Candice N. Thompson
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Candice N. Thompson has a total of 17 co-authors. Here are the top co-authors by number of shared publications:
- Allison W. Kurian
Department of Medicine, Stanford University School of Medicine, Stanford, USA
17 shared publications - Esther M. John
Department of Epidemiology and Population Health, Stanford University School of Medicine , Stanford, CA
17 shared publications - Gunita Kashyap
Stanford Healthcare 7 , Cancer Quality, Stanford, California
17 shared publications - Holden Terry Maecker
Stanford University School of Medicine
17 shared publications - Ingrid Luo
Stanford University
17 shared publications - Lidia Schapira
Division of Medical Oncology Department of Medicine Stanford University Stanford California USA
17 shared publications
Latest Publications
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 2 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Figure 2. Time from Diagnosis to minimum ALC
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 2 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Figure 2. Time from Diagnosis to minimum ALC
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Data from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Background:Low absolute lymphocyte count (ALC) is associated with breast cancer–specific mortality (BCM) and overall mortality (OM) in non-Hispanic (NH) White women with triple-negative breast cancer (TNBC). However, little is known about the relationship between ALC and BCM or OM in other breast cancer subtypes, racial, or ethnic groups. In this study, we investigated the association of ALC with BCM and OM by breast cancer subtype and evaluated for modification by race or ethnicity. Methods:We used the Oncoshare database, linking data from electronic medical records of academic and community institutions to data from the California Cancer Registry, to identify women diagnosed with stage I to III breast cancer in 2000 to 2017 who had a post-diagnosis ALC within 5 years. We used logistic regression to identify factors associated with low ALC (<1 K/μL) and Cox models to evaluate the association of minimum ALC (minALC) after diagnosis with BCM and OM. Results:In 11,669 women, low ALC was associated with neutropenia, chemotherapy receipt, advanced stage, more comorbidities, and aggressive tumor features (all P ≤ 0.001). Lower minALC was associated with higher OM [hazard ratio (HR) = 0.96 per 1 K/μL increase; 95% confidence interval (CI), 0.93–0.99], most strongly in TNBC (HR = 0.73; 95% CI, 0.59–0.91). Race and ethnicity modified associations of minALC with BCM and OM (interaction P < 0.001), more strongly in NH Black and Hispanic than NH White women. Conclusions:Low peripheral ALC was associated with higher OM in women with estrogen and/or progesterone receptor–positive, human epidermal growth factor receptor 2 (HER2)–negative breast cancer or TNBC. Impact:Low ALC is more strongly associated with OM and BCM in women from minoritized racial and ethnic groups.
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessData from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Background:Low absolute lymphocyte count (ALC) is associated with breast cancer–specific mortality (BCM) and overall mortality (OM) in non-Hispanic (NH) White women with triple-negative breast cancer (TNBC). However, little is known about the relationship between ALC and BCM or OM in other breast cancer subtypes, racial, or ethnic groups. In this study, we investigated the association of ALC with BCM and OM by breast cancer subtype and evaluated for modification by race or ethnicity. Methods:We used the Oncoshare database, linking data from electronic medical records of academic and community institutions to data from the California Cancer Registry, to identify women diagnosed with stage I to III breast cancer in 2000 to 2017 who had a post-diagnosis ALC within 5 years. We used logistic regression to identify factors associated with low ALC (<1 K/μL) and Cox models to evaluate the association of minimum ALC (minALC) after diagnosis with BCM and OM. Results:In 11,669 women, low ALC was associated with neutropenia, chemotherapy receipt, advanced stage, more comorbidities, and aggressive tumor features (all P ≤ 0.001). Lower minALC was associated with higher OM [hazard ratio (HR) = 0.96 per 1 K/μL increase; 95% confidence interval (CI), 0.93–0.99], most strongly in TNBC (HR = 0.73; 95% CI, 0.59–0.91). Race and ethnicity modified associations of minALC with BCM and OM (interaction P < 0.001), more strongly in NH Black and Hispanic than NH White women. Conclusions:Low peripheral ALC was associated with higher OM in women with estrogen and/or progesterone receptor–positive, human epidermal growth factor receptor 2 (HER2)–negative breast cancer or TNBC. Impact:Low ALC is more strongly associated with OM and BCM in women from minoritized racial and ethnic groups.
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 1 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Figure 1. Consort Diagram
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 1 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Figure 1. Consort Diagram
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 3 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Figure 3. Low ALC by Race, Ethnicity and time windows
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 3 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Figure 3. Low ALC by Race, Ethnicity and time windows
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Figure 4 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Figure 4. Low ALC by time window
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Figure 4 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Figure 4. Low ALC by time window
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table 11 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Table 11. Association between minALC and Mortality, by Race and Ethnicity
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table 11 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Table 11. Association between minALC and Mortality, by Race and Ethnicity
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table 3 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Table 3. Race and Ethnicity-specific Cox Hazard Ratios fro minALC and mortality
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table 3 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Table 3. Race and Ethnicity-specific Cox Hazard Ratios fro minALC and mortality
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table 1 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Table 1. Baseline patient characteristics with and without ALC
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table 1 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Table 1. Baseline patient characteristics with and without ALC
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table 10 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Table 10. Association between minALC and Mortality, by Breast Cancer Subtype.
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table 10 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Table 10. Association between minALC and Mortality, by Breast Cancer Subtype.
- Open Access
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Supplementary Table 2 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Table 2. Cox Hazard Ratios for minALC and Mortality by Landmark Windows
- 2 November 2026
- Published by American Association for Cancer Research (AACR)
Open AccessSupplementary Table 2 from Peripheral Absolute Lymphocyte Count, Breast Cancer–Specific and Overall Mortality According to Race, Ethnicity, and Breast Cancer Subtypes
Supplementary Table 2. Cox Hazard Ratios for minALC and Mortality by Landmark Windows