Skip to main content
Download PDF

Symptoms, problems and quality of life in patients newly diagnosed with oesophageal and gastric cancer – a comparative study of treatment strategy

BMC Cancer volume 22, Article number: 434 (2022) Cite this article

Abstract

Background

Patients with oesophageal and gastric cancer have a low likelihood of being cured and suffer from a broad spectrum of symptoms and problems that negatively affect their quality-of-life (QOL). Although the majority (67–75%) of patients at the time of diagnosis suffer from an incurable disease, research has primarily focused on the pre- and postoperative phase among patients treated with curative intent, with little attention to symptoms and problems in the diagnostic phase, especially in those who cannot be offered a cure.

Methods

In this cross-sectional study 158 patients newly diagnosed with oesophageal and gastric cancer visiting the surgical outpatient department for a preplanned care visit were included consecutively during 2018–2020. The validated instruments QLQ-C30 and QLQ-OG25, developed by the European Organization for Research and Treatment of Cancer (EORTC), and selected items from the Integrated Patient Outcome Scale (IPOS) were used to assess QOL, symptoms and problems. Differences between patients with a curative and a palliative treatment strategy were analysed using t-test and Mann–Whitney U test. The QLQ-C30 and QLQ-OG25 scores were compared to published reference data on the general Swedish population.

Results

Among all, the QOL was markedly lower, compared with general Swedish population (mean ± SD, 55.9 ± 24.7 vs 76.4 ± 22.8, p < 0.001). Compared to general population, the patients had significant impairment in all QOL aspects, particularly for role and emotional functioning and for symptoms such as eating-related problems, fatigue, insomnia and dyspnea. Majority of patients also reported severe anxiety among family and friends. Among patients with oesophageal cancer those with a palliative treatment strategy, compared with curative strategy, reported significantly lower QOL (mean ± SD, 50.8 ± 28.6 vs 62.0 ± 22.9 p = 0.030), physical (65.5 ± 22.6 vs 83.9 ± 16.5, p < 0.001) and role functioning (55.7 ± 36.6 vs 73.9 ± 33.3, p = 0.012), and a higher burden of several symptoms and problems. No significant differences between treatment groups were shown among patients with gastric cancer.

Conclusions

Patients newly diagnosed with oesophageal and gastric cancer, and especially those with incurable oesophageal cancer, have a severely affected QOL and several burdensome symptoms and problems. To better address patients’ needs, it seems important to integrate a palliative approach into oesophageal and gastric cancer care.

Peer Review reports

Introduction

It is well known that timely and efficient care and support is essential to enhance quality of life (QOL) for patients with cancer. To enable such care we need comprehensive knowledge about how problems and needs vary depending on treatment strategy and how these are perceived by the patients at the time of diagnosis.

Patients suffering from oesophageal and gastric cancer have a low expected 5-year survival rate (16–17%) and suffer from severely hampered QOL, manifested in a broad spectrum of symptoms and problems [1,2,3,4]. For the majority of these patients (67–75%), a curatively intended treatment is not possible owing to severe comorbidity and/or advanced disease. This means that they often are offered palliative chemotherapy, radiotherapy or surgery aiming to maintain QOL, mitigate symptoms and prolong survival [2, 5, 6].

Previous research has primarily focused on the pre- and post-treatment period for patients who undergo treatment with curative intent, with little attention to prognosis and/or initial treatment strategy. This despite the fact that those with the poorest prognosis have the greatest risk of receiving poor quality care [7]. This means that the main focus in previous research has been on a subgroup of patients representing only 40% of the patient population while evidence regarding symptoms and problems in the diagnostic phase, and the potential differences with regard to initial treatment strategy, is still lacking. More knowledge about symptoms, problems and QOL, early after diagnosis of oesophageal and gastric cancer, and how these differ across patients with different treatment strategies, is therefore highly relevant to facilitate timely allocation of support for all.

Oesophageal and gastric cancer are among the ten most common malignancies worldwide [8]. In Sweden there are about 1,300 new cases of oesophageal and gastric cancer annually and the diseases cause about 1,000 deaths each year [9, 10]. Regardless of treatment strategy, patients with oesophageal and gastric cancer are burdened by disease-specific and treatment- related symptoms and problems, including dysphagia, fatigue, pain, weight loss, changed bowel habits and psychological distress, which negatively impacts their QOL [3, 11, 12]. Research also indicates that these complex symptoms and problems arise already at an early stage of the disease trajectory, indicating a need for early and proactive symptom management [13,14,15,16]. Proactive symptom management is associated with improved patient QOL, increased treatment compliance, reduced hospitalizations, and use of unplanned care [17, 18]. Early identification of patients with a high level of symptomatology, and timely support, regardless of treatment strategy, are therefore crucial to optimize the patients’ wellbeing and care.

