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- Med J Islam Repub Iran
- v.35; 2021
- PMC8214037
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Med J Islam Repub Iran. 2021; 35: 22.
Published online 2021 Feb 11. doi:10.47176/mjiri.35.22
PMCID: PMC8214037
PMID: 34169034
Farshid Fardad,1 Kobra Bagheri Valami,1 Nafiseh Ansarinejad,1 Bahareh Abbasi,2 Seide Masoomeh Khataii Khosroshahi,1 and Tayeb Ramim*3,4
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Abstract
Background: Lung cancer accounts for about 13% of all cancers and about 60% of patients with lung cancer also experience weight loss during treatment. There seems to be a clear correlation between the therapeutic outcomes of patients based on their weight changes during treatment. The aim of this study was to investigate the relationship between weight changes during and after treatment and the therapeutic outcomes of a patient with metastatic lung cancer.
Methods: This cohort study was performed on patients with the diagnosis of non-surgical metastatic lung cancer referred to Hematology and Oncology Clinic, Rasoul-e-Akram Hospital. Patients were divided into two groups with a weight gain of more than 5% and a weight gain of 5% and less. The information was entered into the SPSS version 21 software. In the descriptive analysis, mean and standard deviation (SD) were used. To compare quantitative variables, independent samples t-test, Mann-Whitney, chi-square or Fisher exact tests were used to compare qualitative variables and correlation test was used to determine the correlation between quantitative data. Survival curves were used to show differences in two groups of studies. A regression model was used to calculate the hazard ratio. The significance level was less than 0.05.
Results: Sixty patients, including 40 males (66.7%) and 20 females (33.3%) were studied. The mean age of patients was 62.22±9.00 years (43-83 years). The mean weight changes in the patients were -1.28±6.11 kg (-16 to 16kg). Forty-seven patients (78.3%) had weight gain less than 5%. There was no significant difference in overall survival (OS) and progression-free survival (PFS) according to weight gain.
Conclusion: Finally, the findings of the study showed that, despite the fact that PFS and OS in the weight gain group were greater than 5% of the original weight; the difference was not statistically significant.
Keywords: Metastatic lung cancer, Weight gain, Overall survival, Progressive free survival
↑ What is “already known” in this topic:
About sixty percent of patients with lung cancer experience weight loss during treatment. There seems to be a correlation between the therapeutic outcomes of patients based on their weight changes during treatment.
→ What this article adds:
This study showed that overall survival and progression-free survival were higher in the weight gain of more than 5% group compared to the other group. However, there was no significant difference in the survival curve between the two groups.
Introduction
Lung cancer is about 13% of all cancers in the world. Its mortality rate is highest among all cancers (1). The tumor status and stage of the disease are two important factors in determining the prognosis of lung cancer (2, 3). The studies about metastatic lung cancer show that appetite loss and weight loss are the new prognostic factors (4, 5). Also, about 60% of patients with lung cancer experience weight loss during treatment (6). It is always the question of whether the continuation of weight loss or its stabilization can be effective in overall survival (OS) or survival without progression of the disease (Progression-free survival, PFS) (7, 8). In some cancers, lowering energy consumption due to inactivity and hormonal abnormalities can lead to weight gain. There are different data on the association of weight gain with worse disease outcomes in some cancers (9, 10). Some studies have shown that instability in weight, including weight gain and weight loss, is associated with worse survival in cancer patients (11).
Some studies show that the PFS and OS in lung cancer patients who had a steady weight during treatment were about two months longer than other patients. In local cases, weight gain was associated with increased survival during the treatment (12, 13). In addition, patients with advanced stages of lung cancer with weight gain after treatment had greater survival rates (14).
There seems to be a correlation between the therapeutic outcomes of patients based on their weight changes during treatment. Therefore, the present study aims to investigate the relationship between weight changes during and after treatment and the outcomes in patients with metastatic lung cancer.
Methods
Study population
This cohort study was performed in patients with a diagnosis of non-surgical metastatic lung cancer, in Rasool Akram Hospital, Tehran, Iran from 2018 to 2019. Upon approval of the Iran University’s Ethics Committee (IR.IUMS.FMD.REC.1396.9411160003), data collection was carried out. Written consent was received from all patients. Patients’ information was collected based on clinical documentation, pathologic report, interview and follow up.
