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  • Cancer cure finally here? Genetically modified T-cells eradicate cancer.

    It seems like every other month a "major breakthrough" in fighting cancer comes out, only to later be dismissed or limited to specific type of cancer, or its success exaggerated, or human trials are years way etc. This one however, seems rather... radical in its speed of effectiveness and claimed success rate. By first extracting then genetically modifying T-cells, then pumping them back into the body to "hunt" cancer cells; cancer in a very large percentage of trial patients at 3 different centers appears to have gone completely into remission.

    I have zero medical background, but this sounds indeed like some kind of significant breakthrough if real. I'm going to email this article to an oncologist friend of mine to see what he thinks of it.


    Source: http://www.cnn.com/2013/12/07/health...html?hpt=hp_t2


    Killing cancer like the common cold


    (CNN) -- Nick Wilkins was diagnosed with leukemia when he was 4 years old, and when the cancer kept bouncing back, impervious to all the different treatments the doctors tried, his father sat him down for a talk.
    John Wilkins explained to Nick, who was by then 14, that doctors had tried chemotherapy, radiation, even a bone marrow transplant from his sister.
    "I explained to him that we're running out of options," Wilkins remembers telling his son.
    There was one possible treatment they could try: an experimental therapy at the University of Pennsylvania.
    He asked his son if he understood what it would mean if this treatment didn't work.
    "He understood he could die," Wilkins says. "He was very stoic."
    A few months later, Nick traveled from his home in Virginia to Philadelphia to become a part of the experiment.
    This new therapy was decidedly different from the treatments he'd received before: Instead of attacking his cancer with poisons like chemotherapy and radiation, the Philadelphia doctors taught Nick's own immune cells to become more adept at killing the cancer.
    Two months later, he emerged cancer-free. It's been six months since Nick, now 15, received the personalized cell therapy, and doctors still can find no trace of leukemia in his system.
    Trusting her intuition led to two cancer diagnoses
    Twenty-one other young people received the same treatment, and 18 of them, like Nick, went into complete remission -- one of them has been disease-free for 20 months. The Penn doctors released their findings this weekend at the annual meeting of the American Society of Hematology.
    "It gives us hope that this is a cure," Nick's father says. "They're really close. I think they're really onto something."
    'A whole new realm of medicine '
    At the conference, two other cancer centers -- Memorial Sloan-Kettering in New York and the National Cancer Institute -- will be announcing results with immunotherapies like the one Nick received. The results are promising, especially considering that the patients had no success with practically every other therapy.
    "This is absolutely one of the more exciting advances I've seen in cancer therapy in the last 20 years," said Dr. David Porter, a hematologist and oncologist at Penn. "We've entered into a whole new realm of medicine."
    In the therapy, doctors first remove the patient's T-cells, which play a crucial role in the immune system. They then reprogram the cells by transferring in new genes. Once infused back into the body, each modified cell multiplies to 10,000 cells. These "hunter" cells then track down and kill the cancer in a patient's body.
    Essentially, researchers are trying to train Nick's body to fight off cancer in much the same way our bodies fight off the common cold.
    Tumor Paint: Changing the way surgeons fight cancer
    In addition to the pediatric patients, Penn scientists tried the therapy out in 37 adults with leukemia, and 12 went into complete remission. Eight more patients went into partial remission and saw some improvements in their disease.
    The treatment does make patients have flulike symptoms for a short period of time -- Nick got so sick he ended up in the intensive care unit for a day -- but patients are spared some of the more severe and long-lasting side effects of extensive chemotherapy.
    Penn will now work with other medical centers to test the therapy in more patients, and they plan to try the therapy out in other types of blood cancers and later in solid tumors.
    A university press release says it has a licensing relationship with the pharmaceutical company Novartis and "received significant financial benefit" from the trial, and Porter and other inventors of the technology "have benefited financially and/or may benefit financially in the future."
    Searching for one-in-a-million cancer cells
    The big question is whether Nick's leukemia will come back.
    Doctors are cautiously optimistic. The studies have only been going on since 2010, but so far relapse rates have been relatively low: of the 18 other pediatric patients who went into complete remission, only five have relapsed and of the 12 adults who went into complete remission, only one relapsed. Some of the adult patients have been cancer-free and without a relapse for more than three years and counting.
    Relapses after this personalized cell therapy may be more promising than relapses after chemotherapy or a bone marrow transplant, Porter explained.
    First, doctors have been delighted to find the reengineered T-cells -- the ones that know how to hunt down and attack cancer -- are still alive in the patients' bodies after more than three years.
    Stigma lingers for deadliest cancer
    "The genetically modified T-cells have survived," Porter said. "They're still present and functional and have the ability to protect against recurrence."
    Second, before declaring patients in remission, Penn doctors scoured especially hard for errant leukemia cells.
    Traditionally, for the kind of leukemia Nick has, doctors can find one in 1,000 to one in 10,000 cancer cells. But Penn's technology could find one in 100,000 to one in a million cancer cells, and didn't find any in Nick or any of the patients who went into complete remission.
    'It's not a fluke'
    One of the best aspects of this new treatment is that it won't be terribly difficult to reproduce at other medical centers, Porter said, and one day, instead of being used only experimentally, it could be available to anyone who needed it.
    "Our hope is that this can progress really quite quickly," he said. "It won't be available to everyone next year, but I don't think it would take a decade, either."
    Right now patients can only get this therapy if they're in a study, but Dr. Renier Brentjens, director for cellular therapeutics at Memorial Sloan-Kettering, says he thinks it could become available to all patients in just three to five years.
    "When you have three centers all with a substantial number of patients seeing the same thing - that these cells work in this disease - you know it's not a fluke," he said.
    Two days ago, Brentjens became the co-founder of Juno Therapeutics, a for-profit biotech start-up company that's working on immunotherapies.
    "Fifteen years ago I was in the lab looking at these cells kill tumor cells in a petri dish and then I saw them kill tumor cells in mice, and then finally in humans," Brentjens said.
    He says he'll never forget the first patient he treated, who initially had an enormous amount of cancer cells in his bone marrow. Then after the therapy, Brentjens looked under the microscope and, in awe, realized he couldn't find a single cancer cell.
    "I can't describe what that's like," he said. "It's fantastic."
    CNN VIDEO: (3 mins... sorry it won't embed)
    http://i.cdn.turner.com/cnn/.element...ncer-study.cnn
    Last edited by Adeptus; December 07, 2013, 03:22 PM.
    Warning: Network Engineer talking economics!

