Journal List > Ann Surg Treat Res > v.102(4) > 1160645

Jung, Lee, and Chung: Quality of life changes in elderly patients after gastrectomy: perspective of an aged Asian society in the 2010s

Abstract

Purpose

The study aimed to investigate how elderly gastric cancer patients do postoperatively in terms of quality of life (QoL) compared to younger patients. We also investigated how the QoL of elderly gastric cancer patients has changed over the last decade in the aging population.

Methods

We included 113 elderly (≥70 years) and 202 younger patients, who underwent distal gastrectomy for stage I gastric cancer during the 2010s. The European Organisation for Research and Treatment of Cancer quality of life questionnaires were used to assess preoperative and postoperative (3-month/1-year) QoL. The baseline QoL and postoperative QoL changes were compared. The elderly patients were further grouped into the early- and late-2010s groups, based on the year of surgery, and their QoL and clinical data were compared.

Results

The baseline QoL was significantly different on some scales (physical/role functionings, and pain/dyspnea/dysphagia) in favor of younger patients. The postoperative QoL changes were not different with the exception of emotional functioning (1-year postoperatively) in favor of younger patients. Compared to the early-2010s group, comorbidities were more frequent, and the proportion of stage IA cancer was higher in the late-2010s group. There were no QoL differences with the exception of insomnia and financial difficulties (3-months postoperatively) in favor of the late-2010s group.

Conclusion

Despite baseline QoL differences, elderly gastric cancer patients did as well as younger patients in terms of postoperative QoL changes. More elderly gastric cancer patients with comorbidities are undergoing gastrectomies nowadays and it does not cause them a significant QoL disadvantage.

INTRODUCTION

Since 2017, South Korea has officially become an aged society, with an aging rate exceeding 14% [123], and it is not uncommon for a surgeon to encounter elderly patients seeking surgical treatment after a cancer diagnosis. A number of organizations or organization subcommittees have been set up for the proper care and management of elderly patients [4], and, as part of this, the Korean Surgical Society has recently launched the Korean Geriatric Surgery Society [5].
The tendency toward a high prevalence of comorbid conditions in elderly patients has frequently been reported [67], and their safety and well-being after cancer surgery have become tremendous concerns. Advanced age has often been reported as one of the influential factors associated with refusing surgery by cancer patients [89]. Concerns regarding disappointing recovery after successful surgery, along with frailty and overall life expectancy, have been suggested to influence their decision.
Although the mortality from gastric cancer alone is decreasing, it still is one of the most common cancers with high mortality in South Korea [1011]. With the rapid aging of the population, cancer incidence and mortality are also increasing proportionally, and we expect to encounter more elderly gastric cancer patients over time. Thus, we need to verify the postoperative quality of life (QoL) of elderly gastric cancer patients to minimize patient dissatisfaction associated with the dismal gap between reality and expectations associated with gastric cancer and related surgery [12].
The aim of this study was to investigate how the QoL of elderly gastric cancer patients differed from that of younger patients during the perioperative period. We also compared the QoL outcomes between the early- and late-2010s to investigate how the QoL of elderly gastric cancer patients has changed over time in the aging population.

METHODS

Study design and participants

QoL and clinical data were retrospectively evaluated with approval from the Institutional Review Board (IRB) of Kyungpook National University Hospital (No. KNUH 2021-10-028). The IRB waived the requirement for informed consent for this study.
Between 2010 and 2019, a total of 566 patients, aged 55 years or older, underwent a distal subtotal gastrectomy for stage I gastric adenocarcinoma in our hospital. The stage grouping was in accordance with the 8th edition of the Union for International Cancer Control classification. The complete set of QoL data from the preoperative, postoperative 3-month, and postoperative 1-year periods were available for 318 of 566 patients. Patients with combined surgeries or histories of gastric resection that could influence their QoL were excluded, and one patient with combined surgery (total proctocolectomy with ileal pouch-anal anastomosis) for familial adenomatous polyposis and 2 patients with previous partial gastrectomies for benign gastric diseases were excluded. After these exclusions, data from 315 patients remained for the final analysis.
The patients were grouped into younger and older groups by age (<70 years vs. ≥70 years), and there were 202 and 113 patients available for each group. To understand the QoL trends in older patients during the 2010s, the older patients were further grouped by their year of surgery into the early-2010s (2010–2014, n = 67) and the late-2010s (2015–2019, n = 46) groups.

