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Dive into the research topics where Michael J. Katin is active.

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Featured researches published by Michael J. Katin.


American Journal of Clinical Oncology | 1997

Small cell anaplastic carcinoma of the prostate : Seven new cases, review of the literature, and discussion of a therapeutic strategy

James H. Rubenstein; Michael J. Katin; Mark M. Mangano; Jean Dauphin; Sharon A. Salenius; Daniel E. Dosoretz; Peter H. Blitzer

Small cell anaplastic carcinoma of the prostate (SCCP) is a rare entity; a literature review disclosed fewer than 150 cases. SCCP has an aggressive course, and both local and distant failure is common. The optimal treatment method has not been clearly established. We review our experience with 7 patients, with attention paid to clinical and pathological details based on a review of the histological specimens. Three patients had mixed tumors of both SCCP and adenocarcinoma, 3 had pure adenocarcinomas that recurred as small cell, and 1 had pure small cell. Our series confirms the aggressive nature of the disease, with all patients dying of their disease < or = 42 months after diagnosis. All patients progressed locally, and at least 5 later developed distant metastases. Treatment with combination chemotherapy and/or hormones resulted in short-lived responses in most patients. We recommend use of hormonal manipulation and combination chemotherapy as well as surgery and/or radiation therapy to the prostate for local control and emphasize that histologic recognition of the entity is important for proper treatment.


Journal of Clinical Oncology | 2009

Risk of Death From Prostate Cancer After Brachytherapy Alone or With Radiation, Androgen Suppression Therapy, or Both in Men With High-Risk Disease

Anthony V. D'Amico; Brian J. Moran; Michelle H. Braccioforte; Daniel Dosoretz; Sharon A. Salenius; Michael J. Katin; Rudi Ross; Ming-Hui Chen

PURPOSE We estimated the risk of prostate cancer (PC) -specific mortality (PCSM) after brachytherapy alone or in conjunction with androgen suppression therapy (AST), external-beam radiation therapy (EBRT), or both in men with high-risk PC. PATIENTS AND METHODS The study cohort comprised 1,342 men with a prostate-specific antigen level more than 20 ng/mL and clinical T3 or 4 and/or Gleason score 8 to 10 disease. Competing risks multivariable regression was performed to estimate the risk of PCSM in men treated with brachytherapy alone or with supplemental AST, EBRT, or both, adjusting for age, year of treatment, and known PC prognostic factors. RESULTS Despite higher baseline probabilities of PCSM after a median follow-up of 5.1 years, there was a significant reduction in the risk of PCSM (adjusted hazard ratio [AHR], 0.32; 95% CI, 0.14 to 0.73; P = .006) in men treated with brachytherapy and both AST and EBRT as compared with neither. When compared with brachytherapy alone, a significant decrease in the risk of PCSM was not observed in men treated with either supplemental AST (AHR, 0.63; 95% CI, 0.27 to 1.47; P = .28) or EBRT (AHR, 0.57; 95% CI, 0.21 to 1.52; P = .26). There was a near-significant reduction (AHR, 0.53; 95% CI, 0.27 to 1.07; P = .079) in the risk of PCSM in men treated with tri- as compared with bimodality therapy. CONCLUSION Supplemental AST and EBRT but not either supplement compared with brachytherapy alone was associated with a decreased risk of PCSM in men with high-risk PC.


International Journal of Radiation Oncology Biology Physics | 2000

Effective palliative radiation therapy in advanced and recurrent ovarian carcinoma

Alfred Tinger; Tanisha Waldron; Nancy Peluso; Michael J. Katin; Daniel E. Dosoretz; Peter H. Blitzer; James H. Rubenstein; Graciela R. Garton; Bruce A Nakfoor; Stephen J. Patrice; Linus Chuang; James W. Orr

