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  • American Association for Cancer Research (AACR)  (48)
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  • 1
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2020
    In:  Clinical Cancer Research Vol. 26, No. 14 ( 2020-07-15), p. 3760-3770
    In: Clinical Cancer Research, American Association for Cancer Research (AACR), Vol. 26, No. 14 ( 2020-07-15), p. 3760-3770
    Abstract: Adults with T-cell lymphoblastic lymphoma (T-LBL) generally benefit from treatment with acute lymphoblastic leukemia (ALL)-like regimens, but approximately 40% will relapse after such treatment. We evaluated the value of CpG methylation in predicting relapse for adults with T-LBL treated with ALL-like regimens. Experimental Design: A total of 549 adults with T-LBL from 27 medical centers were included in the analysis. Using the Illumina Methylation 850K Beadchip, 44 relapse-related CpGs were identified from 49 T-LBL samples by two algorithms: least absolute shrinkage and selector operation (LASSO) and support vector machine–recursive feature elimination (SVM-RFE). We built a four-CpG classifier using LASSO Cox regression based on association between the methylation level of CpGs and relapse-free survival in the training cohort (n = 160). The four-CpG classifier was validated in the internal testing cohort (n = 68) and independent validation cohort (n = 321). Results: The four-CpG–based classifier discriminated patients with T-LBL at high risk of relapse in the training cohort from those at low risk (P & lt; 0.001). This classifier also showed good predictive value in the internal testing cohort (P & lt; 0.001) and the independent validation cohort (P & lt; 0.001). A nomogram incorporating five independent prognostic factors including the CpG-based classifier, lactate dehydrogenase levels, Eastern Cooperative Oncology Group performance status, central nervous system involvement, and NOTCH1/FBXW7 status showed a significantly higher predictive accuracy than each single variable. Stratification into different subgroups by the nomogram helped identify the subset of patients who most benefited from more intensive chemotherapy and/or sequential hematopoietic stem cell transplantation. Conclusions: Our four-CpG–based classifier could predict disease relapse in patients with T-LBL, and could be used to guide treatment decision.
    Type of Medium: Online Resource
    ISSN: 1078-0432 , 1557-3265
    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2020
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  • 2
    In: Cancer Prevention Research, American Association for Cancer Research (AACR), Vol. 10, No. 6 ( 2017-06-01), p. 327-336
    Abstract: Sufficient sleep duration is crucial for maintaining normal physiological function and has been linked to cancer risk; however, its contribution to lung cancer mortality is unclear. Therefore, we evaluated the relationship between average sleep duration in various age-periods across the adult lifecourse, and risk of lung cancer mortality in Xuanwei, China. An ambidirectional cohort study was conducted in 42,422 farmers from Xuanwei, China. Participants or their surrogates were interviewed in 1992 to assess average sleep hours in the age periods of 21–30, 31–40, 41–50, 51–60, 61–70, and ≥71 years, which were categorized as ≤7, 8 (reference), 9, and ≥10 hours/day. Vital status was followed until 2011. Sex-specific Cox regression models were used to estimate hazard ratios (HR) and 95% confidence intervals (CI) for lung cancer mortality in 1994–2011, adjusted for demographic, anthropometric, medical, and household characteristics. J-shaped relationships were found between average sleep duration and lung cancer mortality. The patterns were consistent across sex, age periods, and fuel usage. Compared with sleeping 8 hours/day on average, ≤7 hours/day was associated with significantly increased HRs ranging from 1.39 to 1.58 in ages ≥41 years in men, and 1.29 to 2.47 in ages ≥51 years in women. Furthermore, sleeping ≥10 hours/day was associated with significantly increased HRs ranging from 2.44 to 3.27 in ages ≥41 year in men, and 1.31 to 2.45 in ages ≤60 years in women. Greater and less than 8 hours/day of sleep in various age-periods may be associated with elevated risk of lung cancer mortality in Xuanwei, China. Cancer Prev Res; 10(6); 327–35. ©2017 AACR.
