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CLINICAL STUDY |
Clinic of Psychosomatic Medicine and Psychotherapy and 1 Department of Nuclear Medicine, University of Duisburg-Essen, Essen, Germany and 2 Department of Psychosomatic Medicine and Psychotherapy, Ruhr-University Bochum, Germany
(Correspondence should be addressed to S Tagay, Clinic of Psychosomatic Medicine and Psychotherapy, University of Duisburg-Essen, Virchowstr. 174, 45147 Essen, Germany; Email: sefik.tagay{at}uni-essen.de)
| Abstract |
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Methods: Using patient-completed instruments, we examined the frequency of physical complaints, HRQL, anxiety and depression in 130 DTC patients hospitalized for radioiodine therapy or whole-body diagnostics (age 52 years, female 71%) under short-term hypothyroidism (4 weeks of levothyroxine withdrawal; DTC-H) and in 100 DTC out-patients under TSH-suppressive doses of levothyroxine subsequent to radioiodine therapy (DTC-L; age 49 years, female 81%).
Results: Compared with the German general population, DTC-H as well as DTC-L patients had significantly impaired HRQL. Notably, the decrease in HRQL was significantly higher in DTC-H than in DTC-L patients. Surprisingly, the prevalence of anxiety (44.6%) but not depression (17.7%) was much higher in the DTC-H patients than in the general population. In contrast to expectations, similar results for anxiety (44.0%) and depression (17.6%) were observed in the DTC-L patients.
Conclusions: This mounting evidence suggests that a consistent pattern of HRQL impairment is experienced by patients with DTC. The high frequency of anxiety and the significantly reduced HRQL should be considered in the aftercare of DTC patients.
| Introduction |
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Withdrawal of thyroid hormone therapy with consecutive hypothyroidism has a well-known negative impact on patients HRQL, leading to increased levels of fatigue, decreased appetite, problems with constipation and motor skills, and fluid retention. Although the efficacy and safety of this approach has been demonstrated for decades, patients frequently complain of symptoms of profound hypothyroidism resulting from levothyroxine withdrawal. Furthermore, during withdrawal, patients show associated psychological symptoms and social changes, such as family distress or decreased motivation to work. Patients suffering from non-metastatic DTC have been shown to have worse HRQL during peak thyroid withdrawal (5, 6). Several years ago, recombinant human TSH (rhTSH) was introduced and this avoids the side-effects of thyroid hormone withdrawal (4). The recent availability of rhTSH as a useful method to stimulate radioactive iodine uptake by thyroid remnants (4, 8) has stimulated research into the poor psychological performance and loss of HRQL in patients with DTC during levothyroxine withdrawal. Several studies have demonstrated impairment in tests measuring HRQL and psychometric functionality in patients with DTC during tri-iodothyronine (4) or levothyroxine (5, 8) withdrawal, compared with these tests when the same patients were taking suppressive doses of thyroid hormones (4), and when these patients were given rhTSH (4, 8).
We therefore performed a cross-sectional study to evaluate physical complaints, HRQL, depression and anxiety in cured DTC out-patients during treatment with chronic suppressive doses of levothyroxine (DTC-L) compared with a group of DTC patients under short-term hypothyroidism (DTC-H) hospitalized for radioiodine therapy or whole-body diagnostics. The extent to which HRQL and psychological well-being worsen during levothyroxine withdrawal is still a topic of interest and, more importantly, the possibility that HRQL and mental health may also be impaired by the chronic administration of suppressive doses of levothyroxine has not been satisfactorily explored to date. We hypothesized that DTC-L patients would have significantly better HRQL compared with DTC-H. Further, we expected that DTC-H patients would have significantly more depression and anxiety compared with DTC-L subjects.
| Materials and methods |
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The study consisted of two study samples: a hypothyroid group after 4 weeks of levothyroxine withdrawal (DTC-H) and DTC out-patients subsequent to radioiodine therapy under TSH-suppressive levothyroxine treatment (DTC-L). In the DTC-H group, we asked all thyroid cancer patients hospitalized at our center for diagnostic or therapeutic 131I administration under thyroid hormone withdrawal and hence, hypothyroid conditions, at any time from February to December 2001 to complete instruments rating their physical, HRQL and psychological status. Concerning the DTC-L group, consecutive out-patients from February to December 2001 were invited to participate. These patients completed the same instruments as were employed in the DTC-H study. Eligibility criteria included any patients who had undergone total thyroidectomy for well-differentiated thyroid cancer. For both the DTC-H and DTC-L populations, all patients provided written informed consent and the local ethics committee approved the protocol.
