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E-Poster Display

61P - Gender and race/ethnicity differences in outcomes of biliary cancers (BC): A SEER database analysis

Date

17 Sep 2020

Session

E-Poster Display

Topics

Tumour Site

Hepatobiliary Cancers

Presenters

Heinz Josef Lenz

Citation

Annals of Oncology (2020) 31 (suppl_4): S260-S273. 10.1016/annonc/annonc259

Authors

H.J. Lenz1, C. Luo2, P. Jayachandran1, H. Arai1, J. Wang1, N. Kawanishi1, S. Soni1, A.B. El-Khoueiry1, W. Zhang1, J. Millstein2, F. Battaglin1

Author affiliations

  • 1 Oncology, USC - Norris Comprehensive Cancer Center, 90033 - Los Angeles/US
  • 2 Preventive Medicine, Keck School of Medicine, USC - Norris Comprehensive Cancer Center, 90033 - Los Angeles/US

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Abstract 61P

Background

Strong evidence supports the impact of gender and race/ethnic background on patients (pts) outcomes across several cancer types. Here we present a comprehensive analysis of the Surveillance, Epidemiology, and End Results database (SEER 1975-2016) in BC.

Methods

53718 pts with BC (22068 gallbladder, 12502 intrahepatic bile duct, 16111 extrahepatic bile duct, 3037 unspecified) were included. Primary end point was 5-year survival probability. Log-rank tests were used to evaluate the effects of gender and race/ethnicity on overall survival (OS). Subgroups analyses included primary tumor site, disease stage, and treatment.

Results

43% of pts in our series were male (M) and 57% female (F); 66% were White/Caucasian (W), 15% Hispanic (H), 11% Asian (A), 8% Black/African American (BA). Significant differences in baseline pts characteristics were found between M and F for: age of diagnosis (68 vs 70 yr), stage (25 vs 28% local disease), primary tumor site (38% extrahepatic in M, 50% gallbladder in F), surgical treatment (39 vs 47%), P < .001. Significant differences in gender proportions and age were observed across race/ethnic groups, with youngest mean age at diagnosis and highest prevalence of F pts in H (66 yr, 64%) and BA (66 yr, 61%). Overall, F pts had higher 5-year OS probability compared to M (0.13 vs 0.11, P < .001). This difference was significant regardless of age in F, however, younger F pts showed higher OS probability rates (0.23 in age <50 vs 0.13 in age ≥ 50 yr, P < .0001). Among race/ethnic groups, higher 5-year OS probability was observed for H and A while lower for BA and W (0.16 vs 0.14 vs 0.13 vs 0.12, P < .0001). The gender related survival difference was largest in H (0.17 vs 0.13, P < .001) but was also significant in BA (0.13 vs 0.11, P = .01); no significant difference was found in W and A. When stratified by both gender and ethnicity, the highest survival probabilities were observed for H and A female pts, the lowest for W and BA males (0.17 vs 0.15 vs 0.11 vs 0.11, P < .0001). A subgroup analysis in the metastatic setting showed the lowest 5-year OS probability in BA female pts (0.05), the highest in H (0.07, both M and F) and A females (0.07).

Conclusions

Our data show that outcomes of BC differ by gender and race/ethnicity, favoring F gender and Hispanic and Asian ethnicity.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

National Cancer Institute grant number P30CA014089, the Gloria Borges WunderGlo Foundation-The Wunder Project, the Dhont Family Foundation, the San Pedro Peninsula Cancer Guild, the Daniel Butler Research Fund, the Call to Cure Research Fund and the Fong Research Project.

Disclosure

H.J. Lenz: Honoraria (self), Advisory/Consultancy, Travel/Accommodation/Expenses: Merck Serono; Honoraria (self), Advisory/Consultancy: Roche; Honoraria (self), Advisory/Consultancy, Travel/Accommodation/Expenses: Bayer; Advisory/Consultancy: Bristol-Myers Squibb; Honoraria (self), Advisory/Consultancy: GlaxoSmithKline; Honoraria (self): Boehringer Ingelheim; Honoraria (self): Isofol Medical. A.B. El-Khoueiry: Honoraria (self), Advisory/Consultancy: CytomX Therapeutics; Honoraria (self), Advisory/Consultancy: Bristol-Myers Squibb; Honoraria (self), Advisory/Consultancy: Bayer; Honoraria (self), Advisory/Consultancy: Eisai; Honoraria (self), Advisory/Consultancy: Roche/Genentech; Honoraria (self), Advisory/Consultancy: EMD Serono; Honoraria (self), Advisory/Consultancy, Research grant/Funding (self): Merck; Honoraria (self), Advisory/Consultancy: Exelixis; Honoraria (self), Advisory/Consultancy: Pieris Pharmaceuticals; Honoraria (self), Advisory/Consultancy: Agenus; Honoraria (self), Advisory/Consultancy: Gilead Sciences; Honoraria (self), Advisory/Consultancy, Research grant/Funding (self): AstraZaneca/MedImmune; Research grant/Funding (self): Astex Pharmaceuticals; Advisory/Consultancy: Novartis; Advisory/Consultancy: BMSCelgene. F. Battaglin: Travel/Accommodation/Expenses: Caris Life Sciences. All other authors have declared no conflicts of interest.

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