barre

High intensity interval training (HIIT) workout

 

Incorporate high intensity interval training into your workouts to increase fat loss and maximise your results. Exercise scientist Johann Ruys shares his favourite HIIT workout.

 

 

3 x 1km runs with 2-minute rest in between each (work-to-rest ratio = 2:1)

2-minute rest

 

4 x 500m runs with 2-minute rest between each (work-to-rest ratio = 1:1)

2-minute rest

 

4 x 150m runs with 1-minute rest in between each (work-to-rest ratio = 1:2)

 

6 x 30m sprints with 10-second rest between each (finisher)

 

Join the movement on Instagram and hashtag #myWHF so we can see what you're up to!

 

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Childhood Vaccinations Rarely Spur Seizures, Study Finds

By Amy Norton
HealthDay Reporter

MONDAY, June 6, 2016 (HealthDay News) — Certain vaccines can trigger fever-related seizures in young children, but the risk is so low that pediatricians might see one case every five to 10 years, a new study estimates.

It has long been known that some vaccines carry a small seizure risk. But the researchers said the new report offers some hard numbers.

And it suggests that even when babies and toddlers get three vaccines at once, they only develop fever-related seizures at a rate of 30 per 100,000 — at most.

The findings should be “reassuring” to parents, said lead researcher Dr. Jonathan Duffy, of the U.S. Centers for Disease Control and Prevention.

“Looking at the big picture, the benefits of vaccination are much greater than the risk of febrile [fever-related] seizures,” Duffy said.

Up to 5 percent of young children will have a fever-related seizure at some point, according to the CDC. It usually happens when they have the flu, a cold or other infection, the agency said.

But while the seizures are scary for parents, Duffy said, they do not cause lasting harm.

According to Dr. Mark Sawyer, a member of the American Academy of Pediatrics Committee on Infectious Diseases, “This study is an important contribution to our understanding of how common — or how rare — this vaccine side effect is.”

Sawyer wrote an editorial accompanying the study, which was published online June 6 in the journal Pediatrics.

He said it’s common for parents to worry about the safety of giving multiple vaccines on the same day.

The new findings do suggest that the risk of fever-related seizure is higher when certain vaccines are given together. “But it’s still quite small,” Sawyer said.

For the study, Duffy’s team combed through a health care database with information on nearly 10 million Americans. The investigators focused on 333 cases of fever-related seizures among babies and toddlers aged 6 months to 23 months.

Overall, the study found, a child’s risk of fever-related seizure was no greater than normal after the flu shot or the DTaP vaccine for diphtheria, tetanus and whooping cough.

There was, however, a small excess risk linked to the pneumococcal vaccine, the findings showed. The risk increased further when the flu shot was given with the pneumococcal vaccine or DTaP — or both.

When all three are given, the CDC estimated, seizures may happen at a rate of up to 30 per 100,000 children.

Sawyer put it another way: Over five to 10 years, the average pediatrician would see one case of fever-related seizure connected to the vaccine trio.

“The total risk is still very small,” Duffy agreed.

The CDC recommends that the DTaP and pneumococcal vaccines be given on the same day. The flu shot is seasonal, so it may be given alone, Sawyer pointed out. But if the timing is right, he said, it is given on a day when a child is getting other routine vaccinations.

Sawyer acknowledged that if there is no extra risk of seizure when the flu shot is given alone, some parents may want the vaccine on a separate day.

“But we know that if we don’t give simultaneous vaccinations, some kids always fall through the cracks,” Sawyer said.

Parents get busy, children get sick and appointments get canceled or delayed, he noted. That’s a problem even if a child eventually catches up on the recommended vaccinations, according to Sawyer.

“When you space out vaccinations,” he said, “your child is at risk of infection during that time.”

Those infections can come with complications, including fever-induced seizure. “So if you want to avoid febrile [fever-related] seizure,” Sawyer said, “delaying vaccinations is not the way to do it.”

More information

The CDC has more on vaccines and febrile seizures.





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U.S. Pays Highest Prices for Cancer Meds: Study

By Dennis Thompson
HealthDay Reporter

MONDAY, June 6, 2016 (HealthDay News) — The United States pays the highest prices in the world for generic and brand-name cancer drugs, a new study has found.

