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Journal of Physiotherapy 66 (2020) 70–72

j o u r n a l h o m e p a g e : w w w. e l s ev i e r. c o m / l o c a t e / j p hy s

Editorial

Cancer rehabilitation
Amy M Dennett a,b, Mark R Elkins c,d
a
Allied Health Clinical Research Office, Eastern Health, Melbourne, Australia; b La Trobe Sport and Exercise Medicine Research Centre, La Trobe University, Melbourne, Australia;
c
Editor, Journal of Physiotherapy; d Faculty of Medicine and Health, University of Sydney, Sydney, Australia

This editorial introduces another of Journal of Physiotherapy’s repeated activities.14,15 The next paper in this collection, however,
article collections.1,2 These are collections of papers in a specific field shows that such guidelines were not based on evidence.
of research, published in the Journal of Physiotherapy within the past Paramanandam et al12 conducted a systematic review of rando-
decade and curated to: facilitate access to recent important findings mised trials of weight training in women with or at risk of developing
in the field; highlight trends in the study designs, methodology, breast cancer-related lymphoedema. Meta-analysing the data from
populations and interventions addressed by the research; and pro- over 1000 women, Paramanandam et al demonstrated that weight
vide a scoping overview of avenues for further research. training did not worsen lymphoedema if it was already present, and
The focus of this article collection is cancer rehabilitation. The weight training did not increase the risk of lymphoedema among
World Health Organization estimates that globally in 2018 there were women who did not have it. Guidelines subsequently changed
18.1 million new cases of cancer and 9.6 million deaths from cancer.3 to remove the restriction on weight training and to encourage exer-
Globally, one in five men and one in six women develop cancer cise.16-18
during their lifetime, and one in eight men and one in eleven women The third breast cancer study in this collection was a randomised
die from cancer.3 This all contributes to its very high disease burden. trial of manual lymph drainage to prevent the development of breast
What these figures also reveal, though, is that a large proportion of cancer-related lymphoedema.13 This is particularly welcome evi-
people diagnosed with cancer survive their cancer. This is reflected in dence, given that the most recent Cochrane review on the topic found
the improved survival data for several types of cancer, particularly in insufficient evidence to make a recommendation about whether
high-income countries.3–6 manual lymph drainage prevents lymphoedema. The long-term trial
Cancer survivors may retain many residual impacts of the disease by Devoogdt et al13 enrolled 160 participants with breast cancer and
and its treatment. Although these impacts are diverse, many of these randomised half of them to undertake manual lymph drainage. Even
impacts are physical, such as cachexia, lymphoedema, dyspnoea and with five years of follow-up, and measurement of lymphoedema in
limited joint range of motion.7 This situation of improving survival multiple ways, the trial was unable to identify any clear preventive
with residual physical impairments creates an enormous need for effect of manual lymph drainage on the risk of developing
acute care and longer-term rehabilitation.8 In response to the need lymphoedema.
for evidence to guide such intervention, there has been an expo- Another type of cancer where physiotherapists have a large role to
nential accumulation of evidence in the oncology subdiscipline of the play is lung cancer. Fortunately for readers of Journal of Physiotherapy,
Physiotherapy Evidence Database (www.PEDro.org.au), as shown in Dr Catherine Granger’s invited topical review19 expertly summarises
Figure 1. Oncology content is constituting an exponentially increasing the available evidence about the burden associated with lung cancer,
percentage of the PEDro database, as shown in Figure 2. Accordingly, the management of lung cancer with a particular focus on physio-
various national guidelines now recommend referral to physiother- therapy interventions, and future directions for research and clinical
apists or other professionals with appropriate expertise for exercise practice.
prescription and other physical interventions to prevent and reduce The remaining articles in this collection relate to exercise for
long-term, adverse effects and disability.9,10 cancer, and studied mixed populations rather than a specific type of
Several of the studies in this article collection relate to breast cancer.20–22 A common sequela of many types of cancer is cancer-
cancer.11–13 The systematic review by Neil-Sztramko et al11 summa- related fatigue. The systematic review by Meneses-Echávez et al20
rises the results of 85 studies of the physical function of women who summarised data on over 1500 participants and showed that super-
had been diagnosed with breast cancer. The results of formal tests of vised physical activity reduces fatigue among people who have been
aerobic fitness were generally very poor compared to predicted diagnosed with cancer. Specifically, combined aerobic and resistance
values, although on functional exercise tests like the 6-minute walk training with or without stretching are effective exercise regimens for
test, the women performed close to their healthy age-matched peers. reducing cancer-related fatigue. This is a welcome addition to the
Upper limb strength was also very poor. Lower limb strength was not other benefits of exercise in cancer, which include reduced anxiety
as affected, with reduced results during active treatment of the and depression, improved muscle strength and mass, physical func-
cancer but improving to above average thereafter. Simple tests of tion and quality of life.23,24 Dennett et al21 extended this evidence by
mobility also showed some impairment. Given the proximity of sur- demonstrating that moderate-intensity exercise safely reduces fa-
gery and radiotherapy, it is not surprising that the upper limb would tigue and improves walking endurance in cancer survivors. This led to
be more affected than the lower limb, but disuse may also be a further investigation into ways to improve the amount of moderate-
contributor. Many of the studies in the review by Neil-Sztramko intensity exercise done by cancer survivors. Dennett et al22 subse-
et al11 were conducted at a time when clinical practice guidelines quently conducted a trial of adding motivational interviewing to
advised against lifting heavy weights or children and to avoid doing oncology rehabilitation to see if it would increase the amount of

