Article Text

Download PDFPDF

Physical activity trajectories following gynecological cancer: results from a prospective, longitudinal cohort study
Free
  1. Steven Fleming1,
  2. Tamara Jones2,
  3. Monika Janda2,3,
  4. Dimitrios Vagenas2,
  5. Leigh Ward4,
  6. Hildegard Reul-Hirche5,
  7. Carolina Sandler2,6,
  8. Andreas Obermair7 and
  9. Sandra Hayes8
  1. 1 College of Public Health, University of Kentucky, Lexington, Kentucky, USA
  2. 2 Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, Queensland, Australia
  3. 3 Centre for Health Services Research, The University of Queensland Faculty of Medicine, Brisbane, Queensland, Australia
  4. 4 School of Chemistry and Molecular Biosciences, The University of Queensland, Saint Lucia, Queensland, Australia
  5. 5 Physiotherapy Department, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia
  6. 6 School of Exercise and Nutrition Sciences, Queensland University of Technology, Brisbane, Queensland, Australia
  7. 7 Queensland Centre of Gynecological Research, Royal Brisbane and Women's Hospital, Brisbane, Queensland, Australia
  8. 8 Menzies Health Institute Queensland, Griffith University, Brisbane, Queensland, Australia
  1. Correspondence to Tamara Jones, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, QLD 4059, Australia; tamara.jones{at}connect.qut.edu.au

Abstract

Background Participating in physical activity after a diagnosis of cancer is associated with reduced morbidity and improved outcomes. However, declines in, and low levels of, physical activity are well documented in the broader cancer population, but with limited evidence following gynecological cancer.

Objective To describe physical activity levels from before and up to 2 years after gynecological cancer surgery; to explore the relationship between physical activity patterns and quality of life; and to describe characteristics associated with physical activity trajectories post-gynecological cancer.

Methods Women with gynecological cancer (n=408) participated in a prospective study that assessed physical activity and quality of life pre-surgery (baseline), at 6 weeks, and 3, 6, 9, 12, 15, 18 and 24 months post-surgery. Validated questionnaires were used to assess physical activity (Active Australia Survey) and quality of life outcomes (Functional Assessment of Cancer Therapy-General). Generalized estimating equation modeling, group-based trajectory analysis, and analysis of variance were used to identify physical activity levels over time, to categorize women into physical activity trajectory groups, and to assess the relationship between physical activity levels and quality of life, respectively.

Results Women had a mean±SD age of 60±11.4 years at diagnosis, with the majority diagnosed with endometrial cancer (n=235, 58%) or stage I disease (n=241, 59%). Most women (80%) started with and maintained low levels of physical activity (1–10 metabolic equivalent task hours per week), reported no physical activity throughout the follow-up period, or reduced physical activity levels over time. Only 19% of women maintained or doubled physical activity levels, so that by 24 months post-diagnosis they were engaging in sufficient levels of physical activity. Women with endometrial cancer (58% of the sample) were more likely to be overweight or obese and to report low levels of physical activity or none at all. Higher physical activity levels were associated with higher quality of life (p<0.05).

Conclusion The low baseline and surveillance levels of physical activity show that the vast majority of gynecological cancer survivors have the ability to improve their physical activity levels. Integration of physical activity advice and support into standard care could lead to gains in quality of life during gynecological cancer survivorship.

  • quality of life (PRO)/palliative care
  • postoperative period
  • miscellaneous
  • gynecology
  • gynecologic surgical procedures
View Full Text

Statistics from Altmetric.com

HIGHLIGHTS

  • Two years post-diagnosis, less than one-third of women met physical activity recommendations.

  • Only 20% of women increased or maintained sufficient levels of physical activity during the survivorship period.

  • Higher levels of physical activity were associated with higher quality of life.

INTRODUCTION

Gynecological cancers (including malignant neoplasms of the ovary, uterus, vulva, vagina, and cervix) account for ~10% of all new cancer diagnoses and are the third most common cancers for women in developed countries, such as Australia and the United States of America.1 However, differences in diagnostic and treatment characteristics between gynecological cancer types, and patient characteristics, may influence post-diagnosis physical activity levels.2

