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Featured researches published by Michele M. Corsini.


American Journal of Clinical Oncology | 2011

Preoperative CA 19-9 level is an important prognostic factor in patients with pancreatic adenocarcinoma treated with surgical resection and adjuvant concurrent chemoradiotherapy.

Christopher L. Hallemeier; Maikel Botros; Michele M. Corsini; Michael G. Haddock; Leonard L. Gunderson; Rob Miller

ObjectivesTo evaluate preoperative CA 19-9 level as a prognostic factor in patients with resected adenocarcinoma of the pancreas. MethodsWe retrospectively reviewed the cases of consecutive patients with pancreatic adenocarcinoma who had CA 19-9 measured preoperatively and underwent potentially curative resection at Mayo Clinic from September 1995 to January 2005. Patients who died within 30 days of resection were excluded. ResultsSearch of our database identified 226 consecutive patients who met all the inclusion criteria. Adjuvant therapy was concurrent chemoradiotherapy (CCRT) in 122 patients, CCRT followed by chemotherapy in 23 patients, chemotherapy alone in 6 patients, and none in 69 patients. Median follow-up for surviving patients was 2.1 years. Median survival in all patients was 1.6 years. Patients with a high preoperative CA 19-9 level (defined as ≥180 U/mL) had a greater chance of having pathologic T3-T4 disease (P=0.03), positive lymph nodes (P=0.01), and histologic grade 3 or 4 (P=0.02). In multivariate analysis, a high preoperative CA 19-9 level (P=0.006) and R1-R2 margin status (P=0.03) were associated with decreased survival. Overall survival was increased for patients who received adjuvant CCRT (vs. those who did not; P=0.002) and for patients with high preoperative CA 19-9 level who received adjuvant CCRT (vs. those who did not; P<0.001). ConclusionsIn patients with resected adenocarcinoma of the pancreas, high preoperative CA 19-9 level was associated with adverse pathologic features and poorer survival. Adjuvant CCRT was associated with a significant survival benefit in patients with high preoperative CA 19-9 but not in those with low CA 19-9.


International Journal of Radiation Oncology Biology Physics | 2009

Review of Adjuvant Radiochemotherapy for Resected Pancreatic Cancer and Results From Mayo Clinic for the 5th JUCTS Symposium

Robert C. Miller; Matthew J. Iott; Michele M. Corsini

PURPOSE To present an overview of Phase III trials in adjuvant therapy for pancreatic cancer and review outcomes at the Mayo Clinic after adjuvant radiochemotherapy (RT/CT) for resected pancreatic cancer. METHODS AND MATERIALS A literature review and a retrospective review of 472 patients who underwent an R0 resection for T1-3N0-1M0 invasive carcinoma of the pancreas from 1975 to 2005 at the Mayo Clinic, Rochester, MN. Patients with metastatic or unresectable disease at the time of surgery, positive surgical margins, or indolent tumors and those treated with intraoperative radiotherapy were excluded from the analysis. Median radiotherapy dose was 50.4 Gy in 28 fractions, with 98% of patients receiving concurrent 5-fluorouracil- based chemotherapy. RESULTS Median follow-up was 2.7 years. Median overall survival (OS) was 1.8 years. Median OS after adjuvant RT/CT was 2.1 vs. 1.6 years for surgery alone (p = 0.001). The 2-y OS was 50% vs. 39%, and 5-y was 28% vs. 17% for patients receiving RT/CT vs. surgery alone. Univariate and multivariate analysis revealed that adverse prognostic factors were positive lymph nodes (risk ratio [RR] 1.3, p < 0.001) and high histologic grade (RR 1.2, p < 0.001). T3 tumor status was found significant on univariate analysis only (RR 1.1, p = 0.07). CONCLUSIONS Results from recent clinical trials support the use of adjuvant chemotherapy in resected pancreatic cancer. The role of radiochemotherapy in adjuvant treatment of pancreatic cancer remains a topic of debate. Results from the Mayo Clinic suggest improved outcomes after the administration of adjuvant radiochemotherapy after a complete resection of invasive pancreatic malignancies.


Pancreas | 2010

Mayo clinic experience with very rare exocrine pancreatic neoplasms

Aaron S. Mansfield; Alfonso Tafur; Patrick Smithedajkul; Michele M. Corsini; Fernando Quevedo; Robert C. Miller