Clinical procedures
Our thyroidectomized DTC patients normally receive levothyroxine in a dose (~2.5 µg/kg body weight) that suppresses endogenous TSH levels. In patients undergoing thyroid hormone withdrawal, levothyroxine treatment was discontinued 4 weeks before radioiodine. According to German radioprotection law, patients receiving radioiodine must be hospitalized for at least 48 h. On day 1 of hospitalization, clinical examination, neck ultrasonography and measurement of TSH, free thyroid hormones, Tg and routine clinical chemistry were performed, and radioiodine was given orally as a capsule in the early afternoon. Radioiodine whole-body scan was performed 310 days after radioiodine administration. All hormones were measured with commercially available kits (B.R.A.H.M.S. Diagnostika GmbH, Henningsdorf, Germany), TSH with an immunoradiometric coated tube sandwich assay (DYNOtest BRAHMS Diagnostica, Henningsdorf, Germany TSH1) and free thyroxine (fT4) and free tri-iodothyronine (fT3) with competitive solid phase antigen radioimmunometric assays (DYNOtest FT4 and DYNOtest FT3). Reference ranges were 0.34.0 mU/l for TSH, 7.819.4 pmol/l for fT4 and 3.58.1 pmol/l for fT3.
Study instruments
The health survey short-form 36 (SF-36) The health survey short-form 36 (SF-36) (9) was used to assess generic HRQL. This generic instrument covers aspects of physical, psychological and social functioning (10). It measures four domains in the area of physical health: physical functioning, role-physical, bodily pain and general health and four domains in the area of mental health: role-emotional, vitality, mental health and social functioning. Two comprehensive indices of HRQL were also computed (physical component summary (PCS) and mental component summary (MCS)). The responses to the questions in each domain are added to provide eight scores between 0 and 100 with higher scores reflecting better HRQL. We compared the SF-36 scores of the present study with those of a large (n = 2911) German general population group (11).
The hospital anxiety and depression scale (HADS) To assess depression and anxiety, the study used the HADS, a 14-item questionnaire that is particularly suitable for somatically ill patients (12). Subjects rate each item on a four-point Likert scale ranging from 0 (not present) to 3 (always present), with higher scores indicating a greater degree of mood disturbance. As recommended by Zigmond & Snaith (12), we grouped our patients according to their subscale scores as non-cases (07 score), as borderline cases (810 score) or as definite cases (1121 score). Data from a German version (HADS-D) from a general German population as well as from large international medically ill populations have been reported (13).
Beck depression inventory (BDI)
Also used to assess depression, specifically, and its cognitive and physical symptoms, was this 21-item questionnaire (14), in which each item is scored on a four-point scale, with higher scores denoting greater severity. Total scores on the instrument of
10 reflect normal mood variation and of
11 increasing degrees of clinical depression.
Profile of mood states (POMS) To assess overall psychological distress and specific mood states, the study used this 65-item scale (15) which asks patients to describe their mood over the previous week with adjectives rated from 0 (not at all) to 4 (extremely). The instrument contains six subscales originally derived from factor analytic studies: fatigueinertia, depressiondejection, vigoractivity, confusionbewilderment, tensionanxiety and angerhostility. To capture the patients overall psychological status on the POMS, we used the total mood disturbance (TMD) score, which is the sum of the five negative mood state subscales, minus the vigor subscale. The validity and reliability of the POMS have been documented extensively, especially in cancer (16).
Hypothyroid physical complaints scale Clinical hypothyroidism was evaluated by a self-rating scale comprising classical hypothyroid symptoms, based on the Zulewski score (17) and Billewicz score (18), which have been used in numerous previous studies (4, 8).
