Literature DB >> 33963457

The impact of gender, age, race/ethnicity, and stage on quality of life in a spectrum of cutaneous lymphomas.

Xochiquetzal U Martinez1, Arnab Chowdhury2, Tracey Stiller2, Joycelynne Palmer2, Matthew Loscalzo3, Estella Barrios3, Farah R Abdulla1, Jasmine Zain4, Steven T Rosen4,5, Christiane Querfeld6,7.   

Abstract

PURPOSE: Cutaneous lymphomas (CLs) are a group of rare, potentially disfiguring and disabling cancers that can have a significant impact on quality of life (QoL). While previous studies have shown that mycosis fungoides (MF) and Sézary syndrome (SS) impair QoL, the effect of other types of CL on QoL has not been evaluated.
OBJECTIVE: To determine the impact of disease on QoL in all CL patients and to assess how QoL between the CL sub-types varies by demographic and clinical factors.
METHODS: The Cutaneous Lymphoma Distress Questionnaire (CL-DQ) was used to assess QoL. All CL patients seen in a multidisciplinary CL clinic were screened for eligibility. Questionnaire responses were collected over a 22-month period between 2017 and 2019. A cross-sectional analysis of CL-DQ scores from an initial visit was performed to determine the effect of disease on QoL across CL sub-types and the potential impact of patient demographics, CL sub-type, and type of treatment.
RESULTS: The study population consisted of 151 patients presenting with distinct types of cutaneous B- and T-cell lymphomas. Notable across the study population were the findings of frustration (44%), worry about progress/spread (43%), itching/pruritus (32%), and embarrassment/shame (28%). QoL was found to be most negatively affected in SS patients, females, younger patients, Black patients, and those with advanced stages of MF/SS.
CONCLUSIONS: Impairment of QoL due to CL correlates with gender, age, race/ethnicity, and stage of MF/SS. While the negative impact on QoL is most pronounced in SS patients, other CL sub-types also affect QoL and impact psychosocial distress. Our findings highlight the need for QoL assessment in all CL patients and further examination of disparities noted across demographic groups.
© 2021. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Cutaneous lymphoma; Mycosis fungoides; Psychosocial impact; Quality of life; Racial/ethnic disparities; Sézary syndrome

Mesh:

Year:  2021        PMID: 33963457      PMCID: PMC8801163          DOI: 10.1007/s00520-021-06241-6

Source DB:  PubMed          Journal:  Support Care Cancer        ISSN: 0941-4355            Impact factor:   3.603


  28 in total

1.  Quality of life of African-American and white long term breast carcinoma survivors.

Authors:  K Ashing-Giwa; P A Ganz; L Petersen
Journal:  Cancer       Date:  1999-01-15       Impact factor: 6.860

2.  Likert scales, levels of measurement and the "laws" of statistics.

Authors:  Geoff Norman
Journal:  Adv Health Sci Educ Theory Pract       Date:  2010-02-10       Impact factor: 3.853

3.  Health-related quality of life in patients with cutaneous T-cell lymphoma?

Authors:  Heather M Holahan; Ronda S Farah; Sara Fitz; Sarah L Mott; Nkanyezi N Ferguson; Julie McKillip; Brian Link; Vincent Liu
Journal:  Int J Dermatol       Date:  2018-08-03       Impact factor: 2.736

4.  Patients' Illness Perception as a Tool to Improve Individual Disease Management in Primary Cutaneous Lymphomas.

Authors:  Stefanie Porkert; Eva Lehner-Baumgartner; Julia Valencak; Robert Knobler; Elisabeth Riedl; Constanze Jonak
Journal:  Acta Derm Venereol       Date:  2018-02-07       Impact factor: 4.437

Review 5.  To be young, Black, and living with breast cancer: a systematic review of health-related quality of life in young Black breast cancer survivors.

Authors:  Cleo A Samuel; Laura C Pinheiro; Katherine E Reeder-Hayes; Jennifer S Walker; Giselle Corbie-Smith; Shekinah A Fashaw; Cheryl Woods-Giscombe; Stephanie B Wheeler
Journal:  Breast Cancer Res Treat       Date:  2016-09-06       Impact factor: 4.872

6.  Incidence and survival patterns of cutaneous T-cell lymphomas in the United States.

Authors:  Muhammad Hassaan Imam; Pareen J Shenoy; Christopher R Flowers; Adrienne Phillips; Mary Jo Lechowicz
Journal:  Leuk Lymphoma       Date:  2013-01-07

7.  Quality of life and psychological distress in patients with cutaneous lymphoma.

Authors:  F Sampogna; M Frontani; G Baliva; G A Lombardo; G Alvetreti; C Di Pietro; S Tabolli; G Russo; D Abeni
Journal:  Br J Dermatol       Date:  2008-12-16       Impact factor: 9.302

8.  Outcomes and prognostic factors in African American and black patients with mycosis fungoides/Sézary syndrome: Retrospective analysis of 157 patients from a referral cancer center.

Authors:  Shamir Geller; Emily Lebowitz; Melissa P Pulitzer; Steven M Horwitz; Alison J Moskowitz; Steve Dusza; Patricia L Myskowski
Journal:  J Am Acad Dermatol       Date:  2019-09-06       Impact factor: 11.527

Review 9.  On the importance of race, socioeconomic status and comorbidity when evaluating quality of life in men with prostate cancer.

Authors:  Scott D Ramsey; Steven B Zeliadt; Ingrid J Hall; Donatus U Ekwueme; David F Penson
Journal:  J Urol       Date:  2007-06       Impact factor: 7.450

10.  Willemze R, Cerroni L, Kempf W, et al. The 2018 update of the WHO-EORTC classification for primary cutaneous lymphomas. Blood. 2019;133(16):1703-1714.

Authors: 
Journal:  Blood       Date:  2019-09-26       Impact factor: 22.113

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  1 in total

1.  Top Ten Tips Palliative Care Clinicians Should Know About Caring for Patients with Cutaneous T Cell Lymphoma.

Authors:  Jennifer A Salant; Niloufer Khan; Judith E Nelson; Moe Norton-Westbrook; Anjali V Desai
Journal:  J Palliat Med       Date:  2021-12-31       Impact factor: 2.947

  1 in total

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