Alice R. T. Bergin
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Alice R. T. Bergin has a total of 87 co-authors. Here are the top co-authors by number of shared publications:
Anand Murugasu
15 shared publications- Andrew W. Roberts
Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia
15 shared publications - François Vaillant
ACRF Cancer Biology and Stem Cells Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, Australia
15 shared publications G. Bruce Mann
15 shared publications- Geoffrey J. Lindeman
Cancer Biology and Stem Cells Division, The Walter and Eliza Hall Institute of Medical Research, Parkville, Australia
15 shared publications - Gordon K. Smyth
The Walter and Eliza Hall Institute of Medical Research, Parkville, VIC 3050, Australia
15 shared publications
Latest Publications
- 20 September 2026
- Published by Wiley in Medical Journal of Australia
- Vol. 224 (9)
Sovereignty and Survival: Understanding Lung Cancer Outcomes for Aboriginal and Torres Strait Islander People in Australia, a Case–Control Study
Objective: To identify factors contributing to the known increased age‐standardised incidence and mortality rates for lung cancer for Aboriginal and Torres Strait Islander people in Victoria, Australia. Study Type: Retrospective, population‐based, case–control study using Victorian Cancer Registry (VCR) data and linked health administrative datasets. Setting and Participants: Self‐identified Aboriginal and Torres Strait Islander people (respectfully referred to hereon as Aboriginal) and non‐Aboriginal people (aged > 18 years) diagnosed with lung cancer from 1 January 2008 to 31 December 2022. Main Outcome Measures: Clinical, pathological, demographic, socio‐economic factors and biomarkers (programmed cell death‐ligand 1 [PD‐L1], anaplastic lymphoma kinase [ ALK ] and c‐ros oncogene [ ROS1 ]) were assessed. Endpoints were all‐cause and lung cancer‐specific mortality. Survival analyses were conducted using Cox regression. Results: Aboriginal people ( N = 512) were younger ( p < 0.001), more likely to live outside a major city ( p < 0.001) and in areas of greatest disadvantage ( p < 0.001) than non‐Aboriginal people ( N = 43,468). More Aboriginal females had small cell lung cancer compared with non‐Aboriginal females (17% vs. 10%), more Aboriginal males had adenocarcinomas (41% vs. 36%) and squamous cell carcinomas (26% vs. 20%), compared with non‐Aboriginal males. There were no differences in the proportions of PD‐L1‐positive disease nor ALK or ROS1 gene rearrangements. A higher risk of all‐cause mortality (hazard ratio, 1.12; 95% CI, 1.01–1.24; p = 0.03) for Aboriginal people after stratification for age, sex and lung cancer subtype was identified. Conclusion: This study identified that Aboriginal people were younger, more likely to be living outside of major cities and in areas of greatest inequity than non‐Aboriginal people, which is an ongoing manifestation of colonisation. Aboriginal people diagnosed with lung cancer had an increased all‐cause mortality compared with non‐Aboriginal people.
- 20 September 2026
- Published by Wiley in Medical Journal of Australia
- Vol. 224 (9)
Sovereignty and Survival: Understanding Lung Cancer Outcomes for Aboriginal and Torres Strait Islander People in Australia, a Case–Control Study
Objective: To identify factors contributing to the known increased age‐standardised incidence and mortality rates for lung cancer for Aboriginal and Torres Strait Islander people in Victoria, Australia. Study Type: Retrospective, population‐based, case–control study using Victorian Cancer Registry (VCR) data and linked health administrative datasets. Setting and Participants: Self‐identified Aboriginal and Torres Strait Islander people (respectfully referred to hereon as Aboriginal) and non‐Aboriginal people (aged > 18 years) diagnosed with lung cancer from 1 January 2008 to 31 December 2022. Main Outcome Measures: Clinical, pathological, demographic, socio‐economic factors and biomarkers (programmed cell death‐ligand 1 [PD‐L1], anaplastic lymphoma kinase [ ALK ] and c‐ros oncogene [ ROS1 ]) were assessed. Endpoints were all‐cause and lung cancer‐specific mortality. Survival analyses were conducted using Cox regression. Results: Aboriginal people ( N = 512) were younger ( p < 0.001), more likely to live outside a major city ( p < 0.001) and in areas of greatest disadvantage ( p < 0.001) than non‐Aboriginal people ( N = 43,468). More Aboriginal females had small cell lung cancer compared with non‐Aboriginal females (17% vs. 10%), more Aboriginal males had adenocarcinomas (41% vs. 36%) and squamous cell carcinomas (26% vs. 20%), compared with non‐Aboriginal males. There were no differences in the proportions of PD‐L1‐positive disease nor ALK or ROS1 gene rearrangements. A higher risk of all‐cause mortality (hazard ratio, 1.12; 95% CI, 1.01–1.24; p = 0.03) for Aboriginal people after stratification for age, sex and lung cancer subtype was identified. Conclusion: This study identified that Aboriginal people were younger, more likely to be living outside of major cities and in areas of greatest inequity than non‐Aboriginal people, which is an ongoing manifestation of colonisation. Aboriginal people diagnosed with lung cancer had an increased all‐cause mortality compared with non‐Aboriginal people.
