Daily Mail

Jab that conquered my ‘terminal’ skin cancer

It saved Ruth’s life and doctors hope it could be a dramatic advance for all cancer patients

- By CAROLINE SCOTT

WHEN Ruth Retter was told her cancer had spread and she was unlikely to survive longer than six months, she wrote letters to her three girls, Abigail, then 12, Kayla, six, and Jenna, four, and started to prepare memory boxes for them.

As her condition was terminal, her life insurance policy paid out in full, meaning she could get much-needed work done on her house. She also visited a funeral director.

‘I’m the most disorganis­ed person in the world, but I was a single mum and I felt an overwhelmi­ng drive to sort everything out,’ she says.

‘Then, once I’d done all that, I wanted to crack on and enjoy the time we had left together. I had to face the fact that I wasn’t going to be around to see them grow up.’

Eight years on, Ruth, now 41, has defied that grim prognosis, as one of the very first patients in the UK to benefit from a breakthrou­gh in cancer treatment: harnessing the body’s own immune system to attack the disease.

Ruth, who lives in Somerset, was diagnosed with malignant melanoma, an aggressive skin cancer, just after Jenna was born in 2006. A spot appeared on her ankle when she was pregnant.

‘It started flat and dark, but got higher as it grew,’ Ruth says.

‘By the end of the pregnancy, it was the size of a pencil rubber tip, with some lighter patches. It was also itchy and red on the edges.’

Her GP thought it was nothing to worry about, but after Jenna was born, it began to look angry and then bleed. Ruth mentioned it during her postnatal check-up. This time she was seen by a new GP, who’d worked in Australia, where melanoma is a common cancer.

RUTH was immediatel­y referred to a dermatolog­ist. Sitting in outpatient­s three weeks later, she gazed at a poster covered with pictures of different kinds of melanoma and saw that her ‘spot’ looked exactly like the most serious of all: nodular melanoma. This spreads quickly and has a very poor prognosis.

‘I thought, “How can this be happening to me?” ’ she says. ‘I was absolutely petrified, but at the same time it seemed unreal.’

The dermatolog­ist removed the ‘spot’ there and then, and called back members of staff who were preparing to go home for the evening. A week later tests confirmed it was nodular melanoma and its depth, 2.3 mm, meant it was likely to have spread.

‘My whole world rocked,’ Ruth recalls. Every year, around 13,500 people in the UK are diagnosed with melanoma — more than 2,000 die from it. Around a quarter of cases are in those under 50 — Ruth was 29, and Jenna was three months.

The most common symptoms are changes in the shape, size or colour of an existing mole, but nodular melanomas — around 15 per cent of all cases — often appear as a firm, raised round pimple or blister which grows over a matter of months, four times quicker than other melanomas. Sometimes, but not always, they change from flesh- coloured to almost black.

They are unusually aggressive — in as little as three months they can spread internally — and account for nearly half of all melanoma deaths.

Chemothera­py and radiothera­py have little effect. Ruth was immediatel­y referred to a specialist team at St George’s Hospital in South-West London, who excised a 6 cm area around the mole.

They also removed cancer cells from her groin and the back of her knee. Ruth recovered well but within months was doubled over with pelvic pain.

‘I’d get a stabbing pain on my left side just above my bikini line,’ she says. ‘I could also feel a lump, which was terrifying.’

A scan in January 2009 revealed a 10 cm tumour around a major artery. This was removed and Ruth was offered a place on the trial of a drug, Avastin, which had shown promising results in breast and bowel cancer and was being evaluated for melanoma.

But a year later, while still on the trial, scans showed a new tumour near her stomach and pockets in her abdomen.

‘It was at that point, four years after I was diagnosed that I thought, “OK, it’s going to get me”,’ says Ruth. She began planning her funeral — again. But at a regular appointmen­t with Professor Angus Dalgleish, her oncologist at St George’s and principal of the Institute for Cancer Vaccines and Immunother­apy, she was offered the chance to join a trial of a new cancer vaccine — a type of immunother­apy called IMM-101.

Immunother­apy works by harnessing the body’s own immune response to fight cancer.

The type being trialled, IMM101, given as a simple monthly injection, was initially developed as a vaccine for tuberculos­is.

‘I wanted to trial it in cancer patients because its effect is more of an immune booster than a vaccine,’ explains Professor Dalgleish. ‘The idea is to kick- start the immune system so other therapies have a chance to work better. I had been keen to move onto more exciting areas — including gene therapy. ‘But the patients who had this simple vaccine — a heat-killed bug injected into their skin — are the ones surviving the longest, particular­ly when combined with other therapies.

‘It’s a bit like dropping a grenade into a sleeping immune system to wake it up to attack the cancer.’

‘I was so desperate, I was happy to try anything,’ says Ruth.

‘Especially as Professor Dalgleish said there’d be no side- effects except site.’ team melanoma the were time in Professor began complete a Ruth slightly patients joined, IMM-101 Dalgleish remission. sore in some 2006 injection trials patients and and his by in

I says ‘I could couldn’t Ruth. possibly But allow three myself be months that to believe lucky,’ later a pockets scan showed of cancer that in the Ruth’s inoperable abdomen had stopped growing, then they actually started to shrink.

After a year, no tumours were visible anywhere — and, over eight years later, they’ve not returned.

‘I didn’t really believe it at first,’ says Ruth. ‘For a long time, I thought every ache and pain was another tumour, but each time I had a scan there was no cancer.’

PROFESSOR Dalgleish believes most cancer types could benefit from IMM-101. It can be used alone but works best in conjunctio­n with other immunother­apy drugs. As he explains: ‘It wakes the immune system up and makes tumours more vulnerable to chemothera­py, radiothera­py and targeted treatments.’

These targeted treatments include other forms of immunother­apy, which work by blocking the proteins that cancer cells use to ‘hide’ from the immune system. Although these checkpoint inhibitors,

as they’re called, have been a huge advance in the treatment of melanoma and lung cancer, many patients don’t respond to them. This is where IMM-101 could help, given in conjunctio­n with immunother­apy. Professor Dagliesh says that two of his patients with advanced melanoma given this combinatio­n had ‘a complete shrank to response: the point that their we tumours can no longer see them on a scan’. ‘But what’s amazing about Ruth Retter is her complete response without any other treatment. She was riddled with cancer and she is now completely disease-free.’ Although the figures involved are small — 150 patients to date — Professor Dalgleish believes we’re on the cusp of a cancer treatment revolution, and he’s now running a new trial with melanoma patients combining a checkpoint inhibitor drug, nivolumab, with IMM-101.

‘I’ve worked on many immunother­apies over the past 20 years, but I think this one could be a massive breakthrou­gh. I could see a cancer moving IMM- inexpensiv­e. advantage apart injection Unlike time from 101 patient when onto site, other a could is red other I he its on would But immunother­apy, mark says. lack IMM-101 be treatments.’ its start of around relatively toxicity, unique before every the

while (she’s redundancy), Ruth life remains weathered hasn’t she’s in always remission, divorce astonished been easy and and she’s grow: and Jenna, Abigail lived 12. to is see now her 20, Kayla, children 14

month,’ ‘I still she have says. injections ‘But instead every of living from week to week, I’ve allowed myself to think I might be here year after year.’

‘I’m conscious that people with my disease are still dying,’ she says. ‘I’m just so grateful I was one of the lucky ones.’

 ??  ?? Grateful: Ruth with two of her girls, Jenna (left) and Kayla
Grateful: Ruth with two of her girls, Jenna (left) and Kayla

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