Renato Zambello

ORCID: 0000-0002-8799-5324
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About
Contact & Profiles
Research Areas
  • Multiple Myeloma Research and Treatments
  • Chronic Lymphocytic Leukemia Research
  • Lymphoma Diagnosis and Treatment
  • Immune Cell Function and Interaction
  • Protein Degradation and Inhibitors
  • Cancer Treatment and Pharmacology
  • Immunodeficiency and Autoimmune Disorders
  • T-cell and B-cell Immunology
  • Peptidase Inhibition and Analysis
  • Interstitial Lung Diseases and Idiopathic Pulmonary Fibrosis
  • HIV Research and Treatment
  • Acute Myeloid Leukemia Research
  • Sarcoidosis and Beryllium Toxicity Research
  • Chronic Myeloid Leukemia Treatments
  • Viral-associated cancers and disorders
  • Pneumocystis jirovecii pneumonia detection and treatment
  • T-cell and Retrovirus Studies
  • Cancer therapeutics and mechanisms
  • Monoclonal and Polyclonal Antibodies Research
  • Acute Lymphoblastic Leukemia research
  • HIV/AIDS drug development and treatment
  • Myeloproliferative Neoplasms: Diagnosis and Treatment
  • Peripheral Neuropathies and Disorders
  • Heat shock proteins research
  • CNS Lymphoma Diagnosis and Treatment

University of Padua
2016-2025

Veneto Institute of Molecular Medicine
2016-2025

Azienda Ospedaliera di Padova
2014-2023

Sarah Cannon
2023

Institute of Molecular Medicine
2019-2022

Fondazione Gimema Onlus
2009-2021

Multiple Myeloma Research Foundation
2021

March of Dimes
2021

The University of Texas MD Anderson Cancer Center
2019

Consorci Institut D'Investigacions Biomediques August Pi I Sunyer
2019

Michel Attal Paul G. Richardson S. Vincent Rajkumar Jesús F. San Miguel Meral Beksaç and 95 more Ivan Špıčka Xavier Leleu Fredrik Schjesvold Philippe Moreau Meletios Α. Dimopoulos Jeffrey Shang-Yi Huang Jiří Minařík Michèle Cavo H. Miles Prince Sandrine Macé Kathryn P. Corzo Frank Campana Solenn Le-Guennec Franck Dubin Kenneth C. Anderson Michel Attal Paul G. Richardson S. Vincent Rajkumar Jesús F. San Miguel Meral Beksaç Ivan Špıčka Xavier Leleu Fredrik Schjesvold Philippe Moreau Meletios Α. Dimopoulos Jeffrey Shang-Yi Huang Jiří Minařík Michèle Cavo H. Miles Prince Sandrine Macé Kathryn P. Corzo Frank Campana Solenn Le-Guennec Franck Dubin Kenneth C. Anderson Simon J. Harrison Wojt Janowski Ian Kerridge Andrew Spencer Michel Delforge Karel Fostier Philip Vlummens Ka Lung Wu Richard LeBlanc Michel Pavic Michaël Sébag Roman Hájek Vladimír Maisnar Luděk Pour Henrik Gregersen Lotfi Benbouker Denis Caillot Martine Escoffre‐Barbe Thierry Façon Laurent Frenzel Cyrille Hulin Lionel Karlin Brigitte Kolb Brigitte Pegourié Aurore Perrot Mourad Tiab Laure Vincent Dietger Niederwieser Αchilles Anagnostopoulos Sosana Delimpasi Marie‐Christine Kyrtsonis Argiris Symeonidis Árpád Illés Gábor Mikala Zsolt Nagy Sara Bringen Paolo Corradini Fabio Ciceri Roberto M. Lemoli Anna Marina Liberati Chiara Nozzoli Renato Zambello Shinsuke Iida Takashi Ikeda Satoshi Iyama Morio Matsumoto Chihiro Shimazaki Kazutaka Sunami Kenshi Suzuki Michihiro Uchiyama Youngil Koh Kihyun Kım Jae Hoon Lee Chang‐Ki Min Hillary Blacklock Hugh J. B. Goodman Annette Neylon David Simpson Sebastian Grosicki Artur Jurczyszyn

