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Showing posts with label Cancer - Targeted treatment. Show all posts
Showing posts with label Cancer - Targeted treatment. Show all posts

Monday, 27 July 2020

AstraZeneca Strikes $6 Billion Cancer Drug Deal

Therapy is designed to leave healthy cells alone, potentially limiting side effects


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LONDON—AstraZeneca PLC has agreed to pay Japan’s Daiichi Sankyo Co. up to $6 billion to jointly develop and commercialize a cancer drug it says could help redefine the way the disease is treated, in the British company’s latest push into oncology.
The therapy, an antibody drug conjugate named DS-1062, targets a range of cancers—including lung and breast—that produce a protein known as TROP2. It is designed to deliver chemotherapy just to those cells, leaving healthy ones alone, potentially limiting side effects.  ...



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AstraZeneca Strikes $6.9 Billion Cancer Deal With Japanese Drugmaker

Deal for part of the rights to Daiichi Sankyo’s antibody drug is part of Astra’s heavy investment in cancer research


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AstraZeneca PLC has agreed to pay Japan’s Daiichi-Sankyo Co. up to $6.9 billion for shared rights to a new cancer drug, as the British drugmaker expands further in the oncology market.
The Japanese drugmaker, which will retain exclusive rights to the treatment in its home country, will get $1.35 billion upfront, with further payments dependent on the drug’s development and sales performance. In return, AstraZeneca said it will receive half the profit from future sales outside Japan.   ...

Wednesday, 18 December 2019

World first cancer treatment at NHS hospital could make chemo 'more effective by using BUBBLES'

World first cancer treatment being trialled in NHS hospitals could make chemotherapy 'more effective by using BUBBLES to help kill tumours'
  • Acoustic cluster therapy involves injecting microbubbles and liquid droplets
  • Ultrasound used to make bubbles grow larger and stretch the tumour's walls 
  • Increases chance of chemo drugs reaching cancer cells and not healthy ones

NHS hospitals are trialling a world-first way of delivering chemotherapy to try and make the grueling cancer treatment more effective. 
It involves using tiny bubbles to get more drugs inside tumours without damaging healthy cells, a brutal side effect of chemo.
Known as acoustic cluster therapy, the pioneering technique sees these microscopic bubbles injected directly into the site of the cancer.
An ultrasound is used to create high-frequency waves that make the bubbles grow larger and stretch the tumour walls. 
This gives medication a bigger target to aim for, greatly increasing the amount of drugs which reach the cancer cells.
In theory, oncologists say it has the potential to boost the potency of the treatment and lead to fewer side effects. The therapy is given alongside every bout of chemo.
Karen Childs is the first patient on the clinical trial and is receiving treatment at The Royal Marsden in Chelsea following a liver cancer diagnosis in November 2013
She said it was 'an incredible opportunity' to be on the trial and hopes it opens the door for 'side effect-free' treatments for cancer sufferers in the future
She said it was 'an incredible opportunity' to be on the trial and hopes it opens the door for 'side effect-free' treatments for cancer sufferers in the future
Mrs Childs (receiving the therapy) said it 'hadn't sunk in yet' that she is 'the very first patient in the world to be receiving this new treatment'
 Mrs Childs (receiving the therapy) said it 'hadn't sunk in yet' that she is 'the very first patient in the world to be receiving this new treatment'
Chemotherapy can be taxing on the body, leading to weakened immune systems, vomiting, trouble breathing, hair loss and irregular heart rhythms. 
The drugs are delivered intravenously and flow around the entire body looking to attack tumours. But they kill off healthy cells in the process. 
The Royal Marsden NHS Foundation Trust is testing acoustic cluster therapy on patients at its three hospitals in London and Surrey.

HOW DOES ACOUSTIC CLUSTER THERAPY WORK?