QoL assessment

The Korean version of the European Organisation for Research and Treatment of Cancer quality of life questionnaire (EORTC QLQ) core (-C30) and gastric cancer-specific (-STO22) modules were used to assess QoL [13]. All patient responses were self-reported without clinician intervention. Preoperative QoL was evaluated upon admission of the patient for surgery. Postoperative QoL was evaluated at scheduled visits to our outpatient department at 3-months and 1-year postoperatively. The patients were asked to respond to 52 items for each time period, and the responses were transformed into 24 scale scores of 0–100 in accordance with the scoring manual provided by the EORTC. A lower score indicated better QoL with 6 exceptions. For the global health status/QoL scale and the 5 functional scales (physical, role, cognitive, emotional, and social), a lower score indicated worse QoL.

Statistical analysis

The clinical and QoL outcomes of the younger (<70 years) and older (≥70 years) groups were compared. In the older group, the outcomes in the early and late 2010s were further compared. The demographic values were compared using chi-square tests for categorical variables and Student t-tests for continuous variables. The QoL outcomes were compared using Student’s t-tests. A P-value of less than 0.05 was considered statistically significant. All statistical analyses were performed using IBM SPSS Statistics for Windows, ver. 25.0 (IBM Corp., Armonk, NY, USA).

RESULTS

Patient characteristics

The mean ages of the younger and older patients were 62.1 ± 4.5 and 74.4 ± 3.4, respectively (P < 0.001). There were 20 (9.9%) and 25 patients (22.1%) with comorbidities among the younger and older patients, respectively (P = 0.005). Cardiac conditions and histories of other malignancies were 2 of the most common comorbidities in both groups (Table 1).
There were no significant differences in surgical procedures and treatment outcomes between the groups. There were 13 younger patients (6.4%) and 7 older patients (6.2%) with postoperative complications, and the difference was not statistically significant. Among the grade III complications, there were 2 cases of wound closures in younger patients, and 1 case of bleeding control in older patients. The rest were cases of fluid collection controlled by percutaneous catheter drainage.

Baseline quality of life and postoperative shifting

During the preoperative period, the global health status/QoL was not significantly different between the younger and older patients (Table 2). However, the older patients exhibited significantly worse QoL on scales evaluating physical functioning (P = 0.001), role functioning (P = 0.011), pain (P = 0.011), and dyspnea (p = 0.045) on the EORTC QLQ-C30, and dysphagia (P = 0.035) on the EORTC QLQ-STO22.
Regarding the extent of postoperative QoL shifts after surgery, there were no significant differences between the younger and older patients with the exception of emotional functioning at 1-year postoperatively (P = 0.046).

Early vs. the late 2010s: older patients

The patient characteristics in the early- and late-2010s groups of older patients are summarized in Table 3. Comorbidities were more common in the late-2010s group than in the early-2010s group (16 patients [34.8%] vs. 9 patients [13.4%], respectively; P = 0.007). The proportion of stage IA gastric cancer was higher in the late-2010s groups (P = 0.025). The surgical procedures and treatment outcomes were not significantly different between the groups with the exception of the number of retrieved lymph nodes (33.5 ± 16.5 and 26.6 ± 11.8 in the early- and late-2010s groups, respectively; P = 0.017). In terms of baseline QoL assessed in the preoperative period, there were no significant differences between the groups (Table 4). Regarding the extent of QoL shifting after surgery, there were no significant differences between the groups with the exception of differences during the 3-month postoperative period in favor of the late-2010s group for insomnia (P = 0.044) and financial difficulties (P = 0.021).

