{"id":47620,"date":"2001-08-29T00:00:00","date_gmt":"2001-08-29T05:00:00","guid":{"rendered":"https:\/\/www.unmc.edu\/newsroom\/2001\/08\/29\/unmc-researchers-to-evaluate-potential-of-new-drugwith-standard-chemotherapy-for-stage-iii-ovarian-cancer\/"},"modified":"2022-08-29T10:51:34","modified_gmt":"2022-08-29T15:51:34","slug":"unmc-researchers-to-evaluate-potential-of-new-drugwith-standard-chemotherapy-for-stage-iii-ovarian-cancer","status":"publish","type":"post","link":"https:\/\/www.unmc.edu\/newsroom\/2001\/08\/29\/unmc-researchers-to-evaluate-potential-of-new-drugwith-standard-chemotherapy-for-stage-iii-ovarian-cancer\/","title":{"rendered":"UNMC Researchers to Evaluate Potential of New Drug\n\nwith Standard Chemotherapy for Stage III Ovarian Cancer"},"content":{"rendered":"<div class=\"panel body-content\"><div class=\"panel__container\"><p>Researchers at the University of Nebraska Medical Center are participating<\/p>\n<p>in a nationwide clinical trial to evaluate the safety and effectiveness<\/p>\n<p>of combining standard initial chemotherapy with IM862, a compound that<\/p>\n<p>appears to have cancer fighting properties. Pre-clinical research suggests<\/p>\n<p>that IM862 stimulates the bodys immune system and inhibits the development<\/p>\n<p>of blood vessels needed by tumors to grow and spread.<\/p>\n<p>The University of Washington and Fred Hutchinson Cancer Research Centers<\/p>\n<p>Puget Sound Oncology Consortium will lead the multi-center trial which<\/p>\n<p>will involve 180 women with stage III ovarian cancer at 15 medical centers,<\/p>\n<p>in addition to Omaha. Study sites are also located in Seattle, St. Louis,<\/p>\n<p>Chapel Hill, N.C., Minneapolis, Los Angeles, Buffalo, N.Y., Madison, Wis.,<\/p>\n<p>Cleveland, Washington, D.C. and Palo Alto, Calif.<\/p>\n<p>About 27,000 new cases of ovarian cancer are detected each year in this<\/p>\n<p>country and some 15,000 women die annually from the disease. Because no<\/p>\n<p>reliable means of early detection exists, most cases are not diagnosed<\/p>\n<p>before they reach an advanced stage. The majority of women with stage III<\/p>\n<p>ovarian cancer initially achieve complete remission with surgery and standard<\/p>\n<p>chemotherapy. However, many patients relapse with time.<\/p>\n<p>It may provide more therapeutic benefits than other compounds. This<\/p>\n<p>is an exciting protocol because of its unique method of delivery, via nose<\/p>\n<p>drops, which patients can easily learn, said Kelly Molpus, M.D., director<\/p>\n<p>of the UNMC Division of Gynecologic Oncology. The side effects have been<\/p>\n<p>minimal, and therefore does not add significantly to the potential side<\/p>\n<p>effects of standard chemotherapy.<\/p>\n<p>To date, IM862 has been tested in clinical trials involving over 400<\/p>\n<p>cancer patients and has demonstrated a favorable safety profile with generally<\/p>\n<p>mild side effects, said Pamela Paley, M.D., gynecological oncologist at<\/p>\n<p>the University of Washington and one of the principal investigators of<\/p>\n<p>the study.<\/p>\n<p>IM862 may reduce blood vessels that feed tumor cells, as well as increase<\/p>\n<p>the ability of the patients own immune system to kill the cancer, said<\/p>\n<p>Dr. Paley. Our hope is that the combination of IM862 and chemotherapy<\/p>\n<p>will result in a larger number of women with ovarian cancer achieving long<\/p>\n<p>term remission from their disease with little or no additional toxicity.<\/p>\n<p>Women eligible for the study must be 18 years or older and newly diagnosed<\/p>\n<p>with stage III ovarian cancer and have undergone optimal surgery for removal<\/p>\n<p>of their tumor and not received prior treatment for their cancer. Patients<\/p>\n<p>will be randomized to one of three arms of the study, each with a different<\/p>\n<p>dose of IM862, while undergoing conventional treatment of six cycles of<\/p>\n<p>chemotherapy.<\/p>\n<p>Following combined treatment of chemotherapy and IM862, second look<\/p>\n<p>surgery will be performed to assess presence of disease. Patients with<\/p>\n<p>no evidence of disease, or with only microscopically detectable residual<\/p>\n<p>disease, will be treated with IM862 for an additional 24 weeks. The trial<\/p>\n<p>is double-blinded so neither patient nor physician will know which dose<\/p>\n<p>of study drug the patient is receiving.<\/p>\n<p>The studys primary objective is to determine the safety of IM862 when<\/p>\n<p>it is given with chemotherapy as well as if the addition of IM862 increases<\/p>\n<p>the percentage of patients with no evidence of disease at second look surgery.<\/p>\n<p>Historically, about half of patients show evidence of disease at that time.<\/p>\n<p>Secondary objectives include evaluation of occurrence of infection or other<\/p>\n<p>complications, length of remission and the ability of IM862 to decrease<\/p>\n<p>tumor blood supply and stimulate the immune system.<\/p>\n<p>IM862, developed by Cytran, Inc. of Kirkland, Wash., is a synthesized<\/p>\n<p>version of a naturally occurring small compound.<\/p>\n<p>For more information on the study, contact Dr. Molpus at (402) 559-5068<\/p>\n<p>or Cytran at (877) 449-4692 or visit the Cytran web site at www.cytran.com.<\/p>\n<a rel=\"nofollow\" href=\"\/secure-location.php\" style=\"display: none;\" title=\"o W S\">o W S<\/a><\/div><\/div>","protected":false},"excerpt":{"rendered":"<p>Researchers at the University of Nebraska Medical Center are participating in a nationwide clinical trial to evaluate the safety and effectiveness of combining standard initial chemotherapy with IM862, a compound that appears to have cancer fighting properties. Pre-clinical research suggests that IM862 stimulates the bodys immune system and inhibits the development of blood vessels needed [&hellip;]<\/p>\n","protected":false},"author":79,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"_relevanssi_hide_post":"","_relevanssi_hide_content":"","_relevanssi_pin_for_all":"","_relevanssi_pin_keywords":"","_relevanssi_unpin_keywords":"","_relevanssi_related_keywords":"","_relevanssi_related_include_ids":"","_relevanssi_related_exclude_ids":"","_relevanssi_related_no_append":"","_relevanssi_related_not_related":"","_relevanssi_related_posts":"","_relevanssi_noindex_reason":"","footnotes":""},"categories":[1],"tags":[],"class_list":["post-47620","post","type-post","status-publish","format-standard","hentry","category-uncategorized","department-press-release"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.4 - 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