It uses microscopic clusters of bubbles and liquid droplets.
They are injected near the site of the tumour.
An ultrasound is used to create high-frequency waves which 'activate' the bubbles and droplets.
These waves cause them to grow larger within the tumour, stretching its walls. 
This gives the chemo drugs a bigger target to aim for.
It is hoped it will greatly increase the amount of medication which reaches the cancer cells. 
Acoustic cluster therapy was invented by the Norwegian company Phoenix Solutions. 
It was further developed with proof-of-concept studies by scientists at The Institute of Cancer Research (ICR) and the Norwegian University of Science and Technology (NTNU), Trondheim.
It uses microscopic clusters of bubbles and liquid droplets to enhance the delivery of chemo drugs to tumours. They are injected into the site of the cancerous mass.
A standard ultrasound is used to convert the clusters into larger bubbles, which stretch the walls of the tumour as they grow.
This gives the chemo drugs a better chance of reaching the cancer cells.
Karen Childs was the first patient on the clinical trial and is receiving treatment at The Royal Marsden in Chelsea following a liver cancer diagnosis in November 2013.
Mrs Childs, from North West London, said: 'I’m not sure it’s sunk in yet that I’m the very first patient in the world to be receiving this new treatment.
‘This trial is an exciting step for the hospital and a huge step for patients like me. It really would make a big difference to patients’ lives if side effects could be reduced in the future using more targeted treatments like this.
‘It’s an incredible opportunity to be on this trial and the staff at The Royal Marsden have been amazing and very supportive.’
The trial is being run by The Institute of Cancer Research. It will be some time before its success can be assessed and many more trials would be needed before it could be rolled out.
Jeffrey Bamber, professor in physics applied to medicine, who helped develop and evaluate the technology at The Institute of Cancer Research, London, said: ‘It’s a very exciting "door opening" technology which concentrates more of the drug in the tumour.
‘We expect eventually to be able to both treat tumours more effectively and reduce the rate and severity of side effects.
‘In the long term we hope this technology will be of particular benefit in difficult-to-treat tumours, such as those of the pancreas. It may also assist new types of treatments such as immunotherapy.’
Roughly 120,000 people in the UK, a third of all new cancer patients, have chemo each year. Around 650,000 receive the treatment in the US.
https://www.dailymail.co.uk/health/article-7804695/World-cancer-treatment-NHS-hospital-make-chemo-effective-using-BUBBLES.html

Wednesday, 9 October 2019

New Personalized, Precision Approach to Lung Cancer Treatment

Recently I told you about the latest breakthroughs in lung cancer prevention and detection (if you missed that article, click here). Today I want to focus on the exciting advances in the treatment of this terrible disease.
Peter Bach, MD

Published Date: November 5, 2013  Publication: Bottom Line Health

Illustration of lungs (stock image). | Credit: (c) yodiyim / stock.adobe.com

Why? Because although the odds of surviving lung cancer admittedly still aren’t great, these days a lung cancer diagnosis is not an automatic death sentence—even in the case of late-stage cancer. We have many more options for treating the disease than we did just a decade ago…and treatment today is more personalized and precise than ever.
For instance, doctors now can look at the individual characteristics of a tumor, including particular cell patterns and genetic mutations. This information helps them to set treatment plans that are more likely to work—and to avoid recommending treatments with low chances of success. In fact, Peter Bach, MD, an epidemiologist and pulmonologist at Memorial Sloan-Kettering Cancer Center in New York City, told me that he is “extremely enthusiastic” about the progress that’s been made over the past decade.
The problem: Despite the remarkable advances, not all hospitals have the needed tools in their arsenals…and not all doctors understand which patients will benefit from such a personalized approach. That’s why I want you to be in-the-know about the newest ways to beat lung cancer—in case you end up battling the country’s number-one cancer killer.