DISCUSSION

Even though QoL disadvantages in elderly gastric cancer patients were apparent by the absolute values in some scales, the extent of postoperative QoL shifting was not very different from that of the younger patients. Compared to the first half of the 2010s, more elderly patients with comorbidities underwent surgery with equivalent or better (insomnia and financial difficulties at 3-months) QoL outcomes during the second half of the 2010s.
While there are a number of studies on general surgical outcomes in elderly gastric cancer patients, very little is known about their QoL. In terms of surgical outcomes, several studies suggested comparable outcomes for complications or morbidities in elderly and younger patients [141516]. While these studies defined the elderly groups by an age of 70 years or older, one study defined the elderly group using the age of 80 years or older [17], which showed higher complication rates for pneumonia, delirium, and urinary tract infections in the elderly group. While the same may not be true for patients with extreme age, at least in patients in their 70s, there were consistent results, showing surgical morbidities at a rate comparable to that of younger patients.
However, unlike surgical morbidities, the reported outcomes on the QoL of elderly patients were inconsistent. Before the widespread use of generic QoL tools in the form of a self-answered questionnaire [1819], several tools were used to attempt to measure QoL, and the Spitzer QoL index was one of them [20]. A previous report assessed postoperative QoL in elderly gastric cancer patients using the Spitzer QoL index [21] and found that both younger (65–74 years) and older (>74 years) age groups showed good QoL outcomes, which were comparable to the outcomes reported by another study in much younger patients (<65 years) [22].
There have been more recent attempts to assess the QoL of elderly gastric cancer patients using the EORTC QLQs, which are designed in the form of self-answered questionnaires and are commonly used currently. In an attempt to assess the QoL of elderly gastric cancer patients after laparoscopic gastrectomy [15], QoL comparisons were made up to 1-year postoperatively in 21 elderly patients and 50 young patients, which showed no QoL disadvantage for elderly patients. In contrast, in a study comparing the QoL of 57 elderly and 74 young patients up to a year after surgery, QoL disadvantages in elderly patients with significant postoperative deteriorations on multiple scales were reported [14]. The study included patients in more physically demanding circumstances, such as those with advanced-stage gastric cancer or undergoing adjuvant chemotherapy, and the results were somewhat inconsistent with the outcomes of other studies, including ours. We constructed a larger pool of patients consisting of 113 elderly and 202 younger patients during a longer time period of a decade. We also controlled the homogeneity of the study group and minimized external influences by limiting our inclusion criteria to those with stage I gastric cancer only. Having a larger pool of homogeneous patients in our study might have resulted in conflicting outcomes without disadvantages for elderly patients in terms of the extent of postoperative QoL deteriorations on most scales.
The reason we designed this study to cover the long study period of a decade was to explore the shift in social and medical trends regarding elderly gastric cancer patients over the last decade. It has been reported that people undergo health screening when beneficial health outcomes are expected by doing so [2324]. Due to the increased comorbidities and shorter life expectancy of older people, there are concerns about unmet expectations among older people, which is known to have a strong influence on their decisions not to undergo health screening. As we had a higher percentage of stage IA gastric cancer (92.1%) in the younger group, compared to 81.4% in the older group, we could presume that more younger people are undergoing screening endoscopies, enabling the earlier detection of gastric cancer. However, we found a huge increase in the percentage of stage IA gastric cancer in the older group from 74.6% in the early 2010s to 91.3% in the late 2010s. Based on similar reasoning, we could presume that this was reflected in the trends of higher desires for health among older people during the late 2010s, which led to more screening endoscopies.
Despite a higher percentage of comorbidities (34.8%) in elderly patients in the late-2010s group compared to 13.4% in the early-2010s group, patients in the late-2010s had comparable outcomes in terms of hospital stays, complications, and QoL. This indicates that the decision-making trends for surgical treatment in older gastric cancer patients have shifted over the last decade with more of them opting for surgery, and that the current practice of performing more surgeries on older gastric cancer patients is producing comparable outcomes in terms of their surgical outcomes and QoL.
Our study highlighted the QoL of elderly gastric cancer patients which showed that the extent of their postoperative deterioration did not surpass that of the younger patients. Having this result drawn from a larger pool of homogeneous gastric cancer patients during a decade of clinical practice was the strength of our study. We often encounter elderly gastric cancer patients refusing surgery because of concerns regarding disappointing postoperative recovery. The current findings could become an essential piece of information that could influence their decisions. Moreover, evaluation of our responsiveness to the population aging was another strength of this study.
Our study had some limitations. First, this was a retrospective analysis based on those who had QoL outcomes available for the preoperative, 3-month, and 1-year postoperative periods. While it may be appropriate to discuss postoperative QoL and morbidities, conclusions regarding mortality cannot be made from our study because those who did not survive could not be included in the study as no QoL responses were available. Second, our study considered the patients aged 70 years and over as elderly reflecting the more traditional definition of the elderly rather than age 80 years and older. In fact, more studies are defining the elderly as age 80 years and older to reflect the real clinical practice in the aging population; however, we still do not have enough QoL data collected in patients aged 80 years and over to make a conclusion. We plan to investigate the QoL of patients in their 80s in the future when the sufficient sample size is obtained in the specific age group. Third, our focus was on the QoL of elderly gastric cancer patients, and we did not have data on other parameters such as nutritional profiles and body composition. Even though those were not the focus of our study, having them available for background information could assist in our understanding. Devising a prospective study with such parameters would provide a better understanding, including the mortality, of elderly gastric cancer patients.
Our findings must not be misunderstood as equivalent QoL scores in older and younger patients. The baseline QoL itself during the preoperative period favored younger patients on 2 functional scales (physical and role) and 3 symptom scales (pain and dyspnea on the EORTC QLQ-C30, and dysphagia on the EORTC QLQ-STO22) while the extent of the postoperative changes was not different.
In conclusion, despite baseline QoL differences, elderly gastric cancer patients did as well as younger patients in terms of relative QoL changes after surgery. More elderly gastric cancer patients with comorbidities underwent surgeries in the late 2010s; nonetheless, they did not suffer disadvantages in QoL changes. Thus, the fear of disappointing QoL after surgery alone should not be regarded as a critical determinant in refusing gastrectomy by elderly patients. We need to continue to keep up with the higher desire for health, manifesting in elderly patients.

