Cervical cancer research
This page is about research into cervical cancer. You can find information below about
Cervical cancer research
All treatments must be fully researched before they can be adopted as standard treatment for everyone. This is so that we can be sure they work better than the treatments we already use. And so we know that they are safe.
First of all, treatments are developed and tested in laboratories. Only after we know that they are likely to be safe to test are they tested in people, in clinical trials. Cancer Research UK supports a lot of UK laboratory research into cancer and also supports many UK and international clinical trials.
There is research looking into HPV vaccines and tests, surgery, chemotherapy, radiotherapy and biological therapies.
You can view and print the quick guides for all the pages in the Treating cervical cancer section.
All treatments have to be fully researched before they can be adopted as standard treatment for everyone. This is so that
- We can be sure they work
- We can be sure they work better than the treatments that are available at the moment
- They are known to be safe
First, treatments are developed and tested in laboratories. For ethical and safety reasons, experimental treatments must be tested in the laboratory before they can be tried in people. If a treatment described here is said to be at the laboratory stage of research, it is not ready for patients and is not available either within or outside the NHS. Cancer Research UK supports a lot of UK laboratory research into cancer.
Research studies involving patients are called clinical trials. Cancer Research UK supports many UK and international clinical trials.
Our trials and research section has information about what trials are, including information about the 4 phases of clinical trials. If you are interested in taking part in a clinical trial, visit our searchable database of clinical trials recruiting in the UK. If there is a trial you are interested in, print it off and take it to your own specialist. If the trial is suitable for you, your doctor will need to make the referral to the research team. The database also has information about closed trials and trial results.
All the new approaches covered here are the subject of ongoing research. Until studies are completed and new effective treatments are found, these treatments cannot be used as standard therapy for cervical cancer.
Here is a video on what it's like to take part in a clinical trial:
View a transcript of the video (Opens in a new window)
A UK study wanted to find out more about the symptoms and experiences that young women had before being diagnosed with cervical cancer. The study team found that many of the women (aged 18 to 29) did not know the symptoms of cervical cancer and delayed going to see the doctor about them. The team suggested that information about symptoms should be improved and this could help cervical cancer to be diagnosed earlier.
We have information about the symptoms of cervical cancer.
We know there is a link between cervical cancer and infection with the human papilloma virus (HPV). Researchers have developed tests to check liquid based cytology (smear test) samples for the different types of human papilloma virus. There are many different types (strains). Types 16 and 18 are the strains most commonly linked to cervical cancer.
HPV testing has recently been introduced as part of the NHS cervical screening programme in England and Wales. If you have borderline or mild cell changes, the laboratory will check your sample for HPV. If HPV is found, you will have further tests. In some areas of England, the screening programme is looking at testing for HPV first. So if HPV is found, the woman's sample is then checked for abnormal cells. Researchers think this may be better as HPV testing picks up more abnormal cells in the cervix. Also, if your sample has no HPV it is unlikely that cervical cancer will develop in the next few years. So these women may not have to go for screening as often. But more studies are needed to know this for sure.
Researchers continue to look into other ways of testing for HPV for cervical screening. One trial looked at whether women could collect their own samples for HPV testing. The researchers found no real difference in test results between the HPV sample taken by the women themselves, and those done by a doctor or nurse. Most women preferred doing the HPV test themselves and would use the self sampling test again if they were offered it.
A recent review of studies has shown that a urine test to pick up HPV may be useful for screening women. More studies are needed. But if this simple test is found to be accurate in picking up HPV more women may want to take part in screening.
Vaccines, such as Cervarix and Gardasil, have been developed to prevent HPV infection. There are many different HPV strains. HPV types 16 and 18 are known to be high risk for cervical cancer. Several research trials have tested vaccines as a way of preventing infection with HPV. The trials have shown that the vaccines help to prevent abnormal changes in the cervix that may develop into cancer. In the UK, HPV vaccination is offered in school to all girls aged 12 to 13.
Research suggests that this vaccination programme will dramatically lower the number of cases of cervical cancer. It will also reduce the need for colposcopy.
You can read about HPV vaccines and cervical cancer.
From September 2012, the vaccination programme will use Gardasil. This protects against HPV types 6 and 11, as well as 16 and 18. HPV 6 and 11 are known to cause warts on the vulva or around the anus.
