SEER Program Coding and Staging Manual 2018
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Is There Anything New in Prostate Cancer Screening?
IS THERE ANYTHING NEW IN PROSTATE CANCER SCREENING? ANDREW M.D. WOLF, MD, FACP ASSOCIATE PROFESSOR OF MEDICINE UNIVERSITY OF VIRGINIA SCHOOL OF MEDICINE No financial disclosures Case Presentation 62 yo white man without significant past medical history presents for annual preventive visit. He has no family history of prostate cancer. He has mild urinary hesitancy and his prostate is mildly enlarged without induration or nodules. His PSA has been gradually rising: - 2011: 2.35 - 2013: 2.17 - 2017: 3.75 - 2019: 4.51 Where do we go from here? What’s New in Prostate Cancer Screening? Key Questions • Do we have any new evidence for or against screening? • Do we have anything better than the PSA? • What about the good old digital rectal exam? • Are we doing any better identifying who needs to be treated? • What do the experts recommend? Prostate Cancer Incidence & Mortality Over the Decades Source: Seer 9 areas & US Mortality Files (National Center for Health Statistics, CDC, Feb 2018 CA Cancer J Clin 2019;69:7-34. Do we have any new evidence for or against prostate cancer screening? Is Prostate Screening Still Controversial? ERSPC Results • Prostate cancer death rate 27% lower in screened group (p = 0.0001) at 13 yrs • Number needed to screen to save 1 life: 781 • NNS to prevent 1 case of metastatic cancer: ~350 • Number needed to diagnose to save 1 life: 27 • Major issue of over-diagnosis & over-treatment Schroder FH, et al. Lancet 2014;384: 2027–2035 • Controlled for differences in study design • Adjusted for lead-time • Both studies led to a ~ 25-32% reduction in prostate cancer mortality with screening compared with no screening Ann Intern Med 2017;167:449-455 • 415,000 British men 50-69 randomized to a single offer to screen vs usual care (info sheet on request) • One-time screen & then followed for 10 yrs • Men dx’d with prostate cancer randomized to treatment vs active surveillance JAMA 2018;319(9):883-895. -
QUEST Provider Bulletin
HMSA Provider Bulletin HMS A ’ S P L an fo R Q U E S T M embe R S Bulletin Q08-01 January 15, 2008 A MESSAGE FROM OUR appointments, ensuring the collection and forwarding of MEDICAL DIRECTOR necessary information, obtaining prior authorizations, educating the parents, and following up to ensure appointments are kept is Children with Special Health Care Needs guaranteed to be difficult and time consuming. Children with chronic illnesses are Other examples include children with diabetes, congenital heart challenging for pediatricians and other defects, seizure disorders, asthma, cancer (even if in remission), primary care providers entrusted with and juvenile rheumatoid arthritis. Also included are children their care. This is especially so for with multiple diagnoses, related or otherwise. those children whose management The Hawaii Department of Health has a service dedicated to requires the services of various assisting such children, their families and their caregivers. This medical specialists, allied health care is the Children with Special Health Needs Program, under the providers, organizations, and institutions. A child with Family Health Services Division. Children and youth under 21 a cleft palate, for example, may require the services of years of age residing in Hawaii are eligible if they have chronic an ENT surgeon, oral surgeon, dentist, audiologist, health conditions lasting (or expected to last) at least one year, speech therapist, DME provider (for hearing aids), for which specialized medical care is required. and the Department of Education. Locating these The Children with Special Health Needs Program can assist providers, making the necessary referrals, coordinating QUEST members who are having difficulty in coordinating or obtaining health care services, or who cannot obtain certain Happy New Year 2008 services through QUEST, with the following: IN THIS ISSUE: • Coordination of health care referrals and appointments. -
Follicular Lymphoma
Follicular Lymphoma What is follicular lymphoma? Let us explain it to you. www.anticancerfund.org www.esmo.org ESMO/ACF Patient Guide Series based on the ESMO Clinical Practice Guidelines FOLLICULAR LYMPHOMA: A GUIDE FOR PATIENTS PATIENT INFORMATION BASED ON ESMO CLINICAL PRACTICE GUIDELINES This guide for patients has been prepared by the Anticancer Fund as a service to patients, to help patients and their relatives better understand the nature of follicular lymphoma and appreciate the best treatment choices available according to the subtype of follicular lymphoma. We recommend that patients ask their doctors about what tests or types of treatments are needed for their type and stage of disease. The medical information described in this document is based on the clinical practice guidelines of the European Society for Medical Oncology (ESMO) for the management of newly diagnosed and relapsed follicular lymphoma. This guide for patients has been produced in collaboration with ESMO and is disseminated with the permission of ESMO. It has been written by a medical doctor and reviewed by two oncologists from ESMO including the lead author of the clinical practice guidelines for professionals, as well as two oncology nurses from the European Oncology Nursing Society (EONS). It has also been reviewed by patient representatives from ESMO’s Cancer Patient Working Group. More information about the Anticancer Fund: www.anticancerfund.org More information about the European Society for Medical Oncology: www.esmo.org For words marked with an asterisk, a definition is provided at the end of the document. Follicular Lymphoma: a guide for patients - Information based on ESMO Clinical Practice Guidelines – v.2014.1 Page 1 This document is provided by the Anticancer Fund with the permission of ESMO. -