Given the poor prognosis, a palliative care approach that aims to improve QOL and decrease suffering associated with the life-threatening illness, by anticipating, preventing and treating pain and other symptoms and problems, is particularly important for patients with oesophageal and gastric cancer [19]. The American Society of Clinical Oncology (ASCO) advocates integration of a palliative care approach within 8 weeks of diagnosis [20] to ensure proactive support and optimize QOL in patients with poor prognosis. Findings from several studies indicate that a palliative care approach integrated early in the disease trajectory not only improves QOL but also enhances symptom control and reduces health care service use [21,22,23]. Temel et al. noted differential effects of a specific early palliative care intervention in patients with different cancer diagnoses, suggesting that effective palliative care needs to be tailored to the specific symptoms, problems and care needs of each unique patient [24]. In the early stage of a cancer disease, symptoms and problems can differ based on disease and patient-related factors, such as age, gender and cancer stage, but treatment-related aspects can also play a role [16, 25, 26]. It has, for instance, been reported that patients receiving palliative treatment have a poorer QOL, higher symptom burden and more problems related to physical, social and emotional function, in comparison with patients with a curative treatment strategy [27]. Among patients newly diagnosed with oesophageal and gastric cancer it has been shown that symptoms and problems differ depending on age and gender, but whether and to what extent there are differences with regard to the patients’ planned treatment needs to be further investigated [13,14,15,16]. Such knowledge is important to comprehensively understand patients’ care needs in the early phase of the oesophageal and gastric cancer trajectory and to enable an anticipatory care approach tailored to the patients’ needs.

The aim of this study was to describe and compare symptoms, problems and quality of life among patients newly diagnosed with oesophageal and gastric cancer with a curative or palliative treatment strategy.

Method

Design

This study had a cross-sectional design.

Study population and setting

The sample comprised 158 patients with newly diagnosed oesophageal and gastric cancer. The patients were recruited at their first visit to the surgical outpatient department at a university hospital in Sweden during 2018–2020. At this stage the decision about treatment strategy is not final, meaning that included patients are still not informed about their treatment regimen. Inclusion criteria were: patients newly diagnosed with oesophageal or gastric cancer, age ≥ 18 years, cognitive ability to participate, and ability to communicate in Swedish.

Inclusion

All patients who met the inclusion criteria were consecutively invited to participate by a nurse or a research assistant in connection with a pre-planned care visit. At inclusion all patients were given both verbal and written information about the study.

Patients who consented to participate were asked to complete a questionnaire at the outpatient department or at home, depending on their preference. A free-postmarked envelope was given to patients who chose to return the questionnaire by mail. Patients who did not return the questionnaire within 2 weeks were reminded by telephone up to two times by a nurse or research assistant. In total 288 patients were eligible for inclusion; 251 were approached and 158 were included in the study (Fig. 1).

Fig. 1
figure 1

Flow diagram of the recruitment procedure. *Not approached because of administrative factors (research assistant unavailable and insufficient time for recruitment)

Full size image

Data collection

Data were collected at inclusion through questionnaires comprising validated instruments, as well as through the patients’ medical records.

The questionnaires included the European Organization for Research and Treatment of Cancer (EORTC) validated instruments QLQ-C30 [28] and QLQ-OG25 [29], which were used to assess QOL. The cancer-specific health-related QOL questionnaire QLQ-C30 consists of 30 questions in 15 subscales: five scales focusing on function (physical, social, role, and cognitive and emotional), one scale for global QOL, three symptom scales (fatigue, pain, vomiting/nausea) and six single-item scales (insomnia, appetite loss, dyspnoea, constipation, diarrhoea, financial difficulties). The QLQ-OG25 is an oesophago-gastric-specific module comprising 25 questions in six subscales (dysphagia, eating restrictions, reflux, odynophagia, pain and anxiety). All items are scored on a 4-point Likert scale ranging from 1 (not at all) to 4 (very much), with the exception of two global QOL-related items, which use a 7-point Likert scale. Both questionnaires have demonstrated good psychometric properties [28, 29].

Data regarding clinical characteristics: tumour site, clinical M stage (M1 = the cancer has metastasized; M0 = no metastasis), histology, American Society of Anesthesiologists (ASA) score (1–6, with lower values representing better physical status) [30], and whether the initially planned treatment strategy was curative (tumour-directed treatment such as surgery/ chemotherapy/radiotherapy with a curative intent) or palliative (tumour-directed treatment or no tumour-directed therapy in non-curative patients) were collected from the medical records.

As part of the clinical routine, symptoms, problems, performance status and need for information and support are assessed by a contact nurse. The assessment is based on the Swedish Palliative Care Guide (S-PCG), which comprises single items, and the instrument Integrated Patient Outcome Scale (IPOS) [31]. The single items include questions concerning need for support and performance status according to the Eastern Cooperative Oncology Group scale (0–5, with lower values representing better function) [32]. The IPOS comprises eight items relating to physical symptoms, and psychological, emotional and spiritual, and information and support needs. All items are scored on a 5-point Likert scale ranging from “not at all” to “overwhelming/all the time” [33]. The instrument has been translated into and validated in a Swedish context [34]. Data on problems that were not covered by the QLQ-C30 and QLQ-OG25 were collected from the IPOS, using the items on anxiety among family and friends, feeling at peace, sharing feelings, information, and practical matters.

Statistical analysis

The sample (n = 158) was divided into four groups according to site of primary tumour (oesophageal or gastric cancer) and the initially planned treatment strategy (curative or palliative).

Data on demographic and clinical characteristics were analysed with descriptive and analytical statistics. Differences were calculated using t-test for numerical data and chi-square test or Fisher’s exact test for nominal data.