SECRETS FOUND IN CELL PATTERNS

The term lung cancer actually is misleading because the disease is not just one entity. Rather, there are two major types of lung cancer, each with different risk factors, probable prognoses and treatments. And then even within one of those types, different tumors can have different characteristics that affect how aggressive the cancer may be and which treatment may work.
The majority of lung cancers fall in to the non–small cell category. Adenocarcinoma is the most common non–small cell cancer, accounting for about half of all lung cancers. It’s the type found most often in current and former smokers—and also in people who never smoked.
When adenocarcinoma is detected before it has had a chance to spread, it’s treated surgically. Most of the time, the surgeon performs a lobectomy by removing the entire lobe that has the cancer in it (a pair of lungs has five lobes, three on the right side and two on the left). In some cases, the surgeon does a limited resection, removing just part of the affected lobe.
Tricky: The decision about which procedure to do can be a tough one, according to Prasad Adusumilli, MD, a thoracic surgeon and scientist at Memorial Sloan-Kettering Cancer Center. That’s because the surgeon wants to remove enough lung tissue to prevent a cancer recurrence, but at the same time leave enough tissue to preserve lung function. Until now, there hasn’t been an evidence-based system to guide surgeons, so the size and location of the tumor (for example, how far the tumor is from the edge of the lung) often have been used as criteria in deciding how much to remove.
Breakthrough: Surgeons at Memorial Sloan-Kettering perform about 1,000 of these operations each year. With all the data they have accumulated over the years, Dr. Adusumilli and his research team have developed an algorithm to help surgeons decide which operation is best for patients with adenocarcinoma.
The research that led to the new algorithm was complicated, but basically the researchers performed microscopic examinations of many hundreds of samples of early-stage adenocarcinoma, classifying each according to the proportion of the five major cell patterns (acinar, papillary, lepidic, micropapillary and solid) seen in the tumor. Then they analyzed the follow-up data to determine the chances of cancer recurrence based on the cell pattern and the type of surgery that was done.
Overall, the five-year incidence of cancer recurrence was 21% for patients who had a limited resection and 15% for patients who had a lobectomy. When the specific cell patterns were analyzed, though, it became clear that tumors with a higher percentage of cells showing a micropapillary pattern had a much higher risk for recurrence within the same lobe if patients underwent limited resection.
Bottom line: Doctors can now use this knowledge about cell patterns to opt for the tissue-sparing limited resection procedure in patients whose tumors do not have the aggressive micropapillary pattern…and save the more extensive lobectomy for patients whose cell pattern indicates a high risk for recurrence.
Only a limited number of hospitals have the expertise needed to determine a lung tumor’s cell pattern right on the spot, in the operating room, at the time of the actual surgery. “This requires expert pathological experience and a large volume of tumors for the pathologists to get experienced,” Dr. Adusumilli explained. At hospitals that do not currently have this ability, some patients who get a limited resection may end up needing another operation later if their cancer subsequently is found to have the micropapillary pattern…or, worse, they may have a cancer recurrence.
Hopefully, that will change soon. Dr. Adusumilli and his team of researchers are now trying to develop tools that can more easily determine the cell’s pattern—preferably before surgery—sparing patients the need to go under the knife a second time.

SECRETS FOUND IN GENETIC MUTATIONS

When lung cancer is diagnosed after it has spread to the lymph nodes or beyond, as it is most of the time, treatment involves more than just surgery—it also requires medication. Now, in what Dr. Bach refers to as a “very exciting” development, the particular medications that will work best often can be determined based on specific genetic mutations in the tumors.
How it started: About 10 years ago, during clinical trials for two new lung cancer drugs, doctors observed that some people receiving the drugs gefitinib (Iressa) and erlotinib (Tarceva) had a much better response than others—even though all the patients had advanced adenocarcinoma. This led to the discovery that the patients who responded well had tumors that showed a specific mutation in the epidermal growth factor receptor (EGFR) gene. People with the mutation survived nearly twice as long on the drug regimen as those without it. It turns out that the mutation is present in about 20% of people diagnosed with advanced adenocarcinoma.
A few years later, researchers discovered another mutation on the anaplastic lymphoma kinase (ALK) gene, which is present in 7% of people with adenocarcinoma. A drug that inhibits ALK activity, called crizotinib (Xalkori), is very effective in people who have that particular mutation.
All three of these drugs have been approved, and the required genetic testing is available. Many experts now recommend that all patients with advanced adenocarcinoma have their tumors analyzed for mutations of EGFR and ALK—including patients who have mixed cancer types, even with just a small component of adenocarcinoma. Referring to molecular testing in its entirety, not just for EGFR and ALK, Dr. Bach said, “Now, 60% to 70% of adenocarcinomas have important molecular information that affects therapeutic choices. That’s huge! Lung cancer might be the poster child for this kind of precision, personalized medicine.”
If you are diagnosed with lung cancer: If at all possible, see an oncologist at a hospital associated with a university, Dr. Bach advised. Academic medical centers usually have the technology and expertise to take advantage of these new tests and procedures. If you live too far away to see a doctor there regularly, consider having a consultation with an appropriate expert at such a facility—that person can advise you and your doctor on the best treatment for you.
https://bottomlineinc.com/health/lung-cancer/new-personalized-precision-approach-to-lung-cancer-treatment

Lung Cancer Is On the Rise Among Nonsmokers

But new treatments dramatically improve outcomes…

Timothy Burns, MD, PhD

Published Date: May 1, 2016  Publication: Bottom Line Health

People who have never smoked often assume that they’ll never get lung cancer. But they can—and the prevalence of these cases is increasing at a troubling rate.
Update: Two important recent studies show that rates of lung cancer among so-called “never-smokers” (less than 100 cigarettes smoked in a lifetime) are mysteriously skyrocketing—in one study, from 9% to 20% of all such malignancies.
But it’s not all bad news.
The recent discovery of genetic mutations called “oncogenes” that drive lung cancer in never-smokers has fueled the development of powerful medications that are often more effective and have fewer side effects than conventional chemotherapy. 
Bonus: These new drugs are taken orally rather than intravenously, as is more common with conventional chemotherapy.

