Trajectories of multidimensional worry in survivors of early breast cancer (BC).
Abstract
12051 Background: Worrisome thoughts are common future-oriented behaviors and may affect quality of life (QoL) years removed from BC diagnosis. We aimed to identify trajectories of worry and their determinants, focusing on age-related specificities. Methods: Disease-free stage I-III BC survivors from CANTO (NCT01993498) completed the Impact of Cancer scale v2 at end of treatment (EoT) and years (Y) 1, 3, and 5 post-EoT. Group-based trajectories were identified modeling continuous scores of the worry subscale (range: 1-5, higher = worse), which evaluates uncertainty and worry about the future and health, a sense of time running out, fear of cancer recurrence (FCR), and symptom-triggered FCR. Adjusted multinomial logistic regression incorporating pre-treatment anxiety/depression assessed membership determinants. QoL (EORTC QLQ-C30/BR23) was described by trajectory. Analyses were stratified by age. Results: We included7824 survivors, 31% were ≤50 and 69% > 50 years old. Among those aged ≤50, we identified five worry trajectories: most had high (41%) or very high (18%) worry (mean scores [95% CI] at EoT: 3.57 [3.55-3.60] and 4.37 [4.33-4.41], respectively, stable); 21% showed improvement (2.77 [2.73-2.82] at EoT, 2.14 [2.08-2.21] at Y5); and 12% had low worry (1.58 [1.53-1.63] at EoT, stable). Finally, 7% had moderate worry at EoT (2.21 [2.14-2.28]) that worsened sharply, stabilizing at high levels by Y5 (3.40 [3.29-3.52]). These patterns, especially in the worsening group, were primarily driven by persisting FCR and increasing uncertainty about health. Among those aged > 50, similar trajectories emerged, however worry levels in the worsening group (17%) remained low-to-moderate (2.04 [2.01-2.06] at EoT, 2.34 [2.27-2.40] at Y5). Younger age was a significant determinant of very high worry, both in the ≤50 (Odds Ratio v low worry [95% CI] per 10-year decrease: 1.92 [1.33-2.77]) and in the > 50 age group (1.50 [1.20-1.90]). Partnered status was associated with worsening worry in the ≤50 age group (v not: 2.54 [1.24-5.19]), whereas chemotherapy with very high worry in the > 50 age group (v no chemo: 1.77 [1.14-2.73]). BC grade, stage, BRCA status, family history of cancer, and comorbidities were not linked to worry in either age group. Psychological and physical domains of QoL, including fatigue, sleep, cognitive function, appetite, and gastrointestinal symptoms, were significantly worse in trajectories at higher worry (p < .001 at all time points). Conclusions: More than two-thirds of younger BC survivors report high levels of worry that either remain unchanged or worsen 5 years post-EoT, with a more pronounced decline and different determinants than older counterparts. These patterns appear to be largely driven by the post-traumatic effects of BC on unresolved FCR and by negative projections about health. Early referral to mental health professionals and monitoring strategies focused on reducing anxious arousal are warranted. Clinical trial information: NCT01993498 .
Article Details
Journal Info
Journal of Clinical Oncology
Lippincott Williams & Wilkins
Authors (20)
Antonio Di Meglio
Martina Pagliuca
Scuola Superiore Meridionale (SSM), Naples, Italy
Stefano Maccarone
Breast Cancer Survivorship Group, INSERM Unit 981, Gustave Roussy, Villejuif, France
Julie Havas
Leonor Fasse
Department for the Organization of Patient Pathways, Gustave Roussy, Villejuif, France
Diane Boinon
Department for the Organization of Patient Pathways, Gustave Roussy, Villejuif, France
Marianne Hermand-Deslandes
Gustave Roussy, Villejuif, France
Anne-Laure Martin
Catherine Gaudin
Unicancer, Paris, France
Christelle Jouannaud
Marion Fournier
Institut Bergonie, Bordeaux, France
Laurence Vanlemmens
Centre Oscar Lambret, Lille, France
Anne Kieffer
Institut de Cancerologie de Lorraine, Vandoeuvre, France
Baptiste Sauterey
ICO Institut de Cancerologie de l'Ouest, Angers, France
François Cherifi
Florence Lerebours
Institut Curie, Saint-Cloud, Paris, France
Gwenn Menvielle
Stefan Michiels
Maria Alice Franzoi
Cancer Survivorship Program, INSERM Unit 981, Gustave Roussy, Villejuif, France
Ines Luis
Cancer Survivorship Program, Université Paris-Saclay, UVSQ, Gustave Roussy, Inserm, CESP, Villejuif, France