Can the revised IPSS predict response to erythropoietic-stimulating agents in patients with classical IPSS low or intermediate-1 MDS?

نویسندگان

  • Valeria Santini
  • Jennifer Schemenau
  • Alessandro Levis
  • Enrico Balleari
  • Rosa Sapena
  • Lionel Adès
  • Agnès Guerci
  • Odile Beyne-Rauzy
  • Marie-Pierre Gourin
  • Stephane Cheze
  • Aspasia Stamatoullas
  • Alessandro Sanna
  • Daniela Gioia
  • Gianni Cametti
  • Dario Ferrero
  • Emmanuel Raffoux
  • Christian Rose
  • Antonella Poloni
  • Thomas Prebet
  • Laurence Legros
  • Shanti Natarajan-Amé
  • Pierre Fenaux
  • Ulrich Germing
  • François Dreyfus
  • Sophie Park
چکیده

Can the revised IPSS predict response to erythropoietic-stimulating agents in patients with classical IPSS low or intermediate-1 MDS? The " classical " International Prognostic Scoring System (IPSS), based on cytogenetics, marrow blast percentage, and number of cytopenias, has played a major role in prognosis assessment in myelodysplastic syndromes (MDS). 1 The recently published revised IPSS (IPSS-R), using the same parameters, but with 5 rather than 3 cytogenetic subgroups and new cutoff values for cytopenias and marrow blast percentages, refines the original IPSS prognostic value. 2,3 However, its prognostic value for response to erythropoiesis-stimulating agents (ESA) has not been assessed. We analyzed it retrospectively in 456 IPSS low/intermediate (Int)-1–risk MDS patients treated with ESA in France, Germany, and Italy. Those 456 patients had serum erythropoietin (EPO) ,500 mU/mL and hemoglobin (Hb) <10 g/dL and had received ESA (EPO alfa or b 40 000-60 000 IU/week, or darbepoetin 150-300 mg/week) for at least 12 weeks. In addition to IPSS-R parameters, age, sex, serum EPO level, serum ferritin (SF), red blood cell (RBC) transfusion requirement before ESA onset were assessed for response to ESA (based on International Working Group 2006 criteria), and overall survival (OS) from ESA onset. Characteristics of the 456 patients at ESA onset are listed in Table 1. Seventy-one percent of the patients had never received RBC transfusions, and their median Hb level was 9.3g/dL (range 7.0-10); 29% of patients had received at least 4 RBC concentrates/8 weeks before ESA onset (with a maximum of 12 concentrates). Median SF was 357 ng/mL and serum EPO was 60 mU/mL (range 6-483). IPSS was low in 55% and Int-1 in 45% of patients. IPSS-R was very low in 15%, low in 61%, intermediate in 19%, and high in 4% of the patients. A total of 303 (61%) patients had an erythroid response, including 72% and 52% of low and Int-1 risk patients, respectively (P 5 .001). Using IPSS-R, 85%, 68%, 48%, and 31% of patients had erythroid response in the very low, low, intermediate, and high-risk groups, respectively (P , .0001). Other prognostic factors of erythroid response, in univariate analysis , included individual IPSS-R parameters analyzed according to Applying 1 point to each of the following unfavorable variables of response to ESA, serum EPO .200 mU/mL (51), SF .350 ng/mL (51), and IPSS-R (very low 5 0, low 5 1, intermediate 5 2, and high 5 3) yielded a score ranging from …

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

The revised IPSS is a powerful tool to evaluate the outcome of MDS patients treated with azacitidine: the GFM experience.

The revised IPSS is a powerful tool to evaluate the outcome of MDS patients treated with azacitidine: the GFM experience The International Prognostic Scoring System (IPSS), which is based on cytogenetics, BM blast percentage, and number of cytopenias, has played a major role in prognosis assessment in myelodysplastic syndrome (MDS) since its publication in 1997. The recently published revised I...

متن کامل

Validation of the IPSS-R in lenalidomide-treated, lower-risk myelodysplastic syndrome patients with del(5q)

Myelodysplastic syndromes (MDS) are a heterogeneous group of hematopoietic stem cell disorders with variable clinical outcome. The International Prognostic Scoring System (IPSS) categorizes untreated MDS patients into one of four risk groups (low, intermediate [Int]-1, Int-2 and high) based on the percentage of bone marrow blasts, presence of cytogenetic abnormalities and number of cytopenias. ...

متن کامل

The myelodysplastic syndrome-comorbidity index provides additional prognostic information on patients stratified according to the revised international prognostic scoring system.

The myelodysplastic syndromes are a heterogeneous group of disorders of the hematopoietic stem cell and stem cell niche. The revised version of the International Prognostic Scoring System (IPSS-R), which is based on disease-related factors, was recently published. In 2010, the MDS-specific Comorbidity Index (MDS-CI) was developed by the Italian MDS study group and was validated using data of th...

متن کامل

Rare Cytogenetic Abnormalities in Myelodysplastic Syndromes

The karyotype represents one of the main cornerstones for the International Prognostic Scoring System (IPSS) and the revised IPSS-R (IPSS-R) that are most widely used for prognostication in patients with myelodysplastic syndromes (MDS). The most frequent cytogenetic abnormalities in MDS, i.e. del(5q), -7/del(7q), +8, complex karyotypes, or -Y have been extensively explored for their prognostic ...

متن کامل

Allogeneic stem cell transplantation in patients with myelodysplastic syndrome: outcome analysis according to the International Prognostic Scoring System.

We determined the outcome of patients with myelodysplastic syndrome (MDS) and secondary acute myeloid leukemia (sAML) after allogeneic stem cell transplantation according to their international prognostic scoring system (IPSS) risk categories at diagnosis. A total of 11 females and 7 males, with a median age of 45 years, were transplanted. With a median follow-up of 60 months, the 6-year actuar...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Blood

دوره 122 13  شماره 

صفحات  -

تاریخ انتشار 2013