The QLQ-C30 and QLQ-OG25 answers were linearly transformed to a 0–100 scale and processed using the EORTC scoring manual [35]. A high score for the global and the functional scales indicates better QOL or functioning, while a high score on the symptom scale indicates higher level of symptomatology or problems. The QLQ-C30 summary score was calculated from the mean of the 13 QLQ-C30 scales (the global QOL scale and the financial impact scale were not included). Differences in mean score were analysed using t-test. To ease the interpretation of the QLQ-C30 and the QLQ-OG25 results for the whole study population, a comparison to published reference data on the general Swedish population (reflecting the age and sex distribution of patients with oesophageal or gastric cancer) [25, 36], were tested with t-test, whenever data were available for both groups. No statistical adjustments were made. For statistically significant result, the absolute difference between mean scores were calculated. Based on previous research, a difference in mean score of ≥ 10 on the 0–100 scale of QLQ-C30, was considered clinically relevant [37]. No information on clinical relevance was presented for QLQ-OG25, as data were not available.

The median and interquartile range (IQR) were calculated for the IPOS items; differences in median were analysed using Mann–Whitney U test.

The statistical analyses were performed using version 25 of IBM SPSS Statistics (IBM Corp., Armonk, NY, USA). A p-value of < 0.05 was used to define statistical significance.

Ethical approval and ethical considerations

The study was approved by the Lund Regional Ethics Review Board (REC number: 2018/03, 2018/270, 2020/03596).

Results

Patient characteristics

Of the included 158 patients, 113 (73.4%) were men and the mean age at diagnosis was 71.0 (SD ± 9.1) years. Most patients were married or lived in a civil partnership (113; 73.4%), were pensioners (109; 72.7%) and had children (139; 90.3%). The most common type of residence was single-family house/link house (82; 53.2%). Elementary school was the highest educational level for the majority (77; 51.3%) (Table 1).

Table 1 Clinical characteristics and sociodemographic data, by initial treatment strategy
Full size table

Among all patients, 107 (67.7%) had a tumour originating in the oesophagus and 53 (33.5%) had distant metastases (M1) at the time of diagnosis. Adenocarcinoma and squamous cell carcinoma accounted for 72.5% and 20.9% of all cancers, respectively. Most patients had an ASA score of 2 (47; 45.6%) and a performance status score of 0 (68; 49.6%). The patients had a mean body mass index (BMI) of 25.2 (SD ± 4.1) and had lost 4.8 kg (SD ± 5.0) during the last 6 months prior to diagnosis (Table 1).

Quality of life, symptoms and problems among patients newly diagnosed with oesophageal and gastric cancer

The patients had a mean score of 55.9 (SD ± 24.7) for self-reported global health status/QOL. On the functional scales, the patients reported lowest score for role functioning (mean ± SD, 65.4 ± 36.1), followed by emotional functioning (69.3 ± 24.8) and social functioning (74.9 ± 28.5). Within the symptom scales, the patients reported the highest score for appetite loss (42.1 ± 40.7), fatigue (40.2 ± 27.9) and insomnia (35.5 ± 33.3). The most prominent diagnosis-specific symptoms reported by all participants were anxiety (mean ± SD, 65.1 ± 28.4), eating restrictions (45.8 ± 35.1) and odynophagia (35.6 ± 33.7) (Table 2).

Table 2 Quality-of-life among patients newly diagnosed with oesophageal and gastric cancer compared with general Swedish population
Full size table

Compared to the general Swedish population, the patients reported significantly worse mean scores for all QOL aspects; global QOL, functional performance, and general and diagnose-specific symptoms. Clinically relevant differences were shown for global QOL, all aspects of functioning, except for cognitive functioning, and for several symptoms related to eating, fatigue, insomnia and dyspnea (Table 2).

Patients reported severe anxiety among their family and friends (median 3.0; first to second quartile (Q1–Q2) 2.0–3.0) and that their own feeling of being at peace was slightly affected (1.0; 1.0–2.0). They also reported that they could always share feelings with family and friends (0.0; 0.0–2.0), that they had received as much information as they wanted (0.0; 0.0–2.0) and that their practical matters had been addressed (0.0; 0.0–1.0) (Table 3).

Table 3 Median values for included IPOS items among patients newly diagnosed with oesophageal and gastric cancer
Full size table

Quality of life, symptoms and problems, by treatment strategy in patients with oesophageal cancer

Among patients with oesophageal cancer, patients with a palliative treatment strategy reported a significantly lower global QOL and a lower global health summary score, in comparison with patients planned for a curative treatment strategy (mean ± SD, 50.8 ± 28.6 vs 62.0 ± 22.9 and 69.0 ± 19.9 vs 77.0 ± 17.4, respectively). Physical and role functioning were also lower among patients planned to receive palliative treatment compared with patients planned for curative treatment (65.5 ± 22.6 vs 83.9 ± 16.5 and 55.7 ± 36.6 vs 73.9 ± 33.3, respectively), while no significant differences between the groups were shown for emotional, cognitive and social functioning (Table 4).

Table 4 Mean values for quality of life among patients with oesophageal cancer, by treatment strategy
Full size table

In comparison with patients planned for curative treatment, patients planned for palliative treatment reported significantly higher intensity of fatigue (mean ± SD, 47.1 ± 27.3 vs 32.5 ± 27.5), pain (39.3 ± 37.1 vs 19.8 ± 27.8) and dyspnea (39.5 ± 33.7 vs 22.0 ± 28.3). The mean scores in other symptom scales did not differ with statistical significance between treatment groups (Table 4).

