Background: Oropharyngeal cancer is the most common type of head and neck cancers,
with a 5-years survival of 64.7%. In the last 40 years risk factors and etiology changed, from
the incidence associated mostly with tobacco and alcohol to HPV infection in 70% of the
cases. Treatments that are standard of care for OPSCC include chemotherapy, radiotherapy
or combination of surgery and radiotherapy have a high chronic treatment-related toxicity
and functional loss. These therapies have significant impact on the quality of life (QOL) of
survivors of oropharyngeal squamous cell carcinoma (OPSCC).
Objectives: The objective of this study is to review literature on 1-year evolution of quality of
life of patients treated for OPSCC with standard of care.
Methods: A comprehensive search of the literature of treated OPSCC patients assessed with
EORTC QLQ-30 EORTC H&N-35 at pre-treatment 12-month post treatment.
Results: The first study showed that standard of care treatment produces chronic side
effects, such as xerostomia, poor oral and dental health, dysphagia, feeding tube dependency
in, and other fibrotic changes likely caused by radiotherapy or combination of surgery and radiotherapy.
Conclusions: Standard of care treatment produces chronic side effects, such as xerostomia,
poor oral and dental health, dysphagia, feeding tube dependency in, and other fibrotic
changes.
INTRODUCTION
In 2017 the American Cancer Society reported 49670 news cases of and 9700
deaths from head and neck cancers, respectively, with a 5-year overall survival
of 64.7% (1-3). While the proportion of oropharyngeal squamous cell carcinoma
was approximately 20% of Head and Neck cancers in 1980s in the US, it currently
represents 70% (4,5). The current standard of care for advanced stages (III and IV)
OPSCC- including HPV related OPSCC- includes high doses of chemotherapy
(usually cisplatin based) and radiotherapy. The current standard of care treatment
for patients with locally advanced OPSCC is known to be highly toxic, and
these approaches leave survivors with significant and lifelong morbidity (6-11).
The short-term and long-term sequelae of OPSCC treatment are known to impact survivors quality of life. These include loss of
salivary function, dry mouth, sticky saliva, dental loss,
poor oral health, dysphagia, feeding tube dependency,
neck muscle dystonia, fibrotic loss of lower cranial
nerve function, pharyngeal and laryngeal stenosis, soft
tissue necrosis, chronic mucosal ulcerations, chronic
feeding tube dependency, muscle atrophy, and osteoradionecrosis.
Social, economic, and emotional factors
are permanently changed after cancer is successfully
cured. Even minimal damage to swallowing, talking,
eating and respiration diminish quality of life of the
patients.
Quality of life questionnaires evaluate multiple
dimensions of life that are of importance to patients.
One of the most used questionnaires in more than
3000 studies since 1993, European Organisation for
Research and Treatment of Cancer (EORTC) Quality of
Life Questionnaire (QLQ-C30) is also available in 130
languages.
It has 30 questions in 15 subscales relevant to
people with cancer: five distinct aspects of functioning
(physical, role, emotional, cognitive, social), eight
symptoms (fatigue, nausea/vomiting, pain, dyspnoea,
insomnia, appetite loss, constipation, diarrhoea),
financial difficulties, and global health/quality of life.
Therefore, the current review was undertaken to
provide a summary of the 1-year evolution of quality of
life of patients treated for oropharyngeal cancer. The
review focuses on the studies that used the EORTC
QLQ30 and H&N35 to assess quality of life at diagnosis
and at 12-month post-treatment, to understand how
the current standard of care treatment for OPSCC
impacts patients in the year following treatment.
MATERIALS AND METHODS
Search strategy
With the help of a librarian, we performed an
extensive literature search through Medline and
Cochrane database for studies from 1999 to December
2019. We used the following terms "oropharynx",
"oropharyngeal"," cancer"," neoplasm", "tumour","
quality of life" with databased- specific coding and
combinations. Mesh headings were used in different
combinations. Inclusion criteria were analytical studies
(case-control, cross-sectional, cohort, randomized
control trials, qualitative studies, systematic reviews,
and meta-analyses) that used the EORTC assessment
tool at diagnosis and 12 months after treatment in
OPSCC patients. Articles published in English were
included with no intention of searching unpublished
literature. Additional limits were set for rejecting results
that involved animals or children. HPV status could not
be used as a search criterion because there was no
clear separation in any study.
RESULTS
In total, 206 papers were identified. After reviewing
initially the titles followed by the abstracts of these
papers, only four met the inclusion criteria. We
extracted the following data from the four studies:
author and year of publication, country, sample size,
age, sex, cancer stage, treatment, and quality of life at
diagnosis and 12-months post-treatment.
As described in table 1, 186 patients from three
countries were included in this review. Mean age
ranged between 57 and 64 in 3 studies; in the fourth
study, 69% of patients were under 65 years of age. All studies had more male than female patients. Treatment
included surgery alone, surgery followed by radiotherapy,
surgery and chemoradiotherapy or radiotherapy
alone. Only one study described the presence
of a PEG at 12-month time-point. There was no
information on the HPV status of the tumour.
Table 2 shows the EORTC OLQ-C 30 values at
diagnosis, and 12-months post-treatment of the four
included studies included as well as those of the
general male population aged 50–59.
The Global quality of life improved in all the studies
from diagnosis to 12-month post-treatment
General population scores were comparable to
scores at diagnosis of patients in all four studies.
Some studies reported degradation of quality of life
in different scales. At 12 months, post-treatment
Nordgren et al (14) reported deterioration in social
functioning, an increase in appetite loss, senses
problems, social eating problems, sexuality problems,
as well as remarkable worsening of problems with teeth and dry mouth compared to diagnosis. Petruson
et al (12) reported an increase in problems with teeth
and dry mouth at 12-month post-treatment compared
to diagnosis. Al-Mamgani et al (17) reported worse
scores in appetite, pain related to head and neck,
senses problems, social eating, sexuality, and
remarkable worsening in problems with teeth,
problems opening the mouth, dry mouth and sticky
saliva. Oates (13) reported increases in fatigue and dry
mouth at 12-month post-treatment compared with
values at diagnosis.
Oates et al was the only study that determined the
presence of a PEG at 12 months, which was reported in 25% of patients.
DISCUSSION AND CONCLUSIONS
In summary, this brief literature review showed that
patients with OPSCC treated with standard of care- that
includes surgery followed by RT/CRT, or chemotherapy
and radiotherapy in different combinations- have a QoL
at 12-month post-treatment that is lower compared
with pre-treatment one. Most problems were related
to long term side effects of radiotherapy, such as xerostomia,
sticky saliva, trismus and problems with teeth.
Patients also reported lower role, functioning scores,
and a possible cause for that is the presence of a PEG
that impedes oral diet in all daily life situations. To date,
and likely deterioration in other scales. For now, there
are no data in the literature to assess the impact of HPV
positivity on the quality of life of OPSCC patients following
treatment as these studies included all OPC irrespective
of HPV status, However, the treatment is the
major determinant of the QOL and that being the same
irrespective of HPV status, these results likely apply to
HPV positive OPC. Given the prevalence of HPV positive
oropharyngeal cancer, likely most patients in these
studies were HPV positive OPC.
Acknowledgements
I thank Dr Maida Sewitch, Associate Professor,
Department of Medicine, McGill University and Dr
Nader Sadeghi for their input as supervisors of my
masters degree. I also thank Ibtisam Mahmoud,
Librarian McGill University Health Centre for helping
me with the search of literature.
Conflict of interests
The authors declare no conflicts of interests.
Ethical approval
Ethical approval was not needed for this retrospective
study.
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