Abstract 150P
Background
Gastric cancer (GC) [including gastroesophageal junction cancer (GEJC)] has the second highest incidence and third highest mortality rate of all malignancies in China. For patients diagnosed with unresectable advanced or metastatic (UAM) GC, the prognosis and survival outcomes are extremely poor.
Methods
This was a retrospective real-world observational study using an oncology database operated by Digital China Health (DCH), which is comprehensive electronic health record (EHR) repository of patient demographics, clinical (including imaging, pathology.), medication use, healthcare resource use (HCRU) and cost data. Patients having ≥2 inpatient records with a primary ICD-10 code of GC were selected from Jan 1st, 2012 through Dec 31st, 2018. The first date of inpatient admission was defined as the index date. Patients were followed for a minimum ± 30 days from the index date and were stratified as resectable vs. unresectable advanced or metastatic (UAM). Demographics, clinical parameters, medication utilization, HCRU, and costs incurred were tracked for these cohorts.
Results
A total of 7,464 patients met the inclusion/exclusion criteria, of whom 14.1% (n=1056) had UAM GC. The mean age at index date of patients with UAM GC was 57.7 (SD=11.3) years, with the vast majority male (70.5%). 69.3% (n=732) of patients with UAM GC received first line (1L) chemotherapy, the most frequent being S-1 + oxaliplatin (SOX, 22.7%) fluorouracil + oxaliplatin (FOLFOX, 12.6%) and capecitabine + oxaliplatin (XELOX, 11.2%). The average duration of 1L chemotherapy was 133.8 ± 115.9 days. Of these 1L line patients, 29.5% (n=216) went on to 2L treatment and 25.9 % (n=56) of 2L patients received 3L treatment. The main disease complications due to UAM GC were gastro-intestinal obstructions (7.8%) and ascites (7.5%). The main adverse drug events due to treatment were anemia (45.6%) and liver impairment (41.1%).
Conclusions
The majority of patients with UAM GC received 1L treatment. The top three regimens were SOX, FOLFOX and XELOX which seems consistent with Chinese Society of Clinical Oncology (CSCO) GC treatment guidelines.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
Bristol-Myers Squibb Pharmaceutical Corp.
Funding
Bristol-Myers Squibb Pharmaceutical Corp.
Disclosure
X. Sun, Y. Qu: Research grant/Funding (self): Bristol-Myers Squibb. P. Navaratnam, H.S. Friedman: Research grant/Funding (self): Bristol-Myers Squibb. J. Gricar, H. Xiao: Shareholder/Stockholder/Stock options, Full/Part-time employment: Bristol-Myers Squibb.
Resources from the same session
211P - The impact of low muscle mass to overall survival in bladder cancer patients undergoing chemotherapy: A systematic review and meta-analysis
Presenter: Karunia Japar
Session: e-Poster Display Session
212P - Stage I non-seminoma testicular cancer: Adjuvant management and outcomes
Presenter: Gaik Tin Quah
Session: e-Poster Display Session
213P - Stage I seminoma testicular cancer: Predictors of relapse and outcomes for adjuvant carboplatin vs active surveillance
Presenter: Gaik Tin Quah
Session: e-Poster Display Session
214P - Study of treatment outcome in adults with TFE related RCC
Presenter: Ajaykumar Singh
Session: e-Poster Display Session
215P - Analysis of spatial heterogeneity of responses in metastatic sites with nivolumab in renal cell carcinoma
Presenter: Venkata Pradeep Babu Koyyala
Session: e-Poster Display Session
216P - Clinical profile and treatment outcome of testicular seminoma treated at tertiary care centre in Chennai
Presenter: Sivasubramaniam Kumaravelu
Session: e-Poster Display Session
220P - A cost-effectiveness analysis of systemic therapy for metastatic hormone-sensitive prostate cancer
Presenter: Winnie Sung
Session: e-Poster Display Session
221P - Patient-reported sexual and urinary function in nonmetastatic castration-resistant prostate cancer (nmCRPC) when treated with apalutamide (APA) vs placebo (PBO) and ongoing androgen deprivation therapy (ADT) in SPARTAN
Presenter: Hiroji Uemura
Session: e-Poster Display Session
222P - Tolerability and treatment response to darolutamide (DARO) in patients with non-metastatic castration-resistant prostate cancer (nmCRPC) in the phase III ARAMIS trial
Presenter: Matthew R. Smith
Session: e-Poster Display Session
223P - Overall survival (OS) results of phase III ARAMIS study of darolutamide (DARO) added to androgen deprivation therapy (ADT) for non-metastatic castration-resistant prostate cancer (nmCRPC)
Presenter: Karim Fizazi
Session: e-Poster Display Session