  • #2
    Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

    Another article with more technical details....

    Source: http://www.eurekalert.org/pub_releas...-pmt120613.php
    Contact: Holly Auer
    holly.auer@uphs.upenn.edu
    215-200-2313
    University of Pennsylvania School of Medicine
    Penn Medicine team reports on study of first 59 leukemia patients who received cell therapy

    Genetically modified cells produce long-term remissions, persist in patients' bodies for over 3 years

    IMAGE: This shows the University of Pennsylvania's Perelman School of Medicine researchers, L-R, David Porter, Bruce Levine, Carl June, Stephan Grupp, and Michael Kalos.

    Click here for more information.
    NEW ORLEANS – Three and a half years after beginning a clinical trial which demonstrated the first successful and sustained use of genetically engineered T cells to fight leukemia, a research team from the Perelman School of Medicine at the University of Pennsylvania and the Children's Hospital of Philadelphia will today announce the latest results of studies involving both adults and children with advanced blood cancers that have failed to respond to standard therapies. The findings from the first 59 patients who received this investigational, personalized cellular therapy, known as CTL019, will be presented during the American Society of Hematology's Annual Meeting and Exposition in New Orleans.
    Two of the first three chronic lymphocytic leukemia (CLL) patients who participated in the study, which started in the summer of 2010, remain in remission, with tests revealing reprogrammed cells still circulating in their bodies, on guard to combat tumor cells that may reappear in the future. Additional highlights of the new research results include an 89 percent complete response rate among adult and pediatric patients with acute lymphoblastic leukemia (ALL).
    "In a very short time, we've learned so much about how CTL019 works and how powerful it can be," said the research team's leader, Carl H. June, MD, Richard W. Vague Professor in Immunotherapy in the department of Pathology and Laboratory Medicine and director of Translational Research in Penn's Abramson Cancer Center. "Our findings show that the human immune system and these modified 'hunter' cells are working together to attack tumors in an entirely new way."
    The research team, which includes investigators who treat patients at both the Hospital of the University of Pennsylvania and the Children's Hospital of Philadelphia, will announce findings from trials of three different groups of patients:
    • 15 of 32 adult patients with CLL (47 percent) responded to the therapy, with seven of those experiencing a complete remission of their disease. Results of both the completed pilot study of 14 CLL patients (Abstract #4162) and results thus far of the first 18 patients in a Phase II, dose-optimization trial (Abstract #873) will be presented.
    • 19 of 22 pediatric patients with ALL (86 percent) experienced complete remissions. The first pediatric patient treated with the protocol, who is now 8 years old, remains in remission 20 months later. Five patients have relapsed, including one whose tests revealed new tumor cells that do not express the protein targeted by the reprogrammed cells. (Abstract #67)
    • All five of the first adult ALL patients treated thus far experienced complete remissions, the longest of which continues six months after treatment. One patient subsequently underwent a bone marrow transplant and remains in remission. One patient relapsed after three months with disease that also tested negative for the engineered cell target. (Abstract #67)