Statistics
Data derived from descriptive statistical analyses are presented in the form of percentages or categorial variables and of the mean and S.D. for continuous data. Categorial data were compared using the chi2-test and continuous data by the Students t-test and ANOVA or, if appropriate, by non-parametric tests. Significant post hoc comparisons included the Bonferroni modification (P < 0.01). The level of significance was set at 0.05; all tests were formulated two-tailed. All statistical analyses were made with the Statistical Package for the Social Sciences (SPSS, Release 11.0, Chicago 2001).
| Results |
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The demographic characteristics of the patients in the two samples are shown in Table 1
. Of 160 eligible patients, 141 (88%) agreed to participate in the hypothyroid population study, four (3%) refused and 15 (9%) were excluded because of insufficient German language proficiency to understand the study instruments. Data from five (4%) of the 141 participants had to be discarded because of very incomplete responses. Six patients who received T3 for 2 weeks were eliminated from the study because their period of hypothyroidism and the degree was shorter. Thus, 130 patients (81.2% of eligible patients) were ultimately included in the DTC-H group. All had been thyroidectomized for DTC before study entry. Their median serum TSH concentration on day 1 of hospitalization was 75 mU/l (range: 17192 mU/l). At that time, all patients under thyroid hormone withdrawal were biochemically hypothyroid (fT4, fT3 or both below normal range). Of 140 eligible out-patients under TSH-suppressive levothyroxine treatment, 111 (79.2%) agreed to participate in the L-thyroxine population study, six (4.2%) were excluded because of insufficient German language. Data from five (3.5%) of the 111 patients had to be discarded because of very incomplete responses. There was no statistically significant difference between the DTC-H and DTC-L groups in terms of age, gender, marital status, education and employment status. Thus, both groups were comparable.
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Hypothyroid patients (DTC-H): patients undergoing a diagnostic procedure (whole-body scan) vs patients receiving high-dose radioiodine treatment
Ninety (69%) of the DTC-H patients received 131I treatment and 40 (31%) were undergoing a whole-body scan (Table 2
). Both groups were similar with respect to the studied outcomes. No significant group differences could be found with respect to depression and anxiety, TMD and HRQL. Furthermore, there were no significant differences in age (P < 0.341) and gender (P < 0.168). Only in the domain of the SF-36 bodily pain group were differences found at the 5% significance level. Overall, it is justified to summarize both groups as one subsample.
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As expected, hypoythyroid patients were significantly more likely than L-thyroxine patients to express symptoms of thyroid dysregulation in nine of twelve areas of symptoms (Table 3
). The DTC-H group had higher prevalences in slow movements (P < 0.05), weight increase (P < 0.000), cold skin (P < 0.000), parasthesia (P < 0.000), freeze (P < 0.001), cold intolerance (P < 0.026), periorbital puffiness (P < 0.000), hoarseness (P < 0.024) and constipation (P < 0.023) than the DTC-L group. There were no statistical differences between both groups in the prevalence of coarse skin and hearing impairment. Most frequent symptoms in the DTC-H patients were slow movements, weight increase and cold skin (all 61%).
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No significant difference could be observed between the DTC-H group and the DTC-L group with regard to depression according to HADS-D (4.3 ± 3.6 vs 4.1 ± 3.8; P < 0.682) and BDI (8.4 ± 7.0 vs 7.2 ± 6.9; P < 0.289). Interestingly, for both groups, mean ± S.D. depression scores were in the normal or non-clinically relevant range on the HADS and BDI as well as in POMS depression subscale. Again, differences between both groups failed statistical significance in most cases (Table 4
). Only in the POMS was the subscale tensionanxiety increased significantly in the DTC-H group (1.1 ± 0.80 vs 0.88 ± 0.66; P < 0.012). In contrast, the subscale vigorvitality was decreased in DTC-H patients (1.3 ± 0.41 vs 1.1 ± 0.45; P < 0.000). Overall, there were no group differences between DTC-H patients and DTC-L group population in depression, anxiety and in most areas of current mood disturbances.