Vaccines for HPV don't protect against all the types of HPV that are linked to cervical cancer. So, even if you have been vaccinated you will still need to go to future screening appointments.
Less radical surgery for very early cervical cancer is increasingly available. Either a cone biopsy or a radical trachelectomy may help some women with early stage cervical cancer (stage 1A or 1B) to have children after their treatment. In trachelectomy, the lower part of the cervix is removed, but the womb is left intact. This procedure is being used as standard treatment in some UK hospitals already. You may also have keyhole surgery, so that the lymph nodes around the womb can be examined as well.
In a recent study in Germany, 212 women with early stage cervical cancer (Stage 1 or 2) have had a new type of hysterectomy called a total mesometrial resection (TMMR). The actual tissue removed is based on improved knowledge of where the cancer is most likely to spread. The results are encouraging and suggest this operation could improve rates of survival. It may cause fewer side effects because there is less risk of damage to the nerve supply to the bowel, bladder and vagina. In this trial the women had not been given radiotherapy and this too helps to reduce side effects. Randomised controlled trials are now needed to see if this new technique works better than the standard treatment which is radical hysterectomy followed by radiotherapy.
The SHAPE trial is comparing 2 different operations for early cervical cancer - a radical hysterectomy with a simple hysterectomy. A simple hysterectomy involves less extensive surgery and so may have fewer side effects than a radical hysterectomy. The aim of the trial is to find out if a simple hysterectomy is as good as a radical hysterectomy in treating cervical cancer, and to compare the side effects and quality of life afterwards.
Researchers are testing chemotherapy before surgery. The aim of this neo adjuvant treatment is to shrink the cancer before surgery, making surgery easier, and also to stop the cancer coming back after surgery. We don't know yet if giving chemotherapy before surgery is better than surgery on its own. In 2010, the Cochrane Collaboration reviewed 6 trials that have looked at this so far. They found that neo adjuvant chemotherapy helped women to live longer without cancer and reduced the risk of cancer spreading. However, it was not clear if having chemotherapy before surgery made it easier to remove the cancer or if it reduced the chance of the cancer coming back.
One trial is comparing chemotherapy before surgery with chemotherapy and radiotherapy (chemoradiation). The aim of this trial is to find out which treatment works best for early cervical cancer. This trial has now closed and we are waiting for the results.
Doctors usually treat locally advanced cervical cancer with chemoradiation. But it may be helpful to give some chemotherapy on its own before chemoradiation starts. A phase 2 trial called CXII found that treating locally advanced cervical cancer with chemotherapy followed by chemoradiation was possible and useful. As a result, the trial team designed a phase 3 trial looking into this. The aim of the INTERLACE study is to see if having chemotherapy for 6 weeks before chemoradiation is better than chemoradiation alone for cervical cancer that cannot be removed with surgery.
Chemotherapy is also being tested for advanced cervical cancer. This hasn't been used much in the past, but doctors hope they will find a drug, or combination of drugs, that can help to slow down the cancer or control symptoms. Drugs that have been tested include
The links above take you to information about the side effects of these drugs.
Internal radiotherapy (brachytherapy) has been used for many years to treat cervical cancer and plays a major role in the treatment of this disease. But doctors believe that they can improve on how well this works in cervical cancer. With all cancers, doctors want to give high enough doses to control or cure the cancer, but not so much that they cause unnecessary side effects.
There are different ways of giving internal radiotherapy for cervical cancer. You may have continuous treatment over a few days called low dose rate brachytherapy (LDR) or 2 or more short treatments a few days apart called high dose rate brachytherapy (HDR). Trials around the world have been monitoring the short and long term side effects of high dose brachytherapy, so that doctors and patients will have a complete picture of the pros and cons of this type of treatment.
Most brachytherapy centres in the UK are phasing out the Selectron equipment, which gives low dose rate treatment (LDR). They are switching to a different system that can use either high dose rate brachytherapy (HDR) or pulsed dose rate brachytherapy (PDR). The PDR source is Iridium 192, which is loaded by remote control in a similar way to HDR treatment. And can be interrupted easily so that staff and visitors can enter the room safely. New imaging equipment with HDR and PDR allows doctors to see the tumour and areas of healthy tissue more clearly, so that they can deliver the treatment more accurately and safely.
