scholarly journals Assessment of quality of life in resectable gastric cancer patients undergoing chemoradiotherapy as adjuvant treatmentLetter to the Editor

2018 ◽  
Vol 07 (01) ◽  
pp. 16-20 ◽  
Author(s):  
Deep Shankar Pruthi ◽  
Mushtaq Ahmad ◽  
Meenu Gupta ◽  
Saurabh Bansal ◽  
Vipul Nautiyal ◽  
...  

Abstract Introduction: Quality of life (QOL) is increasingly recognized as an important endpoint in cancer therapies. However, few data are available on QOL in patients who have received radiotherapy as adjuvant treatment for cancer stomach. Methods: Thirty patients who underwent curative resection were enrolled and received chemoradiotherapy (45 Gy in 25 fractions using three-dimensional conformal radiotherapy technique), together with 5-fluorouracil and leucovorin. The European Organization for Research and Treatment of Cancer QOL questionnaire C30 and STO Q22 was assessed at four time points: pre- and postchemoradiotherapy and at 1-month and 6-month follow-up. Results: Mean age of the patients was 54 years. Male:female ratio was 4:1. Stage II and Stage III disease was present in 60% and 30% of patients, respectively. All patients were able to complete the chemoradiotherapy protocol. Our study found out significant impairment in QOL for emotional functioning, fatigue, nausea and vomiting and dyspnea. Results showed that QOL levels decrease postchemoradiotherapy; however, QOL levels returned to baseline at 1-month and 6-month follow-up period. Conclusion: Chemoradiotherapy as adjuvant treatment for cancer stomach patients who have undergone resection with curative intent is a safe and well-tolerated regimen with respect to QOL.

Author(s):  
Karamveer Singh ◽  
Navneet Jain ◽  
Sunil Saini

Background: Oesophageal cancer is sixth most common cause of cancer related deaths worldwide. Despite complete resections, overall survival remained low. To improve the existing treatment combination of chemotherapy and radiotherapy in both neoadjuvant and adjuvant settings was introduced. Impact of treatment on quality of life, morbidities and toxicities associated with multimodality treatment in patients of carcinoma oesophagus was studied prospectively and retrospectively.Methods: A total of 40 patients histologically proven carcinoma of the oesophagus were enrolled in the study. Study included assessment of clinical features, risk factors, biopsy, multimodality treatment and associated morbidities and toxicities. Quality of Life (QOL) in patients of multimodality treatment assessed using European Organization for Research and Treatment of Cancer Quality of Life Questionnaire Core 30 and Core 18 before, immediate post treatment and 6 months after completion of the planned treatment.Results: In 40 patients, male to female ratio was 1.10:1. Dysphagia was the leading complain. 3 patients were treated using neoadjuvant therapy (chemotherapy and radiotherapy followed by surgery) among them 2 patients expired, 1 patient is under regular follow up. 6 patients underwent upfront surgery followed by adjuvant therapy out of which 3 patients expired,15 patients were treated with curative intent by definitive chemotherapy and radiotherapy out of which only 7 patients survived for >1 year. 16 patients were treated with palliative intent (radiotherapy, chemotherapy, oesophageal stenting and feeding procedures) in which only 1 patient survived for 1 year.Conclusions: The present study demonstrates that patients over all QOL was reduced after treatment and in the follow up period which was due to the treatment related toxicities but in contrast symptom improvement was observed simultaneously.


2021 ◽  
Vol 17 (7) ◽  
pp. 817-823
Author(s):  
Gabriella Maggi ◽  
Irene Terrenato ◽  
Luca Giacomelli ◽  
Viviana Bifano ◽  
Alessandra Gravili ◽  
...  

The aim of this study was to investigate symptoms, their variation over time and their relationship with quality of life (QoL)/psychological distress in sarcoma patients, as few data regarding QoL and psychological distress in this set of patients are currently available. A total of 188 sarcoma patients from an Italian referral center were involved. Symptoms and financial difficulties were evaluated with the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire from the first treatment and over the follow-up period, up to 6 years. The authors found that patients with sarcoma experience several symptoms, especially fatigue and pain, which may dramatically worsen QoL and psychological distress. In conclusion, patients with sarcoma often experience fatigue, pain and financial difficulties, which negatively impacts QoL and psychological distress. To ameliorate overall QoL, proper control of symptoms is necessary.


