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Showing posts with label Tumour Markers. Show all posts
Showing posts with label Tumour Markers. Show all posts

Wednesday, 9 October 2019

Pancreatic Cancer? Only 1 in 5 Patients Gets This Critical Test

Pancreatic cancer is deadly—only 7% of patients survive five years after diagnosis. But giving just-diagnosed patients an inexpensive blood test…


Source

Mayo Clinic research to be presented at the annual meeting of the Western Surgical Association in Napa, California.

Date

November 19, 2015

Publication

Bottom Line Health






CANCER

Pancreatic Cancer? Only 1 in 5 Patients Gets This Critical Test

Pancreatic cancer is deadly—only 7% of patients survive five years after diagnosis. But giving just-diagnosed patients an inexpensive blood test…
Pancreatic cancer is deadly—only 7% of patients survive five years after diagnosis. But giving just-diagnosed patients an inexpensive blood test can help doctors choose the treatment that is most likely to improve their chances.
The test measures CA 19-9—a tumor “biomarker” found in the blood of 90% of the population. When researchers at the Mayo Clinic analyzed data on 97,000 pancreatic cancer patients in the National Cancer Data Base, they found that having elevated levels of CA 19-9 predicted a worse outcome from therapy.
The good news: Having chemotherapy before surgery instead of the usual practice of having it afterward eliminated the elevated biomarker’s negative effect. That is, these patients did as well as patients without the elevated risk. The test is widely available and costs less than $200.
https://bottomlineinc.com/health/cancer/pancreatic-cancer-only-1-in-5-patients-get-this-critical-test


Friday, 22 September 2017

'Pen' identifies cancer in 10 seconds

A handheld device can identify cancerous tissue in 10 seconds, according to scientists at the University of Texas.
  • 7 September 2017

Cancer pen
They say it could make surgery to remove a tumour quicker, safer and more precise.
And they hope it would avoid the "heartbreak" of leaving any of the cancer behind.
Tests, published in Science Translational Medicine, suggest the technology is accurate 96% of the time.
The MasSpec Pen takes advantage of the unique metabolism of cancer cells.
Their furious drive to grow and spread means their internal chemistry is very different to that of healthy tissue.

How it works

The pen is touched on to a suspected cancer and releases a tiny droplet of water.
Chemicals inside the living cells move into the droplet, which is then sucked back up the pen for analysis.
The pen is plugged into a mass spectrometer - a piece of kit that can measure the mass of thousands of chemicals every second.
It produces a chemical fingerprint that tells doctors whether they are looking at healthy tissue or cancer.

The challenge for surgeons is finding the border between the cancer and normal tissue.
In some tumours it is obvious, but in others the boundary between healthy and diseased tissue can be blurred.
The pen should help doctors ensure none of the cancer is left behind.
Remove too little tissue, and any remaining cancerous cells will grow into another tumour. But take too much, and you can cause damage, particularly in organs such as the brain.
Livia Eberlin, an assistant professor of chemistry at the University of Texas, Austin, told the BBC: "What's exciting about this technology is how clearly it meets a clinical need.
"The tool is elegant and simple and can be in the hands of surgeons in a short time."

Trials

The technology has been tested on 253 samples as part of the study. The plan is to continue testing to refine the device before trialling it during operations next year.
The pen currently analyses a patch of tissue 1.5mm (0.06in) across, but the researchers have already developed pens that are even more refined and should be able to look at a finer patch of tissue just 0.6mm across.
While the pen itself is cheap, the mass spectrometer is expensive and bulky.
Dr Eberlin said: "The roadblock is the mass spectrometer, for sure.
"We're visioning a mass spectrometer that's a little smaller, cheaper and tailored for this application that can be wheeled in and out of rooms."
Dr James Suliburk, one of the researchers and the head of endocrine surgery at Baylor College of Medicine, said: "Any time we can offer the patient a more precise surgery, a quicker surgery or a safer surgery, that's something we want to do.
"This technology does all three."
The MasSpec Pen is the latest attempt to improve the accuracy of surgery.
A team at Imperial College London have developed a knife that "smells" the tissue it cuts to determine whether it is removing cancer.
And a team at Harvard are using lasers to analyse how much of a brain cancer to remove.
Dr Aine McCarthy, from Cancer Research UK, said: "Exciting research like this has the potential to speed up how quickly doctors can determine if a tumour is cancerous or not and learn about its characteristics.
"Gathering this kind of information quickly during surgery could help doctors match the best treatment options for patients sooner."

http://www.bbc.com/news/health-41162994

Tuesday, 25 July 2017

Should you do a cancer marker test?