    Type of Medium: Online Resource
    ISSN: 1940-6207 , 1940-6215
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2017
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  • 3
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 74, No. 19_Supplement ( 2014-10-01), p. 2184-2184
    Abstract: Introduction: Indoor air pollution (IAP), mostly from coal burning, was responsible for approximately 3.5 million deaths from all-causes and over 100,000 disability-adjusted life years in 2010. The majority of studies conducted in the past have been retrospective, in rural and under developed populations with recent and high levels of exposure. We assessed the association between historic kitchen coal use and various causes of mortality in the prospective Shanghai Women's Health Study cohort. Methods: A cohort of 73,363 women was followed through December 2009 with a combination of in-person surveys every 2-3 years and annual linkage to a vital statistics registry database where all causes of mortality was recorded. A total of 3808 deaths were identified during the follow-up period. Cox proportional hazards models were used to estimate risk of mortality associated with in-home coal use. Models were adjusted for smoking status, family income, environmental tobacco smoke, occupational history, shift work, BMI, hormone therapy, and parity. Results: All-cause mortality was elevated 13% among ever coal users (Hazard Ratio (HR): 1.13; 95% CI: 1.04-1.23) compared to never-coal users. Coal use was most strongly associated with all-cause mortality among women who had more than 15 years of coal use (15-30 years: HR: 1.14; 95% CI: 1.02-1.26; & gt;30 years: HR: 1.15; 95% CI: 1.04-1.26). Women with 15-30 years of coal use had a 21% elevation of cancer mortality (95% CI: 1.04-1.42), but no elevation was observed in women with & gt;30 years of coal use (HR: 1.06; 95% CI: 0.91-1.24) compared to never-coal users. More than 30 years of coal use was associated with a 32% elevated risk of cardiovascular mortality (HR: 1.32; 95% CI: 1.11-1.57), and 62% elevated risk of myocardial infarction mortality (HR: 1.62; 95% CI: 1.01-2.63) compared to never-coal users. All-cause mortality was elevated in women who last lived in a coal burning home up to 20 years ago ( & gt;0-10 years: HR: 1.16; 95% CI: 1.04-1.28; & gt;10-20 years: HR: 1.21; 95% CI: 1.09-1.35). Discussion: This is the first study of mortality and in-home coal use in a prospective study after much of Shanghai transitioned into a developed and urban city. Evidence from this study suggests that previous coal use could be related to excess cardiovascular and cancer deaths among women in Shanghai. Citation Format: Christopher Kim, Xiao-Ou Shu, H. Dean Hosgood, Bryan A. Bassig, Wei Jie Seow, Yongbin Xiang, Bu-Tian Ji, Wei Hu, Wong-Ho Chow, Yutang Gao, Nathaniel Rothman, Qing Lan. Past use of coal for cooking is associated with all-cause mortality in the prospective Shanghai Women's Health Study. [abstract]. In: Proceedings of the 105th Annual Meeting of the American Association for Cancer Research; 2014 Apr 5-9; San Diego, CA. Philadelphia (PA): AACR; Cancer Res 2014;74(19 Suppl):Abstract nr 2184. doi:10.1158/1538-7445.AM2014-2184
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2014
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  • 4
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2014
    In:  Molecular Cancer Therapeutics Vol. 13, No. 6 ( 2014-06-01), p. 1503-1513
    In: Molecular Cancer Therapeutics, American Association for Cancer Research (AACR), Vol. 13, No. 6 ( 2014-06-01), p. 1503-1513
    Abstract: Tumorigenesis is an immortalization process in which the growth of normal cells is uncontrolled and programmed cell death is suppressed. Molecular biologic and immunologic studies have revealed that the aberrant expression of some proto-oncogenes boosts proliferation and inhibits apoptosis, which is vital for tumor development. The hypofunction of the host immune system also drives the development and metastasis of malignant tumors. Pim-3, a member of the Pim family, is aberrantly expressed in several cancers. Data suggest that Pim-3 inhibits apoptosis by phosphorylating the proapoptotic BH3-only protein Bad. Here, we constructed a dual-function small hairpin RNA (shRNA) vector containing an shRNA targeting Pim-3 and a TLR7-stimulating ssRNA. Stimulation with this bi-functional vector in vitro promoted significant apoptosis of Hepa1-6 cells by regulating the expression of apoptosis-related proteins and induced secretion of type I IFNs. Most importantly, this bi-functional vector more effectively inhibited subcutaneous Hepa1-6 cell growth than did single shRNA and ssRNA treatment in vivo. Natural killer (NK), CD4+ T, and CD8+ T cells and macrophages were required for effective tumor suppression, and CD4+ T cells were shown to play a helper role in the activation of NK cells, possibly by regulating the secretion of Th1 or Th2 cytokines. This ssRNA–shRNA bi-functional vector may represent a promising approach for tumor therapy. Mol Cancer Ther; 13(6); 1503–13. ©2014 AACR.