2011 ◽  
Vol 14 (5) ◽  
pp. 612-618 ◽  
Author(s):  
Gerald M. Quan ◽  
Jean-Marc Vital ◽  
Vincent Pointillart

Object This prospective study was undertaken to assess the clinical outcome of 26 consecutive patients who underwent surgery for symptomatic metastases of the cervical or cervicothoracic spine. Methods All patients suffered axial or radicular pain, with or without neurological deficit, including radicular weakness (23%), quadriplegia or paraplegia (12%), and urinary sphincter dysfunction (8%). All patients underwent palliative decompression and stabilization surgery via an anterior (18 patients), posterior (7 patients) or combined approach (1 patient) depending on the topography of the metastases, and were prospectively followed up for 1 year. Thirteen patients received adjuvant chemotherapy and 7 patients received radiotherapy to the cervical lesion. Clinical data as well as data from the European Organization for Research and Treatment of Cancer QLQ-C30 questionnaire were obtained pre- and postoperatively and at regular follow-up intervals. Results Median survival was 6 months and 10 patients were known survivors at 12 months. Postoperatively, 1 patient developed neurological deterioration and died while an inpatient. There were no other early postoperative complications in any patients. From pre- to postoperatively there was an immediate and significant improvement in axial and radicular pain and overall quality of life. There was also overall improvement in cognitive, emotional, social, role, and physical functioning. The observed improvement in pain, functioning, and quality of life was maintained for the duration of the follow-up period. Furthermore, neurological function was improved or preserved until death in the majority of patients. Conclusions Together with adjuvant medical management, surgery for cervical metastases produces low morbidity and can achieve good symptomatic palliation in the majority of patients for their remaining lifetime.


2018 ◽  
Vol 28 (4) ◽  
pp. 818-823 ◽  
Author(s):  
Francesco Plotti ◽  
Corrado Terranova ◽  
Stella Capriglione ◽  
Stefania Crispino ◽  
Alessandra Li Pomi ◽  
...  

AimsThe aim of this study was to evaluate long-term quality of life and urinary and sexual function in long-term cervical cancer survivors previously treated with radical hysterectomy (RH) type C2/type III.MethodsAll patients who presented at Campus Bio-Medico of Rome for RH type C2/type III for cervical cancer were considered eligible for this retrospective study protocol. We included exclusively patients with complete response to primary treatment with at least 36 months of follow up. Included subjects were interviewed with the European Organization for Research and Treatment of Cancer QLQ-CX24 Questionnaire, European Organization for Research and Treatment of Cancer QLQ-C30, and an Incontinence Impact Questionnaire 7.ResultsFrom January 2004 to June 2014, 251 patients affected by locally advanced cervical cancer were treated at Campus Bio-Medico of Rome treated with type C2/type III RH. At time point of March 2017, 90 patients were included with a mean age of 55.6 ± 8.5 years. The questionnaires were administered after a median follow-up of 49 months after the end of therapy. The symptoms of fatigue, nausea and vomiting, appetite loss, pain, insomnia, and dyspnea, as well as a negative financial impact, were reported as not frequent and rarely disabling. On the contrary, patients frequently reported gastrointestinal complaints. Diarrhea was present in 6% of patients and was referred as mild; constipation was present in 75% of women and was reported as mild in 30% of cases, moderate in 30%, and severe in 15%. Concerning sexual activity, data indicated a good level of sexual enjoyment with a slight worsening of sexual activity. Incontinence was reported in 28% of cases and appeared to be mild and rarely disabling (all mean values <2).ConclusionsWaiting for ongoing randomized controlled trials, this study confirmed that RH may be considered as a useful treatment plan, according to its negligible long-term impact on quality of life, urinary dysfunction, and sexual function.


Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 4287-4287 ◽  
Author(s):  
Jennifer L. Kelly ◽  
Chintan Pandya ◽  
Jonathan W. Friedberg ◽  
Supriya G. Mohile