Clinically relevant differences were shown for global QOL, physical and role functioning and fatigue, pain and dyspnea (Table 4).

Patients planned for palliative treatment reported significantly worse body image and speech in comparison with patients planned for curative treatment (mean ± SD, 36.8 ± 34.0 vs 19.4 ± 32.1 and 18.8 ± 31.3 vs 3.8 ± 12.2, respectively). No significant differences between the groups were shown for the other disease-specific symptoms (Table 4).

Among patients with oesophageal cancer, no significant differences in anxiety among family and friends, own feeling at peace, sharing feelings, and information and practical matters were found between patients with a palliative and patients with a curative treatment strategy (Table 5).

Table 5 Median values for included IPOS items in patients with oesophageal cancer, by treatment strategy
Full size table

Quality of life, symptoms and problems, by treatment strategy in patients with gastric cancer

Among patients with gastric cancer, there were no significant differences in QOL, functioning and symptoms between the initial treatment strategies (Table 6).

Table 6 Mean values for quality of life among patients with gastric cancer, by treatment strategy
Full size table

Regarding diagnosis-specific symptoms, there were no significant differences between the treatment groups (Table 6).

Among patients with gastric cancer, no significant differences in anxiety among family and friends, own feeling at peace, sharing feelings, and information and practical matters were found between those with a palliative and those with a curative treatment (Table 7).

Table 7 Median values for included IPOS items in patients with gastric cancer, by treatment strategy
Full size table

Discussion

This is, to the best of our knowledge, the first study to describe symptoms, problems and QOL among patients newly diagnosed with oesophageal and gastric cancer not yet having a final treatment decision and to compare differences between those planned for curative and those planned for palliative treatment. While previous research has demonstrated a long and short-term deterioration in QOL during the course of treatment [1, 38, 39], this study shows that patients with oesophageal and gastric cancer present with a clinically relevant lower QOL and functioning and higher burden from several symptoms in comparison to the general Swedish population.

Among all, the mean global health status/QOL score was 55.9. Patients scored lowest on role and emotional functioning, while anxiety, fatigue and problems related to eating were the most predominant concerns. Although differences in sample selection and study design make comparisons with other studies difficult, these findings are in line with several previous studies [14, 16, 26, 40]. Tomaszewski et al. showed that role functioning was most impaired and that anxiety, fatigue and problems related to eating were the most common concerns in the pre-treatment phase among patients with oesophageal and gastric cancer [16]. Also, EORTC reference data revealed a mean global health status/QOL of 55.6 (SD ± 24.1) and 53.1 (± 26.5) for patients with oesophageal and gastric cancer, respectively, and that patients scored lowest on role functioning and highest on fatigue and problems related to eating [40]. Compared to the general population in Sweden, the newly diagnosed patients QOL are impaired in several ways [25, 36]. For example, their global QOL is more than 20 points and role, emotional and social functioning are about 16 points, below the mean value for the general Swedish population, differences which are considered clinically significant for the QLQ-C30 scale [25, 37]. This large discrepancy in QOL indicates that patients with oesophageal and gastric cancer are severely affected by their illness already at the time of presentation. The patients’ hampered QOL and low chance of cure suggest that a proactive palliative approach, focusing on symptom management and QOL optimization, may be beneficial already from diagnosis of oesophageal and gastric cancer. The patients’ broad spectrum of concerns, ranging from anxiety to problems with eating, also suggest that interdisciplinary support may be important to proactively address the physical and psychological needs of the patients. In the aftermath of an oesophageal or gastric cancer diagnosis, it may be especially important to provide psychological support, as anxiety can lead to fatigue and depression over time. Involvement of dieticians could prevent long-term consequences of problems related to eating [41,42,43]. However, the current health care service often focuses on diagnostics and medical treatment, rather than embracing a holistic approach to patient care, even though there is strong evidence that early palliative care provides benefits for patients in terms of reduced symptom burden and increased QOL [44, 45]. The present study suggests that a proactive palliative approach needs to be integrated in regular treatment regimens.

There were few differences between patients with regard to the initial treatment strategy, indicating that patients are in need of extended support, irrespective of whether they present with a curable or an incurable disease. This is consistent with ASCO guidelines, recommending access to palliative care competence and knowledge for all seriously ill patients, regardless of disease stage and treatment intent [20]. Among patients with oesophageal cancer, those with palliative treatment had a clinically relevant and statistically significant lower QOL and physical and role functioning, and a higher burden of pain, dyspnoea and fatigue, in comparison with patients receiving curative treatment. The result is similar to findings from a study by Tomaszewski et al., which showed that patients with palliative treatment had a lower level of physical functioning and higher burden of fatigue in the early stage of disease, in comparison with patients receiving curative treatment [16]. The lower physical functioning and the higher burden of fatigue, dyspnoea and pain among patients with a palliative treatment strategy could be related to their higher age, more advanced cancer stage and their lower general health status. Several studies have also shown that pain and fatigue are especially common in patients with advanced cancer [46, 47], and research has previously shown that these symptoms occur concurrently and influence patients’ physical functioning [48]. Patients with incurable oesophageal cancer have reported that their symptoms and concerns are interconnected in so far as pain and fatigue prevent them from participating in normal daily activities, and their functional limitations change their sense of identity and provoke a feeling of being a burden to others [49].