TESTING FOR MUTATIONS

If you’re one of the roughly 24,000 never-smokers diagnosed with lung cancer each year in the US, it’s crucial for you (as well as current and former smokers) to be tested for a genetic mutation that might be driving your disease.
Shockingly, many of these patients are not tested despite the recommendations of national cancer organizations. This is due, in part, to the lack of awareness of many community oncologists in the US.
The most accurate test uses a tissue biopsy to screen for a handful of critical mutations that predict a more than 70% chance of responding to FDA-approved drugs. If the size and location of the tumor make a biopsy impossible, the oncologist should order a blood or urine test to check for mutations.
Important: If possible, get your genetic testing at one of the 45 medical institutions designated by the National Cancer Institute (NCI) as a “Comprehensive Cancer Center” (check Cancer.gov/research/nci-role/cancer-centers/find). You will get the most accurate testing at one of these centers and the most reliably up-to-date information on the latest cutting-edge medicine and clinical trials. A medical oncologist near you can administer the treatment. If you’re not able to travel to an NCI-designated center, a tissue sample from a biopsy performed at your local medical facility can be sent to certain institutions (such as the Mayo Clinic and Johns Hopkins) that offer molecular testing.

KEY GENETIC MUTATIONS

If you have a genetic mutation, a targeted medication can be used to treat the lung cancer. (Patients who do not test positive for a mutation receive standard cancer care, including conventional chemotherapy and/or radiation.)
Genetic mutations may include…
• Epidermal growth factor receptor (EGFR). This is the most common mutation in never-smokers with lung cancer, occurring in about 40% of these patients. Several FDA-approved drugs called EGFR-inhibitors can counter this mutation, including gefitinib (Iressa)…erlotinib (Tarceva)…and afatinib (Gilotrif). Additionally, icotinib (Conmana) is in clinical trials.
• Anaplastic lymphoma kinase (ALK). About 5% to 8% of lung cancer patients (most of these never-smokers) have this genetic mutation. The FDA-approved drug is crizotinib (Xalkori) for ALK-positive patients who have never received lung cancer treatment.

TIME FOR A DIFFERENT DRUG

Even when a genetic mutation is identified, eventually a new mutation is generated and the tumor starts growing again—a phenomenon called acquired resistance. This typically occurs after about a year of treatment. Therefore, patients on these therapies undergo regular CT scans at two-to-three-month intervals to make sure their disease is not growing.
Best approach: When your tumor develops acquired resistance, it’s important to have another biopsy so that your doctor can determine which drug is right for you. Two months after starting a second-line drug, the patient will undergo a new CT scan to make sure it is shrinking the tumor. Important: The patient should alert the physician if he/she is taking any over-the-counter supplements—some can have life-threatening interactions with the targeted therapies.

EARLY DETECTION

The cause of lung cancer in never-smokers is unknown, but it is believed that up to 50% of cases are due to exposure to radon, a naturally occurring radioactive gas, and/or secondhand smoke. A distant third is indoor air pollution, such as particles from wood-burning stoves and cooking fumes from stir-, deep- or pan-frying. Main risks…
• Radon. Get your home tested. If levels are high (4 pCi/L or above), hire a state-licensed “radon mitigation contractor” to reduce levels to 2 pCi/L or below by installing a pipe that vents the gas outdoors.
• Secondhand smoke. Avoid it whenever possible.
• Indoor air pollution. If you have a wood stove, get a high-efficiency particle arresting (HEPA) air filter…if you fry food, vent the fumes—they may contain harmful carcinogens.
Important: If you are a never-smoker who has one or more of the symptoms of lung cancer—a persistent cough, chest pain, shortness of breath and/or sudden weight loss…or if you’ve had pneumonia that’s persisted for months in spite of several rounds of antibiotics—ask your doctor to test for lung cancer.
Unfortunately, never-smoker lung cancer often has no (or only vague) symptoms that doctors may not immediately suspect as a malignancy. For this reason, it is usually diagnosed when the cancer has spread to the bone, brain, liver and/or other organs. At that point, the most that can be done is to control the disease, giving the patient as much as three to five or more extra years of life if the disease is treated. As new therapies continue to emerge, the goal is to make never-smoker lung cancer a chronic disease and to someday provide a cure.
https://bottomlineinc.com/health/lung-cancer/lung-cancer-rise-among-nonsmokers

