Gene Therapy Scores Big Wins

   In one of  the biggest advances against leukemia  and other blood cancers in many years,  doctors  are reporting unprecedented success  by using gene therapy to transform patients’ blood cells into soldiers that seek and destroy cancer.  A  few patients  with one type of  leukemia  were given this one-time, experimental therapy several years ago and some remain cancer-free today.

     Now,  at  least  six research groups  have treated more than 120 patients with many types of  blood and bone marrow cancers,  with stunning results. “It’s  really exciting,”  said  Dr. Janis Abkowitz,  blood  diseases  chief  at  the University of  Washington in Seattle  and president of  the American Society of  Hematology. “You can take a cell  that belongs  to a patient  and engineer it to be an attack cell.”

  In one study,  all  five adults and 19 of  22 children with acute lymphocytic leukemia,  or ALL,  had a complete remission,  meaning  no cancer  could  be found after treatment,  although a  few have relapsed since then. These were gravely  ill patients  out of  options.  Some  had  tried  multiple bone marrow transplants and up to 10 types of  chemotherapy or other treatments.

   Cancer was so advanced in 8-year-old Emily Whitehead, Philipsburg, Pa., that doctors said her major organs would fail within days.  She was the  first child  given the gene therapy  and shows no sign of  cancer today, nearly two years  later. “However,  we’re still nervous every day  because  they can’t tell us what’s going to happen tomorrow,”  said Tom Whitehead, Emily’s  father.

   Emily Whitehead  is  one of  the  unlucky  children  whom  was  diagnosed with  lymphoblastic leukemia  at  the  age of  five.  For  a good portion of  the children diagnosed:  chemotherapy  can  cure the disease,  however,  this did not happen for Emily; several rounds of chemotherapy and other treatments all  failed and even threatened to take her ability to walk.

  The University of  Pennsylvania decided to try something a little different. researchers  decided to take the blood out of  her body and pass it through a machine to take the white blood cells out  and put it back in. They then took a modified  form of  the HIV virus and introduced  it to her white blood cells, basically reprogramming them to destroy the cancer. 

   The procedure  did not work out as planned,  this  instead leaving Emily hospitalized because the cells were attacking her own body as well.  It was not until the doctors gave her a rheumatoid arthritis drug that stopped the immune system malfunction  they  saw  improvement.  A  few  weeks  later, when her bone marrow was checked, they were surprised to see … she was completely cancer  free.

   According to data provider IMS Health, spending on oncology drugs was  $91 Billion last year,  tripling  since  2003.  This is something different than all the other drugs  that  have  come out  in recent years.  This treatment has seen  a  100% success rate  with  27 patients so  far.  Also the cancer that was being treated was no longer detectable. While  some are calling this a major  milestone  for humanity  and calling it the cure to cancer.

   There  are  some  hurdles  ahead which include  further testing  as well as  modified versions which will alleviate some of  the side effects which almost killed the  first patient who tried it.  Internal sources  as saying that the new drug will be ready for mass production by 2016 when they  file with the FDA, however,  the technology that goes behind it is economically viable.  

Introduction: Routine Nagalase testing finds cancer early and GcMAF cures it

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