Trial confirms pelvic radiation as standard of care for high-risk endometrial cancer
SAN DIEGO, September 25, 2017 – In a new phase III trial report from the National Clinical Trial Network group, NRG Oncology, recurrence-free and overall survival rates for women with stage I-II high-risk endometrial cancer were not superior following vaginal cuff brachytherapy plus chemotherapy when compared with pelvic radiation therapy. Risks of pelvic and para-aortic nodal recurrence and frequency of short-term side effects were greater for the brachytherapy-chemotherapy approach. High completion rates for each treatment arm suggest that both therapies are well-tolerated by patients. Findings will be presented today at the 59th Annual Meeting of the American Society for Radiation Oncology (ASTRO).
Clinical trials in the early 2000s (e.g., Gynecology Oncology Group (GOG)-99, PORTEC) found that external beam radiation therapy to the pelvis following surgery to remove early-stage endometrial cancer reduced tumor recurrence rates compared with post-surgical observation alone, which established adjuvant pelvic radiation as the standard treatment for stage I-II patients. In recent years, however, many physicians have begun treating early-stage patients at higher risk of recurrence with an alternative approach of vaginal cuff brachytherapy followed by chemotherapy. GOG-249 was designed to directly compare the two approaches.
"Our trial clearly demonstrates that adjuvant pelvic radiation should remain the standard of care for high-risk, early-stage endometrial cancer patients. It also suggests that the trend in our field of abandoning pelvic radiation in favor of chemotherapy-brachytherapy combinations for high-risk patients is premature and not supported by clinical evidence," said Marcus Randall, MD, FASTRO, lead author of the study and a professor of radiation medicine at the University of Kentucky in Lexington. "The cohort of women with high-risk histologies did not demonstrate any benefit from the addition of chemotherapy, but they did experience worse nodal control rates and more short-term side effects."
GOG-249 was a phase III randomized trial designed to test whether adjuvant brachytherapy plus chemotherapy improved recurrence-free survival compared with the standard treatment of pelvic radiation for early-stage, high-risk endometrial cancer. Eligible patients included women with high-risk stage I-II histology, including stage II tumors, stage I-II serous or clear-cell carcinomas and stage I endometrioid tumors if the patient demonstrated clinic-pathologic features associated with a high risk of recurrence, based on criteria established in the GOG-33 trial and used in the GOG-99 trial.
Most patients (74%) had stage I disease and endometrioid histology (71% versus 15% serous and 5% clear-cell carcinomas). The median patient age was 63 years. All patients underwent hysterectomy prior to radiation or chemoradiation therapy.
One of two treatment arms was randomly assigned to patients: adjuvant external beam RT to the pelvis (PXRT) or vaginal cuff brachytherapy plus chemotherapy (VCB/C). The PXRT group (n = 301 patients) received a median radiation dose of 45 Gray (Gy) delivered over five weeks through standard four-field radiation or intensity-modulated radiation therapy (IMRT). Patients with serous, clear-cell or stage II tumors were eligible for a vaginal cuff brachytherapy boost, and 35 percent of the cohort received this additional therapy. The VCB/C group (n = 300 patients) received either high-dose rate (HDR) or low-dose rate (LDR) brachytherapy followed by three cycles of chemotherapy including paclitaxel (175 mg/m 2 – 3 hour) and carboplatin (AUC 6 – 21 days). Nearly all 601 patients accrued for the trial completed treatment (91% PXRT, 87% VCB/C).
There were no statistically significant increases in recurrence-free survival (RFS) or overall survival (OS) in the brachytherapy-chemotherapy arm. At a median follow-up of 53 months, 82 percent of patients were alive and recurrence free at three years for both the VCB/C and PXRT patient groups. Three-year OS rates were 91 percent for pelvic radiation and 88 percent for the brachytherapy-chemotherapy combination, but this difference was not statistically significant (p = 0.57). Survival distributions were estimated using the Kaplan-Meier method and compared using a log rank test.
The cumulative incidence of pelvic or para-aortic nodal recurrence at five years among the VCB/C group (9.2%, 25 recurrences, 20 in the pelvis) was twice that of the pelvic radiation cohort (4.4%; 12 recurrences, 6 in the pelvis) (Hazard Ratio (HR) = 0.47, 95% CI 0.24-0.94). The cumulative incidence of vaginal and distant tumor recurrences, however, did not differ significantly between the groups. The cumulative incidence of distant recurrence at five years was 18 percent for both groups.