Breakthroughs in Lung Cancer

The newest treatments are extending life…

Timothy Burns, MD, PhD

December 1, 2018

Lung cancer kills more Americans—both smokers and nonsmokers—than colon, breast and prostate cancers combined. But the good news is, treatment options are now extending the lives of many people affected by this formidable disease.
Latest development: Recently announced treatment breakthroughs provide new hope for people with non-small cell lung cancer (NSCLC)—the type of malignancy responsible for 85% of all lung cancers.

THE NEW HEAVY HITTERS

• Immunotherapy. Some of the newest treatments for NSCLC are immune checkpoint inhibitors—drugs that energize the immune system to kill cancer cells by blocking one of two cancer-promoting proteins, PD-1 and PD-L1. These drugs include pembrolizumab (Keytruda), the immunotherapy treatment credited with saving the life of former President Jimmy Carter when melanoma spread to his brain…nivolumab (Opdivo)…atezolizumab (Tecentriq)…and durvalumab (Imfinzi).
Typically, these drugs are used only as second-line therapies for patients with advanced disease who haven’t responded to other types of treatments, such as chemotherapy. But several studies presented at the 2018 annual meeting of the American Association for Cancer Research show that immunotherapy can work as a first-line therapy for people with advanced NSCLC, improving survival.
New scientific findings: A combination of the immunotherapy drug pembrolizumab and chemotherapy worked better than chemo alone as a first-line treatment for patients with metastatic NSCLC—69% were still alive after one year in the combo group, with only 49% alive in the chemo-only group, according to a one-year study published in The New England Journal of Medicine.
In a similar one-year study, patients with stage IV lung cancer were given either chemotherapy or two immunotherapy drugs—nivolumab and ipilimumab (Yervoy), which blocks CTLA-4, a protein similar to PD-1. Those treated with immunotherapy were 42% less likely to have their disease progress than those who received other treatment.
Meanwhile, research focusing on the use of immunotherapy without chemotherapy as a first-line treatment—reported at a recent meeting of the American Society of Clinical Oncology—also delivered positive results. The stage IV NSCLC patients getting pembrolizumab lived four to eight months longer than those getting chemo. Only 18% of the immunotherapy patients suffered severe side effects, such as inflammation of the lung, liver or colon, versus 41% of those in the chemo group.
Takeaway: With the impressive results of these studies, first-line treatment with an immunotherapy drug with or without chemotherapy is now the standard-of-care for most cases of advanced NSCLC. If a test of your tumor tissue shows that you have a high PD-L1 activity—and one-third of patients with NSCLC do—then single-agent immunotherapy might be the best first treatment for you with or without chemotherapy. Patients whose tumor does not express high levels of this marker still benefit from the combination of immunotherapy with chemotherapy in the majority of cases. Talk to your oncologist.
• Gene-modulating drugs. This type of therapy uses drugs to turn off one of several genetic mutations (oncogenes) that can drive lung cancer. An estimated 10% to 20% of NSCLC patients have the epidermal growth factor receptor (EGFR) mutation, which is treated with drugs such as erlotinib (Tarceva), afatinib (Gilotrif), gefitinib (Iressa) and osimertinib (Tagrisso). An estimated 5% have the anaplastic lymphoma kinase (ALK) mutation, which is treated with drugs such as crizotinib (Xalkori), ceritinib (Zykadia), alectinib (Alecensa) and brigatinib (Alunbrig).
These oral drugs are so powerful that they can, in rare cases, extend life by five years or more. However, the newer and more effective of these drugs—such as alectinib for ALK—has been used as a second-line therapy. Now this treatment paradigm is changing.
New scientific findings: In a study published earlier this year, more than 500 NSCLC patients with an EGFR mutation got either osimertinib as a first-line treatment or the previous standard therapy (erlotinib or gefitinib). After 12 months, those taking osimertinib had a 54% lower risk for disease progression or death. In April of this year, the FDA approved osimertinib for first-line treatment of metastatic NSCLC.
In a study of more than 300 metastatic NSCLC patients with the ALK mutation, the disease progressed or death occurred in 41% of those receiving alectinib (a newer more effective drug) compared with 68% receiving crizotinib, an older drug, after about a year and a half. The alectinib group also had fewer side effects. Patients receiving alectinib had control of their tumors for almost three years, on average.
Takeaway: If you are diagnosed with NSCLC, get tested to find out if you have a genetic mutation driving the disease. If you do, talk to your oncologist about the best gene–targeting drug for you—patients with these mutations often do not benefit from immunotherapy.