Notes

Fund/Grant Support: None.

Conflicts of Interest: No potential conflict of interest relevant to this article was reported.

Author Contribution:

  • Conceptualization, Project Administration: SSL, HYC.

  • Formal Analysis, Investigation: JHJ, SSL.

  • Methodology: SSL.

  • Writing – Original Draft: JHJ, SSL.

  • Writing – Review & Editing: All authors.

References

1. Korea Statistical Information Service. Projected population by age group (province) [Internet]. Daejeon: Statistics Korea;c2019. cited 2021 Oct 21. Available from: https://kosis.kr/statHtml/statHtml.do?orgId=101&tblId=DT_1BPB003&conn_path=I2 .
2. Han JW, Kim TH, Kwak KP, Kim K, Kim BJ, Kim SG, et al. Overview of the Korean Longitudinal Study on Cognitive Aging and Dementia. Psychiatry Investig. 2018; 15:767–774.
crossref
3. Hyun KR, Kang S, Lee S. Population aging and healthcare expenditure in Korea. Health Econ. 2016; 25:1239–1251. PMID: 26085120.
crossref
4. Yoo HJ. 50 Years of the Korean Geriatrics Society. Ann Geriatr Med Res. 2018; 22:159–166. PMID: 32743268.
crossref
5. Min SK. Geriatric vascular surgery: time to build optimal resources for the perioperative care of elderly and fragile vascular patients. Vasc Specialist Int. 2021; 37:19. PMID: 34210914.
crossref
6. Jørgensen TL, Hallas J, Friis S, Herrstedt J. Comorbidity in elderly cancer patients in relation to overall and cancer-specific mortality. Br J Cancer. 2012; 106:1353–1360. PMID: 22353805.
crossref
7. Williams GR, Mackenzie A, Magnuson A, Olin R, Chapman A, Mohile S, et al. Comorbidity in older adults with cancer. J Geriatr Oncol. 2016; 7:249–257. PMID: 26725537.
crossref
8. Kaltenmeier C, Malik J, Yazdani H, Geller DA, Medich D, Zureikat A, et al. Refusal of cancer-directed treatment by colon cancer patients: risk factors and survival outcomes. Am J Surg. 2020; 220:1605–1612. PMID: 32680623.
crossref
9. Gaitanidis A, Alevizakos M, Tsalikidis C, Tsaroucha A, Simopoulos C, Pitiakoudis M. Refusal of cancer-directed surgery by breast cancer patients: risk factors and survival outcomes. Clin Breast Cancer. 2018; 18:e469–e476. PMID: 28784267.
crossref
10. Guideline Committee of the Korean Gastric Cancer Association (KGCA). Development Working Group & Review Panel. Korean Practice Guideline for Gastric Cancer 2018: an evidence-based, multi-disciplinary approach. J Gastric Cancer. 2019; 19:1–48. PMID: 30944757.
11. Jung KW, Won YJ, Kong HJ, Lee ES. Community of Population-Based Regional Cancer Registries. Cancer statistics in Korea: incidence, mortality, survival, and prevalence in 2015. Cancer Res Treat. 2018; 50:303–316. PMID: 29566481.
crossref
12. Calman KC. Quality of life in cancer patients: an hypothesis. J Med Ethics. 1984; 10:124–127. PMID: 6334159.
13. Yun YH, Park YS, Lee ES, Bang SM, Heo DS, Park SY, et al. Validation of the Korean version of the EORTC QLQ-C30. Qual Life Res. 2004; 13:863–868. PMID: 15129896.
crossref
14. Han DS, Ahn J, Ahn HS. Are the elderly patient’s changes in the health-related quality of life one year after gastrectomy for stomach cancer different from those in young patients? Ann Surg Treat Res. 2021; 100:8–17. PMID: 33457392.
crossref
15. Mohri Y, Yasuda H, Ohi M, Tanaka K, Saigusa S, Okigami M, et al. Short- and long-term outcomes of laparoscopic gastrectomy in elderly patients with gastric cancer. Surg Endosc. 2015; 29:1627–1635. PMID: 25277478.
crossref
16. Biondi A, Cananzi FC, Persiani R, Papa V, Degiuli M, Doglietto GB, et al. The road to curative surgery in gastric cancer treatment: a different path in the elderly? J Am Coll Surg. 2012; 215:858–867. PMID: 23036827.
crossref
17. Takeuchi D, Koide N, Suzuki A, Ishizone S, Shimizu F, Tsuchiya T, et al. Postoperative complications in elderly patients with gastric cancer. J Surg Res. 2015; 198:317–326. PMID: 26033612.
crossref
18. Cella DF, Tulsky DS, Gray G, Sarafian B, Linn E, Bonomi A, et al. The Functional Assessment of Cancer Therapy scale: development and validation of the general measure. J Clin Oncol. 1993; 11:570–579. PMID: 8445433.
crossref
19. 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; 85:365–376. PMID: 8433390.
crossref
20. Spitzer WO, Dobson AJ, Hall J, Chesterman E, Levi J, Shepherd R, et al. Measuring the quality of life of cancer patients: a concise QL-index for use by physicians. J Chronic Dis. 1981; 34:585–597. PMID: 7309824.
21. Wu CW, Lo SS, Shen KH, Hsieh MC, Lui WY, P’eng FK. Surgical mortality, survival, and quality of life after resection for gastric cancer in the elderly. World J Surg. 2000; 24:465–472. PMID: 10706921.
crossref
22. Wu CW, Hsieh MC, Lo SS, Lui WY, P’eng FK. Quality of life of patients with gastric adenocarcinoma after curative gastrectomy. World J Surg. 1997; 21:777–782. PMID: 9276711.
crossref
23. Breslau ES, Gorin SS, Edwards HM, Schonberg MA, Saiontz N, Walter LC. An individualized approach to cancer screening decisions in older adults: a multilevel framework. J Gen Intern Med. 2016; 31:539–547. PMID: 26941042.
crossref
24. Sazlina SG. Health screening for older people-what are the current recommendations? Malays Fam Physician. 2015; 10:2–10.
Table 1

