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. 2023 Jun 20:12:2023-1-7.
doi: 10.7573/dic.2023-1-7. eCollection 2023.

Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR+/HER2- breast cancer treated with CDK4/6 inhibitors and endocrine therapy

Affiliations

Health-related quality of life and clinical complexity of a real-life cohort of patients with advanced HR+/HER2- breast cancer treated with CDK4/6 inhibitors and endocrine therapy

Barbara Tagliaferri et al. Drugs Context. .

Abstract

Background: Advanced breast cancer (ABC) is characterized by multidimensional clinical complexity that is usually not considered in randomized clinical trials. In the present real-life study, we investigated the link between clinical complexity and quality of life of patients with HR+/HER2- ABC treated with CDK4/6 inhibitors.

Methods: We evaluated multimorbidity burden assessed with the Cumulative Illness Rating Scale (CIRS), polypharmacy and patient-reported outcomes (PROs). PROs were assessed at baseline (T0), after 3 months of therapy (T1), and at disease progression (T2) using EORTC QLC-C30 and QLQ-BR23 questionnaires. Baseline PROs and changes between T0 and T1 were evaluated amongst patients with different multimorbidity burden (CIRS <5 and ≥5) and polypharmacy (<2 or ≥2 drugs).

Results: From January 2018 to January 2022, we enrolled 54 patients (median age 66 years, IQR 59-74). The median CIRS score was 5 (IQR 2-7), whilst the median number of drugs taken by patients was 2 (IQR 0-4). No changes in QLQ-C30 final scoring between T0 and T1 were observed in the overall cohort (p=0.8944). At T2, QLQ-C30 global score deteriorated with respect to baseline (p=0.0089). At baseline, patients with CIRS ≥5 had worse constipation than patients without comorbidities (p<0.05) and a lower trend in the median QLQ-C30 global score. Patients on ≥2 drugs had lower QLQ-C30 final scores and worse insomnia and constipation (p<0.05). No change in QLQ-C30 final score from T0 to T1 was observed (p>0.05).

Conclusion: Multimorbidity and polypharmacy increase the clinical complexity of patients with ABC and may affect baseline PROs. The safety profile of CDK4/6 inhibitors seems to be maintained in this population. Further studies are needed to assess clinical complexity in patients with ABC.This article is part of the Tackling clinical complexity in breast cancer Special Issue: https://www.drugsincontext.com/special_issues/tackling-clinical-complexity-in-breast-cancer/.

Keywords: CDK4/6 inhibitors; breast cancer; clinical complexity; comorbidities; polypharmacy; quality of life; real-life population.

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Conflict of interest statement

Disclosure and potential conflicts of interest: The authors declare that they have no conflicts of interest relevant to this article. The International Committee of Medical Journal Editors (ICMJE) Potential Conflicts of Interests form for the authors is available for download at: https://www.drugsincontext.com/wp-content/uploads/2023/05/dic.2023-1-7-COI.pdf

Figures

Figure 1
Figure 1
Barplots describing the frequency of patients who improved, worsened and remained stable from baseline to intermediate times for QLQ-C30 and QLQ-BR23 items. Barplot widths describe the relative frequency (%) of each category. QLQ-BR23, Quality of Life Questionnaire Breast Cancer Questionnaire; QLQ-C30, Quality of Life Questionnaire CORE 30.
Figure 2
Figure 2
Boxplots describing the frequency distribution of QLQ-C30 final scoring at baseline and corresponding change as function of CIRS score and number of therapies. Each boxplot describes from the bottom to the top: lowest non-outlier value, 25th percentile, median value, 75th percentile and top non-outlier value of the corresponding variable’s frequency distribution. Outliers with respect to the corresponding distribution are graphically represented as dots. QLQ-C30, Quality of Life Questionnaire CORE 30.

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