{"id":199773,"date":"2017-06-19T18:45:15","date_gmt":"2017-06-19T22:45:15","guid":{"rendered":"http:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/cancer-precision-medicine-finds-a-new-mantra-cure-is-inside-the-patient-india-today\/"},"modified":"2017-06-19T18:45:15","modified_gmt":"2017-06-19T22:45:15","slug":"cancer-precision-medicine-finds-a-new-mantra-cure-is-inside-the-patient-india-today","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/gene-medicine\/cancer-precision-medicine-finds-a-new-mantra-cure-is-inside-the-patient-india-today\/","title":{"rendered":"Cancer: Precision medicine finds a new mantra &#8211; cure is inside the patient &#8211; India Today"},"content":{"rendered":"<p><p>    He was a ruggedly handsome man in    life: shirt unbuttoned, muscles rippling, cigarette dangling    rakishly from his lips. He was unrecognisable in death:    pinched, pale, almost skeletal. For those who knew him    onscreen, there was shock and despair at the final terror of    his illness. Vinod Khanna, one of the last screen titans of a    generation, battled a lethal form of bladder cancer, resistant    to chemotherapy, for six long years and finally succumbed on    April 27. That very week, however, the world of science    celebrated a \"huge breakthrough\": the discovery of a new drug    based on malaria proteins that can dramatically reduce    hard-to-treat bladder cancers.  <\/p>\n<p>    Another breakthrough, another    life. \"It's finally here. A new ray of hope in the field of    cancer. 'Nivolumab' for aggressive Hodgkin's lymphoma. Spread    the word.\" Mamta Mohandas, 32, calls herself 'Actor. Singer.    Survivor' on Twitter and posts messages of hope to her 495K    followers. Her rising career graph in Malayalam and Telugu    cinema, despite her seven-year-long fight against an aggressive    lymph cancer, Diffuse Large B-Cell Lymphoma, is legend. Ever    since she joined a clinical trial for an experimental drug in    Los Angeles, USA, the southern beauty has been upbeat. \"It's    working for me,\" she informs her fans. \"Brave girl\", \"love u\",    \"jaldi aaja\", they respond.  <\/p>\n<p>    TIME OF    BREAKTHROUGHS  <\/p>\n<p>    It is the best of times, it is the    worst of times, on the cancer front. Scientists continue to be    baffled by the complexity and smartness of cancer cells: that    they find ways to dodge even the most powerful therapies, that    'cancer' encompasses not one but hundreds of distinct diseases,    that each individual cancer behaves differently, that two    people with the same cancer, at the same stage, receiving the    same treatment, can experience radically different outcomes. As    US-based oncologist and Pulitzer-winning writer Dr Siddhartha    Mukherjee says, \"All cancers are alike, but they are alike in a    unique way.\" With all that, cancer is catching up with heart    disease as the leading cause of deaths globally, reports the    World Health Organization. In India, the latest study based on    the National Cancer Registry shows that there are 1.45 million    new cases every year, a prevalence of over 3 million at any    point of time, over 680,000 deaths a year. Although early    detection saves lives, just 12.5 per cent Indians call on a    doctor in the early stages.  <\/p>\n<p>    But it's also a time of    exceptional breakthroughs and innovations. No, there is no    single death-defying magic bullet, but new generations of    life-saving and life-extending 'smart drugs' are currently    being developed and tested. At the root of all this is the idea    that the cure for cancer is inside the patient. And the mantra    in labs around the world is 'precision medicine'. That is, a    line of treatment that is personalised to a patient's genetic    make-up or molecular changes within one's tumour. Up until now,    therapies have all been geared to treat cancer based on where    it is located, say, in the breast, bladder or lung. Now, the    shift is increasingly evident in finding precision medicine    targeted at genetic glitches. On May 23, in a first, a cancer    drug has won approval from the US Food and Drug Administration    (USFDA) that can be given to anyone who harbours specific    genetic abnormalities found in as many as 15 different types of    cancers, all in patients for whom traditional treatment, like    chemotherapy, has failed.  <\/p>\n<p>    There has not been so much    excitement as there is now since 2001, when one of the first    cancer therapies to show the potential for targeted action,    Imatinib, was approved. Thousands of clinical trials are    humming with promising drug pipelines, many of which are being    used by doctors to benefit patients. \"It's an exciting time,\"    says Dr Anil Suri, director of the National Institute of    Immunology in Delhi and the man who discovered SPAG9, the    cancer antigen to be used in India's first anti-cancer vaccine,    now under phase II clinical trial in cervical cancer patients.    \"Cancer research is at the tipping point of major    breakthroughs. Advances in molecular biology, next-generation    gene sequencing, big data and innovative diagnostics are    opening up a whole new world of possibilities.\"  <\/p>\n<p>    THE PARADIGM SHIFTS  <\/p>\n<p>    The war on cancer is now looking    within, at the patient's own arsenal of weapons: genes,    molecules and the immune system. The conventional regimen of    surgery-radiotherapy-chemotherapy is slowly but surely giving    way to targeted, personalised treatments and more intricate    diagnostic tools. Combination therapies to keep cancers in    check are being worked upon. The emerging field of cancer    immunotherapy, or using the body's own immune system to help    fight off the disease, is especially promising. Of the 30 new    drugs for more than a dozen different types of cancers approved    by the USFDA in the past one year, almost all are in    immunotherapy. Indian scientists, too, are engaged in the    battle to unlock the answers on how to prevent, detect and    treat patients, in the best example of 'Make in India'.  <\/p>\n<p>    A paradigm shift is taking place,    with the approach moving toward a regimen where cancer may not    have to be cured, but controlled, say, like diabetes or heart    disease, explains Dr Mammen Chandy, director of Tata Medical    Centre, Kolkata, and chair of the Human Genome Task Force of    the department of biotechnology (DBT), Union ministry for    science and technology. \"With greater knowledge of the    molecular genetics of cancer, we can study genetic mutations in    a patient and target these with specific drugs,\" he says. A    whole range of new drugs today can shrink and kill cancer cells    without collateral damage. \"We can precisely quantify the    extent of the disease at diagnosis with better imaging    techniques.\" The precision and accuracy of radiation technology    make it possible to hit tumours with minimal damage to    surrounding normal cells. \"In several cancers, a patient can    now pop a pill a day and live a normal life for many years. We    are, thus, converting cancer into a chronic disease that one    can live with.\"  <\/p>\n<p>    LANGUAGE OF GENES  <\/p>\n<p>    ATCG. ATCG. AGGCCTT. Oops, a    typographical error. A tiny mistake can change the meaning of a    sentence. What if there's a typo in your genes? Imagine a    social network humming in each of your 37.2 trillion cells,    with up to 100,000 genes talking to each other in a chemical    code of four letters, A, T, C and G-to post, copy, tweak,    repeat, adapt, modify messages and instructions constantly-for    you to function. The proofreading tools inside cells correct    some typos, junk many, but some get overlooked. And they    fester. Like fake news on social media, they spread lies,    sending wrong signals to other cells giving rise to a series of    mistakes, sometimes profoundly altering the biology of cells.    If 10 million cells repeat the same error, a tumour forms, as    big as the head of a pin, and starts shedding bits of its genes    into the bloodstream, like a trail of bread crumbs.  <\/p>\n<p>    Francis S. Collins, geneticist and    head of the National Institutes of Health, US, wrote in his    book Language of God: A Scientist Presents Evidence for Belief:    \"Science reveals that the universe, our own planet and life    itself are engaged in an evolutionary process. The consequences    of that can include the unpredictability of the weather, the    slippage of a tectonic plate, or the misspelling of a cancer    gene in the normal process of cell division.