Literature DB >> 20015241

Treatment response to bortezomib in multiple myeloma correlates with plasma hepatocyte growth factor concentration and bone marrow thrombospondin concentration.

Pour Ludek1, Svachova Hana, Adam Zdenek, Almasi Martina, Kralova Dana, Buchler Tomas, Kovarova Lucie, Krejci Marta, Michalek Jaroslav, Penka Miroslav, Vorlicek Jiri, Hajek Roman.   

Abstract

Multiple myeloma (MM) is associated with increased rate of bone marrow angiogenesis. Increased concentration of hepatocyte growth factor (HGF) is associated with poor prognosis in patients treated with conventional chemotherapy or thalidomide. We have shown previously that decreased level of thrombospondin, an angiogenesis inhibitor, correlates with poor response to high-dose chemotherapy. The aim of our current study was to evaluate association between therapeutic response to bortezomib and thrombospondin and HGF levels. Peripheral blood plasma concentration of HGF and bone marrow plasma concentration of thrombospondin were measured in patients with MM prior to the initiation of bortezomib therapy. Overall, 58 patients were enrolled, 44/58 (76%) of them with relapsed disease. Treatment outcomes were analyzed for possible associations with pretreatment HGF and thrombospondin levels. Patients who achieved complete response had significantly higher pretreatment HGF levels and lower pretreatment thrombospondin levels than others. More than 70% of patients with low pretreatment HGF and high pretreatment thrombospondin concentrations achieved very good partial response or complete response, in contrast to only 20% of patients with high HGF and low thrombospondin levels. High pretreatment thrombospondin and low pretreatment HGF concentrations are associated with therapeutic response to bortezomib in patients with MM.

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Year:  2009        PMID: 20015241     DOI: 10.1111/j.1600-0609.2009.01396.x

Source DB:  PubMed          Journal:  Eur J Haematol        ISSN: 0902-4441            Impact factor:   2.997


  9 in total

Review 1.  Tumor-host cell interactions in the bone disease of myeloma.

Authors:  Jessica A Fowler; Claire M Edwards; Peter I Croucher
Journal:  Bone       Date:  2010-07-13       Impact factor: 4.398

2.  Variation in innate immunity genes and risk of multiple myeloma.

Authors:  Mark P Purdue; Qing Lan; Idan Menashe; Tongzhang Zheng; Yawei Zhang; Meredith Yeager; H Dean Hosgood; Shelia H Zahm; Stephen J Chanock; Nathaniel Rothman; Dalsu Baris
Journal:  Hematol Oncol       Date:  2011-03       Impact factor: 5.271

3.  Inhibition of Transforming Growth Factor-β Activation Diminishes Tumor Progression and Osteolytic Bone Disease in Mouse Models of Multiple Myeloma.

Authors:  Ailing Lu; Manuel A Pallero; Weiqi Lei; Huixian Hong; Yang Yang; Mark J Suto; Joanne E Murphy-Ullrich
Journal:  Am J Pathol       Date:  2016-01-20       Impact factor: 4.307

4.  Lipopolysaccharide-Induced CXCL10 mRNA Level and Six Stimulant-mRNA Combinations in Whole Blood: Novel Biomarkers for Bortezomib Responses Obtained from a Prospective Multicenter Trial for Patients with Multiple Myeloma.

Authors:  Takashi Watanabe; Masato Mitsuhashi; Morihiko Sagawa; Masaki Ri; Kenshi Suzuki; Masahiro Abe; Ken Ohmachi; Yasunori Nakagawa; Shingen Nakamura; Mizuki Chosa; Shinsuke Iida; Masahiro Kizaki
Journal:  PLoS One       Date:  2015-06-26       Impact factor: 3.240

5.  Phase II study of the c-MET inhibitor tivantinib (ARQ 197) in patients with relapsed or relapsed/refractory multiple myeloma.

Authors:  Muhamed Baljevic; Shadia Zaman; Veerabhadran Baladandayuthapani; Yan Heather Lin; Claudia Morales de Partovi; Zuzana Berkova; Behrang Amini; Sheeba K Thomas; Jatin J Shah; Donna M Weber; Min Fu; Charles S Cleeland; Xin Shelley Wang; Christine M Stellrecht; Richard E Davis; Varsha Gandhi; Robert Z Orlowski
Journal:  Ann Hematol       Date:  2017-03-23       Impact factor: 3.673

6.  ARQ-197, a small-molecule inhibitor of c-Met, reduces tumour burden and prevents myeloma-induced bone disease in vivo.

Authors:  Darren L Lath; Clive H Buckle; Holly R Evans; Matthew Fisher; Jenny M Down; Michelle A Lawson; Andrew D Chantry
Journal:  PLoS One       Date:  2018-06-20       Impact factor: 3.240

Review 7.  Targeting multiple-myeloma-induced immune dysfunction to improve immunotherapy outcomes.

Authors:  Sergio Rutella; Franco Locatelli
Journal:  Clin Dev Immunol       Date:  2012-04-11

8.  High MET gene copy number predicted poor prognosis in primary intestinal diffuse large B-cell lymphoma.

Authors:  Wan-Ting Huang; Shih-Sung Chuang
Journal:  Diagn Pathol       Date:  2013-02-04       Impact factor: 2.644

9.  Targeting MET kinase with the small-molecule inhibitor amuvatinib induces cytotoxicity in primary myeloma cells and cell lines.

Authors:  Cornel Joseph Phillip; Shadia Zaman; Shujun Shentu; Kumudha Balakrishnan; Jiexin Zhang; Veera Baladandayuthapani; Pietro Taverna; Sanjeev Redkar; Michael Wang; Christine Marie Stellrecht; Varsha Gandhi
Journal:  J Hematol Oncol       Date:  2013-12-10       Impact factor: 17.388

  9 in total

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