Previous research indicates that patients with incurable cancer can benefit from physical and psychosocial rehabilitation in terms of improved physical functioning, symptom control and increased QOL [50]. This indicates that, through palliative rehabilitation, it is possible to preserve patients’ physical functioning and thus relieve the burden of other symptoms and concerns. A programme for enhanced recovery is provided for patients with a curative disease, and a plan for pre-operative optimization is under development, but a strategy for maintaining physical functioning among patients with an incurable disease is lacking. This illustrates that these patients are managed in surgical care and that the current support system is structured and adapted for patients with a curative disease. However, it is important to provide proactive support also for those with an incurable disease.

In the present study the majority of patients reported severe anxiety among family and friends. This is in line with previous research showing significant levels of psychological distress among family and friends of patients with oesophageal cancer [51]. Research has also shown that anxiety is particularly intense at the time of diagnosis [52], especially if the prognosis is poor [53]. Our findings indicate that patients perceive that their family and friends are anxious early in the illness trajectory. As oesophageal and gastric cancer may progress rapidly, the patients’ family and friends have a very short time to adapt to the new life situation and lack of knowledge about patient care and difficulties to navigate the health care system and receive support are a source of considerable distress [54]. As patients´ and their families’ anxiety are significantly correlated [55], a family-centred approach embedded in palliative care could enhance the wellbeing of the whole family unit, once again highlighting the need to integrate a palliative care approach into standard surgical care.

This study has some strengths and several limitations that need to be addressed. A major strength is that data are based on validated and well-established instruments, the EORTC QLQ-C30 and QLQ-OG25. This ensures that the instruments measure what they are supposed to measure and it facilitates result comparisons with other studies. However, some limitations needs to be mentioned. Given the descriptive cross-sectional design, conclusions about causality/associations cannot be drawn and the results from the sub-groups analysis needs to be interpreted with caution as the small sample size may increase the risk for type II errors. The QOL comparison between the whole study population and the general population was not adjusted by sex and age. However, the published reference data that was used in the analysis was based on a sample that reflect the sex and age distribution of patients with oesophageal and gastric cancer [25, 36]. Another potential limitation is related to the representativeness of the sample in which 30.3% of the patients with oesophageal cancer and 33.3% of the patients with gastric cancer had a palliative treatment strategy. The fact that the proportion of patients receiving palliative treatment is lower in this study compared with register data [2] is likely to be related to the fact that some patients are so severely ill already at diagnosis so that they are not referred to the outpatient specialist clinic for diagnosis. This means that patients with more severe illness are probably underrepresented in this study and it is therefore likely that patients’ symptoms, problems and low QOL are underreported and underestimated. However, we appreciate that the sample is representative of patients diagnosed in outpatient care. Although eligible, some patients were not asked to participate. We experienced that the nurse at the outpatient department did not ask the patients to participate due to lack of time. However, this may not be a serious threat to the study’s validity as this was related to administrative factors, rather than patient-related factors.

Conclusions

This cross-sectional study on patients newly diagnosed with oesophageal and gastric cancer found that patients are severely affected by their illness already at the time of diagnosis, in terms of reduced QOL and functioning, and several burdensome symptoms. Few differences were found between patients planned for a palliative and curative treatment strategy. The findings suggest that to help alleviate symptom burden and increase QOL for this group of patients an early palliative approach is needed for all, regardless of treatment intent.

Availability of data and materials

The datasets generated and/or analysed during the current study cannot be shared publicly due to regulations in the Swedish Data Protection Act (2018:218; 2019; 219) and Ethical Review Act (2003:460), but data are available from the corresponding author on reasonable request.

Abbreviations

QOL:

Quality of life

EORTC:

European Organization for Research and Treatment of Cancer

IPOS:

Integrated Patient Outcome Scale

ASCO:

The American Society of Clinical Oncology

BMI:

Body mass index

SD:

Standard deviation

Q1:

First quartile

Q3:

Third quartile

ASA:

American Society of Anesthesiologists

S-PCG:

Swedish Palliative Care Guide

References

  1. Conroy T, Marchal F, Blazeby JM. Quality of life in patients with oesophageal and gastric cancer: an overview. Oncology. 2006;70(6):391–402.

    Article  PubMed  Google Scholar 

  2. Jeremiasen M, Linder G, Hedberg J, Lundell L, Björ O, Lindblad M, et al. Improvements in esophageal and gastric cancer care in Sweden - population-based results 2007–2016 from a national quality register. Dis Esophagus. 2020;33(3):doz070.

    Article  PubMed  Google Scholar 

  3. Malmstrom M, Ivarsson B, Johansson J, Klefsgard R. Long-term experiences after oesophagectomy/gastrectomy for cancer–a focus group study. Int J Nurs Stud. 2013;50(1):44–52.

    Article  PubMed  Google Scholar 

  4. Schandl A, Lagergren J, Johar A, Lagergren P. Health-related quality of life 10 years after oesophageal cancer surgery. Eur J Cancer. 2016;69:43–50.

    Article  PubMed  Google Scholar 

  5. Lagergren J, Smyth E, Cunningham D, Lagergren P. Oesophageal cancer. Lancet. 2017;390(10110):2383–96.

    Article  PubMed  Google Scholar 

  6. Van Cutsem E, Sagaert X, Topal B, Haustermans K, Prenen H. Gastric cancer. Lancet. 2016;388(10060):2654–64.

    Article  CAS  PubMed  Google Scholar 

  7. Dalhammar K, Malmström M, Schelin M, Falkenback D, Kristensson J. The impact of initial treatment strategy and survival time on quality of end-of-life care among patients with oesophageal and gastric cancer: a population-based cohort study. PLoS ONE. 2020;15(6):e0235045.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  8. Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2018;68(6):394–424.