    Type of Medium: Online Resource
    ISSN: 1535-7163 , 1538-8514
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2014
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    SSG: 12
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  • 5
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2012
    In:  Cancer Research Vol. 72, No. 8_Supplement ( 2012-04-15), p. 646-646
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 72, No. 8_Supplement ( 2012-04-15), p. 646-646
    Abstract: Background: Recent large-scale clinical trials raised concerns regarding increased risk of aggressive lung cancer and lung cancer mortality among users of postmenopausal estrogen therapy. Soy and its phytoestrogens have been shown to act as a natural estrogen antagonist and have cancer-inhibitory activities in experimental studies. Objective: We prospectively evaluated the association of soy food intake with lung cancer risk, overall and by tumor aggressiveness, and perform a meta-analysis of published data. Methods: Included in this analysis were 71,550 women recruited in the Shanghai Women's Health Study, a population-based cohort study. Usual soy food intake was assessed at baseline and re-assessed during follow-up through in-person interviews. Previous studies were identified through a MEDLINE search. Results: During a mean follow-up of 9.1 years, 370 incident lung cancer cases were identified; 340 were lifetime never smokers. After adjustment for potential confounders, soy food intake was inversely associated with subsequent risk of lung cancer; the hazard ratio (HR) for the highest compared with lowest quintile of intake was 0.63 (95% CI: 0.44 - 0.90; P trend = 0.004). This inverse association appeared predominately among women with a later age at menopause (P interaction = 0.01) and varied by tumor aggressiveness as defined by length of survival ( & lt;12 versus β12 months), with corresponding HR of 0.49 for more aggressive lung cancer versus 0.76 for less aggressive lung cancer (P heterogeneity = 0.057). Similar inverse associations were observed for isoflavone intake. A meta-analysis of seven studies conducted among never smokers found a summary odds ratio of 0.59 (95% CI: 0.49 - 0.71) for the highest versus lowest categories of soy or isoflavone intake. Conclusion: This study suggests that soy food consumption may reduce lung cancer risk in nonsmoking women, particularly for aggressive lung cancer, and its effect may be modified by endogenous estrogens. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 103rd Annual Meeting of the American Association for Cancer Research; 2012 Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2012;72(8 Suppl):Abstract nr 646. doi:1538-7445.AM2012-646
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    RVK:
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2012
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  • 6
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2012
    In:  Cancer Research Vol. 72, No. 8_Supplement ( 2012-04-15), p. 1126-1126
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 72, No. 8_Supplement ( 2012-04-15), p. 1126-1126
    Abstract: Mitochondria play an important role in cellular energy metabolism, free radical generation, and apoptosis. Cumulative evidence suggests that mtDNA copy number may be a biomarker for cancer risk. Using a nested case-control design, we evaluated mtDNA copy number in peripheral blood cells in relation to colorectal cancer risk. Included in the study were 436 colorectal cancer cases and 881 matched controls identified from the Shanghai Woman's Health Study, a population-based, prospective cohort study conducted among Chinese women. Relative mtDNA copy number was determined in triplicate by a quantitative real-time PCR assay using peripheral blood cell DNA samples collected at the time of study enrollment, prior to cancer diagnosis. Baseline levels of mtDNA copy number were lower among women who subsequently developed colorectal cancer (geometric mean = 0.271, 95% CI: 0.263-0.279) than those who remained cancer-free (geometric mean = 0.281, 95% CI: 0.275-0.288) (P=0.0274). Multivariate adjusted odds ratios were 1.15 (95% CI: 0.80-1.65), 1.12 (95% CI: 0.78-1.60) and 1.58 (95% CI: 1.10-2.26) for third to the first quartile of mtDNA copy numbers, respectively, comparing with the highest quartile (P for trend = 0.0135). The association varied little by the interval between blood draw and cancer diagnosis. To our knowledge, this is the first large prospective study evaluating the association of mtDNA copy number with subsequent risk of developing colorectal cancer. Our data suggests that decreased mtDNA copy number may be associated with increased colorectal cancer risk, and mtDNA copy number measured in peripheral blood cells may be a potential biomarker useful for colorectal cancer risk assessment. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 103rd Annual Meeting of the American Association for Cancer Research; 2012 Mar 31-Apr 4; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2012;72(8 Suppl):Abstract nr 1126. doi:1538-7445.AM2012-1126
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
    RVK:
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2012
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  • 7
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 71, No. 8_Supplement ( 2011-04-15), p. 1876-1876
    Abstract: Residents in Xuanwei, China have the highest lung cancer incidence rates in China for both men and women, despite the fact that almost all women are non-smokers. Several lines of research have provided strong support that the excess lung cancer rate in this region is caused primarily by emissions from smoky coal exposure. We have carried out a hospital-based case-control study of non-smoking female lung cancer in Xuanwei and its neighboring county, Fuyuan, to identify which constituents of coal combustion emissions and other indoor environmental exposures are causing the high lung cancer rates in this region. In order to develop individual estimates of exposure to known or suspected lung carcinogens, we designed a comprehensive exposure assessment study of 163 households in this region to evaluate exposure to PAHs, PM2.5, silica, and other exposures from coal and wood burning. Homes that used three main fuel types (i.e., smoky coal, smokeless coal and wood), and eight stove types [e.g., firepit, fixed or portable stove, with or without ventilation] were identified and households were sampled on two consecutive days. Up to 30 households were selected for each combination of fuel and stove type. A subgroup of 53 households was measured at two time-points during the st udy year (e.g. summer and winter). The female head of each household was asked to wear a 24-hour personal PM2.5 air sampler at the same time that 24-hour area air sampling was employed in the main living area. Personal and area particulate matter samples (PM2.5) were collected in each home. These samples were also used to quantify particle bound PAHs including BaP (by GC/MS), elemental components (by XRF and ICP/MS), and silica (by XRD). XAD2 samples were collected for the quantification of gaseous PAHs. Other samples, including radon and organic vapor, fuel and ash were also obtained. We also collected information on potential factors that could influence exposure, such as house characteristics, stove type, fuel type and use, amount of fuel used, amount of time spent in each room. Initial analyses show that people using wood burned in firepits were exposed to the highest levels of PM2.5 measured in area (536.3±370.5 µg/m3) and personal samples(419.8±283.3 µg/m3). Burning smokeless coal in a high stove with a chimney was associated with the lowest exposure to PM2.5 (62.2±34.1 µg/m3, 62.5±29.9 µg/m3 for area and personal samples, respectively). These data show that there is a wide range of exposure to PM2.5 in this population. These data and other exposure information from this study will be used in the future to model environmental exposures and risk of lung cancer in this special, high risk population. Citation Format: {Authors}. {Abstract title} [abstract]. In: Proceedings of the 102nd Annual Meeting of the American Association for Cancer Research; 2011 Apr 2-6; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 2011;71(8 Suppl):Abstract nr 1876. doi:10.1158/1538-7445.AM2011-1876
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2011
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  • 8
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2014
    In:  Cancer Epidemiology, Biomarkers & Prevention Vol. 23, No. 11 ( 2014-11-01), p. 2357-2365
    In: Cancer Epidemiology, Biomarkers & Prevention, American Association for Cancer Research (AACR), Vol. 23, No. 11 ( 2014-11-01), p. 2357-2365