Should you do a cancer marker test?

Options to screen for specific types of cancer would be mammogram (breast cancers), colonoscopy (colorectal cancers), Pap smear (cervical cancers) and faecal occult blood tests (colorectal cancers). Photo: Wikimedia Commons



It is undeniable that there is an increasing number of Malaysians being diagnosed with, and battling, cancer.
Based on the National Cancer Registry of Malaysia (NCR) records, an avearge 20,000 Malaysians are diagnosed with cancer every year.
In Malaysia, it is estimated that the risk of males getting cancer is one in 10, and for females, one in nine.
When we talk about early detection, many people would think of cancer markers (better known as tumour markers), which are readily tested at the many commercial health labs.
However, these tests were not developed to be used on its own to screen for any cancer, noted Dr Verna Lee Kar Mun, Family Medicine Specialist and Head of IMU Healthcare Medical Clinic.
What is a tumour marker test?
A tumour marker is a substance that is produced by the body in response to cancer, or is produced by the cancer cell itself.
“Sometimes, these markers are specific to one type of cancer only, while others may not and can be seen in different types of cancer. The substances are usually found in very high levels in the blood, urine or body tissue for individuals with confirmed cancer,” explained Dr Lee.

Tumour marker tests are usually carried out to monitor responses to cancer treatment or to detect recurrence of cancer.

Testing for tumour markers are usually performed by taking a sample of blood or urine to analyse for specific or multiple tumour markers.
These tests are very important and repeated regularly in patients with confirmed cancer, with or without treatment.
They are carried out to monitor responses to cancer treatment (during the treatment process) or to detect recurrence of cancer (after treatment completion) in these patients.
In medicine, this is called tertiary prevention.
“One important thing to note is, even though cancer cells often produce tumour markers in very high levels, healthy normal cells in the body can produce them as well.
“In other words, non-cancerous conditions can cause markers to be elevated above the normal range because these substances are produced naturally in the body.
“There is lack of data or scientific evidence to inform healthcare providers or doctors on how to accurately interpret these tests from screening a healthy population (secondary prevention),” cautioned Dr Lee.
Doctors do not exactly know what the next appropriate step of management is if a healthy individual has an abnormal tumour marker test. Therefore, these tumour marker tests are never used as a screening test for secondary prevention.
Tumour marker tests and cancer
If repeated test results show elevated tumour marker levels, doctors will conduct further tests to confirm recurrence of cancer or treatment failure.
Essentially, tumour markers guide doctors in employing suitable cancer treatment options, for example, deciding whether to incorporate chemotherapy or radiation therapy after surgery, or selecting types of medications that would be most effective, monitoring progress of treatment, forecasting recovery rate, and observing for recurrence.
As mentioned above, different tumour markers are also used to test for different types of cancer.
However, there are also a number of cancers that do not have tumour markers.
Therefore, it would be best to speak to a doctor before deciding whether or not to have the test. Amongst other options to screen for specific types of cancer would be mammogram (breast cancers), colonoscopy (colorectal cancers), Pap smear (cervical cancers) and faecal occult blood tests (colorectal cancers).
Individuals with a high risk of cancer should talk to their family doctor and be educated and empowered on how to reduce their risk from developing the cancer from young (primary prevention).
A tumour marker test is never a screening test for cancer.
Adverse effects of tumour markers as a screening test
One may ask, “My tumour marker test result shows a very low level, therefore, am I free of cancer, right?”
“Even high levels of tumour markers is not diagnostic of cancer, and it applies the same way with a low level reading as well. We cannot rely on it independently to determine that you are free from the disease, as these markers may potentially give false-positive or false-negative results,” advised Dr Lee.
When you become too concerned by the abnormal level of one tumour marker test, you may convince your doctor to focus solely on investigating if you are suffering from one type of cancer, and miss out on other possibilities. Or even worse, despite getting a false-negative after a thorough process of many other invasive tests (with high costs), you may have trouble accepting that you’re truly cancer-free due to the emotional turmoil experienced from believing the tumour marker test.
Thus, psychological complications or adverse effects such as generalised anxiety, excessive fear and even depressive disorders occur.
Limitations of the tumour marker test include:
• Many non-cancerous diseases can also elevate tumour marker levels.
• Some tumour marker levels have high baselines in normal individuals.
• It is difficult to obtain consistent results because tumour marker levels can change over time.
• The level of a tumour marker may not elevate until the cancer spreads (this is not helpful for early detection, screening, or observing for recurrence).
• Many common cancers do not produce tumour markers.
Questions to ask the doctor
When you are considering if a tumour marker test is necessary, here are a few suggested questions from Dr Lee that you should ask your doctor:
• Do you recommend that I undergo any tumour marker tests? If so, which ones?
• How are these tests performed? How often should I get tested?
• Can you explain the impact of the test results?
• If I have abnormal levels of a tumour marker, what does that mean? How does it affect my health?
• How will the tumour marker tests be used in my follow-up care?
• Where can I get more information about tumour markers?
Save yourself from going through unnecessary anxiety by checking with your doctor if the tumour marker tests are necessary for you.
Remember that these tests have their purposes and limitations, therefore, the results may sometimes fluctuate – whether it’s a false-positive or a false-negative.
Should you have taken the test and if the levels are high, keep composed and speak to your doctor for an informed decision.