    Building a Cancer-Killing CAR
    The investigational treatment pioneered by the Penn team begins by removing patients' T cells via an apheresis process similar to blood donation, then reprogramming them in Penn's cell and vaccine production facility with a gene transfer technique using a lentivirus vector. The newly built T cells target tumor cells using an antibody-like protein, called a chimeric antigen receptor (CAR), which is expressed on the surface of the T cells and designed to bind to a protein called CD19, which is found on the surface of the cancerous B cells associated with both CLL and ALL.
    The modified cells are then infused back into the patient's body following lymphodepleting chemotherapy. In the body, these "hunter" T cells both multiply and attack. A signaling domain built into the CAR promotes rapid growth of these cells, building an army of tumor-killing cells that tests reveal can grow to more than 10,000 new cells for each single engineered cell patients receive. Cells in the patient that do not express CD19 are left untouched by the modified T cells, which limits the prolonged, systemic side effects typically experienced during traditional cancer therapies that harm healthy tissue.
    IMAGE: University of Pennsylvania researchers developed a new cancer treatment that engineers cancer patients' own cells to attack their tumors. A bag of reprogramed cells is shown here, ready for infusion.

    Click here for more information.
    Treatment Prompts High Response Rates, Durable Remissions
    Taken together, the newly announced results show promise for a range of tough-to-treat blood cancers. All study patients had exhausted conventional treatment options. In many cases, they were ineligible for bone marrow transplantation or declined that option due to the risks associated with the procedure, which carries at least a 20 percent mortality risk.
    "We are tremendously excited about these results. About half of our CLL patients responded to this therapy, with most of them having several pounds of tumors eradicated by the genetically modified T cells," says study author David L. Porter, MD, the Jodi Fisher Horowitz Professor in Leukemia Care Excellence and director of Blood and Marrow Transplantation in Penn's Abramson Cancer Center, who will present the two CLL trial abstracts during the meeting. "We've now seen remissions lasting for more than three years, and there are clues that the T cells continue to kill leukemia cells in the body for months after treatment: Even in patients who had only a partial response, we often found that all cancer cells disappeared from their blood and bone marrow, and their lymph nodes continued to shrink over time. In some cases, we have seen partial responses convert to complete remissions over several months."
    The research team is especially encouraged by the early results among ALL patients, since that disease progresses rapidly and is very deadly among those who relapse after standard treatments. About 85 percent of pediatric patients with the disease are cured with first-line therapies, but those whose cancers relapse and/or become refractory have limited options. And while most adults with ALL respond to drug treatment, as many as half ultimately relapse, putting the overall cure rate for the disease among adults at only around 40 percent. New therapies for both these groups of high-risk patients are acutely needed.
    "Our results serve as another important milestone in demonstrating the potential of this treatment for patients who have no other therapeutic options," said study author Stephan A. Grupp, MD, PhD, of the Children's Hospital of Philadelphia and a professor of Pediatrics at the Perelman School of Medicine. "These data also demonstrate that these engineered 'hunter' cells greatly expand and then persist in patients, allowing for long-term disease control. We are looking forward to testing these cells in upcoming multicenter pediatric and adult trials."
    During the pilot study for CLL, patients received a wide range of cell doses, but the Penn team saw no relationship between the number of cells infused and the responses or toxicities associated with the therapy. To refine the treatment approach, the Penn team launched a randomized Phase II study comparing two different doses, each of which is given as a single outpatient infusion. So far, however, the team has again seen no difference in which amount of cells is more effective or associated with greater toxicities.
    Tests Pinpoint Cause, Management Technique for Side Effects
    In the trials for both CLL and ALL, all responding patients experienced a cytokine release syndrome that the researchers now know marks the process of the engineered cells multiplying and attacking tumor cells in the body. During this time, patients typically experience varying degrees of flu-like symptoms, with high fevers, nausea, muscle pain, and in some cases, low blood pressure and breathing difficulties. The team has learned this reaction can be managed, if necessary, using tocilizumab, an immunosuppressant drug which tamps down elevated levels of the inflammatory cytokine IL-6, which have been found to spike during the most robust phase of the engineered cells' expansion in the body.
