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Nanomachines that kill cancer cells in 60 seconds developed

By Chukwuma Muanya, Assistant Editor
06 September 2017   |   2:06 am
Scientists have developed nanomachines that can drill into cancer cells, killing them in just 60 seconds.The tiny spinning molecules are driven by light, and spin so quickly that they can burrow their way through cell linings when activated.

PHOTO: istockphoto/ Eraxion

*First tumour gene therapy to treat leukaemia approved

Scientists have developed nanomachines that can drill into cancer cells, killing them in just 60 seconds.The tiny spinning molecules are driven by light, and spin so quickly that they can burrow their way through cell linings when activated.

In one test conducted at Durham University the nanomachines took between one and three minutes to break through the outer membrane of prostate cancer cell, killing it instantly.

The ‘motor’ is a rotor-like chain of atoms that can be prompted to move in one direction, causing the molecule to rotate at high speed.Dr. Robert Pal of Durham University said: “We are moving towards realising our ambition to be able to use light-activated nanomachines to target cancer cells such as those in breast tumours and skin melanomas, including those that are resistant to existing chemotherapy.

“Once developed, this approach could provide a potential step change in non-invasive cancer treatment and greatly improve survival rates and patient welfare globally.”

The scientists, whose work is reported in the journal Nature, created several different light-activated motorised molecules designed to home in on specific cells. They found that the nanomachines needed to spin at two to three million times per second to overcome nearby obstacles and outpace natural Brownian motion, the erratic movement of microscopic particles suspended in fluid.

The molecules could be used either to tunnel into cells carrying therapeutic agents, or to act as killer weapons that blast open tumour membranes. Videos showed the cancer cell membranes bubbling under the assault.

Without an ultraviolet trigger, the motor molecules located target cells but then remained harmlessly on their surfaces.The researchers are already proceeding with experiments in microorganisms and small fish and hope to move to rodents soon, ahead of clinical trials in humans if animal testing is successful.

Also, United States (US) regulators on Wednesday approved the first gene therapy against cancer – a treatment that uses a patient’s own immune cells to fight leukemia – opening a new era in the fight against one of the world’s top killers.

The treatment is made by Novartis and is called Kymriah (tisagenlecleucel).This type of anti-cancer immunotherapy, known as a CAR-T cell therapy, was known by CTL019 until now.”This marks the first-ever CAR-T cell therapy to be approved anywhere in the world,” Novartis CEO Joseph Jimenez told reporters on a conference call.

“It uses a new approach that is wholly personalized by using a patient’s own T-cells.”The US Food and Drug Administration (FDA) approved Kymriah for children and young adult patients up to age 25 with a form of acute lymphoblastic leukemia (ALL).

To qualify for treatment, patients must have B-cell precursor ALL that is refractory, or the patient has relapsed at least twice.The FDA described the approval as “a historic action” and a “new approach to the treatment of cancer and other serious and life-threatening diseases,” said a statement.

The treatment is not a pill or a form of chemotherapy, which can weaken the body’s natural defenses.Instead, it harnesses a patient’s own immune cells, called T-cells and white blood cells, and trains them to recognise and fight cancer.

The patient’s immune cells are removed with a special blood filtration process, sent to a lab, and genetically encoded to be able to hunt down cancer cells. These re-engineered T-cells are then transfused back into the patient, where they can begin attacking leukemia.

Studies have shown that 83 percent of patients responded to the treatment, achieving remission within three months, Novartis said.An application with the European Medicines Agency is expected to be filed by the end of the year.

The price of Kymriah – which is delivered to a patient just once – is $475,000, said Bruno Strigini, CEO of Oncology at Novartis.Patients who do not respond to the treatment within the first month would not be expected to pay, he told reporters.The more common treatment for leukemia – bone marrow transplants – can cost between $540,000 and $800,000 the first year in the United States, Strigini said.

Meanwhile, outside analyses have set a cost-effective price for Kymriah between $600,000 and $750,000, he added.”Recognising our responsibility we set the price below that level,” said Strigini.Most patients who fit the criteria for treatment would likely be covered by insurance, since they are under 25 and would either be on their parents’ insurance or covered by government-sponsored Medicaid, a Novartis spokesman said.

The price tag is high – as are costs throughout the cancer industry – a trend that is “unsustainable,” said Craig Devoe, acting chief of medical oncology and hematology at Northwell Health Cancer Institute in New York.Asked if he thought Novartis’s pricing was reasonable, he told AFP: “It’s not.”

Devoe also said that while the positive results are exciting, many questions remain about how long these novel cancer treatments – developed mainly in the past decade or so – will last.

“Not just responding but staying in response long term is what patients want,” he said.”We really don’t know how long these cells are going to stay active.”
Breakthrough therapy.Carl June pioneered the treatment at the University of Pennsylvania. Its most high-profile patient is Emily Whitehead, now 12.

Six years ago, she was the first child to receive what was widely considered a risky treatment. She has been cancer-free ever since.In 2014, US regulators designated CTL019 as a “breakthrough therapy” and put the experimental immunotherapy agent on the fast track to market approval. It was the first cancer immunotherapy to receive the breakthrough designation. More are expected to follow in the coming years as the field of immunotherapy grows. Last month, an advisory panel to the FDA unanimously urged approval of the cutting-edge cancer therapy.

About two-dozen centres in the United States are expected to be able to treat patients seeking Kymriah, with as many as 35 up and running by the end of the year.
ALL is the most common form of childhood leukemia, with about 3,000 cases diagnosed in the US each year.Of those, 600 US patients would likely meet the criteria of being under 25 and having relapsed or refractory ALL, according to Novartis.

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