Michael White

Dr. Michael White

orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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23 December 2021 in Science
Verified
Journal Article
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CSChristine N. Spencer
Christine N. Spencer
JMJennifer L. McQuade
Jennifer L. McQuade
VGVancheswaran Gopalakrishnan
Vancheswaran Gopalakrishnan
JMJohn A. McCulloch
John A. McCulloch
MVMarie Vetizou
Marie Vetizou
JWJennifer A. Wargo
Jennifer A. Wargo
Another benefit of dietary fiber: The gut microbiome can modulate the immune system and influence the therapeutic response of cancer patients, yet the mechanisms underlying the effects of microbiota are presently unclear. Spencer et al . add to our understanding of how dietary habits affect microbiota and clinical outcomes to immunotherapy. In an observational study, the researchers found that melanoma patients reporting high fiber (prebiotic) consumption had a better response to checkpoint inhibitor immunotherapy compared with those patients reporting a low-fiber diet. The most marked benefit was observed for those patients reporting a combination of high fiber consumption and no use of over-the-counter probiotic supplements. These findings provide early insights as to how diet-related factors may influence the immune response. —PNK

8 July 2021 in Nature Medicine
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Journal Article
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MAMiles C. Andrews
Miles C. Andrews
CDConnie P. M. Duong
Connie P. M. Duong
VGVancheswaran Gopalakrishnan
Vancheswaran Gopalakrishnan
Valerio IebbaValerio Iebba
Valerio Iebba
WCWei-Shen Chen
Wei-Shen Chen
JWJennifer A. Wargo
Jennifer A. Wargo

1 June 2016 in Thyroid®
Verified
Journal Article
Closed access
SSSaaduddin Siddiqui
Saaduddin Siddiqui
MWMichael White
Michael White
TATatjana Antic
Tatjana Antic
RGRaymon H. Grogan
Raymon H. Grogan
PAPeter Angelos
Peter Angelos
NCNicole A. Cipriani
Nicole A. Cipriani
Background: The treatment for patients with papillary thyroid microcarcinoma (PTMC) is controversial because PTMC is often found incidentally and its prognosis is very good. Lymph node metastasis (LNM) is one of the main predictors of recurrence and survival. This retrospective study aimed to identify clinical and pathologic factors that increase the risk of metastasis or recurrence, in order to isolate clinically unfavorable PTMCs to help guide therapy. Methods: Clinical and pathologic data were collected from 273 patients diagnosed with PTMC at The University of Chicago Medical Center between 2000 and 2011. Data points included age, sex, race/ethnicity, tumor size, multifocality, thyroiditis, extrathyroidal extension (ETE), surgical margins, preoperative clinical suspicion of cancer, central/lateral lymph nodes removed and lymph nodes with metastatic carcinoma, treatment, local recurrence, distant recurrence, and survival. Results: Multivariate logistic regression showed that age <45 years (odds ratio [OR] = 3.565 [confidence interval (CI) 1.137–11.177]), multifocality (OR = 3.556 [CI 1.066–11.855]), and ETE (OR = 4.622 [CI = 1.068–20.011]) significantly increased the risk of central LNM (CLNM). However, sex, size of tumor, thyroiditis, positive margins, and clinical suspicion were not correlated with an increased risk for CLNM. Multivariate logistic regression showed that only ETE (OR = 16.066 [CI 1.850–139.488]) significantly increased the risk of lateral LNM. In the cohort of 202 patients with follow-up data, only six recurred. Median time to recurrence was approximately 12 months (range 3.5–120 months), and median follow-up was 42 months. No patient had distant metastasis, and no patients died. Conclusions: PTMC is an indolent disease, but does pose a risk for LNM and local recurrence. More aggressive treatment or more frequent follow-up could be considered for patients with unfavorable features (age <45 years, multifocality, ETE), especially in the setting of involved lymph nodes at the time of surgical resection, as these patients may be at an increased risk for recurrence.

