Relay-Version: version B 2.10 5/3/83; site utzoo.UUCP Posting-Version: version B 2.10.2 9/18/84 exptools; site hlexa.UUCP Path: utzoo!watmath!clyde!cbosgd!ihnp4!hlexa!hsf From: hsf@hlexa.UUCP (Henry Friedman) Newsgroups: net.med Subject: Re: Query on treatment of Hypernephroma and other visceral carcinoma. Message-ID: <4720@hlexa.UUCP> Date: Wed, 20-Nov-85 14:21:10 EST Article-I.D.: hlexa.4720 Posted: Wed Nov 20 14:21:10 1985 Date-Received: Thu, 21-Nov-85 07:27:58 EST References: <1046@gitpyr.UUCP> Distribution: net Organization: AT&T Bell Laboratories, Short Hills, NJ Lines: 21 > I suspect one of the best avenues being researched at present are the > monoclonal antibodies with toxic attachments. Is there current work > being done on visceral carcinoma? Is any at the experimental or field > stage? I'm particularly interested on current work with hypernephroma, > and would appreciate the pooled knowledge of the net. .... > Don Barry (Chemistry Dept) CSnet: cmpbsdb%gitpyr.GTNET@gatech.CSNET I'm not familiar with hypernephroma, but the most promising research for the class of tumors you mention (other than the monoclonal antibody approach) involves the genetic-engineered version of the natural hormone TNF (tumor necrosis factor). Human testing has recently begun in the US (original live testing was in Japan). I believe four different genetic engineering companies are involved. A combination of TNF and interferon also showed promise. The first phases of live testing usually concentrate on issues of safety, but I'd think that some announcements of effectiveness will be due shortly. My sources are articles in the Wall Street Journal over the past few months (some of the best-documented popular medical reporting). --Henry Friedman