http://www.star2.com/health/wellness/2017/07/23/to-test-or-not-to-cancer-marker/

Wednesday, 5 July 2017

'Exciting' blood test spots cancer a year early

Doctors have spotted cancer coming back up to a year before normal scans in an "exciting" discovery.
The UK team was able to scour the blood for signs of cancer while it was just a tiny cluster of cells invisible to X-ray or CT scans.

  • 26 April 2017
Doctors have spotted cancer coming back up to a year before normal scans in an "exciting" discovery.

The UK team was able to scour the blood for signs of cancer while it was just a tiny cluster of cells invisible to X-ray or CT scans.

It should allow doctors to hit the tumour earlier and increase the chances of a cure.

They also have new ideas for drugs after finding how unstable DNA fuels rampant cancer development.

The research project was on lung cancer, but the processes studied are so fundamental that they should apply across all cancer types.


Lung cancer kills more people than any other type of tumour and the point of the study is to track how it can "evolve" into a killer that spreads through the body.


Blood test

In order to test for cancer coming back, doctors need to know what to look for.

In the trial, funded by Cancer Research UK, samples were taken from the lung tumour when it was removed during surgery.

A team at the Francis Crick Institute, in London, then analysed the tumour's defective DNA to build up a genetic fingerprint of each patient's cancer.

Then blood tests were taken every three months after the surgery to see if tiny traces of cancer DNA re-emerged.

The results, outlined in the journal Nature, showed cancer recurrence could be detected up to a year before any other method available to medicine.

The tumours are thought to have a volume of just 0.3 cubic millimetres when the blood test catches them.


'New hope'

Dr Christopher Abbosh, from the UCL Cancer Institute, said: "We can identify patients to treat even if they have no clinical signs of disease, and also monitor how well therapies are working.

"This represents new hope for combating lung cancer relapse following surgery, which occurs in up to half of all patients."

So far, it has been an early warning system for 13 out of 14 patients whose illness recurred, as well as giving others an all-clear.

In theory, it should be easier to kill the cancer while it is still tiny rather than after it has grown and become visible again.

However, this needs testing.

Prof Charles Swanton, from the Francis Crick Institute, told the BBC: "We can now set up clinical trials to ask the fundamental question - if you treat people's disease when there's no evidence of cancer on a CT scan or a chest X-ray can we increase the cure rate?

"We hope that by treating the disease when there are very few cells in the body that we'll be able to increase the chance of curing a patient."




Janet Maitland
Janet Maitland, 65, from London, is one of the patients taking part in the trial.

She has watched lung cancer take the life of her husband and was diagnosed herself last year.

She told the BBC: "It was my worst nightmare getting lung cancer, and it was like my worse nightmare came true, so I was devastated and terrified."

But she had the cancer removed and now doctors say she has a 75% chance of being cancer-free in five years.

"It's like going from terror to joy, from thinking that I was never going to get better to feeling like a miracle's been acted," she said.

And taking part in a trial that should improve the chances for patients in the future is a huge comfort for her.

"I feel very privileged," she added.




Evolution

The blood test is actually the second breakthrough in the massive project to deepen understanding of lung cancer.

A bigger analysis, published in the New England Journal of Medicine, showed the key factor - genetic instability - that predicted whether the cancer would return.

Multiple samples from 100 patients containing 4.5 trillion base pairs of DNA were analysed.