    Tests of both CLL and ALL patients who experienced complete remissions also show that normal B cells, which also express the CD19 protein, have been eliminated along with their tumors. The researchers note that persistent loss of normal B cells is a good surrogate marker for continued activity of the gene-modified T cells. In this way, the cells appear to be providing long-term vaccine-like activity preventing B cells – and presumably tumor cells – from growing back. B cells are important for the body's immune system to fight infection by making antibodies, though it is possible to replace antibodies with gamma globulin treatments as a preventive measure.
    ###
    Michael Kalos, PhD, and Stephan Grupp, MD, PhD, will present findings from these trials (Abstracts #163 and #67) during an American Society of Hematology press briefing at 8 a.m. CST on Saturday, Dec. 7, 2013 in the ASH Press Briefing Room (Room 346-347) at the Ernest N. Morial Convention Center in New Orleans. David Porter, MD, will present Abstract #4162 at 6 p.m. CST on Monday, Dec. 9, in Hall E, and Abstract #873 at 8 a.m. CST on Tuesday, Dec. 10 in Room 293-294.
    The research was supported in part by the National Cancer Institute (CA165206, CA102646 and CA116660), the Leukemia and Lymphoma Society, the Alliance for Cancer Gene Therapy, and Novartis.
    Editor's note: The University of Pennsylvania has licensed technologies involved in this trial to Novartis. Some of the scientists involved in these trials are inventors of these technologies, including Drs. June, Porter, Kalos and Grupp. As a result of the licensing relationship with Novartis, the University of Pennsylvania receives significant financial benefit, and these inventors have benefitted financially and/or may benefit financially in the future.
    Penn Medicine is one of the world's leading academic medical centers, dedicated to the related missions of medical education, biomedical research, and excellence in patient care. Penn Medicine consists of the Raymond and Ruth Perelman School of Medicine at the University of Pennsylvania (founded in 1765 as the nation's first medical school) and the University of Pennsylvania Health System, which together form a $4.3 billion enterprise.
    The Perelman School of Medicine has been ranked among the top five medical schools in the United States for the past 16 years, according to U.S. News & World Report's survey of research-oriented medical schools. The School is consistently among the nation's top recipients of funding from the National Institutes of Health, with $398 million awarded in the 2012 fiscal year. The University of Pennsylvania Health System's patient care facilities include: The Hospital of the University of Pennsylvania -- recognized as one of the nation's top "Honor Roll" hospitals by U.S. News & World Report; Penn Presbyterian Medical Center; Chester County Hospital; Penn Wissahickon Hospice; and Pennsylvania Hospital -- the nation's first hospital, founded in 1751. Additional affiliated inpatient care facilities and services throughout the Philadelphia region include Chestnut Hill Hospital and Good Shepherd Penn Partners, a partnership between Good Shepherd Rehabilitation Network and Penn Medicine. Penn Medicine is committed to improving lives and health through a variety of community-based programs and activities. In fiscal year 2012, Penn Medicine provided $827 million to benefit our community.
    Last edited by Adeptus; December 07, 2013, 03:39 PM.
    Warning: Network Engineer talking economics!

    Comment


    • #3
      Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

      This is very promising...for those who will die without this possible treatment, and need immediate relief.

      I admire mankind's ability to tinker with the structure of life...I merely wonder at their complete disregard for the end result.

      Get back to me in 20 years with the end result of the gene modification, to see what else was altered upon manipulating the gene structure in a body designed to heal itself under the proper conditions.

      I know that those who have cancer now will be helped by getting rid of the immediate threat of their cancer. That part is wonderful.

      I want to know if I also get a second head or something.

      Comment


      • #4
        Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

        How about cancer prevention?

        Oops, off the reservation . . . .

        Comment


        • #5
          Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

          redacted
          Last edited by nedtheguy; October 09, 2014, 04:30 PM.