However, as the world’s wealthiest nation, the United States is better able to pay for those pricey drugs than poorer countries with somewhat lower medication prices, added study lead author Dr. Daniel Goldstein.

People in China and India are much less able to afford cancer drugs than Americans, he said, even though U.S. monthly drug prices are about three to six times higher in the United States.

That doesn’t mean America came out on top in overall drug affordability, however. Developed nations such as Australia, England and Israel had the “best deal” in the world on cancer drugs, thanks to government programs that regulate drug pricing, the study found.

“America is the wealthiest nation, but its drug prices are significantly higher — so much so that cancer medications are less affordable in the U.S. than developed countries like England or Australia,” said Goldstein, who’s a senior medical oncologist at Rabin Medical Center in Petach Tkvah, Israel.

Goldstein was scheduled to present the findings Monday at the American Society for Clinical Oncology annual meeting, in Chicago. Research presented at medical meetings is typically considered preliminary until published in a peer-reviewed journal.

For the study, Goldstein’s group compared the prices for 23 cancer drugs in seven countries: Australia, China, England, India, Israel, South Africa and the United States.

The analysis included 15 generic and eight brand-name cancer drugs used to treat a wide range of different cancers.

Drugs included in the analysis included the leukemia drug Sprycel (dasatinib), which can cost around $12,000 a month in the United States; the lung and pancreatic cancer drug Tarceva (erlotinib), which costs around $7,700 a month; and the breast cancer drug Herceptin (trastuzumab), which costs more than $5,300 a month, the researchers said.

On average, the study found that Americans pay the most per month for both brand-name drugs ($8,694) and generics ($654).

India had the lowest average brand-name cost per month ($1,515), while South Africa had the lowest average generic price per month ($120).

However, drug prices are only one factor in determining affordability, the study authors noted. Some countries have distinct economic advantages, which make their citizens better able to pay for medications, Goldstein explained.

So, to do a more “apples-to-apples” comparison of drug affordability, the researchers employed a global economic measurement called “GDP per capita based on purchasing power parity,” or GDPcapPPP.

The International Monetary Fund supplied each country’s GDPcapPPP — a measure of national wealth that factors in citizens’ cost of living.

Under that statistical filter, the average monthly price of brand-name drugs amounted to 192 percent of the United States’ GDPcapPPP.

By comparison, India’s brand-name drug prices were 313 percent of GDPcapPPP, while China’s prices were 288 percent of GDPcapPPP — meaning people in those countries have to stretch much farther to pay their drug costs.

“Even though the prices are lower, the GDP per capita is a lot lower in those poorer countries,” Goldstein said.

Meanwhile, average monthly brand-name drug prices in England were 78 percent of that nation’s GCPcapPPP, and 71 percent of the GDPcapPPP in Australia.

In some developed nations — like Australia and England — the government has stepped in to regulate drug prices, resulting in a better value for their citizens, Goldstein said.

“In the United States, the system is lacking any assessment of value,” he said. “The FDA approves a drug based on safety and efficacy, but there’s no consideration for cost or value.”

Cancer expert Dr. Sharon Giordano reviewed the new findings. She said she’s worried that “we may eventually hit some kind of breaking point” when it comes to cancer drug prices in the United States.

“The cost of drugs for cancer care has been increasing substantially faster than the cost of the rest of medical care in the United States,” said Giordano, a breast medical oncologist and chair of health services and health disparities research at the University of Texas MD Anderson Cancer Center in Houston.

“While right now we are able to sustain ourselves, there’s a lot of concern that in future years we won’t be able to,” Giordano continued. “Then the U.S. will be forced to confront really difficult questions about how we’re going to afford to pay for cancer care.”

Countries like England and Australia have been able to control drug prices without significantly affecting cancer treatment, Giordano said.

“You may not have access in those countries to every single drug that the United States has access to, but I think they’ve reached more of a compromise,” she said.

More information

For more on cancer drug prices, visit the Memorial Sloan Kettering Cancer Center.





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Pop Stars Often Hawk Unhealthy Foods to Kids: Study

By Alan Mozes
HealthDay Reporter

MONDAY, June 6, 2016 (HealthDay News) — Katy Perry, Justin Timberlake, Maroon 5: Some of America’s biggest pop stars are making millions from ad campaigns for sugar-laden, low-nutrition foods, a new study says.

