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January 31, 2011

Treating Prostate Cancer
By Dan Harvey
For The Record
Vol. 23 No. 2 P. 24

Research focuses on developments in managing the most common cancer in men.

November’s American Society for Radiation Oncology (ASTRO) annual meeting covered cancer from head to toe as far as research and physiology. Presentations provided valuable new information about treatment and outcomes related to lymphoma and breast, lung, bladder, and colorectal cancers. But a major focus of the most recent ASTRO meeting involved prostate cancer, a common male problem that can often prove to be a manageable disease.

“Treatment is complex and needs to be individualized based on disease characteristics, the patient, and available treatment modalities,” explains Kevin S. Choe, MD, PhD, a radiation oncologist at the University of Texas Southwestern Medical School in Dallas. “The larger arsenal we have to combat the disease—especially more aggressive prostate cancer—the more treatment options we’ll have and better treatment outcomes we can expect.”

Prostate cancer is often curable, as long as the disease is detected within the treatment window: 98% of patients survive at least five years beyond the initial diagnosis, according to ASTRO. But the prostate cancer issue has fostered debate related to both screening and subsequent treatment, with the topic of one important presentation related to screening.

Contentious Issue
A study developed to determine the benefits and/or drawbacks of prostate cancer screening found that men treated for prostate cancer after routine screening experienced a significantly reduced risk of metastases within 10 years of treatment. “We were able to show that routine screening improves a patient’s quality of life by stopping cancer spread,” says lead author Chandana Reddy, MS, a senior biostatistician at the Cleveland Clinic. “Screening also reduces the burden of care placed on the healthcare system.”

The wide application of routine prostate cancer screening began in 1993 with the use of the prostate-specific antigen (PSA) test, which led to earlier diagnosis. The value of the PSA test remains a topic of debate. Researchers involved with the recent retrospective study believed the best way to measure screening effectiveness was to examine its ability to decrease metastatic prostate cancer within 10 years of treatment for a screened population.

“We based the study on data from 1,721 prostate cancer patients who were treated with either radiation therapy or surgery to remove the prostate gland,” says Reddy. “Patients were treated at Cleveland Clinic between 1986 and 1996.”

Researchers divided patients into two groups: those treated in a prescreening era (1986 to 1992) and those treated in a postscreening era (1993 to 1996). Patients were classified as having high-, intermediate-, or low-risk disease to determine which groups could potentially benefit from prostate cancer screening. The study revealed that within each of these three risk groups, patients treated in the prescreening era were significantly more likely to develop metastatic disease within 10 years of treatment compared with men in the postscreening era. “We feel this demonstrates that screening is important to catching cancer before its spreads beyond the prostate and becomes incurable,” says Reddy.

She concedes that the study results provide only the initial footprint in a forward direction. “A larger study now needs to be done to support our findings,” she says.

Prostate Cancer and Radiotherapy
Two other studies looked at radiation therapy as it is applied to prostate cancer treatment. The first compared intensity-modulated radiation therapy (IMRT) with 3D conformal radiotherapy (3D-CRT) in terms of side effects. Researchers found that patients treated with IMRT experienced fewer gastrointestinal complications compared with patients treated with CRT.

As prostate cancer patients are now living many years after treatment, it’s important to minimize side effects to enhance quality of life, notes Justin E. Bekelman, MD, an assistant professor of radiation oncology at the University of Pennsylvania and a lead study author.

“Policy makers, clinicians, and the media have highlighted the need for comparative evaluation of prostate cancer treatment. Attention has been particularly focused on radiation oncology, especially IMRT, for its potential to minimize radiation side effects and costs,” he says. “However, no one has done a large-population study to assess the outcomes of IMRT and 3D-CRT. So we compared patients who received IMRT with patients who received 3D-CRT between 2002 and 2004. We followed them to 2006 and compared the outcomes.”

This study used the Surveillance, Epidemiology, and End Results (SEER)-Medicare database to compare complications of prostate cancer in patients aged 65 or older. The researchers specifically examined common gastrointestinal side effects such as proctitis (inflammation of the rectal lining), rectal bleeding, cystitis (inflammation of bladder tissue), and hematuria (blood in the urine). Researchers found that patients treated with IMRT experienced fewer gastrointestinal complications than patients treated with CRT. However, they found minimal differences with urinary side effects. “But that didn’t surprise us,” adds Bekelman. “We expected that.”

He explains why IMRT provides added benefit: “An evolution of conformal radiation, IMRT uses beams of nonuniform radiation intensity to deliver radiation dose distributions that better conform to targets with irregular shapes, like the prostate. Also, as the prostate is adjacent to the rectum and bladder, clinicians need to restrict the volume of radiation dose to normal tissues to reduce complications. Our study shows that in a very large patient cohort, IRMT does just that.”