    Article  PubMed  Google Scholar 

  9. Socialstyrelsen statistikdatabas för cancer [Internet]. [cited April 20, 2020]. Available from: https://sdb.socialstyrelsen.se/if_can/val.aspx.

  10. Statistikdatabas för dödsorsaker [Internet]. 2017 [cited November 6, 2019]. Available from: www.sdb.socialstyrelsen.se/if_dor/val.aspx.

  11. Bergquist H, Ruth M, Hammerlid E. Psychiatric morbidity among patients with cancer of the esophagus or the gastro-esophageal junction: a prospective, longitudinal evaluation. Dis Esophagus. 2007;20(6):523–9.

    Article  CAS  PubMed  Google Scholar 

  12. Blazeby JM, Farndon JR, Donovan J, Alderson D. A prospective longitudinal study examining the quality of life of patients with esophageal carcinoma. Cancer. 2000;88(8):1781–7.

    Article  CAS  PubMed  Google Scholar 

  13. Calderón C, Jimenez-Fonseca P, Jara C, Hernández R, de Martínez Castro E, Varma S, et al. Comparison of coping, psychological distress, and level of functioning in patients with gastric and colorectal cancer before adjuvant chemotherapy. J Pain Symptom Manage. 2018;56(3):399–405.

    Article  PubMed  Google Scholar 

  14. Hong J, Wei Z, Wang W. Preoperative psychological distress, coping and quality of life in Chinese patients with newly diagnosed gastric cancer. J Clin Nurs. 2015;24(17–18):2439–47.

    Article  PubMed  Google Scholar 

  15. Jacobs M, Anderegg MC, Schoorlemmer A, Nieboer D, Steyerberg EW, Smets EM, et al. Patients with oesophageal cancer report elevated distress and problems yet do not have an explicit wish for referral prior to receiving their medical treatment plan. Psychooncology. 2017;26(4):452–60.

    Article  CAS  PubMed  Google Scholar 

  16. Tomaszewski KA, Püsküllüoğlu M, Biesiada K, Bochenek J, Ochenduszko S, Tomaszewska IM, et al. Main influencing factors and health-related quality of life issues in patients with oesophago-gastric cancer - as measured by EORTC tools. Contemp Oncol. 2013;17(3):311–6.

    Google Scholar 

  17. Cheville AL, Alberts SR, Rummans TA, Basford JR, Lapid MI, Sloan JA, et al. Improving adherence to cancer treatment by addressing quality of life in patients with advanced gastrointestinal cancers. J Pain Symptom Manage. 2015;50(3):321–7.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Mills S, Buchanan D, Guthrie B, Donnan P, Smith B. Factors affecting use of unscheduled care for people with advanced cancer: a retrospective cohort study in Scotland. Br J Gen Pract. 2019;69(689):e860–8.

    Article  PubMed  PubMed Central  Google Scholar 

  19. World Health Organization. WHO Defenition of Palliative Care. 2018. (https://www.who.int/cancer/palliative/definition/en/).

    Google Scholar 

  20. Ferrell BR, Temel JS, Temin S, Alesi ER, Balboni TA, Basch EM, et al. Integration of palliative care into standard oncology care: American Society of Clinical Oncology clinical practice guideline update. J Clin Oncol. 2017;35(1):96–112.

    Article  PubMed  Google Scholar 

  21. Merchant SJ, Brogly SB, Goldie C, Booth CM, Nanji S, Patel SV, et al. Palliative care is associated with reduced aggressive end-of-life care in patients with gastrointestinal cancer. Ann Surg Oncol. 2018;25(6):1478–87.

    Article  PubMed  Google Scholar 

  22. Qureshi D, Tanuseputro P, Perez R, Pond GR, Seow HY. Early initiation of palliative care is associated with reduced late-life acute-hospital use: a population-based retrospective cohort study. Palliat Med. 2019;33(2):150–9.

    Article  PubMed  Google Scholar 

  23. Temel JS, Greer JA, Muzikansky A, Gallagher ER, Admane S, Jackson VA, et al. Early palliative care for patients with metastatic non-small-cell lung cancer. N Engl J Med. 2010;363(8):733–42.

    Article  CAS  PubMed  Google Scholar 

  24. Temel JS, Greer JA, El-Jawahri A, Pirl WF, Park ER, Jackson VA, et al. Effects of early integrated palliative care in patients with lung and GI cancer: a randomized clinical trial. J Clin Oncol. 2017;35(8):834–41.

    Article  PubMed  Google Scholar 

  25. Derogar M, van der Schaaf M, Lagergren P. Reference values for the EORTC QLQ-C30 quality of life questionnaire in a random sample of the Swedish population. Acta Oncol. 2012;51(1):10–6.

    Article  PubMed  Google Scholar 

  26. Suk H, Kwon OK, Yu W. Preoperative quality of life in patients with gastric cancer. J Gastric Cancer. 2015;15(2):121–6.