- Open Access
- 1 July 2025
- Published by American Association for Cancer Research (AACR)
Figure S1 from Aboriginal and Torres Strait Islander Females and Survival from Breast Cancer
Bar charts showing significantly more Aboriginal females live in areas of greatest socioeconomic disadvantage and outside the greater metropolitan area
- 1 July 2025
- Published by American Association for Cancer Research (AACR)
Open AccessFigure S1 from Aboriginal and Torres Strait Islander Females and Survival from Breast Cancer
Bar charts showing significantly more Aboriginal females live in areas of greatest socioeconomic disadvantage and outside the greater metropolitan area
- Open Access
- 1 July 2025
- Published by American Association for Cancer Research (AACR)
Table S2 from Aboriginal and Torres Strait Islander Females and Survival from Breast Cancer
Analysis of co-variates for Aboriginal females and females from TCGA
- 1 July 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S2 from Aboriginal and Torres Strait Islander Females and Survival from Breast Cancer
Analysis of co-variates for Aboriginal females and females from TCGA
- Open Access
- 1 July 2025
- Published by American Association for Cancer Research (AACR)
Table S1 from Aboriginal and Torres Strait Islander Females and Survival from Breast Cancer
Immune-biology data for Aboriginal females and females from TCGA with breast cancer
- 1 July 2025
- Published by American Association for Cancer Research (AACR)
Open AccessTable S1 from Aboriginal and Torres Strait Islander Females and Survival from Breast Cancer
Immune-biology data for Aboriginal females and females from TCGA with breast cancer
- 29 April 2025
- Published by American Association for Cancer Research (AACR) in Cancer Epidemiology, Biomarkers & Prevention
- Vol. 34 (7) , 1167-1176
Aboriginal and Torres Strait Islander Females and Survival from Breast Cancer
Background: Despite access to universal health care, Aboriginal and Torres Strait Islander females (hereafter respectfully referred to as Aboriginal) in Australia have higher breast cancer incidence and mortality rates. We investigated the factors contributing to these survival disparities. Methods: Aboriginal females (n = 395; 0.7%) and non-Aboriginal females (n = 57,618; 99.3%) with breast cancer were identified from Victoria, Australia. Clinical, pathologic, demographic, and socioeconomic variables were analyzed. Endpoints were all-cause and breast cancer–specific mortality. HRs were estimated using Cox regression. Stromal tumor–infiltrating lymphocytes were evaluated from a subset of Aboriginal females and compared with females in The Cancer Genome Atlas. Results: Registry data revealed that Aboriginal females were younger (P < 0.001), had more advanced stage disease (P = 0.007), and were more likely to live in nonmetropolitan areas (P < 0.001) and in areas of greater disadvantage (P < 0.001) compared with other females at diagnosis. Age-adjusted multivariate analysis revealed a higher all-cause mortality risk (HR 1.27; 95% confidence interval, 1–1.61) for Aboriginal females, but this risk diminished for breast cancer–specific mortality and after adjustment for stage and grade. Breast cancers from Aboriginal females had significantly reduced stromal tumor–infiltrating lymphocytes in the luminal and triple-negative subtypes compared with The Cancer Genome Atlas. Conclusions: Mortality for females with breast cancer was influenced by socioeconomic, geographic, and clinical factors. Notably, Aboriginal females with tumor features typically associated with favorable outcomes experienced poorer outcomes. The reduced immune infiltrate warrants further investigation. Impact: These findings highlight the need to address socioeconomic inequities and ensure culturally safe cancer care. Further research should explore biological and environmental factors influencing outcomes for Australian Aboriginal females.