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Comparison of HRQL in DTC patients with a German reference population
Mean values for all domains of the SF-36 scales for the three groups are depicted in Table 6
. The representative German reference group consisted of 2914 subjects. The mean age of all participants was 47.3 years, ranging in age from 14 to 74 years; 55.6% were women and 77.6% of the subjects were married or cohabiting. Approximately 30% had a Secondary General School Certificate. Almost 30% were in a full-time job, nearly 30% were retired (11). Both study samples ware compared with the reference population matching for age. In seven of eight domains of the SF-36, DTC-H patients reported significantly reduced HRQL compared with the German reference group adjusted for age (each variable P < 0.001, expect bodily pain with P < 0.01). There was no significant difference between DTC-H patients and the reference group with regard to general health. Overall, mental health, as reflected by the SF-36 MCS, was significantly lower in the hypothyroid DTC patients compared with the reference group. Furthermore, compared with the German reference population, the DTC-L patients had significantly lower scores in seven of eight SF-36 domains and in the MCS of SF-36. The difference between the German reference population and the DTC-L group failed statistical significance with regard to bodily pain and PCS.
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| Discussion |
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We found that the short-term hypothyroidism resulting from thyroid hormone withdrawal causes physical symptoms in the majority of patients. Compared with DTC-L patients, DTC-H patients had a significantly higher prevalence of virtually all hypothyroid symptoms listed on the test instrument. These observations are in line with those of quantitative (4, 8, 20, 21) and qualitative (7, 22) studies in the same setting. It is generally known that patients with thyroid cancer suffer troublesome physical symptoms relating to short-term hormone withdrawal (5, 7). The less-apparent negative psychological, family and work sequelae have also been demonstrated (5, 6). These sequelae include physical symptoms, impaired psychological well-being, family distress, decreased motivation to work and decreased quality of work.
Our assessment of depression and anxiety in the present study revealed two surprising findings. First, as measured by the mean HADS depression subscale score, the severity of depressive symptoms in our large DTC-H patient population and in the DTC-L survivals was in the normal range for healthy reference populations (12). Additionally, depression case prevalence as defined by HADS criteria was comparable between our thyroid cancer patients and the reference population (12). Moreover, there was no significant difference in the severity or case prevalence of depression between the DTC-H and the DTC-L groups.
The lack of an abnormal degree of depression in both study groups, hypothyroid and DTC survival populations, was confirmed by the mean POMS depression and BDI scores, both fell into the not clinically relevant range. In contrast to our findings, other studies have found significantly (20) and numerically (4) higher scores on the POMS depression subscale in DTC patients when they undergo short-term hypothyroidism than when they are euthyroid. The association between long-term thyroid hormone deficiency and clinical depression, even when the hypothyroidism is subclinical, has long been known and is well documented (23): clinical depression occurs in >40% of chronically hypothyroid patients. Hypothyroidism, even in a mild form, is clearly associated with neurocognitive dysfunction including memory loss and depression (24). Taken together with the results of earlier DTC studies (4, 20), our observations suggest that the association between short-term hypothyroidism and depression is less clear. Multiple factors may be involved for the different prevalence of depression in short-term hypothyroidism, including differences in diagnostic criteria, assessment procedures and the sample characteristics. The heterogeneity of depression is probably an important factor as well. Additional possible factors are unclear sources of the reference values used and small sample sizes.
The second unexpected finding of the psychological testing in our study is the high prevalence of anxiety symptoms in DTC patients. We found that both the DTC-H and DTC-L patients had higher anxiety scores than the German reference population, as assessed by the HADS anxiety score.
While, in general, anxiety is even more frequent in oncological patients than is depression (25), the high rate of HADS anxiety cases in our study groups compared with both selected and unselected samples of cancer patients (26) is remarkable. We found a 23% prevalence of borderline cases in our DTC-H population while, for example, Moorey et al. (27) reported a 27% and Skarstein et al. (26) a 13% prevalence within patients with non-thyroid cancers, although most of these cancer types are associated with poorer prognoses and more invasive interventions. We noted that another 21% of our DTC-H population were definite HADS anxiety cases, while the analogous prevalences ranged from 6% in successfully treated patients with testicular cancer (28) to 19% in patients with various types of non-thyroid cancers in a radiotherapy unit (25). Moreover, DTC-L patients in our study showed similar frequencies in borderline cases (26%) as well as in definite cases (18%).