Taking part in 150 min moderate-intensity physical activity each week (10 metabolic-equivalent-task hours/week (MET-hours/week))3–5 represents a message consistently promoted to cancer survivors by cancer organizations worldwide.6 7 Research demonstrates that meeting physical activity recommendations is associated with reduced morbidity and improvements in physical function, psycho-social outcomes, and quality of life during and post-treatment.8 9 A recent systematic review and meta-analysis has demonstrated that participating in higher levels of pre- or post-diagnosis physical activity is associated with improved all-cause mortality for 10 cancer types, including gynecological cancer, in comparison with those in the lowest physical activity category.10 Post-diagnosis physical activity has also been associated with greater reductions in all-cause mortality, compared with pre-diagnosis physical activity.11

Despite these benefits, declines in, and low levels of, physical activity have been documented in people with cancer, with reductions associated with the development of additional, more severe treatment-related side effects, poorer treatment response, and reduced quality of life.12 13 Findings from a population-based breast cancer cohort study suggest that while ~50% of cancer survivors are sufficiently active at diagnosis, by 12 months post-diagnosis only one in three is sufficiently active.4 Furthermore, 60% experience declines in physical activity from pre- to post-diagnosis (5.7±2.9 months) by an average of 15 MET-hours/week.4

Few studies to date have focused on women with gynecological cancer. Those that have were largely cross-sectional, with few high-quality prospective studies.14–16 Furthermore, of the limited prospective evidence, two of three studies used retrospective recall of pre-diagnosis physical activity.14–16 Findings from the limited evidence involving women with gynecological cancer indicate that the majority are insufficiently active or sedentary post-treatment and experience declines in physical activity of a similar magnitude to those reported in breast cancer cohort studies.16–21 There is a clear dearth of prospective information regarding physical activity pre- and post-treatment of gynecological cancer and whether the relationship between physical activity and quality of survival is consistent with other cancer types. Thus, the purpose of this study was to: (1) describe physical activity levels from before and up to 2 years after gynecological cancer surgery; (2) explore the relationship between patterns of physical activity post-gynecological cancer surgery and quality of life; and (3) describe diagnostic and treatment characteristics associated with patterns of physical activity post-gynecological cancer.

METHODS

Study Design and Subjects

The Lymphoedema Evaluation in Gynecological cancer Study is a prospective, longitudinal cohort study that followed up 408 women from before to 24 months after surgery for gynecological cancer (endometrial, ovarian, and other: n=233, 112 and 59, respectively).22 23 Women with newly diagnosed gynecological cancer (International Classification of Diseases Codes C51–C58) between June 1, 2008 and February 28, 2011, aged 18 years or older, and treated (surgery with or without adjuvant therapy) at one of six hospitals in Australia, were eligible for enrolment. Lower-limb lymphedema was the primary outcome for this cohort study, but physical activity and quality of life were two of several secondary outcomes. Ethical approval was obtained from hospital human research ethics committees (approval numbers: 2008000211, 2007/168, 200842, 1189A/P, 08/16, 10/14, 10/10/RPAH/28).

Timing of Data Collection

Following written informed consent, data were collected at baseline during the pre-operative visit (survey 1,~1 week pre-diagnostic surgery), and during hospital follow-up visits, at 6 weeks, and 3, 6, 9, 12, 15, 18, 21, and 24 months post-surgery (surveys 2–10, respectively). Follow-up assessments were coordinated with each participant’s scheduled appointments; therefore, data were collected a maximum of 10 times over the follow-up period.

Data Collection

Physical activity was measured using the Active Australia Survey.24 This reliable and valid survey asks respondents to estimate the time spent during the previous week walking, and engaging in moderate- and vigorous-intensity physical activity.24 Reported minutes are weighted by the MET value, the ratio of energy expended from physical activity compared with sitting quietly. MET weights of 3.0, 4.0, and 7.5 for walking, moderate- and vigorous-intensity activity, respectively, are used to estimate MET-hours/week of physical activity.25 A clinically relevant difference between groups or over time was defined a priori as >2 MET-hours/week.3 4

Participants provided quality of life information using the Functional Assessment of Cancer Therapy–General Survey.26 This 27-item validated survey assesses well-being in physical, social/family, emotional, and functional domains and total quality of life. A clinically relevant difference between groups or over time was defined a priori as >5 units27 We expected patients reporting higher physical activity would also have better quality of life. Relevant diagnostic, treatment, and patient characteristics were abstracted from medical records by trained research nurses. Patient characteristics relating to socioeconomic status and marital status were collected via a participant-administered questionnaire.