PURPOSE To retrospectively review our experience using radiation therapy as a palliative treatment in ovarian carcinoma. METHODS AND MATERIALS Eighty patients who received radiation therapy for ovarian carcinoma between 1983 and 1998 were reviewed. The indications for radiation therapy, radiation therapy techniques, details, tolerance, and response were recorded. A complete response required complete resolution of the patients symptoms, radiographic findings, palpable mass, or CA-125 level. A partial response required at least 50% resolution of these parameters. The actuarial survival rates from initial diagnosis and from the completion of radiation therapy were calculated. RESULTS The median age of the patients was 67 years (range 26 to 90 years). A median of one laparotomy was performed before irradiation. Zero to 20 cycles of a platinum-based chemotherapy regimen were delivered before irradiation (median = 6 cycles). The reasons for palliative treatment were: pain (n = 22), mass (n = 23), obstruction of ureter, rectum, esophagus, or stomach (n = 12), a positive second-look laparotomy (n = 9), ascites (n = 8), vaginal bleeding (n = 6), rectal bleeding (n = 1), lymphedema (n = 3), skin involvement (n = 1), or brain metastases with symptoms (n = 11). Some patients received treatment for more than one indication. Treatment was directed to the abdomen or pelvis in 64 patients, to the brain in 11, and to other sites in 5. The overall response rate was 73%. Twenty-eight percent of the patients experienced a complete response of their symptoms, palpable mass, and/or CA-125 level. Forty-five percent had a partial response. Only 11% suffered progressive disease during therapy that required discontinuation of the treatment. Sixteen percent had stable disease. The duration of the responses and stable disease lasted until death except in 10 patients who experienced recurrence of their symptoms between 1 and 21 months (median = 9 months). The 1-, 2-, 3-, and 5-year actuarial survival rates from diagnosis were 89%, 73%, 42%, and 33%, respectively. The survival rates calculated from the completion of radiotherapy were 39%, 27%, 13%, and 10%, respectively. Five percent of patients experienced Grade 3 diarrhea, vomiting, myelosuppression, or fatigue. Fourteen percent of patients experienced Grade 1 or 2 diarrhea, 19% experienced Grade 1 or 2 nausea and vomiting, and 11% had Grade 1 or 2 myelosuppression. CONCLUSIONS In this series of radiation therapy for advanced ovarian carcinoma, the response, survival, and tolerance rates compare favorably to those reported for current second- and third-line chemotherapy regimens. Cooperative groups should consider evaluating prospectively the use of radiation therapy before nonplatinum and/or nonpaclitaxel chemotherapy in these patients.


BJUI | 2012

Radical prostatectomy vs radiation therapy and androgen-suppression therapy in high-risk prostate cancer

Kenneth D. Westover; Ming-Hui Chen; Judd W. Moul; Cary N. Robertson; Thomas J. Polascik; Daniel E. Dosoretz; Michael J. Katin; Sharon A. Salenius; Anthony V. D'Amico

Study Type – Therapy (retrospective cohort analysis)


Cancer | 2010

Prostate cancer‐specific mortality and the extent of therapy in healthy elderly men with high‐risk prostate cancer

Karen E. Hoffman; Ming-Hui Chen; Brian J. Moran; Michelle H. Braccioforte; Daniel Dosoretz; Sharon A. Salenius; Michael J. Katin; Rudi Ross; Anthony V. D'Amico

The risk of prostate cancer‐specific mortality (PCSM) in healthy elderly men may depend on extent of treatment. The authors of this report compared the use of brachytherapy alone with combined brachytherapy, external‐beam radiation to the prostate and seminal vesicles, and androgen‐suppression therapy (CMT) in this population.


The Journal of Urology | 2011

Diabetes Mellitus, Race and the Odds of High Grade Prostate Cancer in Men Treated With Radiation Therapy

Timur Mitin; Ming-Hui Chen; Yuanye Zhang; Brian J. Moran; Daniel E. Dosoretz; Michael J. Katin; Michelle H. Braccioforte; Sharon A. Salenius; Anthony V. D'Amico

PURPOSE Black men present more frequently with high grade prostate cancer and are more likely to have diabetes mellitus. We evaluated whether there is an independent association between diabetes mellitus and the risk of high grade prostate cancer in men diagnosed with prostate cancer and treated with radiation therapy. MATERIALS AND METHODS A polychotomous logistic regression analysis was performed to evaluate whether a diagnosis of diabetes mellitus was associated with the odds of Gleason score 7 or 8-10 prostate cancer in a cohort of 16,286 men, adjusting for black race, advancing age, prostate specific antigen and digital rectal examination findings. RESULTS Black men (adjusted OR 1.84, 95% CI 1.08-3.13, p = 0.024) and nonblack men (adjusted OR 1.59, 95% CI 1.33-1.89, p <0.001) with diabetes were more likely to have Gleason score 8-10 vs 6 or less prostate cancer than nondiabetic men. However, this was not true for Gleason score 7 vs 6 or less prostate cancer. Black race was significantly associated with Gleason score 7 vs 6 or less prostate cancer in men without and with diabetes (adjusted OR 1.38, 95% CI 1.17-1.63, p <0.001 and 1.61, 95% CI 1.17-2.21, p = 0.003, respectively). Black race was also associated with Gleason score 8-10 vs 6 or less prostate cancer in men without and with diabetes (adjusted OR 1.36, 95% CI 1.01-1.83, p = 0.04 and 1.58, 95% CI 0.98-2.53, p = 0.06, respectively). CONCLUSIONS In a cohort of men undergoing radiotherapy for prostate cancer the diagnosis of diabetes mellitus was significantly associated with an increased risk of being diagnosed with Gleason score 8-10 prostate cancer independent of black race.