    Abstract: Background: Mitochondria play an important role in cellular energy metabolism, free radical production, and apoptosis, and thus may be involved in cancer development. Methods: We evaluated mitochondrial DNA (mtDNA) copy number in peripheral leukocytes in relation to colorectal cancer risk in a case–control study of 444 colorectal cancer cases and 1,423 controls nested in the Shanghai Women's Health Study, a population-based, prospective cohort study. Relative mtDNA copy number was determined by a quantitative real-time PCR assay using peripheral leukocyte DNA samples collected at the time of study enrollment, before cancer diagnosis. Results: We found that baseline mtDNA copy number was lower among women who subsequently developed colorectal cancer [geometric mean, 0.277; 95% confidence interval (CI), 0.269–0.285] than among women who remained cancer-free (geometric mean, 0.288; 95% CI, 0.284–0.293; P = 0.0153). Multivariate adjusted ORs were 1.26 (95% CI, 0.93–1.70) and 1.44 (95% CI, 1.06–1.94) for the middle and lower tertiles of mtDNA copy number, respectively, compared with the upper tertile (highest mtDNA copy number; Ptrend = 0.0204). The association varied little by the interval between blood collection and cancer diagnosis. Conclusions: Our data suggest that mtDNA copy number measured in peripheral leukocytes may be a potential biomarker useful for colorectal cancer risk assessment. Impact: If confirmed, mtDNA copy number measured in peripheral leukocytes may be a biomarker useful for colorectal cancer risk assessment. Cancer Epidemiol Biomarkers Prev; 23(11); 2357–65. ©2014 AACR.
    Type of Medium: Online Resource
    ISSN: 1055-9965 , 1538-7755
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2014
    detail.hit.zdb_id: 2036781-8
    detail.hit.zdb_id: 1153420-5
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  • 9
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 77, No. 13_Supplement ( 2017-07-01), p. 5315-5315
    Abstract: Xuanwei and Fuyuan are rural counties in China that have the highest lung cancer rates in the country among non-smoking women. This alarming public health burden has been attributed to the combustion of smoky (bituminous) coal for heating and cooking, which can produce carcinogenic emissions such as polycyclic aromatic hydrocarbons (PAHs). Previous studies found that green leafy vegetables could absorb PAHs through air and direct soil contamination. Further, oral ingestion of PAHs was found be to associated with pulmonary adenoma development in animal feeding studies. Therefore, we investigated the associations between lung cancer risk and dietary intake of specific green leafy vegetables and other foods in non-smoking women of this farming region. We conducted a hospital-based case-control study of 1,074 female lung cancer patients and 977 frequency-matched controls from Xuanwei and Fuyuan, China in 2006-2013. Dietary intake was self-reported on questionnaires and categorized as never, several times/year, several times/month, several times/week, and every day. Unconditional logistic regression models were used to estimate the odds ratios (OR) and 95% confidence intervals (CI) of lung cancer in relation to intake of specific green leafy vegetables (i.e. lettuce, cabbage, fennel, spinach, hollow vegetables), corn, buckwheat, carrots, tomatoes, dried and fresh chili, pickled vegetables, bean curd, mushrooms, and preserved meats. Models were adjusted for age, county, first-degree relative with lung cancer, passive smoke exposure, education, lifetime smoky coal tonnage, respiratory disease history, time spent indoors, and menopausal status. Separate models were fitted for each dietary factor. We found that increased consumption of several green leafy vegetables was associated with increased risk of lung cancer. Eating hollow vegetables every day was associated with 2.50 (95% CI: 1.18, 5.27) times the odds of lung cancer compared to never. Similarly, eating lettuce (OR=2.13, 95% CI: 1.41, 3.21) and cabbage (OR=1.82, 95% CI: 1.21, 2.69) every day was associated with increased risks compared to several times a year or less. Conversely, eating bean curd (OR=0.54, 95% CI: 0.40, 0.72) several times a week was associated with decreased risk compared to several times a year or less; while eating buckwheat (OR=0.59, 95% CI: 0.40, 0.89) several