The DEPICT trial is looking at increasing the radiation dose when giving external radiotherapy for cancer of the cervix. It uses Intensity Modulated Radiotherapy (IMRT). IMRT shapes the radiation beams to closely fit the shape of the cancer. But it also changes the radiotherapy dose, according to the shape of the cancer. This means that the central part of the cancer receives the highest dose of radiotherapy and a surrounding area of tissue gets lower doses. The aim of this trial is to see if doctors can increase the radiation dose to the cancer, without causing more side effects than standard radiotherapy treatment.
There is also research looking into using different chemotherapy drugs alongside radiotherapy for cervical cancer. Combined chemoradiation is the accepted best treatment for most stages of cervical cancer, but researchers think they may be able to improve results further still by investigating other combinations of drugs.
Radiotherapy side effects
The HOT II trial looked at whether using a high pressure oxygen treatment called hyberbaric oxygen (HBO) therapy could help relieve the long term side effects of radiotherapy to the area between the hip bones (the pelvis). Side effects of radiotherapy include frequent bowel movements, diarrhoea, pain, bleeding from the bowel and the forming of scar tissue in the bowel (radiation fibrosis). 84 people took part in the trial. The trial team found no evidence that HBO helped people with bowel side effects from radiotherapy. These results disagree with other reports that say HBO is helpful. So the trial team felt larger trials were needed to know for sure.
The PPALM trial is looking at the use of a palm oil supplement and a drug called pentoxifylline to relieve symptoms caused by pelvic radiotherapy. Doctors think these may work well together to reduce thickening of the tissue (fibrosis) in the treatment area. The trial team want to find out if this combination of treatment helps, and to learn more about the side effects.
The PREDICT study wants to find out if an electronic nose can predict long term changes in bowel function after pelvic radiotherapy. Everyone has bacteria in their gut. Radiotherapy can change the number of different types of bacteria. Each type of bacteria has an individual smell, which can be picked up by an electronic nose. Looking at the way bacteria changes may help researchers to understand and predict who will and won't experience bowel problems long term.
Biological therapies are treatments that can control the growth of cancer cells by changing or blocking chemical pathways in the cells. We have detailed information about biological therapies.
Research is looking into different types of biological therapies for cervical cancer, including
These drugs are being tested in trials outside the UK. They are being looked at alone or in combination with radiotherapy or chemotherapy to treat cervical cancer.
A trial has looked at bevacizumab (Avastin) with chemotherapy for advanced cervical cancer. 452 women from America and Spain took part in the trial. They all had cervical cancer that had either spread to another part of their body such as the lungs, had come back since it was first treated, or had not responded to treatment. Half the women had chemotherapy and the other half had chemotherapy with bevacizumab. The results of the trial were published in 2014.
The trial team found that the women who had bevacizumab and chemotherapy lived for almost 4 months longer on average than the women who had chemotherapy alone. The women who had the combination of drugs had more side effects. But the trial team found that adding bevacizumab to chemotherapy did not reduce the women's quality of life compared to having chemotherapy on its own.
Doctors already use bevacizumab to treat some other types of cancer such as breast and bowel cancer. But it is not widely available to treat cervical cancer. The Scottish Medicines Consortium (SMC) have approved bevacizumab for advanced cervical cancer. You may have bevacizumab with the chemotherapy drugs paclitaxel and cisplatin or paclitaxel and topotecan. The National Institute for Health and Care Excellence (NICE) have not looked at bevacizumab for cervical cancer. So it may not be available in England and Wales.
Pazopanib is a type of biological therapy called a tyrosine kinase inhibitor. It is taken as a tablet and stops tumour cells developing blood vessels. It has been used to treat kidney and ovarian cancer and is in early stage clinical trials for bowel and cervical cancer.
In the UK, a trial called CIRCCa has looked at cediranib and chemotherapy for advanced cervical cancer. Cediranib is a type of anti angiogenic drug. These drugs stop cancers growing new blood vessels. The trial team found that cediranib with carboplatin and paclitaxel was a useful treatment for cervical cancer that had spread or come back. You can read the results of the CIRRCa trial.
You can search for cervical cancer trials on our clinical trials database.
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