Abstract 247P
Background
Adjuvant radiation therapy (RT) is standard-of-care following breast-conserving surgery in patients with early-stage breast cancer, while adjuvant chemotherapy is recommended for patients at higher risk of distant recurrence. Data on the ideal sequencing of both adjuvant treatment modalities is limited. Hence, we sought to investigate whether concurrent or sequential delivery of chemotherapy and RT provides superior oncologic outcomes.
Methods
PubMed, Embase, and Cochrane were systematically searched for randomized controlled trials (RCTs) comparing concurrent with sequential administration of adjuvant chemotherapy and RT. Outcomes of interest included locoregional recurrence (in-breast, contralateral breast, and nodal recurrence), distant recurrence, disease-free survival (DFS) and overall survival (OS). Statistical analyses employed random or fixed-effects models with 95% confidence intervals (CI).
Results
From 1,477 initially identified studies, four phase III RCTs with 3,835 patients were selected, of whom 1,932 (50.4%) received concurrent chemotherapy and RT. Locoregional recurrence was lower in patients undergoing concurrent chemoradiation compared to sequentially delivered therapy (OR 0.58; 95% CI 0.43-0.78; P < 0.01). Subgroup analysis excluding T4 tumors yielded similar results. No differences between the sequencing approaches were observed in contralateral breast recurrence (OR 0.78; 95% CI 0.44-1.39; P = 0.46), distant recurrence (OR 1.04; 95% CI 0.82-1.32; P = 0.76), OS (HR 1.02; 95% CI 0.87-1.19; P = 0.82) or DFS (HR 1.00; 95% CI 0.87-1.14; P = 0.95). Concurrent therapy was associated with moderate or severe breast subcutaneous fibrosis (OR 2.38; 95% CI 1.15-4.91; P <0.01; I2 = 33%) and telangiectasia (OR 1.96; 95% CI 1.00-3.44; P = 0.05), while no statistically significant difference was observed regarding lymphedema and severe skin toxicity.
Conclusions
Adjuvant therapy delivered via concurrent chemoradiation improved locoregional control at a cost of increased breast fibrosis and telangectasia. No differences were observed in DFS or OS. Further RCTs using more modern systemic and radiation therapy regimens are warranted.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.
Resources from the same session
54P - BL-B01D1, an EGFR x HER3 bispecific antibody-drug conjugate (ADC), in patients with locally advanced or metastatic biliary tract carcinoma (BTC)
Presenter: Zhihao Lu
Session: Poster session 13
55P - Subsequent anticancer therapy (SAT) analysis from 3-year follow-up of the phase III TOPAZ-1 study of durvalumab plus gemcitabine and cisplatin in biliary tract cancer (BTC)
Presenter: Arndt Vogel
Session: Poster session 13
56P - Multi-omic profiling in cholangiocarcinoma to enable scientific advancement within the DKFZ/NCT/DKTK MASTER study
Presenter: Federico Nichetti
Session: Poster session 13
57P - Integrative analysis of the genomic and transcriptomic landscape identifies ciliary genes as a therapeutic target in bile duct cancer
Presenter: Pietro Carotenuto
Session: Poster session 13
58P - Efficacy and safety of liposomal irinotecan (nal-IRI) plus fluorouracil (5-FU) and leucovorin (LV) versus 5-FU/LV alone for advanced biliary tract cancer (BTC) after progression on gemcitabine-based therapy: A pooled analysis of the NIFTY and NALIRICC trials
Presenter: Changhoon Yoo
Session: Poster session 13
59P - Prognostic score to predict recurrence after pancreaticoduodenectomy for ampullary carcinoma: Results from the French prospective FFCD cohort
Presenter: Gael Roth
Session: Poster session 13
60P - Baseline characteristics and molecular testing of patients with IDH1-mutated cholangiocarcinoma: Initial results from the phase IIIb ProvIDHe study
Presenter: Lorenza Rimassa
Session: Poster session 13
61P - Addressing racial disparities in clinical trials in cholangiocarcinoma
Presenter: Abhinav Vyas
Session: Poster session 13
Resources:
Abstract
62TiP - HERIZON-BTC-302: A phase III study of zanidatamab with standard-of-care (SOC) therapy vs SOC alone for first-line (1L) treatment of human epidermal growth factor receptor 2 (HER2)-positive advanced/metastatic biliary tract cancer (BTC)
Presenter: Teresa Macarulla Mercade
Session: Poster session 13
240P - Efficacy and safety of ribociclib (RIB) + nonsteroidal aromatase inhibitor (NSAI) in older patients (pts) with HR+/HER2− early breast cancer (EBC) in NATALEE
Presenter: Michael Untch
Session: Poster session 13