- 29 April 2025
- Published by American Association for Cancer Research (AACR) in Cancer Epidemiology, Biomarkers & Prevention
- Vol. 34 (7) , 1167-1176
Aboriginal and Torres Strait Islander Females and Survival from Breast Cancer
Background: Despite access to universal health care, Aboriginal and Torres Strait Islander females (hereafter respectfully referred to as Aboriginal) in Australia have higher breast cancer incidence and mortality rates. We investigated the factors contributing to these survival disparities. Methods: Aboriginal females (n = 395; 0.7%) and non-Aboriginal females (n = 57,618; 99.3%) with breast cancer were identified from Victoria, Australia. Clinical, pathologic, demographic, and socioeconomic variables were analyzed. Endpoints were all-cause and breast cancer–specific mortality. HRs were estimated using Cox regression. Stromal tumor–infiltrating lymphocytes were evaluated from a subset of Aboriginal females and compared with females in The Cancer Genome Atlas. Results: Registry data revealed that Aboriginal females were younger (P < 0.001), had more advanced stage disease (P = 0.007), and were more likely to live in nonmetropolitan areas (P < 0.001) and in areas of greater disadvantage (P < 0.001) compared with other females at diagnosis. Age-adjusted multivariate analysis revealed a higher all-cause mortality risk (HR 1.27; 95% confidence interval, 1–1.61) for Aboriginal females, but this risk diminished for breast cancer–specific mortality and after adjustment for stage and grade. Breast cancers from Aboriginal females had significantly reduced stromal tumor–infiltrating lymphocytes in the luminal and triple-negative subtypes compared with The Cancer Genome Atlas. Conclusions: Mortality for females with breast cancer was influenced by socioeconomic, geographic, and clinical factors. Notably, Aboriginal females with tumor features typically associated with favorable outcomes experienced poorer outcomes. The reduced immune infiltrate warrants further investigation. Impact: These findings highlight the need to address socioeconomic inequities and ensure culturally safe cancer care. Further research should explore biological and environmental factors influencing outcomes for Australian Aboriginal females.
- 12 May 2023
- Published by American Association for Cancer Research (AACR) in Cancer Immunology Research
- Vol. 11 (6) , 705-706
Ethnicity, Immunity, and Outcomes: Biology versus Socioeconomic Status
Substantial advances in our understanding of breast cancer disease biology have led to marked improvements in cancer outcomes over the past two decades. These advances have largely focused on women from developed, high-income countries and as a result, significant disparities exist. In this issue, Bauer and colleagues provide new insight into the breast cancer immune microenvironment from women across geographic regions in sub-Saharan Africa, despite inherent infrastructure limitations. The study amassed data from 1,497 women from sub-Saharan Africa, and 117 women from Germany with breast cancer, suggesting regional variation in immune composition but with no significant prognostic impact. These important findings require validation in large, codesigned prospective studies to fully understand the impact of biology, ethnicity, and socioeconomic status on breast cancer outcomes.See related article by Bauer et al., p. 720 (2) .
- 12 May 2023
- Published by American Association for Cancer Research (AACR) in Cancer Immunology Research
- Vol. 11 (6) , 705-706
Ethnicity, Immunity, and Outcomes: Biology versus Socioeconomic Status
Substantial advances in our understanding of breast cancer disease biology have led to marked improvements in cancer outcomes over the past two decades. These advances have largely focused on women from developed, high-income countries and as a result, significant disparities exist. In this issue, Bauer and colleagues provide new insight into the breast cancer immune microenvironment from women across geographic regions in sub-Saharan Africa, despite inherent infrastructure limitations. The study amassed data from 1,497 women from sub-Saharan Africa, and 117 women from Germany with breast cancer, suggesting regional variation in immune composition but with no significant prognostic impact. These important findings require validation in large, codesigned prospective studies to fully understand the impact of biology, ethnicity, and socioeconomic status on breast cancer outcomes.See related article by Bauer et al., p. 720 (2) .