Weighing
Patients were weighed and their topographic characteristics, including weight, height and body mass index, were recorded before the treatment. The patients were weighed at the beginning of each treatment period and the body mass index was calculated in the highest weight. Weight changes and body mass index were calculated after treatment, and their ratio was calculated based on the initial values. According to a similar study (15), patients were divided into two groups including weight gain of more than 5% (group 1) and weight gain of 5% and less (group 1). Progression-free survival (PFS) and overall survival (OS) were calculated at the beginning of the treatment.
Statistical analysis
After completing the checklist, their information was entered into the SPSS version 21 software. In the descriptive analysis, mean and standard deviation (SD) were used. To compare quantitative variables, independent t-test or Mann-Whitney, chi-square or Fisher exact tests were used to compare qualitative variables and correlation test was used to determine the correlation between the quantitative variables. Survival curves were used to show survival differences in the two groups of study. Univariate Cox regression was used to calculate the hazard ratio. The significance level was less than 0.05.
Results
Sixty patients with metastatic lung cancer were enrolled in the study. Forty cases (66.7%) were male, and 20 (33.3%) were female. The mean age of patients was 62.82±9.006 years (43-83 years). The mean weight changes in the patients were -1.28±6.11 kg (-16 to 16kg). Forty-seven patients (78.3%) had weight gain less than 5% and 20 cases (21.7%) had weight gain more than 5%. The median survival in both groups is shown in Table 1.
Table 1
Distribution of overall survival (OS) and disease-free survival (PFS) Median according to weight gain
Variables | Groups | |
Weight gain ≤ 5% | Weight gain > 5% | |
PFS (months) (median (95%CI)) | 6 (5-10) | 7 (6-11) |
OS (months) (median (95%CI)) | 9 (6-12) | 9 (6-24) |
Open in a separate window
There was no statistically significant difference in mean of PFS and OS in terms of percent overweight. PFS and OS are shown in two groups (Charts 1 and and22).
Fig. 1
Survival analysis of PFS in two groups
Fig. 2
Survival analysis of OS in two groups
According to log-rank test, weight gain of 5% and less has no risk to reduce OS or PFS (HR= 1.18: 95%CI: 0.610-2.285).
Discussion
In the present study, it was not found that the weight gain of more than 5% could be associated with increased OS and PFS. In other studies, obesity was one of the major causes of increased mortality due to gastric and prostate cancer in men and breast, endometrial, cervical and ovarian cancers, with 14% and 20% of case fatality rate in men and women, respectively (16, 17).
However, the progression of the disease in cancer patients and the development of metastasis can lead to complications such as bowel obstruction and metabolic problems, which can lead to severe weight loss for these patients. This situation can be effective in reducing the life expectancy of patients (18, 19). Also, the patients may become overweight due to reduced physical activity and the administration of certain chemotherapy drugs during the diagnosis and treatment of cancer (20-23). Overall, weight gain results from the patient's nutritional status and physical activity (24, 25). Many studies have shown that the occurrence or progression of underlying diseases such as diabetes and hypertension can lead to weight gain and obesity during chemotherapy in cancer patients (26, 27).
It was no significant relationship between weight gain and OS and PFS in the present study. But in some studies, such as the Patel et al, patients with breast cancer who gained more than 5% of their initial weight had more survival compared to the other patients (27). A similar finding was also observed in patients with ovarian cancer that the OS of patients with weight gain more than 5% of the initial weight was greater than the patients without weight gain (25). In this study, it seems that the responsiveness of patients to treatment and increased appetite has led to improved patient nutrition and weight gain. Also, OS and PFS increased. In group I (≤ 5 %), OS was 11.26±8.43 m and in group II (>5%), OS was 12.54±10.61 m.
Conclusion
Finally, the findings of the study showed that OS and PFS were higher in group I compared to the group II. However, there was no significant difference in the survival curve between the two groups.
Acknowledgment
This study was supported by the Vice-Chancellor for research of Iran University of Medical Sciences, Tehran, Iran. (Ethics code number: IR.IUMS.REC.1394.277).
Conflict of Interests
The authors declare that they have no competing interests.