In contrast to our hypothesis, significant differences in depression and anxiety between DTC-H and DTC-L groups were not observed. The data in the literature concerning this topic are inconsistent and only published for chronic hypothyroidism in non-DTC patients, which is not necessarily comparable with short-term hypothyroidism after 4 weeks of levothyroxine withdrawal in DTC patients. In a consecutive sample, Monzani et al. (29) found increased anxiety in subclinical hypothyroid patients. The authors claimed that the cause of higher anxiety scores in subclinical hypothyroid subjects might be minor neurobehavioral disturbances. Another study related to subclinical hypothyroidism and anxiety was reported by Baldini et al. (30) who evaluated the effect of subclinical hypothyroidism on psychopathological functions including anxiety in female patients and euthyroid female goiter controls. No significant difference in anxious symptomatology was detected between the groups. More recently, Engum et al. (31) performed a field research study in Norway. They reported that there is no significantly increased risk of anxiety in subclinical hypothyroidism and hyperthyroidism. The results of the study by Engum et al. (31) is consistent with that by Baldini et al. (30). Demet et al. (32) determined the prevalence and severity of depression and anxiety in patients with hypothyroidism and compared these with euthyroid patients. Thirty patients with hypothyroidism and 30 euthyroid controls were recruited. There was no difference between the two groups. Therefore, depression and anxiety were not outstanding features in hypothyroidism. However, depression was more significant in the chronically hypothyroid than in the euthyroid group. In conclusion, these findings demonstrated that the relations between thyroid functional state and anxiety are less clear.
Environmental factors such as uncertainty about the diagnostic results (i.e. detection of relapses) and especially for the DTC-H group hospitalization under radiation protection and surrounding radioiodine diagnostic and treatment procedures may help to explain the high rate of anxiety in our study populations. As Dow et al. (5) and Stajduhar et al. (22) point out, patients awaiting the results of the diagnostic procedures or kept in isolated conditions are usually extremely stressed; anxiety could be a correlative of this stress. A causal relationship between short-term hypothyroidism and anxiety seems unlikely, since the mean degree and the case frequency of anxiety were similar in the DTC-L study. Future investigation is necessary to analyze the cause of anxiety in the DTC patients. A clinical implication of our findings is that depression and anxiety appear and therefore should be treated independently from the thyroid functional state. Moreover, given its surprisingly high prevalence in both DTC-H and DTC-L patients, anxiety should be strongly considered in the aftercare of DTC patients. We found that HRQL is considerably reduced both in physical and psychosocial dimensions in thyroid cancer patients undergoing short-term hypothyroidism as well as in DTC-L patients, compared with a healthy reference population. These HRQL impairments appear to be largely due to hypothyroidism, since our DTC survivals had reduced HRQL scores compared with those of the reference population. Moreover, the DTC-L patients had significantly better HRQL in most domains of the SF-36 than did their DTC-H counterparts.
Compared with the general population, DTC-H group scored lower in all domains of the SF-36. Thus, based upon the now available data, there is irrefutable evidence for a significant impairment of HRQL in DTC patients. This impairment is at least as severe as the impairment in other chronic diseases.
