www.CriteriumInc.com
JULY 2011

 This Month's Clinical Focus:  ONCOLOGY  

 Short-Term ADT Improves Prostate Cancer Survival
The addition of short-term androgen-deprivation therapy (ADT) to conventional radiotherapy was associated with a survival benefit for men with localized prostate cancer.

According to a study published in the July 14 issue of the New England Journal of Medicine, the 10-year overall survival rate was 62% among men who received radiotherapy plus short-term ADT compared with 57% among men who received radiotherapy alone. Adding ADT also decreased the 10-year disease-specific mortality rate from 8% to 4%.

However, when the authors reanalyzed the data according to risk subgroups, they found that the improvements in overall survival and reductions in disease-specific mortality were primarily limited to patients in the intermediate-risk subgroup.

The authors note that they also saw reductions in the secondary endpoints of biochemical failure, distant metastases, and the rate of positive findings on repeat biopsies at 2 years.

"For men with high-risk prostate cancer, previous studies have shown us that adding short-term ADT to radiation therapy is not enough," said lead author Christopher U. Jones, MD, from Radiological Associates of Sacramento in California. "We need to add long-term ADT to radiation therapy for maximum benefit for these patients."  The data from this study support these previous findings, he added.

"But for men with intermediate-risk prostate cancer, treated with conventional doses of radiation, the standard of care now should be to add short-term ADT to the radiation therapy," Dr. Jones told Medscape Medical News.

However, the authors point out that despite the favorable results seen in their study, the adoption of new and advanced modalities in radiotherapy may put the value of adding short-term ADT in patients treated with these new radiation therapy techniques in doubt.

"What complicates the issue is that most men are now treated with modern techniques, which allows considerably higher doses of radiation to be administered safely and with improved efficacy against prostate cancer," Dr. Jones explained. "We do not know if the addition of short-term ADT will still be needed for patients treated with these higher doses of radiation."

He added that the Radiation Therapy Oncology Group (RTOG) has opened a new clinical trial, RTOG 0815, to answer this question.

Further Studies Needed     Even though combination therapy appears to be indicated in men with intermediate risk for prostate cancer, it is unclear whether a radiation dose larger than 66.6 Gy or longer durations of hormonal therapy can further reduce mortality, commented Anthony V. D'Amico, MD, PhD, chair, Division of Genitourinary Radiation Oncology, Dana-Farber Cancer Institute in Boston, Massachusetts.

He points out in an accompanying editorial that 2 previous randomized trials (MRC RT018 and DFCI 950964) have provided evidence that these interventions may further increase survival in this subgroup of men.

Another randomized trial, ICORG 97-0110, which evaluated a 70-Gy radiation dose to the prostate and 8 vs 4 months of hormonal therapy, showed no difference in outcome. However, only 16% of the study cohort had intermediate-risk disease, "which was not sufficient to address the question of the duration of hormonal therapy in these men," Dr. D'Amico writes.

"Therefore, radiation therapy and 4 or 6 months of hormonal therapy remain treatment options for men with intermediate-risk disease," he concludes. "Whether 4 or 6 months of hormonal therapy for intermediate-risk disease is best requires further study."

SOURCE:  The study was supported by grants from the National Cancer Institute. Coauthor Michael Chetner, MD, reports receiving lecture fees from and serving on the advisory boards of Amgen, Ferring, GlaxoSmithKline, and Eli Lilly and receiving fees for the development of educational presentations from Amgen and GlaxoSmithKline. Coauthor Howard Sandler, MD, received consulting fees from Calypso Medical and Varian. N Engl J Med. 2011;365:107-118, 169-171. http://www.nejm.org/doi/full/10.1056/NEJMoa1012348 


 Unpublished Cancer Trials May Affect Clinical Practice
A "substantial" number of phase 3 clinical trials of systemic cancer treatments with potential influence on clinical practice remain unpublished after 6.5 years or more, according to a new report from Canadian researchers.

The investigators also found that "many" other trials are published after a delay of 5 years or more. Their paper was published online July 11 in the Journal of Clinical Oncology.  The findings have potential ramifications in oncology practice, say the authors.  "Nonpublication of clinical trials predominantly reporting negative results can lead to overestimation of treatment benefits and may adversely influence clinical practice," write the authors, led by Vincent C. Tam, MD, from the University of Toronto, in Ontario.

The researchers considered phase 3 trials of systemic cancer treatments that were presented at the annual meeting of the American Society of Clinical Oncology (ASCO) from 1989 to 2003.

A total of 709 phase 3 trials were identified, and 66 (9.3%) of those remain unpublished at a minimum follow-up of 6.5 years. In addition, 94 (13%) were published 5 years or more after their initial presentation. Thus, nearly a quarter of all the trials were either unpublished or their publication was greatly delayed.

Perhaps not surprisingly, 71% of these clinical trials reported negative results.  There is an ethical issue at stake in all of this, suggest the authors. "Nonpublication also breaks an implicit contract that investigators make with study participants," they write.

Dr. Tam and colleagues explain further: "Approximately 23,770 patients participated in the unpublished trials listed in our compendium - an astounding number of patients with cancer who participated in trials after being informed that the results would contribute to public knowledge, and might improve cancer treatment."

SOURCE: J Clin Oncol. Published online July 11, 2011.
Abstract
http://jco.ascopubs.org/content/early/2011/07/06/JCO.2010.33.3922.abstract


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