scholarly journals PCN208 REAL WORLD TREATMENT PATTERNS ANALYSIS FOR PATIENTS WITH ADVANCED OR METASTATIC LUNG CANCER IN THEIR INITIAL TREATMENT: A NATIONWIDE, MULTI-CENTER, RETROSPECTIVE MEDICAL CHART REVIEW IN CHINA (PASSION STUDY)

2019 ◽  
Vol 22 ◽  
pp. S95
Author(s):  
B. Qiu ◽  
L. Fan ◽  
Z. Tang ◽  
J. He ◽  
P.F. Wang
2014 ◽  
Vol 32 (31_suppl) ◽  
pp. 126-126 ◽  
Author(s):  
Jessica Ruth Bauman ◽  
Zofia Piotrowska ◽  
Emily Scribner ◽  
Brandon Temel ◽  
Rebecca Suk Heist ◽  
...  

126 Background: Metastatic lung cancer is the leading cause of cancer-related death in the US. In the last decade, however, patients (pts) with EGFR mutations have benefitted from improved outcomes with EGFR-directed targeted therapy. We hypothesized that this improvement might impact EOL care. The objective of this chart review was to describe the care of EGFR mutant pts with attention to EOL care, health care utilization, and palliative care use. Methods: With IRB approval, we retrospectively reviewed medical records of pts at our center diagnosed with advanced EGFR-mutant lung cancer from January 2009 to June 2012. We limited the review to pts who had at least one cancer therapy at MGH, and to those who died by June 2014. Results: 44 pts were included. 30 pts (68%) were female. 32 pts (73%) received cancer-directed therapy within 30 days of death. Of these, 30 pts (68%) received oral chemotherapy and 5 (11%) received IV chemotherapy. 30 pts (68%) were hospitalized within 30 days of death. Over their entire disease course, the median number of hospitalizations was 2 (0-8), and the median number of total inpatient days was 12 (0-88). 21 pts (48%) had a palliative care outpatient visit and 34 (77%) had an inpatient palliative care consult at some point during their care. 24 pts (54%) enrolled on hospice prior to death, 15 (34%) were never on hospice, and the hospice status of 5 (11%) was unknown. Of the 39 pts with known hospice status, median length of stay was 6 days (0-206). 23 pts (52%) died at home with hospice or in an inpatient hospice, 16 (36%) died in the hospital, 2 (4%) died at home without hospice, and the location of death was unknown for 3 (7%). Conclusions: Pts with EGFR mutations had high rates of hospitalization and chemotherapy use in the last month of life, and many died in the hospital. Palliative care utilization was high, but it is unclear how this affected EOL care. Designing innovative care models to support this unique population and understand EOL decision-making should be a priority.


2016 ◽  
Vol 34 (15_suppl) ◽  
pp. 6567-6567
Author(s):  
Catherine Labbe ◽  
Erin L. Stewart ◽  
Catherine Brown ◽  
Andrea Perez Cosio ◽  
Ashlee Vennettilli ◽  
...  

2020 ◽  
Vol 38 (29_suppl) ◽  
pp. 93-93
Author(s):  
Atul Batra ◽  
Shiying Kong ◽  
Rodrigo Rigo ◽  
Winson Y. Cheung

93 Background: Due to highly selective enrollment in clinical trials, the generalizability of results may be limited. This study aimed to identify the proportion of real-world patients with metastatic lung cancer (MLC) eligible to participate in a clinical trial. Methods: We identified patients diagnosed with MLC in a large Canadian province from 2004 to 2017. Ineligibility to participate in a clinical trial was defined by common exclusion criteria: age > 75 years, anemia, comorbid conditions (heart disease, uncontrolled diabetes, kidney disease, or liver disease) and history of a prior malignancy or immunosuppression. Logistic regression models were used to describe the likelihood of receiving systemic therapy and Cox regression models were constructed to determine the association of trial ineligibility with overall survival (OS). Results: A total of 13,996 patients were included; the median age was 70 years and 46.9% were women. Of these, 8,615 (61.6%) were trial-ineligible. The common reasons for ineligibility were age > 75 years (11.5%), abnormal renal function (8.3%) and prior immunosuppression (3.2%). Further, 32.3% of patients were ineligible by multiple exclusion criteria. In the real-world, 40.6% and 21.8% of trial-eligible and ineligible patients received systemic therapy (P < .001), respectively. After adjusting for age and sex, trial-ineligible patients had lower odds of receiving systemic therapy (odds ratio, .84; 95% confidence interval [CI], .76-.92; P < .001). At a median follow-up of 66.2 months, the median OS of trial-eligible patients was 5.1 months as compared to 2.9 months in those deemed ineligible (P < .001). Receipt of systemic therapy was associated with longer OS in both trial-eligible (10.5 vs 2.7 months, P < .001) and ineligible (9.3 vs 2.1 months, P < .001) patients. In a Cox regression model that adjusted for age, sex and systemic therapy, ineligibility was predictive of worse OS. Conclusions: More than half of patients with MLC are ineligible to participate in clinical trials. Real-world use of systemic therapy was generally low, but its use was associated with improvement in OS even among individuals considered trial-ineligible. Clinical trials should broaden their eligibility criteria to better represent the phenotype of real-world patients so that findings are more generalizable. [Table: see text]


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