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International Myeloma Working Group consensus criteria for response and minimal residual disease assessment in multiple myeloma.
Kumar, Shaji; Paiva, Bruno; Anderson, Kenneth C; Durie, Brian; Landgren, Ola; Moreau, Philippe; Munshi, Nikhil; Lonial, Sagar; Bladé, Joan; Mateos, Maria-Victoria; Dimopoulos, Meletios; Kastritis, Efstathios; Boccadoro, Mario; Orlowski, Robert; Goldschmidt, Hartmut; Spencer, Andrew; Hou, Jian; Chng, Wee Joo; Usmani, Saad Z; Zamagni, Elena; Shimizu, Kazuyuki; Jagannath, Sundar; Johnsen, Hans E; Terpos, Evangelos; Reiman, Anthony; Kyle, Robert A; Sonneveld, Pieter; Richardson, Paul G; McCarthy, Philip; Ludwig, Heinz; Chen, Wenming; Cavo, Michele; Harousseau, Jean-Luc; Lentzsch, Suzanne; Hillengass, Jens; Palumbo, Antonio; Orfao, Alberto; Rajkumar, S Vincent; Miguel, Jesus San; Avet-Loiseau, Herve.
Afiliación
  • Kumar S; Division of Hematology, Mayo Clinic, Rochester, MN, USA. Electronic address: kumar.shaji@mayo.edu.
  • Paiva B; Clinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Pamplona, Spain.
  • Anderson KC; Dana-Farber Cancer Institute, Boston, MA, USA.
  • Durie B; Cedars-Sinai Comprehensive Cancer Center, Los Angeles, CA, USA.
  • Landgren O; Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Moreau P; University Hospital, Nantes, France.
  • Munshi N; Dana-Farber Cancer Institute, Boston, MA, USA.
  • Lonial S; Department of Hematology and Medical Oncology, Winship Cancer Institute, Emory University School of Medicine, Atlanta, GA, USA.
  • Bladé J; Hospital Clinic, Barcelona, Spain.
  • Mateos MV; University Hospital of Salamanca/IBSAL, Salamanca, Spain.
  • Dimopoulos M; Department of Clinical Therapeutics, University of Athens, School of Medicine, Athens, Greece.
  • Kastritis E; Department of Clinical Therapeutics, University of Athens, School of Medicine, Athens, Greece.
  • Boccadoro M; Myeloma Unit, Division of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Citta della Salute e della Scienza di Torino, Torino, Italy; Mount Sinai Cancer Institute, New York, NY, USA.
  • Orlowski R; MD Anderson Comprehensive Cancer Center, Houston, TX, USA.
  • Goldschmidt H; Department of Hematology, Oncology and Rheumatology, University of Heidelberg, Heidelberg, Germany.
  • Spencer A; The Alfred Hospital, Melbourne, VIC, Australia.
  • Hou J; Chang Zheng Hospital, Shanghai, China.
  • Chng WJ; National University Health System, Singapore.
  • Usmani SZ; Levine Cancer Institute, Carolinas HealthCare System, Charlotte, NC, USA.
  • Zamagni E; Seragnoli Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
  • Shimizu K; Tokai Central Hospital, Kakamigahara, Japan.
  • Jagannath S; Mount Sinai Cancer Institute, New York, NY, USA.
  • Johnsen HE; Department of Hematology, Clinical Cancer Research Center, Aalborg University Hospital, Aalborg, Denmark.
  • Terpos E; Department of Clinical Therapeutics, University of Athens, School of Medicine, Athens, Greece.
  • Reiman A; Dalhousie University Medical School, Dalhousie, Nova Scotia, Canada.
  • Kyle RA; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Sonneveld P; Erasmus Medical Center, Rotterdam, Netherlands.
  • Richardson PG; Dana-Farber Cancer Institute, Boston, MA, USA.
  • McCarthy P; Roswell Park Cancer Institute, Buffalo, NY, USA.
  • Ludwig H; Wilhelminenspital Der Stat Wien, Vienna, Austria.
  • Chen W; Beijing Chaoyang Hospital, Beijing, China.
  • Cavo M; Seragnoli Institute of Hematology, Bologna University School of Medicine, Bologna, Italy.
  • Harousseau JL; University Hospital, Nantes, France.
  • Lentzsch S; Columbia University, New York, NY, USA.
  • Hillengass J; Department of Hematology, Oncology and Rheumatology, University of Heidelberg, Heidelberg, Germany.
  • Palumbo A; Myeloma Unit, Division of Hematology, University of Torino, Azienda Ospedaliero-Universitaria Citta della Salute e della Scienza di Torino, Torino, Italy.
  • Orfao A; University Hospital of Salamanca/IBSAL, Salamanca, Spain.
  • Rajkumar SV; Division of Hematology, Mayo Clinic, Rochester, MN, USA.
  • Miguel JS; Clinica Universidad de Navarra, Centro de Investigacion Medica Aplicada (CIMA), Pamplona, Spain.
  • Avet-Loiseau H; University of Toulouse, Toulouse, France.
Lancet Oncol ; 17(8): e328-e346, 2016 08.
Article en En | MEDLINE | ID: mdl-27511158
ABSTRACT
Treatment of multiple myeloma has substantially changed over the past decade with the introduction of several classes of new effective drugs that have greatly improved the rates and depth of response. Response criteria in multiple myeloma were developed to use serum and urine assessment of monoclonal proteins and bone marrow assessment (which is relatively insensitive). Given the high rates of complete response seen in patients with multiple myeloma with new treatment approaches, new response categories need to be defined that can identify responses that are deeper than those conventionally defined as complete response. Recent attempts have focused on the identification of residual tumour cells in the bone marrow using flow cytometry or gene sequencing. Furthermore, sensitive imaging techniques can be used to detect the presence of residual disease outside of the bone marrow. Combining these new methods, the International Myeloma Working Group has defined new response categories of minimal residual disease negativity, with or without imaging-based absence of extramedullary disease, to allow uniform reporting within and outside clinical trials. In this Review, we clarify several aspects of disease response assessment, along with endpoints for clinical trials, and highlight future directions for disease response assessments.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Guías de Práctica Clínica como Asunto / Neoplasia Residual / Mieloma Múltiple Tipo de estudio: Guideline / Prognostic_studies Límite: Humans Idioma: En Revista: Lancet Oncol Asunto de la revista: NEOPLASIAS Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Protocolos de Quimioterapia Combinada Antineoplásica / Guías de Práctica Clínica como Asunto / Neoplasia Residual / Mieloma Múltiple Tipo de estudio: Guideline / Prognostic_studies Límite: Humans Idioma: En Revista: Lancet Oncol Asunto de la revista: NEOPLASIAS Año: 2016 Tipo del documento: Article