\" With the Human    Genome Project (HGP), a massive international effort to unlock    the secrets of our genetic script, taking off in 1991, cancer    research got a massive leg up. Genes could be isolated from    cells in pure form, analysed in full detail, multiplied    manifold in the lab, changed at will. They could also be used    to discover defects in the blueprint of one's body and to take    proactive measures to stem the consequences, most    significantly, the processes that give rise to cancers. The    2015 Nobel Prize in Chemistry was awarded to three scientists    for explaining precisely how cells make mistakes, repair those    and predispose people to cancer when repair mechanisms    fail.  <\/p>\n<p>    THE NEW STRATEGY  <\/p>\n<p>    Now cancer researchers from Johns    Hopkins University and Harvard Medical School have published a    new study on the biology of cancer cells (Science, March 2017)    that has kicked up a new debate. Based on the mathematical    modelling of 32 types of cancers from 69 countries, they argue    that about 66 per cent of cancers occur due to random mistakes    during cell division, with only 29 per cent due to    environmental factors (say, smoking or sun exposure) and 5 per    cent to inherited genetic traits. These percentages, however,    vary from cancer to cancer. In some lung tumours, environmental    factors account for 65 per cent, while in prostate, brain and    bone cancers, more than 95 per cent are due to random errors in    cells. The study, despite the fears that its conclusions would    undercut prevention efforts, has evoked the need for a new    strategy, one that would emphasise early detection and    treatment, in addition to prevention.  <\/p>\n<p>    The problem with early detection    is that when tumours form, they do not shed enough of a \"bread    crumbs trail\" that can be picked up by CT-MRI-PET scans or by    needle biopsies for possible malignancy. But what if cancer can    be detected at such an early stage? The idea of a simple blood    test as an alternative has come up recently. In India,    Bengaluru-based genetic diagnostics company, Strand Life    Sciences, has started offering the first phase of liquid    biopsies: a simple, non-invasive diagnostic test using    circulating tumour genes in a patient's blood, the first such    test in India. \"In the case of cancer patients, such blood    tests can provide early information about tumour presence,    relapse after therapy and response to therapy,\" explains Dr    Vijay Chandru, CEO of Strand, who launched the test in April in    association with the Mazumdar Shaw Centre for Translational    Research, also in Bengaluru.  <\/p>\n<p>    But what about therapies? Ever    since former US president Jimmy Carter announced in 2015 that    he was free of a deadly form of skin cancer after receiving    surgery, radiation and \"a new kind of treatment\", he became a    poster boy for the exciting new field: immunotherapy. Dr Suri    explains that normal cells of the body die when they are not    needed, are damaged, or are infected with virus, bacteria,    parasites or fungi. \"The immune system, the body's first line    of defence, keeps track and as soon as it detects anything    abnormal or unknown, it attacks and kills it,\" he says. But    cancer cells trick the immune system into not recognising them    as a threat. \"This allows the tumours to grow and spread,\" he    says. In immunotherapy, the immune system is enlisted to attack    and force cancer cells to kill themselves.  <\/p>\n<p>    MAKE IN INDIA  <\/p>\n<p>    Where does India stand in all    this? Indian cancer patients have been the key partners in    discovery of cancer antigen SPAG9, which is being used for    personalised intervention by modulating the immune response,    says Dr Suri. \"Most new technologies are available in the    country,\" says Dr Thangarajan Rajkumar, head of molecular    oncology, Cancer Institute (WIA), Adyar, Chennai. \"It is the    cost of the newer therapies that is the major impediment. But    that's true not only for India. Even some developed countries    are finding it difficult to provide cancer care to people    because of the prohibitive costs.\" The institute is conducting    clinical trials of India's first therapeutic anti-cancer    vaccine, SPAG9, in collaboration with Dr Suri and funded by the    department of biotechnology and department of science and    technology, Government of India. \"Rather than directly    attacking cancer cells, this therapy involves priming a    patient's own immune cells to fight the cancer,\" he says. \"Our    immune system prevents most of us from developing cancer, but    once cancer develops, the immune system becomes very subdued.    The newer immunotherapies are addressing precisely this area,    with great results.