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A systematic review of contemporary phase I trials in patients with lymphoma.
Griguolo, G; Zorzi, M F; Pirosa, M C; Treglia, G; Bertoni, F; Kuruvilla, J; Zucca, E; Stathis, A.
Afiliação
  • Griguolo G; Department of Surgery, Oncology and Gastroenterology, University of Padova, Padova, Italy; Division of Oncology 2, Istituto Oncologico Veneto IRCCS, Padova, Italy.
  • Zorzi MF; Faculty of Biomedical Sciences, Università della Svizzera Italiana, Lugano, Switzerland.
  • Pirosa MC; Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland.
  • Treglia G; Faculty of Biomedical Sciences, Università della Svizzera Italiana, Lugano, Switzerland; Faculty of Biology and Medicine, University of Lausanne, Lausanne, Switzerland; Academic education, Research and Innovation Area, General directorate, EOC, Bellinzona, Switzerland.
  • Bertoni F; Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland; Institute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera Italiana, Bellinzona, Switzerland.
  • Kuruvilla J; Department of Medicine, Division of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University of Toronto, Toronto, Canada.
  • Zucca E; Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland; Institute of Oncology Research, Faculty of Biomedical Sciences, Università della Svizzera Italiana, Bellinzona, Switzerland.
  • Stathis A; Faculty of Biomedical Sciences, Università della Svizzera Italiana, Lugano, Switzerland; Oncology Institute of Southern Switzerland, EOC, Bellinzona, Switzerland. Electronic address: anastasios.stathis@eoc.ch.
Crit Rev Oncol Hematol ; 180: 103860, 2022 Dec.
Article em En | MEDLINE | ID: mdl-36265547
ABSTRACT
We performed a systematic review of phase I trials specifically designed for lymphoma patients. PubMed and Cochrane Library databases were searched using (lymphoma*) AND (phase 1) and publication date 2015-2020 to identify phase I dose-finding trials including a majority of lymphoma patients. Eighty-two trials (n = 3289 lymphoma patients) were included 46 (55%) enrolled only lymphoma patients, 34 (41%) included also other hematologic malignancies, 2 (2%) solid tumors. Forty-six trials (56%) evaluated a combination (in 25 addition of experimental drug to standard therapy). Seven trials (9%) enrolled untreated patients. Among trials reporting activity in lymphoma patients, 74% (n = 57) reported an overall response rate ≥ 30%. All trials reported grade ≥ 3 adverse events; however, rates were not comparable across trials. Thirty-one treatment-related deaths in lymphoma patients were reported (overall treatment-related grade 5 adverse events rate 0.94%). Phase I trials designed for lymphoma patients were generally safe and the majority reported overall response rate ≥ 30%.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma Tipo de estudo: Prognostic_studies / Systematic_reviews Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article