“Given current obesity rates among teens, it’s incredibly problematic that the majority of music celebrities’ drink endorsements — 71 percent — were for sugary beverages like soda,” said study lead author Marie Bragg.

“Most food endorsements — 81 percent — were for unhealthy products like fast food, candy, and nutritionally poor snacks,” she added.

Bragg’s team at NYU Langone Medical Center in New York City said that about $2 billion is spent every year on food and drink advertising aimed at the young. Each year, the average American preteen sees about 4,700 such ads, while the average teenager views about 5,900, Bragg’s group noted.

Many of the ads feature a (paid) pitch from one of a number of pop music personalities. To track which celebrities are endorsing which products, Bragg’s team focused on ads featuring hit-makers from Billboard magazine’s “Hot 100” listings in 2013 and 2014, adding in “Teen Choice Award” winners, and artists with popular videos featured on YouTube.

The investigators then compiled a list of all celebrity food/drink endorsements across all media between 2000 and 2014.

The result: 163 pop stars endorsed a total of 590 products during that 14-year period. About one-fifth (107 endorsements) were for food and non-alcoholic drinks, the study found.

Some of the biggest music stars were involved in these pitches. Katy Perry lent her fame to Pepsi and PopChips; Maroon 5 appeared in ads for Coca-Cola and Snapple; One Direction hyped Nabisco and Pepsi; and Justin Timberlake helped advertise Chili’s, McDonald’s and Pepsi.

Country music stars played their part, too: Carrie Underwood was featured in ads for Vitamin Water and Hershey’s chocolate, while Blake Shelton appeared in ads for Pepsi and Pizza Hut.

The study authors said that four-fifths of the endorsed foods could be classified as unhealthy (or “nutrient poor”), while nearly three-quarters of the endorsed drinks were sugar-sweetened.

Full-calorie sodas were the most frequently hawked beverage, Bragg’s team reported.

“Companies like Coca-Cola have been using celebrities, especially professional athletes, to promote products since the early 1900s, so it’s not a new phenomenon,” said Bragg, who is assistant professor of population health at the NYU College of Global Public Health.

“Our study didn’t assess whether music celebrity endorsements of foods and beverages has been gaining steam over time,” she said. “But it’s estimated that many of these contracts are worth millions of dollars — suggesting companies think celebrity endorsements are an incredibly valuable tool for promoting their products.”

No pop star endorsed fruits, vegetables or whole grains, the nutritionists noted.

That’s no surprise, according to Bragg, since “industries that sell fruits and vegetables can’t afford to hire celebrities.”

Still, inroads on behalf of healthier foods are being made.

“Partnership for a Healthier America recently teamed up with some celebrities — mostly professional athletes — to promote fruits and vegetables through an advertising campaign called FNV,” Bragg said. Their goal is “to make produce cool and edgy,” she explained.

Lona Sandon is program director and assistant professor of clinical nutrition at the University of Texas Southwestern Medical Center at Dallas. She agreed with Bragg that getting kids to eat better is always an uphill battle, even with advertisers on your side.

“The ‘Got Milk’ campaign by the dairy industry was fairly successful with getting celebrity athletes and pop stars on board to promote milk,” Sandon said. “It likely had some influence on milk drinking among kids.”

However, “there is more money to be made promoting less healthy food choices,” she added, and parents simply don’t hold all the cards when it comes to nutritional messaging.

“Teens want to make their own decisions and be independent, and start looking to others such as pop stars as role models,” Sandon said. “They want to try things that they see their role models doing, things that maybe their parents do not approve of, like drinking a soda or energy drink.”

And, Sandon pointed out, “Eating an apple or bowl of broccoli is just not rebellious.”

Parents aren’t powerless, however. They should “set limits on how often unhealthful foods and beverages are served” at home, she suggested. A child’s age matters, too.

“Parents are likely to have the most influence as role models of healthy eating up to about the age of 12 to 13,” Sandon said. That means that “it is important to instill healthy eating choices early on in life.”

The study was published online June 6 in the journal Pediatrics.

More information

The American Academy of Pediatrics has more on nutrition and teens.