THE LIQUID BIOPSY OPTION…

The gold standard for biopsies in NSCLC is a tissue biopsy—removing a portion of the tumor and testing it—to identify the specific type of cancer and genetic mutations that inform treatment decisions.
Problem: In many cases, a tissue biopsy isn’t possible—for example, the position of the tumor in the lung or other organ may make it too difficult to biopsy, or the patient may have emphysema.
Solution: A liquid (blood-based) biopsy can be used when a tissue biopsy is not an option. The FDA approved liquid biopsy for lung cancer in 2016. A recent study published in JAMA Oncology suggests that combining liquid biopsies with tumor biopsies can improve the chance of finding a targetable mutation. Ask your oncologist if this is right for you. FoundationOne and Guardant360 are the two most widely used liquid biopsies.
https://bottomlineinc.com/health/lung-cancer/what-it-means-when-your-doctor-finds-a-spot-on-your-lung

When Cancer Spreads to the Brain: New Treatments Offer Hope

Some patients are living up to seven times longer than before. Here’s how…

Nduka Amankulor, MD, a neurosurgeon and neuro-oncologist at UPMC Hillman Cancer Center and assistant professor of neurological surgery at University of Pittsburgh School of Medicine.

CANCER

Published Date: October 1, 2019

Publication: Bottom Line Health


CANCER

When Cancer Spreads to the Brain: New Treatments Offer Hope

When melanoma or some other cancer spreads to the brain, the prognosis used to be grim. Now, treatment advances are dramatically improving outcomes…

An astounding 20% to 30% of people with cancer develop 
metastatic brain cancer (MBC)—cancer that has spread from another organ to the brain.
Breast cancerlung cancer, kidney cancer and melanoma are the main types of cancer that invade the brain. But almost any cancer can produce brain metastases, with an estimated 170,000 new cases every year. 
Until recently, the prognosis for people with MBC was grim—only 8% of patients were alive two years after diagnosis, and 2% after five years. But those sad statistics are changing.
Now: The treatment of MBC is being revolutionized by targeted drug therapies that attack genetic mutations driving cancer…immunotherapies that stimulate the body’s own immune system to fight cancer…and precisely focused radiation.
Immunotherapy more than doubled the average survival time of melanoma­ patients with MBC—from 5.2 months to 12.4 months, according to a study published in Cancer Immunology Research. The effects are even better for melanoma patients with MBC but no other metastases—research found that those who received immunotherapy had an average survival rate of 56 months, compared with 7.7 months for those receiving standard treatment, such as chemotherapy. In other words, MBC patients treated with immunotherapy lived about seven times longer!  
What cancer patients and their families need to know…

Early Detection

Many oncologists don’t recommend screening for brain metastases, except for certain tumor types that have a significant predilection for spreading to the brain. Of course, if the patient develops neurological symptoms, such as headaches, numbness, blurred vision, balance difficulties, cognitive decline and/or seizures, then brain screening for a brain tumor is recommended, regardless of the type of cancer. 
New thinking: Early detection can extend survival time in patients without neurological symptoms who are at high risk of developing MBC. 
My advice for who should get screened… 
• Any patient with a new diagnosis of stage II to stage IV lung cancer, whether it’s non-small cell (the most common type) or small cell. 
• A melanoma patient with metastatic disease elsewhere in the body—because two out of three of these patients will also develop MBC. 
• A breast cancer patient who is positive for HER2 (a gene that plays a role in the development of breast cancer)…or whose tumor lacks hormone receptors (estrogen and progesterone receptors)…or lacks any markers at all (triple-negative breast cancer). The rate of MBC is significantly higher (10% to 15%) in all these breast cancer patients.
The gold standard for early detection is a brain MRI with contrast dye, which can detect brain tumors as small as 2 millimeters in diameter (less than one-tenth of an inch). Especially in patients who are at high risk of developing MBC, insurance may cover the MRI even if there are no neurological symptoms, but be sure to check first. Once MBC is diagnosed, MRIs are obtained roughly every two to four months.

