikum Jena, Am Klinikum 1, 07747 Jena, Germany;(J.H.);(S.M.L.)
Lang, Susanne M.

Background : Patients with lung cancer face an increased incidence of venous (VTE) and arterial (ATE) thromboembolism. Risk factors for thrombosis remain unclear, particularly the impact of the use of immune checkpoint inhibitors (ICIs). We sought to compare the incidence of VTE and ATE in lung cancer patients receiving platinum-based therapy versus those receiving ICIs alone or in combination with chemotherapy and to validate the Khorana risk score for predicting VTE in the era of ICIs.

Methods : A retrospective single-institution data analysis of 173 patients diagnosed with locally advanced or metastatic lung cancer at the Jena University hospital between 2015 and 2021.

Results : The study revealed a high incidence of VTE (17.9%) and ATE (5.8%). The VTE risk was higher in patients diagnosed with adenocarcinoma (OR 0.29, 95% CI 0.09–0.93) than in patients with other histological types. A prior venous event was associated with an increased risk of recurrent VTE (OR 4.46, 95% CI 1.20–16.63). The incidence of thrombosis under first-line platinum-based chemotherapy did not differ from the incidence under ICIs ( p = 0.19). There were no differences in the subgroup of patients who received ICIs alone or combined immunochemotherapy ( p = 0.43). The Khorana score failed to predict the risk of VTE correctly.

Conclusions : We did not find evidence supporting the theory that ICI therapy (alone or combined) increases the risk of thrombotic events. Adenocarcinoma and a prior history of VTE were strongly associated with an increased risk of VTE. Other scores for thrombotic risk assessment in lung cancer patients should be tested in prospective studies.

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