          Comment


          • #6
            Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

            Originally posted by Adeptus View Post
            It seems like every other month a "major breakthrough" in fighting cancer comes out, only to later be dismissed or limited to specific type of cancer, or its success exaggerated, or human trials are years way etc. This one however, seems rather... radical in its speed of effectiveness and claimed success rate. By first extracting then genetically modifying T-cells, then pumping them back into the body to "hunt" cancer cells; cancer in a very large percentage of trial patients at 3 different centers appears to have gone completely into remission.

            I have zero medical background, but this sounds indeed like some kind of significant breakthrough if real. I'm going to email this article to an oncologist friend of mine to see what he thinks of it.


            Source: http://www.cnn.com/2013/12/07/health...html?hpt=hp_t2


            Killing cancer like the common cold




            CNN VIDEO: (3 mins... sorry it won't embed)
            http://i.cdn.turner.com/cnn/.element...ncer-study.cnn
            This is how the zombie apocalypse starts....

            Even the bible predicted it!

            "And ye shall eat the flesh of your sons, and the flesh of your daughters shall ye eat." -- Leviticus 26:29

            "And I will cause them to eat the flesh of their sons and the flesh of their daughters, and they shall eat every one the flesh of his friend." -- Jeremiah 19:9

            Comment


            • #7
              Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

              Originally posted by Adeptus View Post
              Killing cancer like the common cold
              umm, the first thing that strikes me about this is that we can't actually kill the common cold

              As far as the treatment goes. This sounds like similar research done 20 years ago, only then, they were using the strep virus. After the initial report I never heard about it again. My suspicion is that the "hunters" could not be controlled once let lose in the body.

              ie if 10,000 cells are let lose in the body and hunt with 99.99% accuracy; that leaves you with 1 cell with 0% accuracy that then multiplies into 10,000 cells with 0% accuracy. Wash, rinse, repeat, until your patient is reduced to a puddle of mush.

              I'll wait for the peer review on this one thanks.

              Comment


              • #8
                Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

                Originally posted by ProdigyofZen View Post
                This is how the zombie apocalypse starts....
                Even the bible predicted it!
                "And ye shall eat the flesh of your sons, and the flesh of your daughters shall ye eat." -- Leviticus 26:29
                "And I will cause them to eat the flesh of their sons and the flesh of their daughters, and they shall eat every one the flesh of his friend." -- Jeremiah 19:9
                LOL !!! Ok, now I gotta post this meme from MATT 27:52-53

                Now back to the serious discussion of curing cancer...
                Warning: Network Engineer talking economics!

                Comment


                • #9
                  Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

                  Well they better get moving on that cure for overpopulation then!

                  Comment


                  • #10
                    Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

                    Treating cancer is profitable. Preventing cancer threatens profits.

                    Comment


                    • #11
                      Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

                      My Oncologist friend has replied to my query (i.e. Is this for real?)

                      His response:
                      Yes, targeted immune therapy is a novel way to treat cancer. The [SNIP] research Centre on the third floor of where I work does research on cancer immunology. Our understanding of the role of immune system in surveillance and destruction of bad cells in our body and how to enhance tumor killing by the immune system is expanding.
                      Warning: Network Engineer talking economics!

                      Comment


                      • #12
                        Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

                        Our understanding of the role of immune system in surveillance and destruction of bad cells in our body and how to enhance tumor killing by the immune system is expanding.
                        No offense to your friend but 40 years and $100 Billion into the "war on cancer" and that's what we have to show for it?

                        Comment


                        • #13
                          Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

                          Originally posted by swgprop View Post
                          No offense to your friend but 40 years and $100 Billion into the "war on cancer" and that's what we have to show for it?

                          No offense swgprop, but we should expect that very entrenched and very important problems might take generations to solve.
                          In those cases we ought to get started early, apply lots of cash and talent, and keep at it through the years.

                          Comment


                          • #14
                            Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

                            Yes it is an important problem. But as Don alludes to above, treatment has evolved into a multibillion dollar industry to which a cure would be quite disruptive.

                            Yes I'm a cynic. That's why I'm here.

                            Comment


                            • #15
                              Re: Cancer cure finally here? Genetically modified T-cells eradicate cancer.

                              Originally posted by swgprop View Post
                              No offense to your friend but 40 years and $100 Billion into the "war on cancer" and that's what we have to show for it?
                              Jobs?

                              Comment

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