CHICAGO, June 6, 2011 /PRNewswire/ -- Cell Therapeutics, Inc. ("CTI") (NASDAQ: CTICDJorge Cortes, M.D. and discussed at the 2011 Annual Meeting of the American Society of Clinical Oncology (ASCO) by Farhad Ravandi, M.D., who presided over the ASCO discussion session, both of the University of Texas M.D. Anderson Cancer Center. They concluded that once daily oral tosedostat was well-tolerated and demonstrated encouraging response rates at the interim evaluation time point including a high response rate among patients who received prior hypomethylating agents, which suggests combination studies of tosedostat with hypomethylating agents in first-line elderly AML patients should be investigated. Tosedostat is a novel, orally administered AADR (amino acid deprivation response) inducer, which targets and deprives sensitive tumor cells of amino acids by blocking protein recycling resulting in tumor cell death.
"While only interim response evaluation data is available, the results are very encouraging especially when one considers the fragile and difficult to treat nature of the patient population studied," said Jorge Cortes, M.D., of the University of Texas M.D. Anderson Cancer Center, an investigator on the tosedostat study. "An interesting observation is that 9 of the 15 responders were observed in patients who received prior hypomethylating agent therapy. These preliminary results support the preclinical data and suggest a rationale for exploring tosedostat in the types of patient usually treated with hypomethylating agents like decitabine or azacytidine in both elderly AML and MDS (myelodysplastic syndrome)."
The phase II study enrolled 73 patients randomized to two tosedostat dose regimens — 120 mg once daily for six months or 240 mg once daily for two months followed by 120 mg once daily for four months. The median age of the patients was 72 years old. Prior primary induction therapy for AML included 61% of the patients treated with Ara-C plus anthracycline or other Ara-C regimens, 33% of the patients treated with hypomethylating agents and 4% of the patients treated with other regimens. Fifty-two percent had been refractory to primary induction therapy and 21% had shown a response of less than six months. The overall response rate to tosedostat was 21% and was similar between treatment arms. In patients who were evaluable (i.e., had a post-baseline bone marrow assessment) (n=50) the response rate was 30%. Nine of the 15 responders (60%) had received prior hypomethylating agents suggesting that these patients were more likely to respond to tosedostat than those treated with traditional AML therapy. Tosedostat was generally well-tolerated. The most common grade >/= 3 treatment-related adverse events were febrile neutropenia (in 29% of patients) and thrombocytopenia (in 22% of patients).
"While being only interim data, the observed disease control rate at 3 months of 51% (bone marrow CR/PR/SD) with 30% of evaluable patients having a bone marrow response are encouraging results in such a difficult to treat disease," said Jack Singer, M.D., Chief Medical Officer of CTI. "Of great interest, tosedostat was most active in patients with prior hematologic disorders such as myelodysplastic syndromes that had evolved into AML and was particularly active in patients that had failed prior therapy with standard hypomethylating agents. If these data continue to hold up on the six month evaluation, we believe these results would support exploration of tosedostat combination with a hypomethylating agent as first-line therapy for elderly patients with AML and MDS"
The poster from the conference is available at www.celltherapeutics.com/investor_updates.
Tosedostat is an oral, AADR inducer that has demonstrated significant anti-tumor responses in blood-related cancers and solid tumors in phase I-II clinical trials. CTI has exclusive marketing and co-development rights to Chroma Therapeutics Ltd.'s drug candidate tosedostat in North, Central and South America.
About Cell Therapeutics, Inc.
Headquartered in Seattle, CTI is a biopharmaceutical company committed to developing an integrated portfolio of oncology products aimed at making cancer more treatable.
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This press release includes forward-looking statements that involve a number of risks and uncertainties, the outcome of which could materially and/or adversely affect actual future results. Specifically, the risks and uncertainties that could affect the development of tosedostat include risks associated with preclinical and clinical developments in the biopharmaceutical industry in general and with tosedostat in particular including, without limitation, the potential failure of tosedostat to prove safe and effective for the treatment of AML, the potential failure of combination studies of tosedostat with hypomethylating agents in treating AML and/or MDS, determinations by regulatory, patent, and administrative governmental authorities, competitive factors, technological developments, costs of developing, producing, and selling tosedostat, and the risk factors listed or described from time to time in CTI's filings with the Securities and Exchange Commission including, without limitation, CTI's most recent filings on Forms 10-K, 8-K, and 10-Q. Except as may be required by law, CTI does not intend to update or alter its forward-looking statements whether as a result of new information, future events, or otherwise.
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SOURCE Cell Therapeutics, Inc.
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