Treatment of higher risk myelodysplastic syndrome patients unresponsive to hypomethylating agents with ON 01910.Na

التفاصيل البيبلوغرافية
العنوان: Treatment of higher risk myelodysplastic syndrome patients unresponsive to hypomethylating agents with ON 01910.Na
المؤلفون: Liwen Xu, John P. Renschler, Mai Tran, Alice C. Fan, Kunju Sridhar, Francois Wilhelm, Dean W. Felsher, Mahesh Seetharam, Peter L. Greenberg
المصدر: Leukemia research. 36(1)
سنة النشر: 2011
مصطلحات موضوعية: Oncology, Male, IV Infusion, Cancer Research, CD34, Drug resistance, Trisomy 8, Biochemistry, Gastroenterology, Stable Disease, Drug tolerance, Bone marrow sampling, DNA (Cytosine-5-)-Methyltransferases, Sulfones, Enzyme Inhibitors, Aged, 80 and over, Rigosertib, Hematology, Treatment Outcome, Female, medicine.drug, DNA (Cytosine-5-)-Methyltransferase 1, Risk, medicine.medical_specialty, Immunology, Glycine, Decitabine, Antineoplastic Agents, Biology, Article, Disease course, Internal medicine, medicine, Humans, In patient, Survival analysis, Aged, business.industry, Myelodysplastic syndromes, Cell Biology, DNA Methylation, medicine.disease, Survival Analysis, Surgery, Clinical trial, Hypomethylating agent, Drug Resistance, Neoplasm, Myelodysplastic Syndromes, Cancer research, business
الوصف: Abstract 4010 Patients with IPSS intermediate or high risk myelodysplastic syndrome (MDS) have few treatment options once their disease fails to respond to hypomethylating agent therapy. The styryl sulfone mitotic inhibitor ON 01910.Na, inhibits Polo-1 kinase, PI3-kinase and AKT pathways, and the drug has shown promising results in patients (pts) with advanced solid tumors (Jimeno et al, J Clin Onc 26:5504, 2008) and in Phase I/II studies of MDS pts, including those with trisomy 8 (Sloand at al, Proc ASH 2007, #822, Proc ASH 2008, #1651). In an ongoing Phase II clinical trial, we have treated 10 MDS pts unresponsive to at least 4 cycles (range 4–12 cycles) of hypomethylating agent therapy (5 post-azacytidine, 4 post-decitabine, and 1 pt treated with both agents) with ON 01910.Na. The pts had IPSS Intermediate-1 (n=3), Intermediate-2 (n=4) and High (n=3) risk MDS. The study cohort comprised pts with RAEB-1 (4 pts), RAEB-2 (3 pts) and RAEB-T (3 pts), with a median age of 80 years (range 65–86) and 2.3 year median (range 0.4–5.4) prior duration of MDS. Their cytogenetic profile included 5 pts with Good, 4 with Intermediate [t(8,10), t(14,18), +8, and (8+, 19+)], 1 with Poor risk cytogenetics (+8, 5q-, 1p-). At baseline, all pts were red blood cell transfusion-dependent. After the initial 2 pts were treated with 800mg/m2/day × 2day continuous IV infusion (CIVI)/week × 3weeks/month, the subsequent 8 patients received 1800mg/day × 3day CIVI q2weeks/month × 2 months, then monthly. Patients underwent bone marrow sampling and evaluation after every other cycle of treatment. To date, 7 pts have completed at least 2 cycles of therapy, with 2 pts having completed the full treatment course of 7 monthly cycles (median 4.7 for all pts). Responses according to IWG 2006 criteria were: Marrow CR (mCR) (2), Partial response (1), stable disease (SD) with hematologic improvement (HI) (2; 1 HI-E, N, 1 HI-P, N) = 5/10 overall responses (50%). Four pts had SD without HI, 1 pt progressed to AML. mCRs occurred in those with Disclosures: Off Label Use: The drug ON01910.Na is an investigational agent. Felsher:Cell Bioscience: On The Advisory Board. Wilhelm:Onconova Therapeutics Inc: Employment, Equity Ownership. Greenberg:Onconova Therapeutics Inc: Research Funding.
تدمد: 1873-5835
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e415b223b5135a6d4050beae55b40496
https://pubmed.ncbi.nlm.nih.gov/21924492
Rights: OPEN
رقم الانضمام: edsair.doi.dedup.....e415b223b5135a6d4050beae55b40496
قاعدة البيانات: OpenAIRE