Long-Term Cancer Outcomes From Study NRG Oncology/RTOG 9517: A Phase 2 Study of Accelerated Partial Breast Irradiation With Multicatheter Brachytherapy After Lumpectomy for Early-Stage Breast Cancer
Creators
- 1. Department of Radiation Oncology, The James, Ohio State University, Columbus, Ohio (United States)
- 2. NRG Oncology Statistics and Data Management Center, Philadelphia, Pennsylvania (United States)
- 3. Department of Radiation Oncology, Arizona Breast Cancer Specialists, Scottsdale, Arizona (United States)
- 4. Department of Radiation Oncology, Oschner Clinic, New Orleans, Louisiana (United States)
- 5. Department of Radiation Oncology, Virginia Commonwealth University, Richmond, Virginia (United States)
- 6. Department of Radiation Oncology, University of Colorado Denver, Aurora, Colorado (United States)
- 7. Department of Radiation Oncology, Medical College of Wisconsin, Milwaukee, Wisconsin (United States)
- 8. Mount Sinai Comprehensive Cancer Center, Miami, Florida (United States)
- 9. Department of Radiation Oncology, Botsford Hospital, Farmington Hills, Michigan (United States)
- 10. Department of Radiation Oncology, Memorial Sloan-Kettering Cancer Center, New York, New York (United States)
Description
Purpose: To examine 10-year rates of local, regional, and distant recurrences, patterns of recurrence, and survival rates for breast cancer patients enrolled on Study NRG Oncology/Radiation Therapy Oncology Group 9517, a multi-institutional prospective trial that studied one of the earliest methods of accelerated partial breast irradiation (APBI), multicatheter brachytherapy (MCT). Methods and Materials: Eligibility included stage I/II unifocal breast cancer <3 cm in size after lumpectomy with negative surgical margins and 0 to 3 positive axillary nodes without extracapsular extension. The APBI dose delivered was 34 Gy in 10 twice-daily fractions over 5 days for high-dose-rate (HDR); and 45 Gy in 3.5 to 5 days for low-dose-rate (LDR) brachytherapy. The primary endpoint was HDR and LDR MCT reproducibility. This analysis focuses on long-term ipsilateral breast recurrence (IBR), contralateral breast cancer events (CBE), regional recurrence (RR), and distant metastases (DM), disease-free, and overall survival. Results: The median follow-up was 12.1 years. One hundred patients were accrued from 1997 to 2000; 98 were evaluable; 65 underwent HDR and 33 LDR MCT. Median age was 62 years; 88% had T1 tumors; 81% were pN0. Seventy-seven percent were estrogen receptor and/or progesterone receptor positive; 33% received adjuvant chemotherapy and 64% antiendocrine therapy. There have been 4 isolated IBRs and 1 IBR with RR, for 5.2% 10-year IBR without DM. There was 1 isolated RR, 1 with IBR, and 1 with a CBE, for 3.1% 10-year RR without DM. The 10-year CBE rate was 4.2%, with 5 total events. Eleven patients have developed DM, 8 have died of breast cancer, and 22 have died from other causes. The 10-year DFS and OS rates are 69.8% and 78.0%, respectively. Conclusion: This multi-institutional, phase 2 trial studying MCT-APBI continues to report durable in-breast cancer control rates with long-term follow-up.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.ijrobp.2016.03.037Additional details
Identifiers
- DOI
- 10.1016/j.ijrobp.2016.03.037;
- PII
- S0360-3016(16)30004-9;
Publishing Information
- Journal Title
- International Journal of Radiation Oncology, Biology and Physics
- Journal Volume
- 95
- Journal Issue
- 5
- Journal Page Range
- p. 1460-1465
- ISSN
- 0360-3016
- CODEN
- IOBPD3
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 48097362
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- BRACHYTHERAPY; CHEMOTHERAPY; GY RANGE 10-100; IRRADIATION; MAMMARY GLANDS; NEOPLASMS; PATIENTS
- Descriptors DEC
- ABSORBED DOSE RANGE; BODY; DISEASES; GLANDS; GY RANGE; MEDICINE; NUCLEAR MEDICINE; ORGANS; RADIATION DOSE RANGES; RADIOLOGY; RADIOTHERAPY; THERAPY
Optional Information
- Copyright
- Copyright (c) 2016 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.