Notes
Cite this article as: Fardad F, Bagheri Valami K, Ansarinejad N, Abbasi B, Khataii Khosroshahi SM, Ramim T. Relationship between weight gain and survival rate in patients with metastatic lung cancer. Med J Islam Repub Iran. 2021 (11 Feb);35:22. https://doi.org/10.47176/mjiri.35.22
Footnotes
Conflicts of Interest: None declared
Funding:None
References
1. Peek RM, Blaser MJ. Helicobacter pylori and gastrointestinal tract adenocarcinomas. Nature Rev Cancer. 2002;2(1):28–37. [PubMed] [Google Scholar]
2. Suerbaum S, Michetti P. Helicobacter pylori infection. N Engl J Med. 2002;347(15):1175–86. [PubMed] [Google Scholar]
3. Fazeli A, Nafisi MR, Hazeghi K, Ghavaminejad A. Accuracy of whole-cell ELISA and HM-cap ELISA in the diagnosis of Helicobacter pylori infection. Kaums J. 2000;3(4):30–7. [Google Scholar]
4. Peek RM, Moss SF, Wang S, Holt PR, Tham KT, Blaser MJ. et al. Helicobacter pylori cagA+ strains and dissociation of gastric epithelial cell proliferation from apoptosis. J Natl Cancer Inst. 1997;89(12):863–68. [PubMed] [Google Scholar]
5. Gonzalez CA, Figueiredo C, Lic CB, Ferreira RM, Pardo ML, Ruiz Liso JM. et al. Helicobacter pylori cagA and vacA genotypes as predictors of progression of gastric preneoplastic lesions: a long-term follow-up in a high-risk area in Spain. Am J Gastroenterol. 2011;106(5):867–74. [PubMed] [Google Scholar]
6. Ogiwara H, Sugimoto M, Ohno T, Vilaichone RK, Mahachai V, Graham DY. et al. Role of deletion located between the intermediate and middle regions of the Helicobacter pylori vacA gene in cases of gastroduodenal diseases. J Clin Microbiol. 2009;47(11):3493–3500. [PMC free article] [PubMed] [Google Scholar]
7. Evans DG, Queiroz DM, Mendes EN, Evans DJ. Helicobacter pylori cagA status and s and m alleles of vacA in isolates from individuals with a variety of H pylori-associated gastric diseases. J Clin Microbiol. 1998;36(11):3435–37. [PMC free article] [PubMed] [Google Scholar]
8. Bakhti SZ, Latifi‐Navid S, Mohammadi S, Zahri S, Bakhti FS, Feizi F. et al. Relevance of Helicobacter pylori vacA 3ʹ‐end Region Polymorphism to Gastric Cancer. Helicobacter. 2015;1-12 [PubMed] [Google Scholar]
9. Vagenas D, DiSipio T, Battistutta D, Demark-Wahnefried W, Rye S, Bashford J. et al. Weight and weight change following breast cancer: evidence from a prospective, population-based, breast cancer cohort study. BMC Cancer. 2015 Jan 31;15:28. [PMC free article] [PubMed] [Google Scholar]
10. Schvartsman G, Gutierrez-Barrera AM, Song J, Ueno NT, Peterson SK, Arun B. Association between weight gain during adjuvant chemotherapy for early-stage breast cancer and survival outcomes. Cancer Med. 2017 Nov;6(11):2515–2522. [PMC free article] [PubMed] [Google Scholar]
11. Liu W, Qdaisat A, Lee E, Yeung J, Vu K, Lin JZ. et al. The association between weight stability and parenteral nutrition characteristics and survival in patients with colorectal cancer. Gastroenterol Rep (Oxf) 2019 Jun 17;7(6):419–425. [PMC free article] [PubMed] [Google Scholar]
12. Abdi E, Latifi‐Navid S, Latifi‐Navid H, Safarnejad B. Helicobacter pylori vacuolating cytotoxin genotypes and preneoplastic lesions or gastric cancer risk: a meta‐analysis. J Gastroenterol Hepatol. 2015;31(4):734–44. [PubMed] [Google Scholar]
13. Mottaghi B, Safaralizadeh R, Bonyadi M, Latifi-Navid S, Somi MH. Helicobacter pylori vacA i region polymorphism but not babA2 status associated to gastric cancer risk in northwestern Iran. Clin Exp Med. 2016 Feb;16(1):57–63. [PubMed] [Google Scholar]