Statistical Analysis

Analyses were conducted using statistical analysis software (SAS) (SAS Institute, Gary, North Carolina, USA). Proportions were used to describe patient, diagnostic, and treatment characteristics within gynecological cancer groups (endometrial, ovarian, and other, including cervical and vulva/vaginal cancer). Using all available data at each data collection period (baseline plus up to nine follow-up periods), generalized estimating equations with exchangeable correlation structures were used to identify statistically significant trends over time in physical activity, including total physical activity (MET-hours/week) and hours/week of walking, moderate- and vigorous-intensity activity. Women were then categorized into physical activity trajectories based on total MET-hours/week and group-based modeling theory. The application of such a theory has been used for over 25 years in the development of abnormal psychology and criminology literature,28 29 but only more recently in epidemiology.30 31 Descriptive statistics (n, %) were used to identify relationships between physical activity trajectory groups and patient, diagnostic, and treatment characteristics deemed clinically relevant (>20% difference between groups).

Analysis of variance was applied to determine if there were differences in mean quality of life (data were normally distributed) between physical activity groups over time. For this analysis, we used baseline data from survey 1 but for the other three time periods, we averaged physical activity and quality of life measures over multiple surveys (surveys 2–3 for period 2, surveys 4–6 for period 3, and surveys 7–10 for period 4).

RESULTS

All participants completed baseline assessment, with retention rates of 86%, 84%, and 78% at time periods 2, 3, and 4, respectively. Characteristics of those with complete (all four time periods) and those with incomplete follow-up data were similar, except that those with incomplete data were more likely to die during the study period, have received chemotherapy, and been diagnosed with stage III disease.22 Descriptive statistics of characteristics of the sample (n=408) are presented in Table 1 (a more extensive summary has been previously presented).22 In summary, women had a mean±SD age of 60±11.4 years at diagnosis, with the majority diagnosed with endometrial cancer (n=235, 58%) or stage I disease (n=241, 59%). Most were post-menopausal (n=326, 80%) and either overweight or obese (body mass index ≥25 kg/m2; n=307, 75%). Higher proportions of women with cervical or vulva/vaginal cancer were aged <60 years, compared with those with ovarian or endometrial cancer. Compared with other gynecological cancers, higher proportions of women with ovarian cancer were diagnosed with stage III+ disease and higher proportions of overweight and obese women were diagnosed with endometrial cancer. Overall, these characteristics are representative of the wider gynecological cancer population. Baseline physical activity was similar across gynecological cancers, with up to 68% of women who provided baseline physical activity data classified as sedentary (<0.67 MET-hours/week) or participating in low levels (0.67–10 MET-hours/week) of weekly physical activity.3–5

Table 1

Descriptive characteristics of the study sample (n=408 women with gynecological cancer)

Table 2 reports descriptive statistics on physical activity from baseline to 24 months post-diagnosis, showing that mean total physical activity (MET-hours/week) increased from baseline to >15 months post-diagnosis (p<0.002), with increases in moderate- (including walking, p<0.002) and vigorous-intensity activity (p<0.02) contributing to these changes. A steady increase in physical activity was observed between baseline and 6–12 months post-diagnosis, equating to a twofold increase in MET-hours/week. When calculating this increase according to means, the increase in MET-hours/week is largely driven by increases in walking, as only small changes in moderate- and vigorous-intensity physical activity were observed. Group-based trajectory analysis of physical activity from baseline to 15–24 months post-diagnosis found five groups provided the best fit, and quadratic trajectories provided the most parsimonious model. Figure 1 shows the five trajectories of physical activity summarizing MET-hours/week including walking, moderate- and vigorous-intensity activity. Group 1 (labeled ‘sedentariates’) and group 2 (labeled ‘physically inactive’) remained flat over the post-diagnosis study period. Sedentariates (n=15, 3.7%) reported virtually no physical activity and experienced no change over the 2 year follow-up. The physically inactive (n=297, 72.8%) started and remained at a relatively low level (<10 MET-hours/week). Group 3, labeled ‘doublers’ (n=70, 17.2%) started at ~14 MET-hours/week but doubled physical activity over the 2-year study period, while group 4, ‘downsizers’ (n=16, 3.9%) reported high levels of baseline physical activity but reduced activity by two-thirds over the 2-year follow-up period. Group 5 (labeled ‘enthusiasts’; n=10, 2.5%) started and remained at high physical activity levels (~55 MET-hours/week) throughout the follow-up period.

