TY - JOUR
T1 - Preoperative Partial Breast Irradiation in Patients with Low-Risk Breast Cancer
T2 - A Systematic Review of Literature
AU - Civil, Yasmin A.
AU - Jonker, Lysanne W.
AU - Groot Koerkamp, Maartje P. M.
AU - Duvivier, Katya M.
AU - de Vries, Ralph
AU - Oei, Arlene L.
AU - Slotman, Berend J.
AU - van der Velde, Susanne
AU - van den Bongard, H. J. G. Desirée
N1 - Funding Information:
This article is supported by a grant from KWF Dutch Cancer Society (Grant Number 12138).
Publisher Copyright:
© 2023, The Author(s).
PY - 2023/6
Y1 - 2023/6
N2 - Background: Preoperative instead of standard postoperative partial breast irradiation (PBI) after breast-conserving surgery (BCS) has the advantage of reducing the irradiated breast volume, toxicity, and number of radiotherapy sessions and can allow tumor downstaging. In this review, we assessed tumor response and clinical outcomes after preoperative PBI. Patients and Methods: We conducted a systematic review of studies on preoperative PBI in patients with low-risk breast cancer using the databases Ovid Medline, Embase.com, Web of Science (Core Collection), and Scopus (PROSPERO registration CRD42022301435). References of eligible manuscripts were checked for other relevant manuscripts. The primary outcome measure was pathologic complete response (pCR). Results: A total of eight prospective and one retrospective cohort study were identified (n = 359). In up to 42% of the patients, pCR was obtained and this increased after a longer interval between radiotherapy and BCS (0.5–8 months). After a maximum median follow-up of 5.0 years, three studies on external beam radiotherapy reported low local recurrence rates (0–3%) and overall survival of 97–100%. Acute toxicity consisted mainly of grade 1 skin toxicity (0–34%) and seroma (0–31%). Late toxicity was predominantly fibrosis grade 1 (46–100%) and grade 2 (10–11%). Cosmetic outcome was good to excellent in 78–100% of the patients. Conclusions: Preoperative PBI showed a higher pCR rate after a longer interval between radiotherapy and BCS. Mild late toxicity and good oncological and cosmetic outcomes were reported. In the ongoing ABLATIVE-2 trial, BCS is performed at a longer interval of 12 months after preoperative PBI aiming to achieve a higher pCR rate.
AB - Background: Preoperative instead of standard postoperative partial breast irradiation (PBI) after breast-conserving surgery (BCS) has the advantage of reducing the irradiated breast volume, toxicity, and number of radiotherapy sessions and can allow tumor downstaging. In this review, we assessed tumor response and clinical outcomes after preoperative PBI. Patients and Methods: We conducted a systematic review of studies on preoperative PBI in patients with low-risk breast cancer using the databases Ovid Medline, Embase.com, Web of Science (Core Collection), and Scopus (PROSPERO registration CRD42022301435). References of eligible manuscripts were checked for other relevant manuscripts. The primary outcome measure was pathologic complete response (pCR). Results: A total of eight prospective and one retrospective cohort study were identified (n = 359). In up to 42% of the patients, pCR was obtained and this increased after a longer interval between radiotherapy and BCS (0.5–8 months). After a maximum median follow-up of 5.0 years, three studies on external beam radiotherapy reported low local recurrence rates (0–3%) and overall survival of 97–100%. Acute toxicity consisted mainly of grade 1 skin toxicity (0–34%) and seroma (0–31%). Late toxicity was predominantly fibrosis grade 1 (46–100%) and grade 2 (10–11%). Cosmetic outcome was good to excellent in 78–100% of the patients. Conclusions: Preoperative PBI showed a higher pCR rate after a longer interval between radiotherapy and BCS. Mild late toxicity and good oncological and cosmetic outcomes were reported. In the ongoing ABLATIVE-2 trial, BCS is performed at a longer interval of 12 months after preoperative PBI aiming to achieve a higher pCR rate.
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85149740755&origin=inward
UR - https://www.ncbi.nlm.nih.gov/pubmed/36869253
U2 - 10.1245/s10434-023-13233-9
DO - 10.1245/s10434-023-13233-9
M3 - Review article
C2 - 36869253
SN - 1068-9265
VL - 30
SP - 3263
EP - 3279
JO - Annals of Surgical Oncology
JF - Annals of Surgical Oncology
IS - 6
ER -