DNA is packaged up into sets of chromosomes containing thousands of genetic instructions.

The team at the Francis Crick Institute showed tumours with more "chromosomal chaos" - the ability to readily reshuffle large amounts of their DNA to alter thousands of genetic instructions - were those most likely to come back.

Prof Charles Swanton, one of the researchers, told the BBC News website: "You've got a system in place where a cancer cell can alter its behaviour very rapidly by gaining or losing whole chromosomes or parts of chromosomes.

"It is evolution on steroids."

That allows the tumour to develop resistance to drugs, the ability to hide from the immune system or the skills to move to other tissues in the body.

'Exciting'

The first implication of the research is for drug development - by understanding the key role of chromosomal instability, scientists can find ways to stop it.

Prof Swanton told me: "I hope we'll be able to generate new approaches to limit it and bring evolution back from the brink, perhaps reduce the evolutionary capacity of tumours and hopefully stop them adapting.

"It's exciting on multiple levels."

The scientists say they are only scratching the surface of what can be achieved by analysing the DNA of cancers.

http://www.bbc.co.uk/news/health-39658680

Friday, 5 May 2017

Chinese scientists use drop of blood to detect cancer

‍Scientists around the world are striving for effective detection of cancer in the early stages, and a Chinese scientist may have found a quick way of knowing whether malignant tumors exist in a patient's body, with just one drop of blood.
By Xie Zhenqi
2017-05-01 15:08 GMT+8
13km to Beijing
Luo Yongzhang and his team in Tsinghua University's School of Life 
Sciences in Beijing have successfully invented a reagent test kit of 
Hsp90α for clinical use, which can diagnose multiple kinds of cancer 
by analyzing a drop of human blood. 
Luo and his team members in a lab. / CCTV Photo
Malignant tumors in early phases can be cured but once they 
have spread all over the patient's body there is no way to save the 
person's 
life. 
However, it's extremely difficult to be aware of cancer in its early 
stages, as patients don't show obvious symptoms and thus it can 
only be found in its later stages, which is already too late, so to 
detect cancer early remains a global challenge for scientists. 
Scientists around the globe are working to find ways to detect cancer in its early stage. 
/ VCG Photo
Back in 1989, scientists have found a kind of heat shock proteins 
(HSP), named Hsp90α, which existed in human bodies and can 
be used as a cancer biomarker detection kit. 
Scientists around the globe have been working on it since then, 
and more than 10,000 journals have been published on accredited magazines, yet no one has actually turned their research results 
into medical products. 
However, Luo and his team seemed to have cracked the code, after 
working on the problem since 2009. The team has produced an 
artificial Hsp90α protein that gains structural stability by regrouping proteins. This means they are able to "create" the protein, in any 
quantity, and at any time ‍they wish to. 
The kit has since been used in clinical trials involving 2,347 patients 
at eight hospitals in China. It was the first clinical trial in the world 
to test if the protein could be a useful tumor biomarker for lung 
cancer, and it succeeded.
Now, the kit has been certified to enter the Chinese and European
 markets, 24 years after Hsp90α was discovered.
The final product that has been approved by government and ready to enter 
markets in China and Europe. / CCTV Photo
Cancer is a group of diseases involving abnormal cell growth with 
the potential to invade or spread to other parts of the body. 
In 2015, about 90.5 million people had cancer in the world, with 
roughly 14.1 million new cases occurring each year. Approximately 
8.8 million human deaths, or 15.7 percent of all deaths in the world, 
are caused by cancer. 
In China alone, 4.29 million people were detected as having cancer 
in 2015, and 2.8 million of them died in that year. 

Monday, 12 May 2014

World Ovarian Cancer Day: One voice for every woman

Thursday May 8, 2014

Today is World Ovarian Cancer Day, and on this day, ovarian cancer organisations from around the world unite to educate their communities about ovarian cancer and its symptoms

BY DR SURESH KUMARASAMY

Working at it: There is ongoing research evaluating a combination of blood tests for tumour markers together with ultrasound scans with the hope of developing a screening test for ovarian cancer in the future. — AFP
Working at it: There is ongoing research evaluating a combination of blood tests for tumour markers together
with ultrasound scans with the hope of developing a screening test for ovarian cancer in the future. — AFP