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Immune-Based Drug May Help Some With Advanced Bladder Cancer

By Dennis Thompson
HealthDay Reporter

SUNDAY, June 5, 2016 (HealthDay News) — Patients with advanced bladder cancer can sometimes be too old or unhealthy to withstand standard chemotherapy. However, some may gain hope from a new drug that unleashes the immune system to attack tumor cells, researchers reported Sunday.

Patients who responded to the drug Tecentriq (atezolizumab) had an average survival of nearly 15 months, about 5 to 6 months longer than people usually gain from platinum-based chemotherapy, said lead researcher Dr. Arjun Balar.

The treatment didn’t help everyone, however: Only about a quarter of patients responded to the drug.

Still, any advance for this patient population is sorely needed, experts say. That’s because about half of advanced bladder cancer patients cannot receive chemotherapy because they’re too old to withstand chemo’s toxic effects, explained Balar, who is assistant professor of medicine at NYU Langone Medical Center in New York City.

He noted that the average patient age for this disease is 70.

Other patients can’t receive chemotherapy because they’re suffering from kidney failure or other health problems, said Dr. Elizabeth Plimack, who reviewed the study findings. She directs genitourinary clinical research at Fox Chase Cancer Center in Philadelphia.

This means that chemo is currently the only approved first-line treatment for bladder cancer.

“After that, there are no other standard therapies,” Balar said. “These patients are really out of other options.”

But, the new results suggest Tecentriq may serve as a significant advance for at least some of those patients, he said.

The drug’s maker, Genentech, helped fund the study, which was presented Sunday at the American Society for Clinical Oncology annual meeting in Chicago.

As the researchers explained, cancers evade the immune system by switching off the ability of immune system cells to recognize tumor cells as a harmful intruder. Immunotherapy drugs like Tecentriq essentially remove cancer’s “cloaking device” — allowing the immune system to identify, target and destroy malignant cells.

The U.S. Food and Drug Administration approved Tecentriq last month for use in treating bladder cancer for patients who’ve already gone through chemotherapy. It’s the first new medication approved in more than three decades for bladder cancer, Balar said.

His team wanted to see whether the drug might also help patients who’ve never had chemotherapy due to frail health.

Almost 77,000 Americans will be diagnosed with bladder cancer in 2016, the researchers said in background notes. Fewer than 15 percent survive past five years if the disease — which is closely tied to smoking — is in its advanced stages when diagnosed.

The new clinical trial involved 119 bladder cancer patients averaging 73 years of age. None had been deemed eligible for chemotherapy.

About 24 percent of patients — 28 out of 119 — responded to Tecentriq, which shrank their tumors by at least 30 percent and in some cases caused their cancer to disappear. Their average overall survival was just under 15 months.

Tecentriq had a lower response rate than platinum-based chemotherapy, which typically helps about 40 percent of patients, Balar said. However, people who respond to chemo have an average overall survival of about 9 to 10 months, lower than that achieved with Tecentriq.

Most patients taking Tecentriq also appeared to remain in remission. Of the 28 for whom the drug worked, 21 are still in remission, the researchers reported. The longest duration of response so far is more than 18 months.

Seven of the patients who initially saw their cancer respond to the drug experienced tumor recurrence, the study found.

Also, about 10 to 15 percent of patients experienced severe side effects from Tecentriq, which could include hypothyroidism (underactive thyroid), liver function problems, rash or diarrhea. Despite this, only 6 percent of patients dropped out of the trial due to side effects, the researchers reported.

For her part, Plimack believes further clinical trials are needed to better understand Tecentriq, given that the response rate was lower than chemotherapy but overall survival appeared to be increased.

“The overall survival numbers do exceed what we’ve seen in the past, but overall survival can be affected by many factors other than the study agents,” Plimack said.

A larger follow-up trial already is planned, as Genentech hopes to develop the drug as a first-line new standard of care for people unable to receive chemotherapy, Balar said.

Experts note that research presented at medical meetings is typically considered preliminary until published in a peer-reviewed journal.

More information

For more on bladder cancer, visit the American Cancer Society.





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Immune-Based Drug May Help Some With Advanced Bladder Cancer

By Dennis Thompson
HealthDay Reporter

SUNDAY, June 5, 2016 (HealthDay News) — Patients with advanced bladder cancer can sometimes be too old or unhealthy to withstand standard chemotherapy. However, some may gain hope from a new drug that unleashes the immune system to attack tumor cells, researchers reported Sunday.