    Article  PubMed  PubMed Central  Google Scholar 

  27. Beernaert K, Pardon K, Van den Block L, Devroey D, De Laat M, Geboes K, et al. Palliative care needs at different phases in the illness trajectory: a survey study in patients with cancer. Eur J Cancer Care. 2016;25(4):534–43.

    Article  CAS  Google Scholar 

  28. Aaronson NK, Ahmedzai S, Bergman B, Bullinger M, Cull A, Duez NJ, et al. The European Organization for Research and Treatment of Cancer QLQ-C30: a quality-of-life instrument for use in international clinical trials in oncology. J Natl Cancer Inst. 1993;85(5):365–76.

    Article  CAS  PubMed  Google Scholar 

  29. Lagergren P, Fayers P, Conroy T, Stein HJ, Sezer O, Hardwick R, et al. Clinical and psychometric validation of a questionnaire module, the EORTC QLQ-OG25, to assess health-related quality of life in patients with cancer of the oesophagus, the oesophago-gastric junction and the stomach. Eur J Cancer. 2007;43(14):2066–73.

    Article  PubMed  Google Scholar 

  30. American society of anesthesiologists Apcs. American society of anesthesiologists. 2014. (https://www.asahq.org/standards-and-guidelines/asa-physical-status-classification-system).

    Google Scholar 

  31. The Institute for Palliative Care. NVP-Nationell vårdplan för palliativ vård [Available from: https://palliativtutvecklingscentrum.se/utveckling/vardutveckling/nationell-vardplan-nvp/.

  32. ECOG-ACRIN Cancer Research Group. ECOG Performance Status [Available from: www.ecog-acrin.org/resources/ecog-performance-status.

  33. Schildmann EK, Groeneveld EI, Denzel J, Brown A, Bernhardt F, Bailey K, et al. Discovering the hidden benefits of cognitive interviewing in two languages: the first phase of a validation study of the Integrated Palliative care Outcome Scale. Palliat Med. 2016;30(6):599–610.

    Article  PubMed  Google Scholar 

  34. Beck I, Olsson Moller U, Malmstrom M, Klarare A, Samuelsson H, Lundh Hagelin C, et al. Translation and cultural adaptation of the Integrated Palliative care Outcome Scale including cognitive interviewing with patients and staff. BMC Palliat Care. 2017;16(1):49.

    Article  PubMed  PubMed Central  Google Scholar 

  35. Fayers PMAN, Bjordal K, Groenvold M, Curran D, Bottomly A; on behalf of the EORTC Quality of Life Group. The EORTC QLQ-C30 Scoring Manual. 3rd ed. 2001.

  36. van der Schaaf M, Derogar M, Lagergren P. Reference values of oesophago-gastric symptoms (EORTC QLQ-OG25) in a population-based setting. Eur J Cancer. 2012;48(11):1602–7.

    Article  PubMed  Google Scholar 

  37. Osoba D, Rodrigues G, Myles J, Zee B, Pater J. Interpreting the significance of changes in health-related quality-of-life scores. J Clin Oncol. 1998;16(1):139–44.

    Article  CAS  PubMed  Google Scholar 

  38. Djarv T, Lagergren J, Blazeby JM, Lagergren P. Long-term health-related quality of life following surgery for oesophageal cancer. Br J Surg. 2008;95(9):1121–6.

    Article  CAS  PubMed  Google Scholar 

  39. Jacobs M, Macefield RC, Elbers RG, Sitnikova K, Korfage IJ, Smets EM, et al. Meta-analysis shows clinically relevant and long-lasting deterioration in health-related quality of life after esophageal cancer surgery. Qual Life Res. 2014;23(4):1097–115.

    Article  CAS  PubMed  Google Scholar 

  40. Scott NW, Fayers P, Aaronson NK, Bottomley A, de Graeff A, Groenvold M, et al. EORTC QLQ-C30 reference values manual. 2008.

    Google Scholar 

  41. Fosså SD, Dahl AA, Loge JH. Fatigue, anxiety, and depression in long-term survivors of testicular cancer. J Clin Oncol. 2003;21(7):1249–54.

    Article  PubMed  Google Scholar 

  42. Jacobson NC, Newman MG. Anxiety and depression as bidirectional risk factors for one another: A meta-analysis of longitudinal studies. Psychol Bull. 2017;143(11):1155–200.

    Article  PubMed  Google Scholar 

  43. Minnella EM, Awasthi R, Loiselle SE, Agnihotram RV, Ferri LE, Carli F. Effect of exercise and nutrition prehabilitation on functional capacity in esophagogastric cancer surgery: a randomized clinical trial. JAMA Surg. 2018;153(12):1081–9.

    Article  PubMed  PubMed Central  Google Scholar 

  44. Haun MW, Estel S, Rücker G, Friederich HC, Villalobos M, Thomas M, et al. Early palliative care for adults with advanced cancer. Cochrane Database Syst Rev. 2017;6(6):Cd011129.

    PubMed  Google Scholar 

  45. Vanbutsele G, Van Belle S, Surmont V, De Laat M, Colman R, Eecloo K, et al. The effect of early and systematic integration of palliative care in oncology on quality of life and health care use near the end of life: A randomised controlled trial. Eur J Cancer. 2020;124:186–93.

    Article  PubMed  Google Scholar 

  46. Al Maqbali M, Al Sinani M, Al Naamani Z, Al Badi K, Tanash MI. Prevalence of fatigue in patients with cancer: a systematic review and meta-analysis. J Pain Symptom Manage. 2021;61(1):167-89.e14.

