Outcomes of Different Quality of Life Assessment Modalities After Breast Cancer Therapy

Author:

Kastora Stavroula Lila12,Holmquist Alexander3,Valachis Antonios4,Rocco Nicola56,Meattini Icro78,Somaiah Navita9,Peled Anne10,Chatterjee Abhishek11,Catanuto Giuseppe612,Tasoulis Marios Konstantinos913,Nava Maurizio Bruno,Poortmans Philip1415,Pusic Andrea16,Masannat Yazan217,Karakatsanis Andreas318

Affiliation:

1. University College London, UCL EGA Institute for Women’s Health, London, United Kingdom

2. School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, United Kingdom

3. Department of Surgical Sciences, Faculty of Medicine, Uppsala University, Uppsala, Sweden

4. Department of Oncology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden

5. Department of Advanced Biomedical Sciences, University of Naples Federico II, Naples, Italy

6. G.RE.T.A. Group for Reconstructive and Therapeutic Advancements, Milan, Naples, and Catania, Italy

7. Department of Experimental and Clinical Biomedical Sciences M. Serio, University of Florence, Florence, Italy

8. Radiation Oncology Unit, Oncology Department, Florence University Hospital, Florence, Italy

9. Division of Radiotherapy and Imaging, Institute of Cancer Research, London, United Kingdom

10. Sutter Health California Pacific Medical Center, San Francisco

11. Division of Surgical Oncology and Plastic Surgery, Tufts Medical Center, Boston, Massachusetts

12. Humanitas, Institute Clinico Catanese–Misterbianco, Catania, Italy

13. Breast Unit, Royal Marsden NHS Foundation Trust, London, United Kingdom

14. Department of Radiation Oncology, Iridium Netwerk, Wilrijk-Antwerpen, Belgium

15. Faculty of Medicine and Health Sciences, University of Antwerp, Wilrijk-Antwerpen, Belgium

16. Division of Plastic and Reconstructive Surgery, Brigham and Women’s Hospital, Boston, Massachusetts

17. Aberdeen Royal Infirmary, Breast Surgery, NHS Grampian, Aberdeen, United Kingdom

18. Section for Breast Surgery, Department of Surgery, Uppsala University Hospital (Akademiska), Uppsala, Sweden

Abstract

ImportanceImprovement in clinical understanding of the priorities of patients with breast cancer (BC) regarding postoperative aesthetic outcomes (AOs) is needed.ObjectiveTo assess expert panel and computerized evaluation modalities against patient-reported outcome measures (PROMs), the gold standard of AO assessment, in patients after surgical management of BC.Data SourcesEmbase, MEDLINE, PsycINFO, PubMed, the Cochrane Central Register of Controlled Trials, the World Health Organization International Clinical Trials Registry Platform, and ClinicalTrials.gov were interrogated from inception through August 5, 2022. Search terms included breast conserving AND aesthetic outcome AND breast cancer. Ten observational studies were eligible for inclusion, with the earliest date of database collection on December 15, 2022.Study SelectionStudies with at least 1 pairwise comparison (PROM vs expert panel or PROM vs computerized evaluation with Breast Cancer Conservation Treatment cosmetic results [BCCT.core] software) were considered eligible if they included patients who received BC treatment with curative intent. Studies reporting solely on risk reduction or benign surgical procedures were excluded to ensure transitivity.Data Extraction and SynthesisTwo independent reviewers extracted study data with an independent cross-check from a third reviewer. The quality of included observational studies was assessed using the Newcastle-Ottawa Scale, and the level of evidence quality was assessed using the Grading of Recommendations Assessment, Development and Evaluation tool. Confidence in network meta-analysis results was analyzed with the Confidence in Network Meta-analysis semiautomated tool. Effect size was reported using random-effects odds ratios (ORs) and cumulative ratios of ORs with 95% credibility intervals (CrIs).Main Outcomes and MeasuresThe primary outcome of this network meta-analysis was modality (expert panel or computer software) discordance from PROMs. Four-point Likert responses across PROMs, expert panel assessment, and BCCT.core evaluation of AOs were assessed.ResultsA total of 10 observational studies including 3083 patients (median [IQR] age, 59 [50-60] years; median [range] follow-up, 39.0 [22.5-80.5] months) with reported AOs were assessed and homogenized in 4 distinct Likert response groups (excellent, very good, satisfactory, and bad). Overall network incoherence was low (χ22 = 0.35; P = .83). Overall, panel and software modalities graded AO outcomes worse than PROMs. Specifically, for excellent vs all other responses, the panel to PROM ratio of ORs was 0.30 (95% CrI, 0.17-0.53; I2 = 86%) and the BCCT.core to PROM ratio of ORs was 0.28 (95% CrI, 0.13-0.59; I2 = 95%), while the BCCT.core to panel ratio of ORs was 0.93 (95% CrI, 0.46-1.88; I2 = 88%).Conclusions and RelevanceIn this study, patients scored AOs higher than both expert panels and computer software. Standardization and supplementation of expert panel and software AO tools with racially, ethnically, and culturally inclusive PROMs is needed to improve clinical evaluation of the journey of patients with BC and to prioritize components of therapeutic outcomes.

Publisher

American Medical Association (AMA)

Subject

General Medicine

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