Abstract Abstract 4287 Introduction: Greater than 50% of newly diagnosed non-Hodgkin lymphoma (NHL) cases are ≥ age 60, and the numbers of older patients with NHL will grow as the population ages. NHL treatment may significantly impact health related quality of life (HRQOL) in older patients and thereby have long-term adverse physical and mental consequences. One recent evaluation of HRQOL following a cancer diagnosis among patients age '65 indicated a significant decrease following any NHL diagnosis, particularly in the physical health component. However, NHL is a collection of distinct disease entities, with widely varied clinical course. Diffuse large B-cell lymphoma (DLBCL) is a prevalent subtype often treated with curative intent. In this analysis, we evaluate HRQOL among patients diagnosed with DLBCL, using a novel nationally representative population-based dataset, and describe patterns in HRQOL by time from diagnosis. Methods: The National Cancer Institute sponsored Surveillance, Epidemiology, and End Results-Medical Health Outcomes Survey (SEER-MHOS) linkage database is a research resource that allows for evaluation of HRQOL in cancer patients and survivors. The MHOS was administered annually to cohorts of patients randomly selected from Medicare Advantage health plans; each cohort was surveyed at baseline and 2 years later in follow-up. The MHOS measured HRQOL using the SF-36, an instrument with established reliability and validity for patients with cancer. The questions of the SF-36 capture data on 8 dimensions of general health that are grouped into physical (PCS) and mental (MCS) summary scores, capturing physical function and emotional well-being, respectively. Patients included in 6 cohorts (baseline 1998–2003; last follow-up on cohort 6 in 2005) were linked to the SEER database. For this cross-sectional analysis, we selected all patients age ≥65 that had a diagnosis of DLBCL (ICD-O-3 8680, 8684); HRQOL responses from the first available survey after DLBCL were used. SF-36 PCS and MCS (both scales range from 0–100) and poor self-rated health (self –reported fair or poor general health compared to other people your age) were compared among DLBCL patients by time from diagnosis to survey: 0–1, 1–3, and 3–5 years. HRQOL was also compared to patients that had MHOS data >1 year prior to a DLBCL diagnosis. Differences in PCS and MCS median scores were tested using the Wilcoxon rank sum test, and differences in the proportions of participants reporting fair or poor self-rated health were tested using the χ2statistic. Results: Median age and range for patients surveyed before, 0–1 (n=62), 1–3 (n=76), or 3–5 (n=31) years after their DLBCL diagnosis was similar (medians 73, 75, 74, and 78 years old, respectively; p=0.37). Date ranges for DLBCL diagnoses are as follows: 1997–2005, 1995–2004, and 1993–1998 for those surveyed 0–1, 1–3, and 3–5 year after diagnosis. HRQOL and self-rated health were low among the patients surveyed prior to their DLBCL diagnosis (n=296; PCS median=45.0, MCS median=56.3, poor self-rated health: 22.3%). In comparison, patients surveyed 0–1 year after DBCL diagnosis have even worse HRQOL scores (PCS median=33.6, MCS median=40.8, poor self-rated health: 51.6%; p=<0.0001 for all three comparisons). While older DLBCL patients surveyed 3–5 years from diagnosis have better quality of life (PCS median=36.0, MCS median=53.3, poor self-rated health fair: 29.0%) in comparison to the participants surveyed 0–1 year after diagnosis, PCS is still significantly different from the similarly aged group that was surveyed before their DLBCL (p=0.021). Conclusion: In this SEER-MHOS population of older patients with a history of DLBCL, HRQOL is surprisingly low. Older patients prior to DLBCL had low scores on both the physical and mental components of the SF-36, indicating vulnerability prior to diagnosis and treatment. HRQOL and self-rated health was statistically and clinically worse among DLBCL patients less than a year out from diagnosis, possibly due to therapy. Notably, HRQOL remains low, compared to pre-diagnosis, in patients surveyed 3–5 years out from diagnosis, particularly in the physical domains. This study provides a benchmark for HRQOL among older patients with DLBCL, an NHL subtype in which aggressive treatment with curative intent is a standard approach, and further research that evaluates HRQOL prospectively in vulnerable older patients receiving treatment for DLBCL is critical. Disclosures: No relevant conflicts of interest to declare.


2017 ◽  
Vol 35 (4_suppl) ◽  
pp. 24-24
Author(s):  
Young-Il Kim ◽  
Young Ae Kim ◽  
Chan Gyoo Kim ◽  
Keun Won Ryu ◽  
Young Woo Kim ◽  
...  

24 Background: The aim of this study was to compare the serial changes of health-related quality of life (HRQOL) after Endoscopic submucosal dissection (ESD) with those after surgery in patients with early gastric cancer (EGC). Methods: Gastric cancer patients were prospectively enrolled from 2004 through 2007. HRQOLs of 161 EGC patients were prospectively assessed by European Organization for Research and Treatment of Cancer Quality of Life Questionnaire-Core 30 (EORTC-QLQ-C30) and the stomach cancer-specific module EORTC-QLQ-STO22 at the baseline, 1, 6, 12, 18 and 24 months after treatments. Analysis was done using the generalized linear model and paired- ttests. Results: Of 161 patients, 48 (29.8%) underwent ESD (ESD group) and 113 (70.2%) underwent surgery (surgery group). The median age of stomach cancer patients was 57 years. Surgery group had poorer scores compared with those of ESD group in the most HRQOL factors one month after treatments ( P< 0.05), except for emotional and cognitive functioning, financial problems, anxiety, and hair loss. However, most of the functional and symptom scales after surgery subsequently improved and became insignificant until 24 months of follow up. Only 3 parameters including physical functioning, diarrhea and body image in ESD group still remained better until 24 months after treatment ( P< 0.05). Conclusions: Because poorer HRQOLs after surgery in the early post-treatment periods become insignificant during long-term follow-up, surgical treatment should not be discouraged in EGC treatment solely based on the QOL aspects.


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