The study demonstrates that IMRT accomplishes what it was designed to do: reduce bowel complications compared with conformal radiation, says Bekelman. “Hopefully, our study leads to further similar studies. We now need to look at proton therapy vs. IMRT, brachytherapy vs. CRT or IMRT, and prostatectomy vs. radiation therapy. We hope our study fosters further research in these directions,” he says.

Bekelman reports that the University of Pennsylvania has already partnered with Massachusetts General Hospital in Boston to conduct a randomized study that compares proton therapy with IMRT. “This is an important step,” he says. “Does proton therapy reduce treatment complications compared to IMRT? If so, this needs to be documented. That’s our next step.”

Combined Therapies: Radiation and Hormones
Another significant radiotherapy-related study presented at ASTRO involved the addition of radiation therapy to hormone therapy to increase prostate cancer patients’ survival chances. The study showed that patients treated with combination hormone and radiation therapies lived longer compared with patients who received only hormone therapy. Currently, the number of men treated with this combination is on the rise, but many patients are still treated with hormone therapy alone.

These interim results come from the largest randomized trial of its kind. The multicenter study involved the National Cancer Institute of Canada, the United Kingdom Medical Research Council, and the Southwest Oncology Group in the United States. Specifically, researchers examined the effects of external beam radiation treatment added to lifelong androgen deprivation therapy for patients at a high risk of cancer return after treatment. Androgen deprivation therapy lowers the level of male hormones androgens, which shrinks the prostate or slows down prostate cancer growth.

During a 10-year period from 1995 to 2005, 1,205 high-risk prostate cancer patients in the United States, the United Kingdom, and Canada were randomly selected to receive hormone therapy alone or a combination of hormone therapy and radiation treatment. They were followed for six months on average. Interim results revealed that the addition of radiation therapy significantly decreased the risk of death. Further, there were no increased long-term side effects.

If the interim analysis figures are similar to those of the final analysis, the impact could be significant, according to lead author Malcolm Mason, MD, a radiation oncologist at Cardiff University in Wales. Clinicians could witness a 43% reduction in the chance of death, he points out, and this would involve thousands of men throughout the world.
Mason comments that the study results point to paradigm-shifting implications: Standard treatment should include a combination of hormone and radiation therapies.

The Anticoagulant Factor
Another highlighted prostate cancer study indicated that afflicted men who take aspirin for its anticoagulant benefit in addition to radiotherapy or surgery see their death risk reduced by at least 50%. This large study involved more than 5,000 patients with localized prostate cancer.

Choe, the lead author, notes that anticoagulants interfere with cancer growth. “That’s a well-known association,” he says. “We felt that prostate cancer would provide a good study model, as it impacts elderly patients. Older patients typically have other medical problems, such as cardiovascular issues that require an anticoagulant. An association between such medications and prostate cancer would be beneficial, we felt.”

Researchers evaluated data from the Cancer of the Prostate Strategic Urological Research Endeavor (CaPSURE) database to investigate anticoagulation effects of four medications—aspirin, warfarin, clopidogrel, and enoxaparin—related to risk of prostate cancer death among men whose cancer had not metastasized.

The study involved 5,275 men with localized prostate cancer who were treated with surgery or radiation. Of these patients, 1,982 were taking anticoagulants. Results revealed that anticoagulant usage among patients treated with either surgery or radiation reduced the risk of death from 10% to 4% at 10 years. Risk of bone metastasis development was also reduced. Further, study results indicated that the benefit appeared even greater among patients diagnosed with high-risk prostate cancer.

The study also found that the benefit was most prominent with aspirin compared with other anticoagulants. “Still, it’s premature to recommend aspirin to every prostate cancer patient,” says Choe. “But data is certainly encouraging and needs corroboration. If corroborated, it could have a huge impact because aspirin is widely used, and prostate cancer is the most common cancer among men. The benefit could be very large for society.”

Further studies are necessary before the addition of aspirin to prostate cancer therapy becomes standard treatment, Choe says. “That will involve a prospective study instead of going back and looking at the outcomes of previously treated patients. This way, we’ll have better control. One of the downsides of our recent study was the doses or the therapy duration was not part of the trial. So we don’t know the optimal dose or how long to take the medication. But we have revealed the association. Now we need to confirm the association, and that will be best done in a prospective study,” says Choe, who will be part of the next step.

— Dan Harvey is a freelance writer based in Wilmington, Del.