Sanne H. Tonino

ORCID: 0000-0002-3253-8759
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About
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Research Areas
  • Chronic Lymphocytic Leukemia Research
  • Lymphoma Diagnosis and Treatment
  • Viral-associated cancers and disorders
  • CAR-T cell therapy research
  • Immune Cell Function and Interaction
  • Immunodeficiency and Autoimmune Disorders
  • Chronic Myeloid Leukemia Treatments
  • CNS Lymphoma Diagnosis and Treatment
  • Lung Cancer Treatments and Mutations
  • Advanced Breast Cancer Therapies
  • Cancer Immunotherapy and Biomarkers
  • Cancer-related Molecular Pathways
  • Multiple and Secondary Primary Cancers
  • Monoclonal and Polyclonal Antibodies Research
  • Acute Lymphoblastic Leukemia research
  • Immunotherapy and Immune Responses
  • Ovarian cancer diagnosis and treatment
  • Galectins and Cancer Biology
  • Vascular Malformations and Hemangiomas
  • Cancer Genomics and Diagnostics
  • PI3K/AKT/mTOR signaling in cancer
  • Glycosylation and Glycoproteins Research
  • Calcium signaling and nucleotide metabolism
  • Histiocytic Disorders and Treatments
  • Genomic variations and chromosomal abnormalities

University of Amsterdam
2010-2025

Amsterdam University Medical Centers
2018-2025

Amsterdam UMC Location University of Amsterdam
2012-2023

Centre for Research and Technology Hellas
2023

Cancer Center Amsterdam
2019-2022

Lymphoma Research Foundation
2019-2021

Hovon
2018

OLVG
2005

Abstract Morbidity and mortality due to immunosuppression remain among the foremost clinical challenges in chronic lymphocytic leukemia (CLL). Although is considered originate within lymph node (LN) microenvironment, alterations T natural killer (NK) cells have almost exclusively been studied peripheral blood (PB). Whereas chemoimmunotherapy further deteriorates immune function, novel targeted agents like B-cell lymphoma 2 inhibitor venetoclax potentially spare nonmalignant lymphocytes;...

10.1182/bloodadvances.2019000360 article EN cc-by-nc-nd Blood Advances 2019-09-10
Thomas Chatzikonstantinou Anargyros Kapetanakis Lydia Scarfò Georgios Karakatsoulis David Allsup and 95 more Alejandro Alonso Cabrero Martin Andres Darko Antić Mónica Baile Panagiotis Baliakas Dominique Bron Antonella Capasso Sofia Chatzileontiadou Raúl Córdoba Juan Gonzalo Correa Carolina Cuéllar‐García Lorenzo De Paoli Maria Rosaria De Paolis Giovanni Del Poeta Christos Demosthenous Maria Dimou D. Donaldson Michael Doubek Maria Efstathopoulou Barbara Eichhorst Shaimaa El‐Ashwah Alicia Enrico Blanca Espinet Lucia Farina Angela Ferrari Myriam Foglietta Henrik Frederiksen Moritz Fürstenau José A. García‐Marco Rocío García‐Serra Massimo Gentile Eva Gimeno Andreas Glenthøj María Gomes da Silva Odit Gutwein Yervand Hakobyan Yair Herishanu José‐Ángel Hernández‐Rivas Tobias Herold Idanna Innocenti Gilad Itchaki Ozren Jakšić Ann Janssens Olga Kalashnikova Elżbieta Kalicińska Linda Karlsson Arnon P. Kater Sabina Kersting Jorge Labrador Deepesh Lad Luca Laurenti Mark‐David Levin Enrico Lista Alberto López‐García Lara Malerba Roberto Marasca Monia Marchetti Juan Marquet Mattias Mattsson Francesca Romana Mauro Ivana Milošević Fatima Mirás Marta Morawska Marina Motta Talha Munir Roberta Murru Carsten Utoft Niemann Raquel Nunes Rodrigues Jacopo Olivieri Lorella Orsucci Maria Papaioannou Miguel Arturo Pavlovsky Inga Piskunova Viola Maria Popov Francesca Maria Quaglia Giulia Quaresmini Kristian Qvist Gianluigi Reda Gian Matteo Rigolin Rosa Ruchlemer Gevorg Saghumyan Amit Shrestha Martin Šimkovič Martin Špaček Paolo Sportoletti Oana Stanca Niki Stavroyianni Tamar Tadmor Doreen te Raa Sanne H. Tonino Livio Trentin Ellen van der Spek Michel van Gelder Roel van Kampen Marzia Varettoni