In the past, various studies have reported a link between reduced HRQL and DTC (8, 21, 33, 34). HRQL is now considered an important endpoint in clincial studies (35). Our results dovetail with those of two studies examining HRQL in the thyroid cancer population. Recently, a Spanish study showed that, when hypothyroid, DTC patients had lower HRQL scores than healthy controls. However, when euthyroid, the same individuals had similar HRQL scores to those of the healthy controls, except on the general health functional scale, which was lower in the DTC patients (21). In an Austrian study (33) of 150 consecutive DTC patients on levothyroxine, SF-36 HRQL functional scores were statistically similar between the DTC patients and sex- and age-matched healthy controls in all SF-36 functional areas except role-emotional and vitality. Of interest, in the Austrian study, the SF-36 role-physical, mental health and social functioning scores were also significantly lower in the subgroup that had been diagnosed with DTC within 1 year of study entry than in controls. This suggested an HRQL improvement in DTC patients with time since diagnosis independent from their metabolic state. Hence, the length of this interval in a given study population could influence the studys HRQL findings. Most studies concerning HRQL issues during withdrawal of thyroid hormone therapy have not used generic or specific HRQL tools (Billewicz scale, POMS) but have included quite small samples (5, 6). These studies have focused especially on impairments of HRQL during withdrawal of thyroid hormone therapy (5, 6). Dow et al. (5) studied HRQL after withdrawal of thyroid hormone therapy, utilizing an instrument designed specifically for this purpose which was tested and validated. The majority of HRQL issues addressed in this instrument were general, applicable to most types and locations of cancer. Meier et al. (4) also noted that the most debilitating period in thyroid cancer surveillance was during the induced hypothyroidism for follow-up scanning. The HRQL as measured by two psychometric scales is far better during rhTSH treatment than after thyroid hormone withdrawal. These findings correspond with the results of the present study which indicate a high distress level for thyroid hormone withdrawal. The previous studies of HRQL in DTC patients cited above (4, 8) showed a consistent worsening of quality of life during withdrawal of thyroid hormone. Meier et al. (4) used the POMS and found that 94% of patients with DTC experienced increased fatigue during thyroid hormone withdrawal, and 89% experienced decreased vigor and activity. Haugen et al. (8) employed the SF-36 health survey and found that many of the parameters evaluated also worsened after levothyroxine withdrawal when compared with treatment with rhTSH. Dow et al. (5) used a specific test for measuring HRQL in patients with DTC during levothyroxine withdrawal (the QoL-thyroid scale), as well as a test for the evaluation of functionality in cancer patients, in a series of 34 patients with DTC. Our present study confirms and expands these results, with the additional advantage of having compared the results of the patients with a control group of DTC patients under L-thyroxine treatment, allowing us to determine the magnitude of the marked deterioration of these variables when compared with DTC controls.
The limitations of the present study should be noted. First, we did not assess the disease-specific HRQL of thyroid cancer. The SF-36 health survey seems to be a very useful instrument to decribe the overall HRQL of patients but, to detect more specific symptoms and HRQL deficits related to different cancer entities, disease-specific questionnaires may be more appropriate (5). Secondly, the psychometric analyses were based on self-rating scales and not on interview data, which may make a difference. Finally, the data are cross-sectional and do not allow us to suggest any causal relationship. Despite these limitations, our results can provide guidance for clinicians dealing with hypothyroid patients, and investigators interested in HRQL impairment in these patients. Patients were drawn consecutively from a large Nuclear Medicine Clinic at a tertiary referral center and should be representative of the DTC general population. All in all, our results have demonstrated a marked deterioration in HRQL and anxiety in patients with DTC during levothyroxine withdrawal as well as in levothyroxine treatment. If confirmed by future studies with DTC patients, the worsening of HRQL and the increased anxiety observed during TSH-suppressive therapy with levothyroxine as well as under short-term hypothyroidism should stimulate research into novel strategies for long-term treatment of patients with DTC.
In summary, our study showed that HRQL was distinctly reduced in DTC patients undergoing thyroid hormone withdrawal to prepare for follow-up diagnostic or therapeutic procedures but in a minor intensity also in DTC patients under TSH-suppressive levothyroxine treatment. Overall, patients with DTC under short-term hypothyroidism had more severely impaired HRQL compared with patients with DTC under levothyroxine treatment. Anxiety is considerably more frequent in DTC patients than in the general population and other cancer patient samples, regardless of whether patients had levothyroxine withdrawal or were under levothyroxine treatment. Since short-term hypothyroidism accounts for a substantial proportion of the HQRL impairment, this situation could be improved by avoiding short-term hypothyroidism and applying rhTSH instead. Furthermore, the results of the present study have demonstrated that the increased prevalence of anxiety should be considered more in the aftercare of DTC patients, e.g. psychooncological support for selected patients. Physicians could help to improve HRQL and reduce the increased anxiety among patients with thyroid cancer by teaching them how to manage these uncomfortable symptoms, informing patients of possible reactions to their cancer, developing a training group for health professionals and designing psychosocial intervention in oncology.
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