Prevalence and risks of intravenous chemotherapy-induced severe neutropenia in solid cancers: a multicenter retrospective cohort study on real-life data.


Journal

Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer
ISSN: 1433-7339
Titre abrégé: Support Care Cancer
Pays: Germany
ID NLM: 9302957

Informations de publication

Date de publication:
13 Sep 2024
Historique:
received: 25 01 2024
accepted: 15 08 2024
medline: 13 9 2024
pubmed: 13 9 2024
entrez: 13 9 2024
Statut: epublish

Résumé

We aimed at identifying prevalence, clinical outcomes and prognostic factors in cancer patients with intravenous chemotherapy-induced severe neutropenia (ICISN). In this multicenter retrospective cohort study on the clinical data warehouse of Greater Paris University Hospitals (AP-HP), we included all adult patients with solid cancer hospitalized between 2016 and 2021 with intravenous chemotherapy within 30 days prior to severe neutropenia (D70 or D611 ICD-10 codes AND a neutrophil count < 500/mm3). The primary endpoint was referral to intensive care unit (ICU) or death within 30 days. We collected cancer, patient, and treatment characteristics. Among 141,586 cancer inpatients, 40,660 received chemotherapy among whom 661 (1.6%) had ICISN. Median age was 63 years (interquartile range (IQR), 54-70) and 330 patients (49%) were female. The median Charlson score was 10 (IQR, 8-11). Main primary cancers were lung (n = 204, 31%) and breast (n = 87, 13%). Advanced cancers were found in 551 patients (83%), 331 (50%) were in 1st line of chemotherapy, 284 (42%) in the 1st cycle of the current line and 149 (22%) had primary G-CSF. Documented bacterial (mostly gram-negative bacilli) and fungal infections were observed in 113 (17%) and 19 (3%) patients; 58 (9%) were transferred to ICU and 82 (12%) died within 30 days, 372 (56%) patients received subsequent chemotherapy. Independent prognostic factors were the level of monocyte, lymphocyte counts or albuminemia and a documented bacterial infection, while Charlson index and primary prophylactic G-CSF were not associated with patient clinical outcomes. Despite the use of primary G-CSF, ICISN remains a frequent event, which leads to ICU death in one on five cases Some prognostic factors of severity have been highlighted and could help clinicians to prevent severe complications.

Identifiants

pubmed: 39269541
doi: 10.1007/s00520-024-08817-4
pii: 10.1007/s00520-024-08817-4
doi:

Substances chimiques

Antineoplastic Agents 0

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

657

Investigateurs

Guillaume Lamé (G)
Christel Daniel (C)
Ariel Cohen (A)
Marie Verdoux (M)
Gilles Galula (G)

Informations de copyright

© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

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Auteurs

Olivia Rohr (O)

Department of Medical Oncology, Henri Mondor and Albert Chenevier Teaching Hospital, Université Paris Est Créteil, Assistance Publique - Hôpitaux de Paris, 1 Rue Gustave Eiffel, 94000, Créteil, France.

Sonia Priou (S)

Innovation and Data, IT Department, Assistance Publique - Hôpitaux de Paris, Paris, France.
Laboratoire Génie Industriel, Université Paris-Saclay, CentraleSupélec, Gif-Sur-Yvette, France.

Gilles Chatellier (G)

Department of Medical Informatics, Université de Paris, Assistance Publique Hôpitaux de Paris, Centre-Université de Paris (APHP-CUP), 75015, Paris, France.

Samy Babai (S)

Department of Pharmacovigilance, Henri Mondor and Albert Chenevier Teaching Hospital, Université Paris Est Créteil, Assistance Publique - Hôpitaux de Paris, Créteil, France.

Sébastien Gallien (S)

Department of Infectious Diseases and Immunology, Henri Mondor Teaching Hospital, Université Paris Est Créteil, Assistance Publique - Hôpitaux de Paris, Créteil, France.

Rémi Flicoteaux (R)

Department of Medical Information, Assistance Publique - Hôpitaux de Paris, Paris, France.

Christophe Tournigand (C)

Department of Medical Oncology, Henri Mondor and Albert Chenevier Teaching Hospital, Université Paris Est Créteil, Assistance Publique - Hôpitaux de Paris, 1 Rue Gustave Eiffel, 94000, Créteil, France.

Emmanuelle Kempf (E)

Department of Medical Oncology, Henri Mondor and Albert Chenevier Teaching Hospital, Université Paris Est Créteil, Assistance Publique - Hôpitaux de Paris, 1 Rue Gustave Eiffel, 94000, Créteil, France. Emmanuelle.kempf@aphp.fr.
Laboratoire d'Informatique Médicale Et d'Ingénierie Des Connaissances Pour La E-Santé, LIMICS, Sorbonne Université, Inserm, Université Sorbonne Paris Nord, Paris, France. Emmanuelle.kempf@aphp.fr.

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