Short-term side effects were more pronounced on the brachytherapy-chemotherapy arm, while long-term side effects were similar for both treatments. Grade 3 or higher adverse events were reported in 187 patients receiving VCB/C, compared with 32 patients in the PXRT group. Severe late effects, or side effects that occurred after treatment ended, were reported in 35 patients who received VCB/C and 37 who received PXRT. Side effects were graded using the Common Terminology Criteria for Adverse Events (CTCAE) version 3.
"Previous GOG trials confirmed that pelvic radiation is an effective, safe and tolerable option to manage early-stage endometrial cancer. The current trial confirms that this standard treatment is preferable to the experimental approach of vaginal cuff brachytherapy followed by chemotherapy, in terms of tumor control in the nodal regions and also in terms of acute toxicity. This finding holds true even for patients at a higher risk of recurrence," said Dr. Randall. "Researchers can focus now on determining the optimal radiation dosing and fractionation schedules for various patient sub-groups, as well as refining the techniques we use to deliver external beam therapy to the pelvis and continue to investigate therapies to decrease distant failures in this high-risk group."
The abstract, "A phase III trial of pelvic radiation therapy versus vaginal cuff brachytherapy followed by paclitaxel/carboplatin chemotherapy in patients with high-risk, early-stage endometrial cancer: A Gynecology Oncology Group study," will be presented in detail during a news briefing and the Plenary Session at ASTRO's 59th Annual Meeting in San Diego (full details below). To schedule an interview with Dr. Randall and/or outside experts in gynecologic cancer, contact ASTRO's media relations team on-site at the San Diego Convention Center September 24 through 27, by phone at 703-286-1600 or by email at [email protected]
ATTRIBUTION TO THE AMERICAN SOCIETY OF RADIATION ONCOLOGY (ASTRO) ANNUAL MEETING REQUESTED IN ALL COVERAGE.
This news release contains additional and/or updated information from the study author(s). Full original abstract and author disclosures available from [email protected] or at http://www.astro.org/annualmeeting.
Study Presentation Details
- News Briefing: Monday, September 25, 11:00 a.m. – 12:00 p.m. Pacific, San Diego Convention Center, room 24C, webcast: http://www.bit.do/astro17-2
- Scientific Session: Plenary, Monday, September 25, 2:15 – 3:45 p.m. Pacific time, San Diego Convention Center, Ballroom 20
Resources on Gynecologic Cancer and Radiation Therapy
- Digital brochure: Radiation Therapy for Gynecologic Cancers
- Videos: Radiation Therapy for Gynecologic Cancers (Spanish version), An Introduction to Radiation Therapy (Spanish version)
- Additional brochures, videos and information on radiation therapy from ASTRO's patient site, RTAnswers.org
- ASTRO's clinical practice statements and guidelines
ABOUT ASTRO'S ANNUAL MEETING
ASTRO's 59th Annual Meeting, the world's largest scientific meeting in radiation oncology, will be held September 24-27, 2017, at the San Diego Convention Center. The 2017 Annual Meeting is expected to attract more than 11,000 attendees from across the globe, including oncologists from all disciplines and members of the entire radiation oncology team. More than 2,800 abstracts sharing results from clinical trials and other research studies will be presented in conjunction with educational sessions and keynote addresses that underscore the meeting's theme, "The Healing Art and Science of Radiation Oncology." Led by ASTRO President Brian Kavanagh, MD, MPH, FASTRO, the 2017 meeting will feature keynote addresses from Richard D. Zane, MD, FAAEM, Chief Innovation Officer for the University of Colorado Health System; Lucy Kalanithi, MD, FACP, widow of Paul Kalanithi, MD, the best-selling author of "When Breath Becomes Air," with Heather Wakelee, MD, Paul's oncologist; and Vinay K. Prasad, MD, MPH, an assistant professor of medicine at the Oregon Health & Science University. During the four-day meeting, more than 200 exhibitors will demonstrate cutting-edge technology and medical device innovations for radiation oncology. Visit us online for more information about ASTRO's 59th Annual Meeting or press opportunities at the meeting.
The American Society for Radiation Oncology (ASTRO) is the world's largest radiation oncology society, with more than 10,000 members who are physicians, nurses, biologists, physicists, radiation therapists, dosimetrists and other health care professionals who specialize in treating patients with radiation therapies. The Society is dedicated to improving patient care through professional education and training, support for clinical practice and health policy standards, advancement of science and research, and advocacy. ASTRO publishes three medical journals, International Journal of Radiation Oncology * Biology * Physics, Practical Radiation Oncology and Advances in Radiation Oncology; developed and maintains an extensive patient website, RT Answers; and created the Radiation Oncology Institute, a nonprofit foundation to support research and education efforts around the world that enhance and confirm the critical role of radiation therapy in improving cancer treatment. To learn more about ASTRO, visit http://www.astro.org and follow us on our blog, Facebook and Twitter.