Figure 1

Trajectories of physical activity levels from pre-diagnosis to 24 months post-diagnosis of gynecological cancer. Group 1 ‘sedentariates’=3.7% of women; group 2 ‘physically inactive’=72.8%; group 3 ‘doublers’=17.2%; group 4 ‘downsizers’=3.9%; group 5 ‘enthusiasts’=2.5%. T1=baseline; T2=6 weeks to 3 months post-diagnosis; T3=6 to 12 months post-diagnosis; T4=15 to 24 months post-diagnosis.

Table 2

Physical activity levels in hours per week from baseline to 24 months post-diagnosis of women with gynecological cancer

Figure 2 presents descriptive quality of life statistics for the five physical activity groups from baseline to 15–24 months post-diagnosis. There were significant differences (p<0.05) in mean quality of life between groups at baseline, with quality of life highest for enthusiasts and lowest for the physically inactive (Tukey honest significant difference test=15.9 (95% CI 0.54 to 31.2). For the three follow-up periods, there were clinically relevant (>5 units) differences between groups, with enthusiasts continuing to report the highest quality of life compared with all other groups, although differences were not supported statistically. Also, of note, the physically inactive (p<0.01) and doublers (p>0.05) reported clinically relevant improvements in mean quality of life over time. Table 3 shows higher proportions of women aged <60 years and obese women in the sedentariates group compared with other groups. Women in the enthusiasts group were more likely to be diagnosed with ovarian cancer, have stage III disease, have had lymph node removal, and/or received chemotherapy as their only form of adjuvant treatment.

Figure 2

Quality-of-life from baseline to 24 months post-diagnosis of women with gynecological cancer by physical activity groups T1= baseline; T2=6 weeks to 3 months post-diagnosis; T3=6 to 12 months post-diagnosis; T4=15 to 24 months post-diagnosis. *FACT-G=functional assessment of cancer therapy–general; †mean (SD).

Table 3

Unadjusted relationships* between diagnostic, treatment and patient characteristics and membership in each of the five physical activity trajectory groups

DISCUSSION

On average, there was an increase in time spent walking and engaging in moderate- and vigorous-intensity physical activity from before to 24 months after surgery for gynecological cancer. However, trajectory analyses showed that these results are due to high and increasing levels of physical activity among a small group. Very few women reported sufficient physical activity pre- or post-gynecological cancer surgery. Almost 70% were sedentary or insufficiently active at diagnosis, and by 24 months post-diagnosis fewer than one in three met physical activity recommendations (that is, >150 min/week of moderate-intensity physical activity, equivalent to ≥10 MET-hours/week). Further, when grouped according to post-cancer physical activity patterns, only 20% increased or maintained sufficient physical activity levels throughout the survivorship period. The majority were insufficiently active (physically Inactive) or sedentary (sedentariates) pre-diagnosis and remained so 24 months post-diagnosis. For 4% of women, diagnosis and/or gynecological cancer treatment was associated with steep declines in physical activity, so that by 6–12 months post-diagnosis their average weekly MET-hours/week were half their pre-diagnosis levels (downsizers, 3.9%). Together, downsizers, sedentariates, and physically inactive accounted for >80% of our gynecological cancer sample.

Findings suggest that physical activity levels are probably associated with quality of life, with those reporting the highest levels of physical activity (enthusiasts) also reporting the highest quality of life from before to 24 months after diagnosis. The positive relationship between physical activity and quality of life has been previously demonstrated among several cancer cohorts, including patient with gynecological cancer.17 32 33 However, longitudinal findings from this paper contribute to the evidence by demonstrating the positive relationship between change in physical activity and quality of life improvements. Results show those reporting increases in physical activity (physically inactive and doublers) achieved commensurate increases in quality of life. Additionally, while the physically inactive failed to meet physical activity recommendations, increases in physical activity were still associated with quality of life improvements. These findings highlight the importance of recommending physical activity and show that some activity is better than no activity, which is in line with internationally endorsed physical activity recommendations.7 34 35 Improvements in quality of life may be achieved through avoiding inactivity, engaging in as many physical activities as possible, and progressing towards and maintaining physical activity levels.

The physical activity levels reported here are consistent with those reported following breast cancer diagnosis,4 but differences between gynecological cancers were identified. Specifically, sedentariates had a higher proportion of women with endometrial cancer and obese women (double that of other groups). In contrast, enthusiasts had a higher proportion of women with ovarian cancer, those >60 years, diagnosed with stage III disease, and receiving chemotherapy. These findings suggest that gynecological cancer type, or characteristics associated with developing particular gynecological cancers may contribute to the relationship observed between characteristics and physical activity behaviors. For example, obesity is a significant risk factor for endometrial cancer36 37 and women in the sedentariates (who exercised less) were more likely to be obese with endometrial cancer; however, this is based on a small subgroup (n=15).