    Article  PubMed  Google Scholar 

  47. Davis MP, Walsh D. Epidemiology of cancer pain and factors influencing poor pain control. Am J Hosp Palliat Care. 2004;21(2):137–42.

    Article  PubMed  Google Scholar 

  48. Laird BJ, Scott AC, Colvin LA, McKeon AL, Murray GD, Fearon KC, et al. Pain, depression, and fatigue as a symptom cluster in advanced cancer. J Pain Symptom Manage. 2011;42(1):1–11.

    Article  PubMed  Google Scholar 

  49. Laursen L, Schønau MN, Bergenholtz HM, Siemsen M, Christensen M, Missel M. Table in the corner: a qualitative study of life situation and perspectives of the everyday lives of oesophageal cancer patients in palliative care. BMC Palliat Care. 2019;18(1):60.

    Article  PubMed  PubMed Central  Google Scholar 

  50. Salakari MR, Surakka T, Nurminen R, Pylkkänen L. Effects of rehabilitation among patients with advances cancer: a systematic review. Acta Oncol. 2015;54(5):618–28.

    Article  PubMed  Google Scholar 

  51. Graham L, Dempster M, McCorry NK, Donnelly M, Johnston BT. Change in psychological distress in longer-term oesophageal cancer carers: are clusters of illness perception change a useful determinant? Psychooncology. 2016;25(6):663–9.

    Article  PubMed  Google Scholar 

  52. Murray SA, Kendall M, Boyd K, Grant L, Highet G, Sheikh A. Archetypal trajectories of social, psychological, and spiritual wellbeing and distress in family care givers of patients with lung cancer: secondary analysis of serial qualitative interviews. BMJ (Clinical research ed). 2010;340:c2581.

    Article  Google Scholar 

  53. Vodermaier A, Linden W, MacKenzie R, Greig D, Marshall C. Disease stage predicts post-diagnosis anxiety and depression only in some types of cancer. Br J Cancer. 2011;105(12):1814–7.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  54. Shaw J, Harrison J, Young J, Butow P, Sandroussi C, Martin D, et al. Coping with newly diagnosed upper gastrointestinal cancer: a longitudinal qualitative study of family caregivers’ role perception and supportive care needs. Support Care Cancer. 2013;21(3):749–56.

    Article  PubMed  Google Scholar 

  55. Götze H, Brähler E, Gansera L, Polze N, Köhler N. Psychological distress and quality of life of palliative cancer patients and their caring relatives during home care. Support Care Cancer. 2014;22(10):2775–82.

    Article  PubMed  Google Scholar 

Download references

Acknowledgements

The authors would like to thank all patients who participated in this study and the research assistant and the nurses at the surgical outpatient department for help with inclusion.

Funding

Open access funding provided by Lund University. This work was supported by the ALF (governmental founding from the Swedish NHS; grant number ALF 2018:0092; URL:https://www.med.lu.se/intramed/styrning_organisation/ekonomi_alf/alf) and the Sjöberg Foundation (grant number Sjöberg F2019/210; URL: https://sjobergstiftelsen.se) awarded to JK. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.

Author information

Authors and Affiliations

  1. Institute for Palliative Care, Lund University and Region Skåne, Lund, Sweden

    Karin Dalhammar, Jimmie Kristensson, Birgit H. Rasmussen & Marlene Malmström

  2. Department of Health Sciences, Faculty of Medicine, Lund University, Lund, Sweden

    Karin Dalhammar, Jimmie Kristensson, Birgit H. Rasmussen & Marlene Malmström

  3. Department of Surgery, Skåne University Hospital, Lund, Sweden

    Dan Falkenback

  4. Department of Clinical Sciences Lund, Faculty of Medicine, Lund University, Lund, Sweden

    Dan Falkenback

Authors
  1. Karin Dalhammar
    View author publications

    You can also search for this author in PubMed Google Scholar

  2. Jimmie Kristensson
    View author publications

    You can also search for this author in PubMed Google Scholar

  3. Dan Falkenback
    View author publications

    You can also search for this author in PubMed Google Scholar

  4. Birgit H. Rasmussen
    View author publications

    You can also search for this author in PubMed Google Scholar

  5. Marlene Malmström
    View author publications

    You can also search for this author in PubMed Google Scholar

Contributions

All authors contributed to the design, analysis, interpretation of data, drafting and critical revision of manuscript. All authors read and approved the final manuscript.

Corresponding author

Correspondence to Karin Dalhammar.

Ethics declarations

Ethics approval and consent to participate

The study was conducted in accordance with the act for ethical review of research involving humans, SFS 2003:460, and ethical approval was obtained from the Regional Ethics Review Board in Lund (REC number: 2018/03, 2018/270, 2020/03596). Participants provided informed written consent prior to participation.

Consent for publication

Participants gave informed consent for data to be published.

Competing interests

The authors declare that no competing interests exist.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visithttp://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Dalhammar, K., Kristensson, J., Falkenback, D. et al. Symptoms, problems and quality of life in patients newly diagnosed with oesophageal and gastric cancer – a comparative study of treatment strategy. BMC Cancer 22, 434 (2022). https://doi.org/10.1186/s12885-022-09536-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12885-022-09536-x

Keywords

BMC Cancer

ISSN: 1471-2407

Contact us