Patient characteristics of younger (<70 years) and elderly (≥70 years) gastric cancer patients from the 2010s

astr-102-214-i001

Values are presented as number only, number (%), or mean ± standard deviation.

a)Stage grouping was based on the 8th edition of the Union for International Cancer Control classification. b)Complications were classified according to the Clavien-Dindo classification.

*P < 0.05, significant difference between the groups.

Table 2

Baseline and postoperative QoL of younger (<70 years) and elderly (≥70 years) gastric cancer patients from the 2010s

astr-102-214-i002

QoL, quality of life; No., number of available responses; SD, standard deviation; EORTC QLQ, European Organisation for Research and Treatment of Cancer quality of life questionnaire; EORTC QLQ-C30, EORTC QLQ core; EORTC QLQ-STO22, EORTC QLQ stomach.

a)Higher scores (or positive changes) represent better (or improved) QoL. b)Lower scores (or negative changes) represent better (or improved) QoL.

*P < 0.05, significant difference between the groups.

Table 3

Patient characteristics of elderly gastric cancer patients from the first and second half of the 2010s

astr-102-214-i003

Values are presented as number only, number (%), or mean ± standard deviation.

a)Stage grouping was based on the 8th edition of the Union for International Cancer Control classification. b)Complications were classified according to the Clavien-Dindo classification.

*P < 0.05, significant difference between the groups.

Table 4

Baseline and postoperative quality of life of elderly (≥70 years) gastric cancer patients from the first and second half of the 2010s

astr-102-214-i004

QoL, quality of life; No., number of available responses; SD, standard deviation; EORTC QLQ, European Organisation for Research and Treatment of Cancer quality of life questionnaire.

a)Higher scores (or positive changes) represent better (or improved) QoL. b)Lower scores (or negative changes) represent better (or improved) QoL.

*P < 0.05, significant difference between the groups.

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