Patients who responded to the drug Tecentriq (atezolizumab) had an average survival of nearly 15 months, about 5 to 6 months longer than people usually gain from platinum-based chemotherapy, said lead researcher Dr. Arjun Balar.

The treatment didn’t help everyone, however: Only about a quarter of patients responded to the drug.

Still, any advance for this patient population is sorely needed, experts say. That’s because about half of advanced bladder cancer patients cannot receive chemotherapy because they’re too old to withstand chemo’s toxic effects, explained Balar, who is assistant professor of medicine at NYU Langone Medical Center in New York City.

He noted that the average patient age for this disease is 70.

Other patients can’t receive chemotherapy because they’re suffering from kidney failure or other health problems, said Dr. Elizabeth Plimack, who reviewed the study findings. She directs genitourinary clinical research at Fox Chase Cancer Center in Philadelphia.

This means that chemo is currently the only approved first-line treatment for bladder cancer.

“After that, there are no other standard therapies,” Balar said. “These patients are really out of other options.”

But, the new results suggest Tecentriq may serve as a significant advance for at least some of those patients, he said.

The drug’s maker, Genentech, helped fund the study, which was presented Sunday at the American Society for Clinical Oncology annual meeting in Chicago.

As the researchers explained, cancers evade the immune system by switching off the ability of immune system cells to recognize tumor cells as a harmful intruder. Immunotherapy drugs like Tecentriq essentially remove cancer’s “cloaking device” — allowing the immune system to identify, target and destroy malignant cells.

The U.S. Food and Drug Administration approved Tecentriq last month for use in treating bladder cancer for patients who’ve already gone through chemotherapy. It’s the first new medication approved in more than three decades for bladder cancer, Balar said.

His team wanted to see whether the drug might also help patients who’ve never had chemotherapy due to frail health.

Almost 77,000 Americans will be diagnosed with bladder cancer in 2016, the researchers said in background notes. Fewer than 15 percent survive past five years if the disease — which is closely tied to smoking — is in its advanced stages when diagnosed.

The new clinical trial involved 119 bladder cancer patients averaging 73 years of age. None had been deemed eligible for chemotherapy.

About 24 percent of patients — 28 out of 119 — responded to Tecentriq, which shrank their tumors by at least 30 percent and in some cases caused their cancer to disappear. Their average overall survival was just under 15 months.

Tecentriq had a lower response rate than platinum-based chemotherapy, which typically helps about 40 percent of patients, Balar said. However, people who respond to chemo have an average overall survival of about 9 to 10 months, lower than that achieved with Tecentriq.

Most patients taking Tecentriq also appeared to remain in remission. Of the 28 for whom the drug worked, 21 are still in remission, the researchers reported. The longest duration of response so far is more than 18 months.

Seven of the patients who initially saw their cancer respond to the drug experienced tumor recurrence, the study found.

Also, about 10 to 15 percent of patients experienced severe side effects from Tecentriq, which could include hypothyroidism (underactive thyroid), liver function problems, rash or diarrhea. Despite this, only 6 percent of patients dropped out of the trial due to side effects, the researchers reported.

For her part, Plimack believes further clinical trials are needed to better understand Tecentriq, given that the response rate was lower than chemotherapy but overall survival appeared to be increased.

“The overall survival numbers do exceed what we’ve seen in the past, but overall survival can be affected by many factors other than the study agents,” Plimack said.

A larger follow-up trial already is planned, as Genentech hopes to develop the drug as a first-line new standard of care for people unable to receive chemotherapy, Balar said.

Experts note that research presented at medical meetings is typically considered preliminary until published in a peer-reviewed journal.

More information

For more on bladder cancer, visit the American Cancer Society.





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Antibody-Based Therapy Shows Promise Against Stomach Cancer

SUNDAY, June 5, 2016 (HealthDay News) — An experimental therapy based on immune-system antibodies is helping some people with advanced stomach cancer live longer, a new study finds.

The phase 2 clinical trial, involving 161 patients, focused on an antibody called IMAB362.

The median survival of people using the treatment plus standard chemotherapy was more than 13 months, compared with 8.4 months for those who received chemotherapy alone, the researchers reported.