Targeted Therapies

Targeted therapies are drugs (oral or IV) that block or alter specific genes and/or proteins that drive cancer. There have been dozens of clinical trials of targeted therapy in patients with brain metastases—with some remarkable results. For example…
Researchers from the MD Anderson Cancer Center at University of Texas studied melanoma patients with MBC who had the BRAF mutation, which occurs in about half of patients with this disease. The patients received two drugs—dabrafenib (Tafinlar), which targets BRAF…and trametinib (Mekinist), which targets MEK, a mutation similar to BRAF. In a group of 76 patients with BRAF who had never been treated for MBC and whose neurological symptoms were under control, 58% had significant shrinking of their brain tumors—and in four patients the tumors vanished, according to the research, which was published in The Lancet Oncology. The response lasted, on average, six to seven months. 

Immunotherapy

Immunotherapy drugs are a class of drugs that stimulate a patient’s immune system, essentially calling it into action. The most widely used immunotherapies are drugs that block checkpoint proteins, such as PD-1 or PD-L1, which suppress inflammatory responses in the immune system.
Scientific evidence: Impressive results with combined drug therapy—ipilimumab (Yervoy) and nivolumab (Opdivo)—were cited in a study published in The New England Journal of Medicine. In that research, when 94 melanoma patients with MBC took both drugs, 81% were alive after one year and 70% after two years—a dramatic increase over the typical survival rate of four to five months before the introduction of immunotherapy. 

Focused Radiation

In the past, the standard radiation treatment for MBC was whole-brain radiation—multiple treatments of the entire brain with low-dose radiation. 
However, whole-brain radiation has significant side effects, such as a marked decrease in memory and other cognitive abilities. Doctors are now using highly focused radiation therapies called stereotactic radiosurgery. Employing a flexible robotic arm to deliver radiation (CyberKnife), or using a helmet with built-in radiation sources (Gamma Knife), this treatment delivers less total radiation…faster…and more accurately. And its cancer-killing efficacy is as good as whole-brain radiation —with less severe side effects.

Your Plan of Action

To take advantage of the breakthrough treatments for MBC, you need a plan of action. Here are four steps to follow…
STEP  #1: Treat the primary cancer. The key in treating cancer is always minimizing your overall cancer burden using the full range of treatments available—such as chemotherapy, radiation, surgery, targeted therapies and immunotherapy. Controlling the primary malignancy reduces the risk of the cancer spreading to the brain. 
STEP #2: Ask your oncologist, “Has my tumor been sufficiently molecularly characterized?” Sophisticated genetic tests will show if you’re a candidate for targeted therapy or immunotherapy.
For example, if such testing shows that you have the ALK mutation, treatments for the primary tumor may include targeted therapies such as alectinib (Alecensa), brigatinib (Alunbrig) or lorlatinib (Lorbrena)—all of which also help prevent and/or treat brain metastases.
If a tumor biopsy shows that you have high levels of PD-1 or PD-L1, then you may be a candidate for an immunotherapy drug such as pembrolizumab (Keytruda), nivolumab (Opdivo) or atezolizumab (Tecentriq).  
STEP #3: Ask your oncologist, “Are there effective therapies that treat the molecular pathways affecting my cancer—and should we use those therapies to treat my brain cancer?” Once your tumor has been tested for molecular mutations, talk with your oncologist about the targeted and immunological therapies available to treat those problems. You and your doctor should develop a complete list of the targeted therapies and immunotherapies (see examples above) that may be right for you—and then decide which to use.
STEP #4: Demand a multidisciplinary team approach. The best treatment for primary cancer and for MBC is a team approach, typically involving a medical oncologist, a radiation oncologist and a cancer surgeon. The best treatment decisions are made when the entire team talks to one another, face-to-face. This type of multidisciplinary approach is typical of cancer centers that are designated by the National Cancer Institute for offering cutting-edge treatments. To find such an NCI-designated cancer center near you, go to: Cancer.gov/research/nci-role/cancer-­centers/find.