\"  <\/p>\n<p>    With cervical cancer rising    dramatically among Indian women-nearly 23 per cent of all    cancers in women and over 100,000 deaths a year-it might just    be a game-changer. One of the patients included in phase I of    the clinical trials at the Cancer Institute, whose persistent    cervical cancer had spread to the lungs even after    radiotherapy, has been disease-free now for over nine years.    The vaccine is being manufactured at a world-class industrial    facility, owned by Biocon. Researchers at the institute have    also developed a simple kit for cervical cancer screening, a    biomarker panel for early diagnosis of ovarian cancer and a    therapy to inhibit an aggressive bone cancer, Ewing's    sarcoma-all awaiting further verification.  <\/p>\n<p>    \"There are major institutions    across the country working on basic, translational and clinical    research as applied to cancer,\" says Dr Rajkumar. New and    potentially therapeutic molecules have been identified at the    Indian Institute of Science, Bangalore, he points out. A    multi-centre study under Professor Partha Majumdar of the    National Institute of Biomedical Genomics at Kalyani, West    Bengal, and Dr Rajiv Sarin of Tata Memorial Centre's ACTREC    (Advanced Centre for Treatment, Research and Education in    Cancer) in Mumbai, are doing promising work in cancer genomics.    Truly cutting edge research may be taking place only at a few    centres, but at hospitals and laboratories across the country,    innovative molecular genetic tests, technology and techniques    are being used. From next generation sequencing (NGS)    technology to detecting genetic change driving a cancer,    molecular diagnosis and monitoring, best-in-class radiotherapy    equipment, new small molecules to specifically target the    tumour cells, stem cell transplantation, hormone therapy to    cellular therapy, it's all happening.  <\/p>\n<p>    RUSH FOR DRUGS  <\/p>\n<p>    In December 2015, when Jimmy    Carter called a press conference to announce that he had been    cured of his cancer, the 'breakthrough' immunotherapy drug,    Pembrolizumab, sold by pharma giant Merck as Keytruda, got a    new moniker, \"the president's drug\". Keytruda, along with    Bristol-Myers Squibb's Opdivo (Nivolumab), is one of a growing    number of 'immuno-onco' drugs that unleash the body's immune    system to fight malignant cells. Keytruda and Opdivo, effective    against some forms of lung, skin, kidney and other cancers, are    set to launch in the Indian market soon. Prohibitively    expensive, above Rs 1 crore for an entire treatment, the drugs    may not be for the general public. But they are shaping up to    be the biggest blockbusters for the global pharma    industry.  <\/p>\n<p>    Most patented medicines are    unaffordable to the average patient in India, even if priced    lower than their western counterparts. But Indian companies,    with their track record in generic drugs, are emerging as    strong global players in the biosimilar (or exact copies of    biological medicines that are already approved) segment of    molecularly targeted cancer drugs. From Biocon, Cipla,    Aurobindo Pharma, Dr Reddy's Laboratories, Intas    Pharmaceuticals to Hetero Drugs, they are all expanding their    biosimilar portfolios. Roche has teamed up with Emcure    Pharmaceuticals to manufacture and sell its breast cancer drug,    Herceptin, at a reduced price in India. \"Biosimilars have made    cancer treatment affordable to the middle class, and most    companies have compassionate usage programmes,\" says Dr    Chandy.  <\/p>\n<p>    Immunotherapy is emerging as a    'sweet spot' among smaller research companies as well as    investors. Biotech company Aurigene Discovery Technologies of    Bengaluru has got into off-licence deals with global pharma    companies like Curis, Orion and Pierre Fabre for its novel    immunotherapy molecules. Delhi-based Curadev, a drug discovery    company, has entered into collaboration with Roche. Ratan Tata,    chairman emeritus of Tata Sons, has invested an undisclosed    amount in biopharmaceutical firm Invictus Oncology, Delhi, to    develop a cancer technology platform.  <\/p>\n<p>    THE NEW NEW  <\/p>\n<p>    Jugnu Jain, molecular geneticist,    cell biologist and inventor with three patents, returned to    India from the US in 2011 and realised, surprisingly, that    India did not have a human biobank. Globally, there are over    350. \"Leftover tissues from surgery or diagnostic procedures,    say, cancer tissue, blood or urine, are precious,\" she says,    \"highly sought after worldwide by researchers, diagnostics,    biotech and pharma companies\" to validate their drug candidates    in target patient population samples, prior to launching    clinical trials. They spur research into diseases: from    identifying risk factors to diagnosing early, screening family    members at risk to customising a patient's treatment to improve    outcomes. Results from such studies can boost, sometimes even    replace, the need to test new drugs. Ultimately, the war    against cancer depends on cancer research.  <\/p>\n<p>    Jain co-founded a health science    firm, Saarum Innovations, and finally set up India's first    commercial biobank and personalised medicine company, Sapien    Biosciences, a joint venture with Apollo Hospitals, in    Hyderabad in 2013. The work is in full flow. Imagine live    cancer cells growing in the lab. Study those to understand the    complexity of a tumour, screen new drug candidates, use    cultured cancer cells as models to investigate the changes that    may have caused cancer, or its spread, or its resistance to a    therapy. There are many other applications of fresh samples in    a biobank, she says. \"Several companies in China have built    thousands of cancer models in biobanks, which are being used by    pharma companies to screen drug molecules. We can too.\"  <\/p>\n<p>    With excitement building around    the innovative research in the cancer space, it's hard not to    think of a cure. \"But to conquer a complicated, costly and    devastating disease such as cancer, many more major scientific    breakthroughs are needed,\" says Mukherjee. Medicine still needs    to catch up. The battle still relies largely on three    brute-force weapons: surgery, radiation and chemotherapy.    Cancer cells are subtle and smart. So the treatment needs to be    more sophisticated. And bringing in the latest and the best are    gene therapies. He points to an important development that took    place in 2013: a unique technology, the CRISPR-Cas9 system,    currently the most versatile method of genetic manipulation.    It's somewhat like conducting a molecular surgery on genes:    remove abnormal sequences, replace them with normal ones, pull    out genes that give an advantage to cancer cells. The idea    comes from some types of bacteria that have a built-in gene    editing system against invaders, say, a virus. \"Your genome has    three billion letters, ATCGs. If it were to be written down, it    would be 66 full sets of Encyclopaedia Britannica,\" he    explains. \"What if you can take out a letter, one that    predisposes you to cancer, erase or tweak it to your    advantage?\"  <\/p>\n<p>    Can that be the future of cancer?    Or, perhaps, our future without cancer?  <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>See the article here:<br \/>\n<a target=\"_blank\" href=\"http:\/\/indiatoday.intoday.in\/story\/cancer-treatment-india-gene-sequencing\/1\/979111.html\" title=\"Cancer: Precision medicine finds a new mantra - cure is inside the patient - India Today\">Cancer: Precision medicine finds a new mantra - cure is inside the patient - India Today<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> He was a ruggedly handsome man in life: shirt unbuttoned, muscles rippling, cigarette dangling rakishly from his lips. He was unrecognisable in death: pinched, pale, almost skeletal. For those who knew him onscreen, there was shock and despair at the final terror of his illness.  <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/gene-medicine\/cancer-precision-medicine-finds-a-new-mantra-cure-is-inside-the-patient-india-today\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":4,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[21],"tags":[],"class_list":["post-199773","post","type-post","status-publish","format-standard","hentry","category-gene-medicine"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/199773"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=199773"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/199773\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=199773"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=199773"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=199773"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}