Each year, nearly a quarter of a million women around the world are diagnosed with ovarian cancer, and the disease is responsible for 140,000 deaths annually.
Statistics show that just 45% of women with ovarian cancer are likely to survive for five years, compared with 89% of women with breast cancer.
Recognising the severity of the disease and the need to raise awareness about ovarian cancer, the first World Ovarian Cancer Day was organised on May 8, 2013.
On this day, ovarian cancer organisations from around the world unite to educate their communities about ovarian cancer and its symptoms.
Today marks the second annual World Ovarian Cancer Day, and for women living with the disease, and their families and friends, this day has built, and will continue to build, a sense of solidarity in the fight against the disease.
The theme for 2014 is “One Voice for Every Woman”.
Ovarian cancer is a cancer of the female reproductive system, and is the fifth most common cancer among Malaysian women.
Approximately 500 women are diagnosed with ovarian cancer every year in our country; of these, 90% are classified as epithelial ovarian cancer.
The remaining 10% consists of germ cell tumours and sex cord stromal tumours, which are less common and generally have a better outlook compared to epithelial ovarian cancer.
Family history is a significant factor as approximately 5-10% of epithelial ovarian cancer cases are due to genetic factors. This means having a close blood relation on either the mother or father’s side of the family who has had breast cancer before the age of 50, or ovarian cancer at any age.
The ovaries, which are two small organs located on both sides of a woman’s uterus, are responsible for releasing eggs every month during a woman’s reproductive years.
They also produce hormones which trigger the secondary sex changes which occur at puberty and maintain reproductive organ function.
When a woman reaches menopause, the ovaries stop releasing the eggs and hormone production decreases.
Epithelial ovarian cancer (hereafter referred to as “ovarian cancer”) in its early stages produces few or non-specific symptoms.
Symptoms and screening
Due to its non-specific symptoms, one of the most significant challenges of ovarian cancer is the absence of a test for early detection which offers a better chance for successful treatment and improved survival rates.
Lack of awareness of symptoms and late stage diagnosis results in many instances of the disease progressing undetected until it reaches an advanced stage – approximately 70% of women are diagnosed at Stage 3 or Stage 4 of the disease, with an overall five-year survival rate of only 30%.
To aid in earlier detection, even vague symptoms should be carefully evaluated. These symptoms include abdominal bloating or fullness, anorexia (poor appetite and loss of weight), nausea, vomiting and urinary symptoms.
However, due to the non-specific nature of these symptoms, most of the women who present themselves with these symptoms would not necessarily be suffering from ovarian cancer.
Unlike the Pap smear which detects pre-cancerous changes in the cervix, or mammograms which detect breast cancer at an early stage, there is no definitive screening test for ovarian cancer.
There is, however, ongoing research evaluating a combination of blood tests for tumour markers together with ultrasound scans with the hope of developing a screening test for the future.
Unfortunately, at the present time, there is not enough scientific evidence to recommend this approach for screening for ovarian cancer.
Screening using the tumour marker CA125 has not been proven to be useful because only 50% of patients with early stages of ovarian cancer have raised levels of CA125. Among patients at an advanced stage of ovarian cancer, 90% of patients have raised CA125 levels, but at such an advanced stage, other signs and symptoms are usually already evident.
Testing for CA125 is also associated with a high false positive rate – i.e. patients may not have cancer, but still exhibit high levels of CA125. In such cases, the patient may needlessly undergo further tests and investigations, which can be costly and invasive.
One percent of healthy women, women in early pregnancy, as well as women with common conditions such as fibroids, endometriosis, kidney disease, lupus, gastrointestinal and liver conditions as well as cancers of the liver, lung, breast and pancreas may have raised levels of CA125.
Hence, this test is not specific enough to detect ovarian cancer and is an ineffective tool.
Diagnosis and treatment
To ensure an accurate diagnosis, a doctor requires the patient’s full medical history to perform a clinical examination, including an abdominal and pelvic examination.
The doctor then arranges other tests such as ultrasound scans, blood tests, including tests for tumour markers, and CT scans. While the number and type of examinations may vary depending on the individual patient, a careful and thorough assessment is essential before embarking on surgery and treatment.
For many patients in the advanced stages of the disease, the tumour often spreads beyond the ovaries to neighbouring organs such as the uterus, bowel and other areas within the abdominal cavity.
Surgery is recommended if cancer is diagnosed; this procedure is called a laparotomy, whereby doctors will remove all or as much of the tumour as possible together with the ovaries, the uterus and omentum (the fat which hangs from the stomach and large intestine).
