Discussion
With regard
to the swallowing mechanism, the
following anatomic structures
were identified: the
superior constrictor muscle (scm),
the
middle constrictor muscle (mcm),
the inferior constrictor muscle
(icm), the cricopharyngeal
muscle (cphm), and the first
centimeter of the muscular
compartment of the esophagus
inlet.
From the
current literature, we know that
the intensification of therapy
for head-and-neck cancer in
general results in improved
locoregional tumor control.
However, late sequelae also
increase, including swallowing
disorder.
Limited data on swallowing
problems are reported before
2005. Recently, increased
attention is given to the
swallowing problem because of
the ongoing randomized clinical
trials in dysphagia. The
prevalence of dysphagia in organ
preservation therapy is reported
to be as high as 50%. A
study by Eisbruch showed
that elevation of the larynx and
pharynx during swallowing is
essential for protection of the
airway and propulsion of the
bolus. After chemoradiation,
there is decreased base of
tongue or posterior pharyngeal
contraction and reduced
pharyngeal contraction,
resulting in impaired bolus
transport through the pharynx.
Logemann et al. concludes
that there is little if any
difference in frequency of
swallowing problems across
different disease sites after
treatment and according to the
same authors that the effects of
the different chemotherapy
agents were seemingly small.
Pretreatment swallowing therapy
may improve dysphagia and reduce
the need for tube feedings. Feng
et al. demonstrated
significant relationships
between dose–volume parameters
of structures and objective and
subjective measurements of
swallowing dysfunction. Other
groups also showed significant
correlations of various
dysphagia endpoints with dose:
the supraglottic lesions and
glottic cancers.
This article
analyzes the dose–volume
relationships for dysphagia (and
xerostomia). It particularly
relates the side effects (QoL)
to different treatment
techniques and to widely
separated anatomic locations;
that is the BOT, the tonsillar
fossa or soft palate, and the
nasopharynx. From our series of
132 patients, chart review
showed that 24 (18%)
patients experienced moderate to
severe dysphagia (Radiation
Therapy Oncology Group Grade 3
and 4) with more problems in
patients with BOT (32%) cancer
as opposed to patients with
cancer of the TF/SP (22%) and NP
(6%). Although
correlations between the
questionnaires were poor,
almost one third of the
patients' complain of
swallowing disorders. Moreover,
patients seem to experience more
complaints of dysphagia with
longer follow-up (this finding
is part of a separate article in
preparation). If grouped by
treatment technique, most severe
dysphagia was found in IMRT/3D-CRT
compared with BT group and SRT/CBK
group. One explanation could be
the cumulative dose in the
swallowing structures. For
example, if treated by EBRT
techniques, the mean dose in the
scm was 70 Gy in case of BOT
tumors, 64 Gy in TF/SP, and 67
Gy in NPC. If the booster is
given by BT, the highest mean
dose in scm is 52 Gy for BOT and
42 Gy for TF/SP. However,
comparing dose distributions in
TF/SP, BOT, and NP, it can be
seen that in the scm and mcm the
highest dose was found in
patients with NPC. The NPC
patient category is always
treated (per protocol) by a
large volume boost dose (so
called first boost) of 24 Gy by
EBRT techniques to a cumulative
dose of 70 Gy to the primary
tumor and positive neck nodes.
It is unclear to us why the
patients with NPC treated by a
high dose to the upper
swallowing muscles do not
complain of dysphagia to the
same extent compared with, for
example, BOT cancer patients.
One possible explanation could
be the infiltrating nature of
the disease itself in the case
of BOT cancers. The BT or SRT/CBK
booster dose in NPC is, however,
of no relevance to the scm and
other muscles given the very
small volume and rapid dose
falloff.
Several dose–effect relationships between dysphagia problems and the dose received by the swallowing muscles were found to be significant. Most significant were the relationships between EORTC H&N35 and the dose in the scm/mcm and the association of the PSS (normalcy of diet) and the dose in the scm (p values < 0.01). The higher the dose, the more chance of complaints of dysphagia. Xerostomia and dysphagia are strongly associated. Particularly highly correlated were the questions of the EORTC H&N35 questionnaire regarding swallowing, dry mouth, and sticky saliva.
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Conclusions
Patients treated with a variety of disease sites (TF/BOT/NPC) and treated by various RT techniques (IMRT/3D-CRT/BT/SRT/CBK) vary in their prevalence of severe dysphagia. Responses to QoL questionnaires in relation to the dose received by scm and mcm demonstrated a dose–effect relationship. Dysphagia is also site (geographic position)-dependent; most dysphagia problems are seen in BOT cancer patients. Although NPC patients receive the highest dose because of the treatment techniques used, dysphagia is still less as opposed to patients with cancer of the BOT. The explanation of this phenomenon remains somewhat unclear; it is speculated that this might have to do with the infiltrative (muscles) nature of the BOT cancers. Dysphagia is obviously multifactorial. In particular, dysphagia is strongly correlated with xerostomia. From the findings of the present research, we would like to emphasize for the future to focus more on treatment planning research (constraints), especially for issues like this frequently underreported dysphagia problem.
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