TY - JOUR
T1 - Patient-reported outcome thresholds and their associations with survival, adverse events, and quality of life in a pooled analysis of breast cancer trials
AU - Menz, Bradley D.
AU - Modi, Natansh D.
AU - Abuhelwa, Ahmad Y.
AU - Kuderer, Nicole M.
AU - Lyman, Gary H.
AU - Swain, Sandra M.
AU - Kichenadasse, Ganessan
AU - Shahnam, Adel
AU - Haseloff, Mark
AU - Vitry, Agnes
AU - Rammant, Elke
AU - Ramsey, Imogen
AU - Chan, Raymond J.
AU - McKinnon, Ross A.
AU - Rowland, Andrew
AU - Sorich, Michael J.
AU - Hopkins, Ashley M.
PY - 2025/11/15
Y1 - 2025/11/15
N2 - Researchers at the EORTC recently recommended clinical thresholds for the QLQ-C30 to facilitate actionable insights in clinical practice. We evaluate the distribution of these thresholds and associations with outcomes in breast cancer. Data were pooled from two early-stage and six advanced-stage breast cancer trials. EORTC thresholds were applied to available QLQ-C30 data to identify clinically important PRO domains. Associations between the number of clinically important PRO domains at baseline with overall survival (OS), invasive-disease-free survival (IDFS), progression-free survival (PFS), grade ≥3 adverse events (AEs), and serious AEs were evaluated using Cox-regression. Data from 8544 breast cancer patients, of whom 2428 (41%) of the 5893 early-stage and 1486 (56%) of the 2651 advanced-stage patients reported ≥3 clinically important PRO domains. In the early-stage, each additional clinically important PRO domain was associated with worsened grade ≥3 AEs (HR, 1.03 [95%CI, 1.01–1.04], p = 0.001) and serious AEs (1.05 [1.03–1.07], p < 0.001). In the advanced-stage, each additional clinically important PRO domain was associated with worsened OS (1.05 [1.03–1.07], p < 0.001), PFS (1.03 [1.01–1.04], p = 0.002), grade ≥3 AEs (1.04 [1.02–1.06], p < 0.001), and serious AEs (1.07 [1.04–1.11], p < 0.001). A substantial proportion of breast cancer patients report clinically important PRO domains at baseline, with increasing numbers associated with worsening AEs, survival, and quality-of-life.
AB - Researchers at the EORTC recently recommended clinical thresholds for the QLQ-C30 to facilitate actionable insights in clinical practice. We evaluate the distribution of these thresholds and associations with outcomes in breast cancer. Data were pooled from two early-stage and six advanced-stage breast cancer trials. EORTC thresholds were applied to available QLQ-C30 data to identify clinically important PRO domains. Associations between the number of clinically important PRO domains at baseline with overall survival (OS), invasive-disease-free survival (IDFS), progression-free survival (PFS), grade ≥3 adverse events (AEs), and serious AEs were evaluated using Cox-regression. Data from 8544 breast cancer patients, of whom 2428 (41%) of the 5893 early-stage and 1486 (56%) of the 2651 advanced-stage patients reported ≥3 clinically important PRO domains. In the early-stage, each additional clinically important PRO domain was associated with worsened grade ≥3 AEs (HR, 1.03 [95%CI, 1.01–1.04], p = 0.001) and serious AEs (1.05 [1.03–1.07], p < 0.001). In the advanced-stage, each additional clinically important PRO domain was associated with worsened OS (1.05 [1.03–1.07], p < 0.001), PFS (1.03 [1.01–1.04], p = 0.002), grade ≥3 AEs (1.04 [1.02–1.06], p < 0.001), and serious AEs (1.07 [1.04–1.11], p < 0.001). A substantial proportion of breast cancer patients report clinically important PRO domains at baseline, with increasing numbers associated with worsening AEs, survival, and quality-of-life.
KW - breast cancer
KW - cancer
KW - EORTC
KW - patient-reported outcomes
KW - survival outcomes
UR - http://www.scopus.com/inward/record.url?scp=105008687607&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/NHMRC/2030913
UR - http://purl.org/au-research/grants/NHMRC/2008119
U2 - 10.1002/ijc.70020
DO - 10.1002/ijc.70020
M3 - Article
AN - SCOPUS:105008687607
SN - 0020-7136
VL - 157
SP - 2135
EP - 2145
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 10
ER -