https://doi.org/10.1016/j.jphys.2020.03.004
1836-9553/© 2020 Australian Physiotherapy Association. Published by Elsevier B.V. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/
licenses/by-nc-nd/4.0/).
Editorial 71

Figure 1. Cumulative oncology content on the Physiotherapy Evidence Database (PEDro) by article type, based on November 2019 update of the database.

Figure 2. Cumulative oncology content on the Physiotherapy Evidence Database (PEDro) as a percentage of the overall database content, based on November 2019 update of the
database.

moderate-intensity physical activity undertaken. This study gener- In summary, this article collection includes a range of important de-
ated clear estimates that motivational interviewing wasn’t effective in velopments in cancer rehabilitation research. The study designs address
this regard; however, possible effects on reducing sedentary behav- the prevelance of cancer sequelae,11 treatment of sequelae,12,20–22 pre-
iour were identified that are worthy of further investigation. Despite vention of sequelae,12,13,19 and adherence to recommended long-term
the known benefits of exercise, low levels of physical activity remain self-management with physical activity.22 Importantly, each paper has
an issue for people after oncology rehabilitation; therefore, support to clear implications for clinical physiotherapists, which are identifiable in
increase physical activity beyond rehabilitation is needed. the paper’s ‘What this study adds’ summary box.
72 Editorial

Ethics approval: Not applicable. 11. Neil-Sztramko SE, et al. J Physiother. 2014;60:189–200.
12. Paramanandam VS, et al. J Physiother. 2014;60:136–143.
Competing interest: Nil. 13. Devoogdt N, et al. J Physiother. 2018;64:245–254.
Source of support: Nil. 14. Cancer Research UK. Breast cancer - UK incidence statistics: Cancer Research UK.
Acknowledgement: Nil. 2011. Available at: http://info.cancerresearchuk.org/cancerstats/types/breast/
incidence/. Accessed December 15, 2011.
Provenance: Invited. Not peer reviewed.
15. Breast Cancer Care. Risk of lymphoedema: Breast Cancer Care. 2011. Available at:
Correspondence: Mark R Elkins, Centre for Education & Workforce http://www.breastcancercare.org.uk/breast-cancer-information/treating-breastca
Development, Sydney Local Health District, Sydney, Australia. Email: ncer/lymphoedema/risk-lymphoedema. Accessed December 16, 2011.
mark.elkins@sydney.edu.au 16. Centre for Clinical Practice at the National Institute for Health and Care Excellence.
Advanced breast cancer: diagnosis and treatment (CG81). 2017. Available at:
https://www.nice.org.uk/guidance/cg81. Accessed November 12, 2019.
17. Centre for Clinical Practice at the National Institute for Health and Care Excellence.
References Early and locally advanced breast cancer: diagnosis and management (NG101).
2018. Available at: https://www.nice.org.uk/guidance/ng101. Accessed November
1. Hush J, et al. J Physiother. 2018;64:208–209. 12, 2019.
2. Bonnevie T, et al. J Physiother. 2020;66:3–4. 18. Stuiver MM, et al. Cochrane Database Syst Rev. 2015;2:CD009765.
3. Bray F, et al. CA Cancer J Clin. 2018;68:394–424. 19. Granger C. J Physiother. 2016;62:60–67.
4. Bosetti C, et al. Ann Oncol. 2013;24:2657–2671. 20. Meneses-Echávez JF, et al. J Physiother. 2015;61:3–9.
5. Torre LA, et al. Cancer Epidemiol Biomarkers Prev. 2015;25:16–27. 21. Dennett AM, et al. J Physiother. 2016;62:68–82.
6. Steliarova-Foucher E, et al. Lancet. 2004;364:2097–2105. 22. Dennett AM, et al. J Physiother. 2018;64:255–263.
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9. Cormie P, et al. Med J Aust. 2018;209:184–187.
10. National Academies of Sciences, Engineering, and Medicine, Division HAM,
Services BOHC, National Cancer Policy Forum. Long-Term Survivorship Care Websites
After Cancer Treatment. National Academies Press 2018. https://doi.org/10.17226/
25043. PEDro www.pedro.org.au

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