10.1016/s0140-6736(19)32556-5 article EN The Lancet 2019-11-14

Purpose In patients with myeloma, thalidomide significantly improves outcomes but increases the risk of thromboembolic events. this randomized, open-label, multicenter trial, we compared aspirin (ASA) or fixed low-dose warfarin (WAR) versus low molecular weight heparin (LMWH) for preventing thromboembolism in myeloma treated thalidomide-based regimens. Patients and Methods A total 667 previously untreated who received thalidomide-containing regimens had no clinical indication...

10.1200/jco.2010.31.6844 article EN Journal of Clinical Oncology 2011-02-01

Bortezomib-melphalan-prednisone (VMP) has improved overall survival in multiple myeloma. This randomized trial compared VMP plus thalidomide (VMPT) induction followed by bortezomib-thalidomide maintenance (VMPT-VT) with patients newly diagnosed myeloma.We randomly assigned 511 who were not eligible for transplantation to receive VMPT-VT (nine 5-week cycles of VMPT 2 years VT maintenance) or without maintenance).In the initial analysis a median follow-up 23 months, complete response rate from...

10.1200/jco.2013.52.0023 article EN Journal of Clinical Oncology 2014-01-22

B cell chronic lymphocytic leukemia (B-CLL) is a neoplastic disorder characterized by accumulation of lymphocytes due to uncontrolled growth and resistance apoptosis. Analysis cells freshly isolated from 40 patients with demonstrated that the Src kinase Lyn, switch molecule couples receptor downstream signaling, displays anomalous properties. Lyn remarkably overexpressed at protein level in leukemic as compared normal lymphocytes, substantial aliquot anomalously present cytosol. Whereas...

10.1172/jci22094 article EN Journal of Clinical Investigation 2005-01-13

B cell chronic lymphocytic leukemia (B-CLL) is a neoplastic disorder characterized by accumulation of lymphocytes due to uncontrolled growth and resistance apoptosis. Analysis cells freshly isolated from 40 patients with demonstrated that the Src kinase Lyn, switch molecule couples receptor downstream signaling, displays anomalous properties. Lyn remarkably overexpressed at protein level in leukemic as compared normal lymphocytes, substantial aliquot anomalously present cytosol. Whereas...

10.1172/jci200522094 article EN Journal of Clinical Investigation 2005-01-13

The ability of NK cells to kill a wide range tumor or virally infected target as well normal allogeneic T cell blasts appears depend upon the concerted action multiple triggering receptors. In this study, using two specific monoclonal antibodies [(mAb) MA152 and LAP171], we identified receptor expressed at surface dimer approximately 80 kDa (NKp80). NKp80 is by virtually all fresh activated minor subset characterized CD56 antigen. expression was also detected in CD3– 6 / 10 CD3+ large...

10.1002/1521-4141(200101)31:1<233::aid-immu233>3.0.co;2-4 article EN European Journal of Immunology 2001-01-01

A multiparameter analysis, which included the evaluation of clinical features, cell morphology, karyo-type, phenotypic and functional immunologic findings, T-cell receptor beta-chain configuration was performed on 34 patients with lymphoproliferative disease granular lymphocytes (LDGL). The two-fold aim study to identify most useful tools that would more accurately characterize these deal problem classifying disorders. data presented in this article suggest a single parameter may not be...

10.1002/1097-0142(19871215)60:12<2971::aid-cncr2820601220>3.0.co;2-o article EN Cancer 1987-12-15

The combination of bendamustine (B) and rituximab (R) is efficacious, with favorable toxicity in mantle-cell lymphoma (MCL). In this phase II study, we combined cytarabine R B (R-BAC) patients MCL age ≥ 65 years who were previously untreated or relapsed refractory (R/R) after one prior immunochemotherapy treatment.In stage one, established the maximum-tolerated dose (MTD) R-BAC. two, received (375 mg/m(2) intravenously [IV] on day 1), (70 IV days 2 3), (MTD to 4) every 28 for four six...