1 February 2016 in Cancer Epidemiology, Biomarkers & Prevention
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Journal Article
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SNSarah M. Nielsen
Sarah M. Nielsen
MWMichael White
Michael White
SHSusan Hong
Susan Hong
BABriseis Aschebrook-Kilfoy
Briseis Aschebrook-Kilfoy
EKEdwin L. Kaplan
Edwin L. Kaplan
RGRaymon H. Grogan
Raymon H. Grogan
Rates of thyroid cancer in women with a history of breast cancer are higher than expected. Similarly, rates of breast cancer in those with a history of thyroid cancer are increased. Explanations for these associations include detection bias, shared hormonal risk factors, treatment effect, and genetic susceptibility. With increasing numbers of breast and thyroid cancer survivors, clinicians should be particularly cognizant of this association. Here, we perform a systematic review and meta-analysis of the literature utilizing PubMed and Scopus search engines to identify all publications studying the incidence of breast cancer as a secondary malignancy following a diagnosis of thyroid cancer or thyroid cancer following a diagnosis of breast cancer. This demonstrated an increased risk of thyroid cancer as a secondary malignancy following breast cancer [OR = 1.55; 95% confidence interval (CI), 1.44–1.67] and an increased risk of breast cancer as a secondary malignancy following thyroid cancer (OR = 1.18; 95% CI, 1.09–1.26). There is a clear increase in the odds of developing either thyroid or breast cancer as a secondary malignancy after diagnosis with the other. Here, we review this association and current hypothesis as to the cause of this correlation. Cancer Epidemiol Biomarkers Prev; 25(2); 231–8. ©2016 AACR.

1 May 2017 in Thyroid®
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Journal Article
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ACAllison Cavallo
Allison Cavallo
DJDaniel N. Johnson
Daniel N. Johnson
MWMichael White
Michael White
SSSaaduddin Siddiqui
Saaduddin Siddiqui
TATatjana Antic
Tatjana Antic
NCNicole A. Cipriani
Nicole A. Cipriani
Thyroid-related mortality has remained constant despite the increasing incidence of thyroid carcinoma. Most thyroid nodules are benign; therefore, ultrasound and fine needle aspiration (FNA) are integral in cancer screening. We hypothesize that increased nodule size at ultrasound does not predict malignancy and correlation between nodule size at ultrasound and pathologic exam is good. Resected thyroids with preoperative ultrasounds were identified. Nodule size at ultrasound, FNA diagnosis by Bethesda category, size at pathologic examination, and final histologic diagnosis were recorded. Nodule characteristics at ultrasound and FNA diagnoses were correlated with gross characteristics and histologic diagnoses. Nodules for which correlation could not be established were excluded. Of 1003 nodules from 659 patients, 26% were malignant. Nodules 6 cm). At ultrasound size cutoffs of 2, 3, 4, and 5 cm, smaller nodules had higher malignancy rates than larger nodules. Of the 455 not subject to FNA, 11% were malignant. Ultrasound size alone is a poor predictor of malignancy, but a relatively good predictor of final pathologic size (R2 = 0.748), with less correlation at larger sizes. In nodules subject to FNA, false negative diagnoses were highest (6-8%) in nodules 3-6 cm, mostly due to encapsulated follicular variant of papillary carcinoma. Thyroid nodule size is inversely related to malignancy risk, as larger nodules have lower malignancy rates. However, the relationship of size to malignancy varies by FNA status. All nodules (regardless of FNA status) demonstrate a risk trough at ≥2 cm. Nodules subject to FNA show step-wise decline in malignancy rates by size, demonstrating that size alone should not be considered as an independent risk factor. Size at ultrasound shows relatively good correlation with final pathologic size. False negative rates are low in this series. Lesions with the appropriate constellation of clinical and radiographic findings should undergo FNA regardless of size. Both size and FNA diagnosis should influence the clinical decision-making process.

15 June 2022 in Nature
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Journal Article
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CVChristopher P. Vellano
Christopher P. Vellano
MWMichael White
Michael White
MAMiles C. Andrews
Miles C. Andrews
MCManoj Chelvanambi
Manoj Chelvanambi
RWRussell G. Witt
Russell G. Witt
JWJennifer A. Wargo
Jennifer A. Wargo