times a week was associated with decreased risk compared to never. No significant associations were found for fennel, spinach, and other foods. Our findings suggest that increased consumption of a variety of green leafy vegetables may be related to elevated lung cancer risk in non-smoking women from Xuanwei and Fuyuan, China, independent of other risk factors. The increased risk may be due to environmental contamination of crops from coal combustion. Conversely, frequent consumption of bean curd and buckwheat was found to be protective. Citation Format: Jason Y. Wong, Bryan A. Bassig, Wei Hu, Jinming Zhang, Wei Jie Seow, Neil E. Caporaso, Bu-tian Ji, Robert S. Chapman, George S. Downward, Jihua Li, Jun He, Kaiyun Yang, Yunchao Huang, Roel Vermeulen, Nathaniel Rothman, Qing Lan. Dietary intake and risk of lung cancer in non-smoking women: a hospital-based case-control study in Xuanwei and Fuyuan, China [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2017; 2017 Apr 1-5; Washington, DC. Philadelphia (PA): AACR; Cancer Res 2017;77(13 Suppl):Abstract nr 5315. doi:10.1158/1538-7445.AM2017-5315
    Type of Medium: Online Resource
    ISSN: 0008-5472 , 1538-7445
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    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2017
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    detail.hit.zdb_id: 1432-1
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  • 10
    Online Resource
    Online Resource
    American Association for Cancer Research (AACR) ; 2023
    In:  Cancer Research Vol. 83, No. 5_Supplement ( 2023-03-01), p. P1-01-01-P1-01-01
    In: Cancer Research, American Association for Cancer Research (AACR), Vol. 83, No. 5_Supplement ( 2023-03-01), p. P1-01-01-P1-01-01
    Abstract: Purpose: There is little evidence determining whether elderly patients (from 70 to 90 years old) with triple-negative breast cancer (TNBC) could benefit from adjuvant chemotherapy (AC). The objective of this study was to explore the effect of AC in these population following surgery. Methods: A total of 4610 patients were identified in the Surveillance, Epidemiology, and End Results database (2010-2018). Inverse probability of treatment weighting (IPTW) was used to reduce the selection bias. IPTW-adjusted Kaplan-Meiers survival analysis and Cox proportional hazards models were performed to compare breast cancer specific survival (BCSS) and overall survival (OS) in the two different treatment groups. Results: All eligible patients were divided into two groups, the chemotherapy (n=1989) and the observation (n=2621) groups. The percentage of patients receiving AC versus observation increased significantly from 2010 to 2018 (estimated annual percentage change, 1.49%; 95%CI, 0.75-2.16%, p=0.002). The 5-year IPTW-adjusted rates of BCSS and OS in AC group were better than that in observation group (BCSS: 82.32% vs. 78.42%, p=0.010; OS: 75.54% vs. 64.65%, p & lt; 0.001). In IPTW-adjusted Cox proportional hazards regression analysis, elderly patients could benefit from AC (BCSS: HR, 0.77, 95%CI, 0.62-0.94, p=0.012; OS: HR, 0.66, 95%CI, 0.57-0.78, p & lt; 0.001). AC was associated with a significant outcome benefit across year at diagnosis, marital status, stage, lymph node, surgery and radiation subgroups (all p & lt; 0.05). Patients with T1ab could not benefit from AC. Conclusions: We show a BCSS and OS benefit from AC in old patients with TNBC. AC may remain a reasonable treatment approach in these specific patients. For the patients with T1ab, de-escalated treatment should be administrated with caution. It requires further randomized controlled trial to ensure the AC effectiveness for elderly TNBC patients. Citation Format: Tian Lan, Qiusheng Guo, Yunyan Lu, Junwei Gu, Xiying Shao, Haibin Xu, Zujian Hu. The Role of Adjuvant Chemotherapy for Elderly Women with Triple-Negative Breast Cancer [abstract]. In: Proceedings of the 2022 San Antonio Breast Cancer Symposium; 2022 Dec 6-10; San Antonio, TX. Philadelphia (PA): AACR; Cancer Res 2023;83(5 Suppl):Abstract nr P1-01-01.
    Type of Medium: Online Resource
    ISSN: 1538-7445
    Language: English
    Publisher: American Association for Cancer Research (AACR)
    Publication Date: 2023
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    detail.hit.zdb_id: 1432-1
    detail.hit.zdb_id: 410466-3
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