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Cancer Meeting Highlights the Good and Bad of the Immune System

http://www.fool.com/investing/general/2013/05/15/cancer-meeting-highlights-the-good-and-bad-of-the.aspx

Brian Orelli
May 15, 2013

Biotech investors rejoice. The ASCO abstracts are here. The annual meeting of the American Society of Clinical Oncology starts on May 31, but the organization releases most of the 4,700 abstracts -- available here -- tonight.

Here's a breakdown of some of two themes we'll see at the meeting.

Harnessing the immune system
In theory, immune cells can recognize and kill tumors, but cancer cells have developed molecular breaks that tell the immune cells that they shouldn't be killed. Drugs developed by Roche (NASDAQOTH: RHHBY) and Bristol-Myers Squibb (NYSE: BMY) are designed to block those breaks, allowing T cells to do their job.

The molecular break involves PD-L1 on the tumor cell binding to two receptors, PD-1 and B7.1, on the T cells, which signals to the T cell not to kill the tumor cell. There's also another molecule in the same family called PD-L2 on tumors that also activates the blocking signal through PD-1.

Roche's MPDL3280A acts on the tumor side, binding to PD-L1 to block the signal. Bristol's nivolumab binds to PD-1 on the T cell to block the signal.

Both trials testing MPDL3280A and nivolumab are phase 1 trials, but they produced fairly remarkable results.

The trial that tested MPDL3280A in patients with lung, melanoma, kidney, head and neck, colorectal, and bladder cancers that had progressed after multiple prior treatment produced a 36% overall response rate in patients whose tumors stained positive for PD-L1. Of the 29 patients who responded to the drug -- PD-L1 negative and positive -- 26 continued to respond some three to 15 months later. That's pretty impressive given the amount of pretreatment.

Nivolumab was combined with Yervoy, Bristol's melanoma drug that stimulates the immune system in a different way. When the drugs were given concurrently, 53% of melanoma patients had an objective response with 41% seeing at least an 80% tumor deduction after just 12 weeks of treatment. Bristol plans to start a phase 3 trial of the combinatio