Cancer | 2011

Coronary Revascularization and Mortality in Men With Congestive Heart Failure or Prior Myocardial Infarction Who Receive Androgen Deprivation

Paul L. Nguyen; M. Chen; Samuel Z. Goldhaber; Neil E. Martin; Clair J. Beard; Daniel E. Dosoretz; Michael J. Katin; Rudi Ross; Sharon A. Salenius; Anthony V. D'Amico

A study was undertaken to determine the impact of prior coronary revascularization (angioplasty, stent, or coronary artery bypass graft) on the risk of all‐cause mortality after neoadjuvant hormonal therapy (HT) for prostate cancer (PC) in men with a history of coronary artery disease (CAD)‐induced congestive heart failure (CHF) or myocardial infarction (MI).


Cancer | 2010

Mortality in men with localized prostate cancer treated with brachytherapy with or without neoadjuvant hormone therapy

Amy M. Dosoretz; Ming-Hui Chen; Sharon A. Salenius; R. Ross; Daniel E. Dosoretz; Michael J. Katin; C.A. Mantz; Bruce M. Nakfoor; Anthony V. D'Amico

Discrepancies exist regarding the impact of neoadjuvant hormone therapy (NHT) on the risk of all‐cause mortality (ACM) in men who receive brachytherapy for localized prostate cancer. Therefore, the objective of the current study was to examine the effect of NHT on the risk of ACM in men with prostate cancer who receive with brachytherapy.


BJUI | 2010

Androgen-suppression therapy for prostate cancer and the risk of death in men with a history of myocardial infarction or stroke

Julia H. Hayes; Ming-Hui Chen; Brian J. Moran; Michelle H. Braccioforte; Daniel E. Dosoretz; Sharon A. Salenius; Michael J. Katin; Rudi Ross; Toni K. Choueiri; Anthony V. D’Amico

Study Type – Prognosis (inception cohort)
Level of Evidence 1b


International Journal of Radiation Oncology Biology Physics | 2011

Type of Diabetes Mellitus and the Odds of Gleason Score 8 to 10 Prostate Cancer

J. Kang; Ming-Hui Chen; Yuanye Zhang; Brian J. Moran; Daniel E. Dosoretz; Michael J. Katin; Michelle H. Braccioforte; Sharon A. Salenius; Anthony V. D'Amico

PURPOSE It has been recently shown that diabetes mellitus (DM) is significantly associated with the likelihood of presenting with high-grade prostate cancer (PCa) or Gleason score (GS) 8 to 10; however, whether this association holds for both Type 1 and 2 DM is unknown. In this study we evaluated whether DM Type 1, 2, or both are associated with high-grade PCa after adjusting for known predictors of high-grade disease. METHODS AND MATERIALS Between 1991 and 2010, a total of 15,330 men diagnosed with PCa and treated with radiation therapy were analyzed. A polychotomous logistic regression analysis was performed to evaluate whether Type 1 or 2 DM was associated with odds of GS 7 or GS 8 to 10 compared with 6 or lower PCa, adjusting for African American race, age, prostate-specific antigen (PSA) level, and digital rectal examination findings. RESULTS Men with Type 1 DM (adjusted odds ratio [AOR], 2.05; 95% confidence interval [CI], 1.28-3.27; p = 0.003) or Type 2 DM (AOR, 1.58; 95% CI, 1.26-1.99; p < 0.001) were significantly more likely to be diagnosed with GS 8 to 10 PCa compared with nondiabetic men. However this was not true for GS 7, for which these respective results were AOR, 1.30; 95% CI, 0.93-1.82; p = 0.12 and AOR, 1.13; 95% CI, 0.98-1.32; p = 0.10. CONCLUSION Type 1 and 2 DM were associated with a higher odds of being diagnosed with Gleason score 8 to 10 but not 7 PCa. Pending validation, men who are diagnosed with Type I DM with GS 7 or lower should be considered for additional workup to rule out occult high-grade disease.

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Sharon A. Salenius

Brigham and Women's Hospital

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Anthony V. D'Amico

Brigham and Women's Hospital

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Ming-Hui Chen

University of Connecticut

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M. Chen

University of Connecticut

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Akash Nanda

University of Texas MD Anderson Cancer Center

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Anthony V. D’Amico

Brigham and Women's Hospital

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