RT and concurrent chemotherapy after surgery is effective treatment for high-risk endometrial cancer

PUBLIC RELEASE DATE:

9-Sep-2014

Contact: Michelle Kirkwood press@astro.org 703-286-1600 American Society for Radiation Oncology http://www.twitter.com/ASTRO_org

Fairfax, Va., September 9, 2014Radiation therapy with concurrent paclitaxel chemotherapy following surgery is an effective treatment for patients with high-risk endometrial cancer, according to a study published in the September 1, 2014 edition of the International Journal of Radiation Oncology Biology Physics (Red Journal), the official scientific journal of the American Society for Radiation Oncology (ASTRO).

Endometrial cancer is the most common gynecologic malignancy. Patients with early-stage disease are typically treated with surgery alone; however, patients with advanced endometrial cancer have higher instances of local or distant recurrence. Concurrent radiation therapy and chemotherapy after surgery is used to reduce the rate of recurrence in patients with advanced disease. This study, "A Phase 2 Trial of Radiation Therapy With Concurrent Paclitaxel Chemotherapy After Surgery in Patients With High-Risk Endometrial Cancer: A Korean Gynecologic Oncology Group Study," evaluates the efficacy and toxicity of concurrent chemoradiation with weekly paclitaxel in patients with stage III and IV endometrial cancer.

From January 2006 to March 2008, 57 patients from 20 institutions in Korea were included in the study. Patients eligible to participate in the study were between 20 and 80 years old, with a histologic diagnosis of International Federation of Gynecology and Obstetrics (FIGO) stage III or IV endometrioid adenocarcinoma with no history of prior surgery, chemotherapy or radiation therapy for the treatment of other cancers. Patients with diagnoses of other cancers or severe infection requiring parenteral antibiotics, with a history of cardiac arrhythmia, congestive heart failure or myocardial infarction within the previous six months, or with uncontrolled infection, diabetes, hypertension or compromised cardiac, renal, liver or bone marrow functions were not included in the study. Of the 57 patients in this study, 12 patients (21.1 percent) had FIGO stage IIIA disease, 40 (70.1 percent) had FIGO stage IIIC disease and five (8.8 percent) had FIGO stage IV disease. Fourteen patients (24.6 percent) had grade 1 tumors, 27 (47.3 percent) had grade 2 tumors, and 16 (28.1 percent) had grade 3 tumors. The average age of the study patients was 52.2 years old.

All eligible patients had a staging laparotomy, including total abdominal hysterectomy, bilateral salpingo-oophorectomy (removal of both ovaries and both fallopian tubes), pelvic and para-aortic lymphadenectomy and peritoneal washing cytology. Patients in the study received a total dose of 45.0 to 50.4 Gy of external pelvic radiation therapy (1.8 to 2.0 Gy daily, five times a week), and 60 mg/m2 of paclitaxel diluted in 500 mL of 5 percent dextrose in water administered intravenously for three hours, once a week, for six weeks. Radiation therapy and chemotherapy were initiated within six weeks of surgery, and radiation therapy began either two days before or two days after the first chemotherapy treatment.

Chemotherapy was suspended due to adverse toxic effects in two patients. Of those two patients, one experienced septic shock, and one had persistent grade 4 neutropenia (an abnormally low count of neutrophils, a type of white blood cell) for more than two weeks. One patient refused treatment after enrollment, and two patients withdrew from treatment prior to completing all six cycles of chemotherapy. Fifty-two patients were included in the study's final analysis.

Patients received follow-up for five years after surgery. Chest X-ray and abdominal-pelvic CT or MRI were conducted every six months for the first two years post-surgery and then annually for the next three years. Patients were also evaluated by pelvic examinations, monitoring CA125 blood serum levels and Papanicolaou tests every three months for the first two years post-surgery and then every six months for the next three years.

Severe toxicities observed during treatment were primarily hematologic toxicities. Of the 312 treatment cycles (52 patients each received six cycles), 52 episodes (16.7 percent) of grade 3 or 4 leukopenia (decrease in number of white blood cells) were observed, and 35 episodes (11.2 percent) of grade 3 or 4 neutropenia were observed. Hematologic toxicity caused 98 cycles to be delayed one week, and a paclitaxel dose reduction was required for eight patients (15.3 percent) who experienced persistent neutropenia for more than one week.