Abstract Patients with chronic lymphocytic leukemia (CLL) may be more susceptible to Coronavirus disease 2019 (COVID-19) due age, disease, and treatment-related immunosuppression. We aimed assess risk factors of outcome elucidate the impact CLL-directed treatments on course COVID-19. conducted a retrospective, international study, collectively including 941 patients CLL confirmed Data from beginning pandemic until March 16, 2021, were collected 91 centers. The case fatality rate (CFR),...

10.1038/s41375-021-01450-8 article EN cc-by Leukemia 2021-11-01

Achieving a metabolic complete response (mCR) before high-dose chemotherapy (HDC) and autologous peripheral blood stem-cell transplant (auto-PBSCT) predicts progression free survival (PFS) in relapsed/refractory classical Hodgkin lymphoma (R/R cHL). We added brentuximab vedotin (BV) to DHAP improve the mCR rate. In Phase I dose-escalation part 12 patients, we showed that BV-DHAP is feasible. This II study included 55 R/R cHL patients (23 primary refractory). Treatment consisted of three...

10.3324/haematol.2019.243238 article EN cc-by-nc Haematologica 2020-04-09

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary point, may be published when key planned co-primary or secondary analyses are not yet available. Trial Updates provide an opportunity to disseminate additional results from studies, in JCO elsewhere, for which point has already been reported. analysis of Early positron emission tomography (ePET) Response–Adapted Treatment localized Hodgkin Lymphoma H10...

10.1200/jco.23.01745 article EN cc-by-nc-nd Journal of Clinical Oncology 2023-11-15

Summary Background Invasive fungal diseases (IFD) are life‐threatening infections most commonly diagnosed in acute leukaemia patients with prolonged neutropenia and uncommonly lymphoproliferative diseases. Objectives Following the initial report of aspergillosis shortly after beginning ibrutinib for chronic lymphocytic leukaemia, a survey was developed to seek additional cases IFD during treatment. Methods Local international physicians groups were approached relevant cases. Patients...

10.1111/myc.13001 article EN Mycoses 2019-09-14

In patients with chronic lymphocytic leukemia (CLL), numbers of CD8 + CD45RA +/- CD27- effector T cells are expanded. We investigated whether this expansion is also present in other B cell malignancies and the possible mechanism underlying these changes. Whereas an increase total CD4+and CD8+ was found only CLL, CD4+ were significantly increased both CLL indolent lymphoma, but not aggressive lymphoma myeloma. Interestingly, PD-1 expression decreased on inversely correlated numbers,...

10.3109/10428194.2012.673224 article EN Leukemia & lymphoma/Leukemia and lymphoma 2012-03-07

Background Bispecific antibodies are promising new therapeutics in B cell malignancies. Whether they lead to potent T activation despite described dysfunction chronic lymphocytic leukemia (CLL), and able effectively target high-risk or venetoclax-resistant samples, is currently unknown. Methods CD19 + lines primary (high-risk) CLL were cocultured vitro with healthy donor (HD) CLL-derived cells the presence of a CD3xCD19 dual affinity retargeting molecule (CD3xCD19 DART). Cell cytotoxicity,...

10.1136/jitc-2019-000218 article EN cc-by-nc Journal for ImmunoTherapy of Cancer 2020-06-01
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