10.1200/jco.2012.45.9842 article EN Journal of Clinical Oncology 2013-02-12

Lymphoproliferative disease of granular lymphocytes (LDGL) is a recently recognized, relatively rare atypical lymphocytosis characterized by the presence over 2000 with cytoplasmic azurophilic granules/mm3 in peripheral blood. The clinical course heterogeneous, varying from spontaneous regression to progressive, malignant disease. As consequence, intervention not standardized. In worldwide multicenter study, authors observed 151 patients LDGL for mean follow-up time 29 months. Forty-three...

10.1002/1097-0142(19900115)65:2<341::aid-cncr2820650227>3.0.co;2-2 article EN Cancer 1990-01-15

Treatment of secondary CNS dissemination in patients with aggressive lymphomas remains an important, unmet clinical need. Herein, we report the final results a multicenter phase II trial addressing new treatment for lymphoma based on encouraging experiences high doses antimetabolites primary and rituximab plus high-dose sequential chemoimmunotherapy (R-HDS) relapsed lymphoma.HIV-negative B-cell involvement at diagnosis or relapse, age 18 to 70 years, Eastern Cooperative Oncology Group...

10.1200/jco.2015.61.1236 article EN Journal of Clinical Oncology 2015-08-18

8002 Background: High and comparable rates of MRD negativity were seen in NDMM pts after 4 28-day induction cycles with KRd followed by ASCT consolidation (KRd_ASCT_KRd) 12 (KRd12), showing the superiority both regimens over KCd induction-ASCT-KCd (KCd-ASCT-KCd) (Gay F ASH 2018). Here we evaluated benefit KRd_ASCT_KRd vs KRd12 specific subgroups pts. Methods: 474 ≤65 years randomized to or KCd_ASCT_KCd. We compared rate ≥VGPR, ≥CR, sCR, (centralized, second generation flow cytometry,...

10.1200/jco.2019.37.15_suppl.8002 article EN Journal of Clinical Oncology 2019-05-20

High levels of circulating tumor plasma cells (CTC-high) in patients with multiple myeloma are a marker aggressive disease. We aimed to confirm the prognostic impact and identify possible cutoff value CTC-high for prediction progression-free survival (PFS) overall (OS), context concomitant risk features minimal residual disease (MRD) achievement.CTC were analyzed at diagnosis two-tube single-platform flow cytometry (sensitivity 4 × 10-5) enrolled multicenter randomized FORTE clinical trial...

10.1200/jco.21.01393 article EN Journal of Clinical Oncology 2022-06-06

Abstract T cell large granular lymphocytic leukemia (T-LGLL) is a rare lymphoproliferative disorder of mature, clonally expanded cells, where somatic-activating STAT3 mutations are common. Although T-LGLL has been described as chronic response to an antigen, the function non-leukemic immune system in this largely uncharacterized. Here, by utilizing single-cell RNA and receptor profiling (scRNA+TCRαβ-seq), we show that irrespective mutation status, clonotypes more cytotoxic exhausted than...

10.1038/s41467-022-29173-z article EN cc-by Nature Communications 2022-04-11

Abstract The accumulation of T cells and monocytes at sites ongoing inflammation represents the earliest step in series events that lead to granuloma formation sarcoidosis. In this study, we evaluated pulmonary production IFN-inducible protein 10 (IP-10), a CXC chemokine stimulates directional migration activated cells. Striking levels IP-10 were demonstrated bronchoalveolar lavage (BAL) fluid 24 patients with sarcoidosis lymphocytic alveolitis, as compared inactive disease or control...

10.4049/jimmunol.161.11.6413 article EN The Journal of Immunology 1998-12-01
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