A phase I trial of inotuzumab ozogamicin in combination with temsirolimus in patients with relapsed or refractory CD22-positive B-cell non-Hodgkin lymphomas.


Journal

Leukemia & lymphoma
ISSN: 1029-2403
Titre abrégé: Leuk Lymphoma
Pays: United States
ID NLM: 9007422

Informations de publication

Date de publication:
01 2022
Historique:
pubmed: 20 8 2021
medline: 18 3 2022
entrez: 19 8 2021
Statut: ppublish

Résumé

This phase I trial evaluated the safety, tolerability, and preliminary activity of inotuzumab ozogamicin in combination with temsirolimus in patients with relapsed/refractory CD22 positive B-cell non-Hodgkin lymphomas. Nineteen patients received at least one dose of both study drugs. Dose-limiting toxicities consisted of thrombocytopenia, hypertriglyceridemia, oral mucositis, clinical deterioration, and the inability to receive at least three doses of temsirolimus during cycle 1. The most common grade ≥3 treatment-related adverse events were thrombocytopenia (

Identifiants

pubmed: 34407735
doi: 10.1080/10428194.2021.1966780
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
CD22 protein, human 0
Sialic Acid Binding Ig-like Lectin 2 0
temsirolimus 624KN6GM2T
Inotuzumab Ozogamicin P93RUU11P7
Sirolimus W36ZG6FT64

Banques de données

ClinicalTrials.gov
['NCT01535989']

Types de publication

Clinical Trial, Phase I Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

117-123

Auteurs

Maria C Pirosa (MC)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.

Lu Zhang (L)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Institute of Hematology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, Hubei, China.

Felicitas Hitz (F)

Department of Oncology and Hematology, Cantonal Hospital, St. Gallen, Switzerland.

Urban Novak (U)

Department of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.

Dagmar Hess (D)

Department of Oncology and Hematology, Cantonal Hospital, St. Gallen, Switzerland.

Tatiana Terrot (T)

Clinical Trial Unit, Ente Ospedaliero Cantonale, Bellinzona, Switzerland.

Mariarosa Pascale (M)

Clinical Trial Unit, Ente Ospedaliero Cantonale, Bellinzona, Switzerland.

Luca Mazzucchelli (L)

Cantonal Institute of Pathology, Locarno, Switzerland.

Francesco Bertoni (F)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Institute of Oncology Research, Bellinzona, Switzerland.
Faculty of Biomedical Sciences, Università della Svizzera Italiana (USI), Lugano, Switzerland.

Franco Cavalli (F)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Institute of Oncology Research, Bellinzona, Switzerland.

Emanuele Zucca (E)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Department of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Institute of Oncology Research, Bellinzona, Switzerland.
Faculty of Biomedical Sciences, Università della Svizzera Italiana (USI), Lugano, Switzerland.

Anastasios Stathis (A)

Oncology Institute of Southern Switzerland, Bellinzona, Switzerland.
Faculty of Biomedical Sciences, Università della Svizzera Italiana (USI), Lugano, Switzerland.

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Classifications MeSH