One specialist in gastric (stomach) cancer care believes therapeutic advances are sorely needed.

“Metastatic gastric cancer carries a poor prognosis and the treatment effectiveness of current chemotherapeutic agents leave a lot to be desired,” said Dr. David Bernstein, chief of hepatology at Northwell Health in Manhasset, N.Y.

While a larger, more rigorous trial is still needed, “this study is quite encouraging that this type of therapy may be effective in treating this disease,” he said.

The IMAB362 antibody employed in this new treatment targets a protein on cancer cells called claudin 18.2. German researchers found that study patients who had the highest levels of this protein in tumors prior to receiving the new treatment had an even longer median overall survival, at almost 17 months.

The study was to be presented Sunday at the annual meeting of the American Society of Clinical Oncology (ASCO), in Chicago. The research was funded by drug maker Ganymed Pharmaceuticals AG.

Study lead researcher Dr. Salah-Eddin Al-Batran directs the Institute of Clinical Cancer Research at Nordwest Hospital in Frankfurt. In an ASCO news release, he said that since “claudin 18.2 is abundant in gastric tumors, we estimate that half of all patients with advanced gastric cancer may be candidates for this new treatment.”

In addition, he said, “this unique target is not present in any healthy tissues except the lining of the stomach, thereby minimizing treatment side effects.”

According to the researchers, a larger, phase 3 study in stomach cancer patients is scheduled to begin in early 2017.

IMAB362 is the first antibody to target claudin 18.2, which is also found in a number of other cancers, including pancreatic, lung, esophageal and ovarian tumors. Because of this, the same research team said it plans a phase 2 study of IMAB362 in patients with pancreatic cancers.

Dr. James Grendell is chief of gastroenterology, hepatology and nutrition at Winthrop-University Hospital in Mineola, N.Y. He agreed that phase 3 studies are needed to confirm the new findings. But he called the new antibody-based approach “exciting.”

The therapy “utilizes agents to break down the barriers that prevent cancers from being recognized and destroyed by our body’s own immune system,” Grendell explained. “These agents — such as IMAB362 in this report — tear off the disguise and expose the cancer as the ‘enemy invader’ it really is.”

Grendell agreed that because the therapy’s target, claudin 18.2, is found in a number of other tumor types, “this therapeutic antibody has the potential to improve the outlook for patients with a variety of currently difficult-to-treat cancers.”

According to the American Cancer Society, more than 26,000 cases of stomach cancer will be diagnosed in Americans this year, and almost 11,000 will die of the disease. Stomach cancer affects men more than women, and typically affects people over the age of 65.

Experts note that findings presented at medical meetings are typically considered preliminary until published in a peer-reviewed journal.

More information

The American Cancer Society has more about stomach cancer.





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Two-Pronged Chemo Helps Some With Advanced Ovarian Cancer

By Dennis Thompson
HealthDay Reporter

SATURDAY, June 4, 2016 (HealthDay News) — Some women with advanced ovarian cancer may fare better if chemotherapy is dripped directly into their abdomens as well as introduced into their bloodstream through traditional IV, a new study finds.

Clinical trial results show the combination of abdominal and IV chemotherapy can slow the progression of ovarian cancer better than IV chemo by itself in women who already have had surgery to remove all or nearly all of their cancer.

Close to 77 percent of women who got combination treatment had at least a nine-month delay in the progression of their cancer, compared with slightly less than 58 percent of women who received IV therapy alone.

Average overall survival also was longer, 59 months versus 38 months, respectively. However, the researchers said the difference was not statistically significant.

Progression-free survival was similar between the two groups, amounting to slightly more than 11 months with IV chemotherapy compared with 12.5 months from IV/abdominal chemotherapy, the findings showed.

Nevertheless, these statistics support using IV/abdominal chemotherapy in certain patients, said Dr. Don Dizon, director of medical oncology for the women’s oncology program at Women & Infants Hospital of Rhode Island. He was not involved in the study.

Women taking this path first receive traditional chemotherapy to reduce the size of their tumor, and then undergo surgery to have as much of their cancer removed as possible, Dizon explained.

A port is then installed into their bellies to allow chemotherapy to drip directly into their abdominal cavities, he said. They also receive chemotherapy via IV.