Objectives: Limited data are available to guide the management of very rare exocrine neoplasms of the pancreas (VREP). Available evidence suggests that VREP have different risk factors and prognoses from those of adenocarcinoma of the pancreas. The primary objectives for this study were to determine the survival, comorbidities, and response to treatment of patients seen at Mayo Clinic with VREP. Methods: We reviewed patients from 1975 to 2005 who had VREP and compared them to patients with adenocarcinomas that were matched for TNM, grade, and decade of treatment. Results: Sixty-six patients with VREP were identified. The most commonly identified neoplasms were acinar cell carcinoma (n = 15), small cell carcinoma (n = 12), and squamous cell carcinoma (n = 8). Abdominal discomfort and jaundice were the most common presenting symptoms. The median overall survival for patients with VREP, 10.4 months (range, 3.7-23 months), was better than that for matched controls, 8.2 months (range, 4-15.4 months) (P = 0.01). There was no difference in the survival of patients with stage 4 disease between cases, 8 months (range, 2.3-21.8 months), and controls, 6.7 months (range, 2.3-10.8 months) (P = 0.17). Conclusions: We present one of the largest series of VREP to date. The overall survival of all patients with VREP was better than matched controls, but no statistical difference was seen between the groups with stage 4 disease.


Clinical Journal of Oncology Nursing | 2008

Evidence-Based Guidelines for Adjuvant Therapy for Resected Adenocarcinoma of the Pancreas

Matthew J. Iott; Michele M. Corsini; Robert C. Miller

Pancreatic cancer, the fourth most common cause of cancer deaths, has a five-year survival rate of 5% or less. Surgical removal of the tumor may improve survival, but survival remains poor even in optimally resected patients. The best adjuvant therapy for patients with resected pancreatic cancer is not clear. Surgical resection followed by chemoradiation and maintenance chemotherapy has been considered the most beneficial treatment for improving survival, but more recent studies have suggested that chemotherapy alone is more effective. The purpose of this article is to review randomized controlled studies of adjuvant chemoradiation or chemotherapy alone in the treatment of resected pancreatic cancer and to determine the optimal adjuvant therapy after curative resection with negative or microscopically positive margins. The outcomes of interest were overall survival and disease-free survival. The results indicate that chemoradiation is an acceptable option for adjuvant treatment. Three of the four randomized controlled trials suggest that adjuvant chemoradiation for resected pancreatic cancer improves overall survival. Adding gemcitabine to the chemoradiation regimen also confers increased disease-free survival. Providers counseling patients regarding treatment options for resected pancreatic cancer should continue to recommend adjuvant therapy--a combination of chemotherapy including gemcitabine and radiotherapy--for appropriately selected patients.


Annals of Surgical Oncology | 2010

Adjuvant Chemoradiation for Pancreatic Adenocarcinoma: The Johns Hopkins Hospital—Mayo Clinic Collaborative Study

Charles C. Hsu; Joseph M. Herman; Michele M. Corsini; Jordan M. Winter; Matthew D. Callister; Michael G. Haddock; John L. Cameron; Timothy M. Pawlik; Richard D. Schulick; Christopher L. Wolfgang; Daniel A. Laheru; Michael B. Farnell; Michael J. Swartz; Leonard L. Gunderson; Robert C. Miller


International Journal of Radiation Oncology Biology Physics | 2007

Adjuvant Radiation and Chemotherapy for Pancreatic Adenocarcinoma: The Mayo Clinic Experience

Michele M. Corsini; Robert C. Miller; Michael G. Haddock; John H. Donohue; Michael B. Farnell; David M. Nagorney; Aminah Jatoi; Robert R. McWilliams; Sumita Bhatia; Leonard L. Gunderson


European journal of Clinical and Medical Oncology | 2010

Adjuvant radiotherapy and chemotherapy for resected pancreatic adenocarcinoma: Review of current evidence

M.A. Neben-Wittich; Michael C. Stauder; Fernando Quevedo; Michele M. Corsini; Matthew J. Iott; Robert C. Miller


International Journal of Radiation Oncology Biology Physics | 2008

Adverse Prognostic Factors Impacting Survival in Resected Invasive, Mucinous Cystadenocarcinomas of the Pancreas

Stephen J. Ko; Michele M. Corsini; Michael G. Haddock; M.B. Wallace; George P. Kim; Aminah Jatoi; Leonard L. Gunderson; Robert C. Miller


International Journal of Radiation Oncology Biology Physics | 2008

Adjuvant Chemoradiation Therapy after Surgical Resection for 1092 Cases of Pancreatic Adenocarcinoma: The Johns Hopkins Hospital - Mayo Clinic Collaborative Study of Pancreatic Cancer

Charles C. Hsu; Joseph M. Herman; Michele M. Corsini; Jordan M. Winter; Matthew D. Callister; John L. Cameron; Timothy M. Pawlik; Michael J. Swartz; Leonard L. Gunderson; Robert C. Miller


International Journal of Radiation Oncology Biology Physics | 2008

Pre-operative CA 19-9 > 90 is Associated with Worse Overall Survival and Marginal Resection Status in Resectable, Invasive Pancreatic Carcinoma

Michele M. Corsini; Robert C. Miller; Michael G. Haddock; Leonard L. Gunderson

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Jordan M. Winter

Thomas Jefferson University

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Joseph M. Herman

University of Texas MD Anderson Cancer Center

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