14. Basiri Z, Safaralizadeh R, Bonyadi MJ, Somi MH, Mahdavi M, Latifi-Navid S. Helicobacter pylori vacA d1 Genotype Predicts Risk of Gastric Adenocarcinoma and Peptic Ulcers in Northwestern Iran. Asian Pac J Cancer Prev. 2014;15(4):1575–79. [PubMed] [Google Scholar]
15. Yang R, Cheung MC, Pedroso FE, Byrne MM, Koniaris LG, Zimmers TA. Obesity and weight loss at presentation of lung cancer are associated with opposite effects on survival. J Surg Res. 2011 Sep;170(1):e75–83. doi:10.1016/j.jss.2011.04.061. Epub 2011 May 23. [PMC free article] [PubMed] [CrossRef] [Google Scholar]
16. Calle EE, Rodriguez C, Walker-Thurmond K, Thun MJ. Overweight, obesity, and mortality from cancer in a prospectively studied cohort of US adults. N Engl J Med. 2003 Apr 24;348(17):1625–38. [PubMed] [Google Scholar]
17. Zhang M, Xie X, Lee AH, Binns CW, Holman CD. Body mass index in relation to ovarian cancer survival. Cancer Epidemiol Biomarkers Prev. 2005 May;14(5):1307–10. [PubMed] [Google Scholar]
18. Gadducci A, Cosio S, Fanucchi A, Genazzani AR. Malnutrition and cachexia in ovarian cancer patients: pathophysiology and management. Anticancer Res. 2001 Jul-Aug;21(4B):2941–7. [PubMed] [Google Scholar]
19. Dell DD. Cachexia in patients with advanced cancer. Clin J Oncol Nurs. 2002 Jul-Aug;6(4):235–8. [PubMed] [Google Scholar]
20. Irwin ML, Crumley D, McTiernan A, Bernstein L, Baumgartner R, Gilliland FD. et al. Physical activity levels before and after a diagnosis of breast carcinoma: the Health, Eating, Activity, and Lifestyle (HEAL) study. Cancer. 2003 Apr 1;97(7):1746–57. [PMC free article] [PubMed] [Google Scholar]
21. Andrykowski MA, Beacham AO, Jacobsen PB. Prospective, longitudinal study of leisure-time exercise in women with early-stage breast cancer. Cance Epidemiol Biomarkers Prev. 2007 Mar;16(3):430–8. [PubMed] [Google Scholar]
22. Takahashi H, Takahashi M, Taguchi K, Sasaki F, Todo S. Weekly pacl*taxel administration in the adjuvant therapy of primary breast cancer. Gan To Kagaku Ryoho. 2003 May;30(5):653–9. [PubMed] [Google Scholar]
23. Hainsworth JD, Urba WJ, Hon JK, Thompson KA, Stagg MP, Hopkins LG. et al. One-hour pacl*taxel plus carboplatin in the treatment of advanced non-small cell lung cancer: results of a multicentre, phase II trial. Eur J Cancer. 1998Apr;34(5):654–8. [PubMed] [Google Scholar]
24. Doyle C, Kushi LH, Byers T, Courneya KS, Denmark-Wahnefried W, Grant B. et al. Nutrition and physical activity during and after cancer treatment: An American Cancer Society guide for informed choices. CA Cancer J Clin. 2006 Nov/Dec;56(6):323–353. [PubMed] [Google Scholar]
25. Hess LM, Barakat R, Tian C, Ozols RF, Alberts DS. Weight Change During Chemotherapy as a Potential Prognostic Factor for Stage Iii Epithelial Ovarian Carcinoma: A Gynecologic Oncology Group Study. Gynecol Oncol. 2007 November;107(2):260–265. [PMC free article] [PubMed] [Google Scholar]
26. Demark-Wahnefried W, Rimer BK, Winer EP. Weight gain in women diagnosed with breast cancer. J Am Diet Assoc. 1997;97(5):519–26. [PubMed] [Google Scholar]
27. Patel JD, Pereira JR, Chen J, Liu J, Guba SC, John WJ. et al. Relationship between efficacy outcomes and weight gain during treatment of advanced, non-squamous, non-small-cell lung cancer patients . Ann Oncol. 2016 Aug;27(8):1612–9. [PubMed] [Google Scholar]
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