“I think this represents a very valid option for this population, who are receiving primary chemotherapy before surgery and then have successful surgery,” Dizon said. “I think you need to mention this option and these data when discussing treatment with those patients.”

The researchers will continue to track the patients in this study in hopes of figuring out the best potential recipients of this combination therapy, said presenting researcher Dr. Helen Mackay. She is divisional head of medical oncology and hematology at the Sunnybrook Odette Cancer Center in Toronto.

“If we can identify the long-term survivors, we hope this will help us better predict who truly benefits from this approach,” Mackay said.

About 22,280 women are expected to receive a diagnosis of ovarian cancer in 2016, and about 14,240 women will die from the disease, according to the American Cancer Society. Ovarian cancer is the fifth most common cause of cancer death among women.

The new clinical trial involved 200 women who first underwent chemo to shrink their tumor, followed by surgery to remove the cancer. Afterward, they were randomly assigned to receive either IV chemotherapy or IV/abdominal chemotherapy.

Researchers were scheduled to present the findings Sunday at the American Society of Clinical Oncology’s annual meeting, in Chicago.

This therapeutic option delivers chemotherapy directly to cancer cells, without having to wend its way through the bloodstream, noted Dr. Linus Chuang. He is a professor of obstetrics, gynecology and reproductive science with the Icahn School of Medicine at Mount Sinai, in New York City.

Chuang pointed out that for nine out of 10 ovarian cancer patients, their cancer is confined to their abdomen when they are first diagnosed.

Delivering chemo directly into the abdomen “may improve efficacy by increasing concentration of the cytotoxic agent directly against the tumor in the abdominal cavity,” Chuang said.

The researchers also noted this technique allows delivery of higher doses of chemotherapy to the tumor, while sparing other parts of the body from side effects.

The rate of severe side effects was slightly lower among women who received the combo therapy, about 16 percent compared to 23 percent. However, the difference was not statistically significant.

More information

For more on ovarian cancer, visit the American Cancer Society.





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Liquid Biopsy May Help Doctors Track Changes in Tumors

By Dennis Thompson
HealthDay Reporter

SATURDAY, June 4, 2016 (HealthDay News) — Biopsies can be arduous and painful for cancer patients, but necessary to accurately diagnose the disease and determine the best course of treatment.

Now, researchers report that a new blood-based “liquid biopsy” seems to be a groundbreaking alternative.

Doctors used blood drawn from a patient’s arm to analyze DNA that tumors typically shed into the bloodstream, explained lead researcher Philip Mack. He is director of molecular pharmacology at the University of California, Davis, Comprehensive Cancer Center.

A study of more than 15,000 patients with 50 different tumor types determined that liquid biopsy can detect mutations in cancer DNA from 94 percent to 100 percent of the time, Mack said.

“If we saw a mutation in the plasma, that meant it was in the tumor,” said Mack, who was to present the findings this weekend at the American Society of Clinical Oncology annual meeting, in Chicago.

Dr. Joshua Brody, director of the Lymphoma Immunotherapy Program at Mount Sinai’s Tisch Cancer Institute in New York City, called the research “a big deal. This will be practice-changing.”

“This is not quite a Star Trek medical magic wand, but it’s getting towards there,” Brody said.

Researchers used a new genetic scan called Guardant360 to analyze cancer DNA in patients’ blood. The study received funding from Guardant Health Inc., which produces the test used in the study.

Liquid biopsies provide valuable information for doctors using targeted therapies to treat cancer, Mack said, because they detect when tumors are developing resistance to a particular therapy.

Tumors develop resistance “through the acquisition of new mutations that allow it to circumvent or otherwise ignore a therapeutic option,” Mack said. “If we identify what that mutation is, we can treat with a different therapy.”

In the study, the most common types of cancer were advanced lung cancer (37 percent), breast cancer (14 percent) and colorectal cancer (10 percent).

It’s been known for decades that tumors release their DNA into the bloodstream, particularly in advanced cases where cancer has spread to other parts of the body, Mack said.

“The question has always been whether this can serve as an alternative to a biopsy for diagnosis and for the assignment of appropriate targeted therapy,” Mack said.

Mack and his colleagues found that genetic analysis of blood-borne cancer DNA very accurately detected cancer-causing mutations that were also found in tumor tissue samples.