Removal of the tumour is called “debulking”, and plays an important role in determining the patient’s survival as there is a very close relationship between the amount of tumour left behind after surgery (residual tumour) and the patient’s survival rate.
Simply put, the lesser the amount of residual tumour, the better the chances of survival. In selected patients where the cancer is still in its early stages and confined to only one ovary, it may be possible to perform conservative surgery, which means removing only the cancerous ovary and preserving the uterus and remaining unaffected ovary so that the patient may still have children in the future.
Surgery should be performed by a specialist with the necessary skill, training and experience in treating and managing ovarian cancer. A gynaecologist who specialises in the treatment of women with cancer of the reproductive organs (uterus, ovaries, fallopian tubes, vagina and vulva) is called a gynaecological oncologist.
Several studies have confirmed that better cure rates are obtained when this complex surgery is carried out by a gynaecological oncologist and both the US National Cancer Institute as well as the National Health Service in the United Kingdom have endorsed this recommendation.
Surgery also helps doctors to determine the stage of the cancer; it’s essential for doctors to understand this so they can create an effective treatment plan for the individual patient.
Chemotherapy
Chemotherapy is the use of drugs to stop the growth of cancer cells, either by killing the cancer cells or preventing the cells from dividing, multiplying and spreading.
Patients with very early cancer (stage 1A Grade 1) don’t require chemotherapy. Those with more advanced cancer will benefit from chemotherapy. Most patients will be treated with six courses of chemotherapy. Each course lasts for five to six hours and a course is repeated every three to four weeks.
Some patients, especially those in poor health, may be advised to have neo-adjuvant chemotherapy. This involves giving three courses of chemotherapy first, followed by surgery, and then a further three courses of chemotherapy.
In conventional chemotherapy for ovarian cancer, the drugs are given intravenously. Known as systemic chemotherapy, this treatment decreases the risk of recurrence, prolongs survival and increases the chances of cure.
The most common chemotherapy drugs used for ovarian cancer are carboplatin and paclitaxel, a combination which is well tolerated.
Common side effects of treatment include hair loss (which grows back after the treatment is over), low blood counts and decreased immunity.
Monitoring for side-effects will be carried out at specific intervals by clinical examination and blood tests.
New treatment approach with anti-angiogenesis therapy
Anti-angiogenesis therapy is a form of targeted therapy that has been found to be effective for patients with ovarian cancer.
Angiogenesis or new vessel formation is a pre-requisite for the progression and metastasis (spread) of cancer cells.
A pro-angiogenetic factor in blood, known as vascular endothelial growth factor (VEGF), is related to the progression of the disease and corresponding poor prognosis for ovarian cancer patients.
In 1971, a scientist named Judah Folkman came up with the concept of using drugs called angiogenesis inhibitors to block the growth of tumours by preventing the formation of new blood vessels.
Since then, this form of therapy has been further refined, and subsequent research with anti-VGEF therapy shows that it slows tumour progression, causes resolution of ascites (fluid in the abdominal cavity related to cancer) and makes chemotherapy work better.
In a nutshell
Ovarian cancer is a challenging disease to treat. The cornerstone of treatment is surgery by a trained and experienced surgeon.
Following surgery, most patients will benefit from chemotherapy.
A relatively recent form of targeted therapy, known as anti-angiogenesis inhibitors, has been found to be effective in reducing the progression and metastasis (spread) of cancer cells.
The best hope for successful treatment, however, lies in early detection. At present, ovarian cancer is difficult to detect in its early stages as its symptoms are few and non-specific and there is lack of an effective and proven screening test, hence most patients are only diagnosed at advanced stages of the disease.
Women should be aware of changes in their body and be alert for unusual symptoms. It is said that “ovarian cancer whispers” – some of the signs and symptoms may be mild or subtle.
Evaluation of women with unusual or suspicious signs and symptoms should include assessment by an experienced gynaecologist.
Women should make it a point to have regular check-ups. At these check-ups, unusual symptoms should be discussed and assessed. A pelvic examination should be carried out during routine Pap smears as this may result in the detection of gynaecological problems, including ovarian cancer.
Dr Suresh Kumarasamy is an obstetrician & gynaecologist/gynaecological oncologist in private practice based in Penang. He is immediate past president of the Obstetrical & Gynaecological Society of Malaysia, a council member of the Asian Society of Gynaecological Oncology and an adjunct associate professor at Penang Medical College.