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Sexual quality of life in the cancer continuum
Author(s) -
Srilatha Balasubramanian,
Leong Jayne Chiara,
Ong Yew Jin
Publication year - 2017
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/cncr.30448
Subject(s) - survivorship curve , quality of life (healthcare) , sexual function , feeling , medicine , population , cancer , clinical psychology , human sexuality , gerontology , psychology , social psychology , nursing , gender studies , environmental health , sociology
In their original article, Jackson et al present impressive descriptive data supporting a nearly equal distribution of sexual function and/or dysfunction in cancer survivors in comparison with a large cancer-free population cohort. Although this new evidence is reassuring, a critical review of the take-home message is imperative from several standpoints. Thus far, the clinical data show reductions (40%-100%) in the multifarious components of sexual health and related quality of life across generic cancer types in both men and women. Not surprisingly, Jackson et al indeed identified significant levels of dissatisfaction in survivors with their sex life after cancer; satisfaction is a multidimensional aspect within sexual health–related quality of life and is often worsened, is at times unchanged, and is rarely enhanced during survivorship. This being so, the presented data still do not explain the role of the type and extent of sexual or other concerns in the genesis of survivors’ dissatisfaction with their overall sex life. On this note, the inclusion characteristics are also constrained. Some pertinent variables affecting quality of life in survivorship may be related to physical ability, emotional intimacy, relationship quality, and social-life adjustments. Furthermore, there is a lack of information on any prevailing psychological impact, which can be as much as 35% to 50% in the cancer continuum. This has negative attributes for sexual quality and satisfaction and leads to feelings of sexual inadequacy. Ideally, a measure of the level of sexual function and/or satisfaction before the diagnosis and treatment of cancer would have been a valid indicator for the control function. In addition, useful corroborative information would have been gathered when both the survivors and their partners were assessed. Even if these were beyond the scope of the study, one may still question the comprehensiveness of preexisting or coexisting morbidities for sexual function and satisfaction. Although the simplified comorbidity score (0-5) used in the study conforms to significant prevalence in the older survivors, data on several classic risk factors for sexual problems, such as obesity (body mass index), anxiety, depression, prescription medications, smoking, and alcohol use, are not available. Taken together, the study findings allow a generalized interpretation of normative sexual behavior after cancer; however, there are some methodological pitfalls. At the outset, the authors indicated that 67% of the study population completed measures of sexual attitudes and behavior (self-report) and were included in the analyses. This may mean an inclusion bias of data collection from only those respondents comfortable with reporting sexual health matters versus those who were, among other possibilities, either too stigmatized or distressed about their sexual problems (33%). Furthermore, the population sampling, though large enough, does not seem to be representative of generic cancer prevalence. With the average incidence of any cancer diagnosis in those aged 50 to 74 years being 53%, a survival rate of 52% also includes data estimates for the proportion of cured patients in survivorship of 21% to 47% for men and 38% to 59% for women. In contrast to these wide-ranging figures, the cancer incidence in the study population was 7.4% for men and 9.2% for women. The sample size became further simplified with stratification by the time since diagnosis (< or 5 years). Matching this small study group with a huge reservoir of control subjects could be a potential shortcoming. For instance, the level of sexual functioning, activities, and concerns of the cancer survivors were matched with data from a vast and variable number of k> 2 cancer-free controls with a probability for larger biases that may preclude precision. Although a huge sample size for the control group can mask any true variability in responses for a meaningful comparison, data from small sample sizes (for survivors) are also likely to be compromised in their statistical power, as agreed by the researchers. The resulting professional concern here is that an extrapolation of sexual normalcy after cancer based on the study data could be misguiding. This is particularly important because the results from a large population study are expected to be more generalizable than those from any narrow representative surveys. Five years after cancer, survivorship is focused on the overall quality of life, and under this umbrella, sexuality still remains an infrequently met clinical concern; this problem occurs far and wide, regardless of cultural or ethnic variability depicted in the literature. Nevertheless, findings of healthy sexuality on par with a normal agematched population will have a substantial impact on the knowledge base. However, because of the limitations, it is difficult at this time to accept the lack of significant differences in estimated measures of sexual functioning in the studied population.

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