They also found that the test could detect genetic changes in a cancer that occur as tumors gain resistance to targeted cancer drugs.

Overall, the liquid biopsy revealed possible treatment options for more than 63 percent of patients tested, including FDA-approved drugs as well as eligibility for clinical trials.

Mack expects the cost of a liquid biopsy to be competitive with that of a traditional tissue biopsy, since a blood draw costs less than the cost of an invasive procedure and subsequent processing of dissected tissue.

However, at this point Mack believes a liquid biopsy cannot replace a tissue biopsy when it comes to an initial diagnosis of cancer.

“At this point, we cannot dispense with that initial tumor biopsy,” he said. “The initial biopsy and subsequent pathology are what allow us to determine what type of cancer it is and whether it is even cancer at all. That will still be necessary.”

“A trained medical pathologist can tell you most of the time what kind of tumor it is based on how the cells look and behave in a tissue sample,” Mack continued. “They can say, ‘Even though we pulled this from a lesion on your liver, it’s actually lung cancer.’ “

Mack believes the real value of liquid biopsy will show itself as a patient’s cancer treatment proceeds.

Most patients never undergo a second tissue biopsy during treatment to check their progress, “unless there’s a compelling therapeutic option available,” he said.

Liquid biopsy provides an easier way to keep track of treatment. “You can get a blood draw basically at any time, so you can really monitor the progression of a patient’s tumor over time,” Mack said.

But Brody believes liquid biopsy can also serve as a valuable alternative to tissue biopsy for cancer diagnosis in particular patients.

“We have lots of older or less healthy patients who simply are not great candidates for surgery,” Brody said. “For them, it’s not this [liquid biopsy] versus tissue biopsy. It’s this versus nothing.”

Dr. Sumanta Pal, a medical oncologist with City of Hope National Medical Center in Duarte, Calif., agreed with Brody, noting that tissue biopsies can be very difficult to perform in cancers that have spread to the brain or the bone. Some patients also may have a bleeding risk that makes tissue biopsy a dangerous option.

“There are many different scenarios where I can imagine this test would be clinically meaningful for diagnosis,” Pal said.

Several competing liquid biopsy tests are currently available or under development, Pal added.

While this study focused on gene-based cancer treatment, Brody believes a liquid biopsy also will prove valuable for therapies that use the body’s immune system to target cancer cells.

“We will be able to develop similar tests to predict patients’ response to immunotherapies,” he said.

More information

Visit the American Cancer Society for more on cancer biopsy.





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Overweight Kids Eat Only a Bit More Per Meal

FRIDAY, June 3, 2016 (HealthDay News) — An extra spoonful or two with each meal may lead to an overweight infant or toddler, a new study suggests.

British researchers found that overweight infants and toddlers don’t eat more often than their normal-weight peers, but they do consume just a little bit more food at each meal.

The overweight youngsters had about 141 calories at each meal. The normal-weight babies and toddlers had about 130 calories at each meal, the study found.

“Although the difference in average meal size between the overweight and healthy-weight children seems small [11 calories, perhaps an extra spoonful of baked beans with a meal] children are eating on average five times per day so the difference over the course of a week is considerable,” study author Hayley Syrad, from University College London, and colleagues, wrote.

The study included data from more than 2,500 children in the United Kingdom. They were between 4 months and 18 months old.

The researchers also noted that overweight and normal-weight children were eating the same types of foods. The overweight kids were just eating more of those foods.

“This small extra intake each meal means that overweight children are consuming approximately two extra days’ worth of energy each month. Given that these children are less than 2 years of age, over time the effects could be substantial,” the study authors concluded.

The study also showed that overweight babies and toddlers didn’t eat more frequently than their normal-weight counterparts.

The risk of overweight or obesity went up 9 percent for every extra 24 calories consumed during each meal, the researchers said.

“Larger portions, rather than eating more often, may be a risk factor for the development of childhood overweight in early life. Further prospective studies that look at the development of excess weight over time are needed to establish causation,” the researchers said.

The study was to be presented Friday at the European Obesity Summit in Sweden. Findings presented at meetings are generally viewed as preliminary until they’ve been published in a peer-reviewed journal.

More information

The U.S. Centers for Disease Control and Prevention has more on childhood overweight and obesity.





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