Understanding the characteristics of physical activity trajectory groups provides insight into how to individually tailor interventions from a behavior change perspective, as well as determining the initial level of physical activity and capacity for change. For example, obese women with endometrial cancer may benefit from the incorporation of physical activity into cancer care by preventing chronic disease and improving survivorship outcomes. Thus, physical activity interventions may focus on understanding lifestyle behaviors (lack of physical activity and obesity) and building self-efficacy. Specifically, the level of physical activity may start low, with the intervention duration period accommodating movement from pre-contemplation through to maintenance and termination stages of behavior change.38 Conversely, women with more advanced ovarian cancer may benefit from interventions focusing on the role of physical activity in the management of physical and psychological side effects during and after treatment. Given the higher proportions of women with ovarian cancer among the enthusiasts, it is plausible that the intervention should target maintenance of physical activity and prevention of declines, together with developing self-efficacy and strategies for overcoming novel exercise barriers arising as a consequence of treatment. However, the vast majority of participants (80%) were insufficiently active and unable to increase or maintain sufficient physical activity levels. Therefore, there is scope for physical activity interventions to be delivered to all women diagnosed with gynecological cancer. Flexible approaches to delivery and individualized interventions could allow for targeted support for women with differing demographic and diagnostic characteristics.

Of equal importance is understanding determinants of physical activity trajectories. Particularly, why some women increase their physical activity (doublers), whereas others decrease (downsizers). Clinical factors, including lymphedema, anthropometric factors (eg, body mass), and social factors (eg, social support networks), may contribute to physical activity trajectory and inform treatment strategies. To date, lifestyle intervention trials in the gynecological cancer setting are scarce. Nonetheless, findings from published trials suggest that physical activity support or exercise intervention during and after gynecological cancer treatment is feasible, safe, and effective at improving physical activity and health outcomes.39 40 Improved understanding of determinants of physical activity trajectories will inform the design and testing of future intervention trials, which if proved to be successful, can be translated to clinical practice.

Key strengths of this work include its prospective, longitudinal design with a 2-year post-diagnosis follow-up, recruitment of a sample with characteristics generalizable to the wider gynecological cancer population, and the classification of women based on post-diagnosis physical activity patterns. Physical activity was not assessed objectively, and self-reported physical activity levels are more likely to be overestimated41, placing these findings in the conservative direction. Additionally, while these data provide insufficient power for adjusted analyses, results provide pilot findings to support future research, including more in-depth analysis of characteristics associated with physical activity trajectories. Thus, these epidemiological findings represent unique and important contributions to the gynecological survivorship field. Furthermore, while findings reflect associations rather than causal relationships, they contribute to a compelling and growing evidence demonstrating the potential for improving cancer survivorship by incorporating physical activity intervention into standard care. Future research must focus on developing and implementing safe and cost-effective strategies to influence changes in physical activity during and beyond cancer treatment.

In summary, findings demonstrate that the vast majority of gynecological cancer survivors are insufficiently active and have significant capacity for improvement in physical activity, highlighting a clear need for the formal integration of physical activity advice and support into standard gynecological cancer care. Understanding how to translate this evidence into practice is an important next step for researchers, clinicians, policy makers and cancer survivors.

Supplemental material

Acknowledgments

We would like to acknowledge the invaluable contributions of the women who participated in this study.

References

View Abstract

Footnotes

  • Contributors All authors have provided a substantial contribution to this work.

  • Funding This work was supported by project grants and fellowships from Cancer Council Australia, Cancer Australia, Greenslopes Hospital Research Foundation, Wesley Research Foundation, National Breast Cancer Foundation (SH), Cancer Council Queensland (SH) and the National Health and Medical Research Foundation (MJ).

  • Competing interests AO is the founder and managing director of SurgicalPerformance Pty Ltd, an Australian, private company that provides surgeons with a platform for collection of surgical outcome audit data; AO received travel grants from the O.R. Company (formerly Tyco Healthcare) and is a consultant for Covidien, NSW, Australia.

  • Patient consent for publication Not required.

  • Ethics approval All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data availability statement Data are available upon reasonable request. Deidentified participant data available from Tamara Jones upon reasonable request (see Corresponding author information).

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.