Profiling Prostate Cancer Therapeutic Resistance
International Journal of Molecular Sciences Review Profiling Prostate Cancer Therapeutic Resistance Cameron A. Wade 1 and Natasha Kyprianou 1,2,3,* 1 Departments of Urology, University of Kentucky College of Medicine, Lexington, Kentucky, KY 40536, USA; [email protected] 2 Department of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, Kentucky, KY 40536, USA 3 Department of Toxicology & Cancer Biology, University of Kentucky College of Medicine, Lexington, Kentucky, KY 40536, USA * Correspondence: [email protected]; Tel.: +1-859-323-9812; Fax: +1-859-323-1944 Received: 1 March 2018; Accepted: 16 March 2018; Published: 19 March 2018 Abstract: The major challenge in the treatment of patients with advanced lethal prostate cancer is therapeutic resistance to androgen-deprivation therapy (ADT) and chemotherapy. Overriding this resistance requires understanding of the driving mechanisms of the tumor microenvironment, not just the androgen receptor (AR)-signaling cascade, that facilitate therapeutic resistance in order to identify new drug targets. The tumor microenvironment enables key signaling pathways promoting cancer cell survival and invasion via resistance to anoikis. In particular, the process of epithelial-mesenchymal-transition (EMT), directed by transforming growth factor-β (TGF-β), confers stem cell properties and acquisition of a migratory and invasive phenotype via resistance to anoikis. Our lead agent DZ-50 may have a potentially high efficacy in advanced metastatic castration resistant prostate cancer (mCRPC) by eliciting an anoikis-driven therapeutic response. The plasticity of differentiated prostate tumor gland epithelium allows cells to de-differentiate into mesenchymal cells via EMT and re-differentiate via reversal to mesenchymal epithelial transition (MET) during tumor progression. -
Radiation Therapy – a Technicians Overview By: Stephanie Corsi, CVT
Radiation Therapy – A technicians overview By: Stephanie Corsi, CVT Senior Radiation Oncology nurse, PennVet What is radiation therapy? Radiation therapy uses high-energy radiation or high energy particle (electrons) to kill cancer cells and shrink tumors. How does radiation therapy work? Radiation kills cancer cells by damaging their DNA. Cells that are rapidly dividing, like cancer cells, are more susceptible to radiation. The damage is by a high energy photon ejecting a high energy electron that then reacts with a water molecule to create charged particle, also called free radicals, within the cell that will damage the DNA. Most cells die what is called a “mitotic death”, meaning the cancer cells whose DNA is damaged beyond repair will stop dividing and die. Goal of Radiation: The purpose of radiation is to maximize the likelihood of tumor control while minimizing side-effects to the patient. Radiation may be used alone or in combination with surgery, chemotherapy, or both. “Curative” intent/ definitive therapy: This is given when the prognosis is good. The hope is that treatment will cure a cancer by eliminating a tumor and preventing recurrence. For tumors that are inherently sensitive, relatively small, and localized. Also used to treat residual cancer left behind after surgery, or before surgery to shrink a tumor. Examples: localized lymphomas, certain mast cell tumors, cutaneous squamous cell carcinomas Palliative intent: Not intended to cure, but rather relieve symptoms and reduce suffering. Given when prognosis is poor and quality of life is the primary focus. Used with bulky tumors. Examples: alleviate bone pain associated with osteosarcoma, a tumor pressing on the spine, tumors pressing on the esophagus interfering with breathing/eating, etc. -
Clinical Outcomes and Prognostic Factors of Cyberknife Stereotactic
Que et al. BMC Cancer (2016) 16:451 DOI 10.1186/s12885-016-2512-x RESEARCH ARTICLE Open Access Clinical outcomes and prognostic factors of cyberknife stereotactic body radiation therapy for unresectable hepatocellular carcinoma Jenny Que1*, Hsing-Tao Kuo2, Li-Ching Lin1, Kuei-Li Lin1, Chia-Hui Lin1, Yu-Wei Lin1 and Ching-Chieh Yang1 Abstract Background: Stereotactic body radiation therapy (SBRT) has been an emerging non-invasive treatment modality for patients with hepatocellular carcinoma (HCC) when curative treatments cannot be applied. In this study, we report our clinical experience with Cyberknife SBRT for unresectable HCC and evaluate the efficacy and clinical outcomes of this highly sophisticated treatment technology. Methods: Between 2008 and 2012, 115 patients with unresectable HCC treated with Cyberknife SBRT were retrospectively analyzed. Doses ranged from 26 Gy to 40 Gy were given in 3 to 5 fractions for 3 to 5 consecutive days. The cumulative probability of survival was calculated according to the Kaplan-Meier method and compared using log-rank test. Univariate and multivariate analysis were performed using Cox proportional hazard models. Results: The median follow-up was 15.5 months (range, 2-60 months). Based on Response Evaluation and Criteria inSolidTumors(RECIST).Wefoundthat48.7%ofpatients achieved a complete response and 40 % achieved a partial response. Median survival was 15 months (4-25 months). Overall survival (OS) at 1- and 2-years was 63. 5 %(54-71.5 %) and 41.3 % (31.6-50.6 %), respectively, while 1- and 2- years Progression-free Survival (PFS) rates were 42.8 %(33.0-52.2 %) and 38.8 % (29.0-48.4 %). -
New Source of Black Rot Disease Resistance in Brassica Oleracea and Genetic Analysis of Resistance
Euphytica (2016) 207:35–48 DOI 10.1007/s10681-015-1524-y New source of black rot disease resistance in Brassica oleracea and genetic analysis of resistance Partha Saha . Pritam Kalia . Munish Sharma . Dinesh Singh Received: 1 May 2015 / Accepted: 22 July 2015 / Published online: 28 July 2015 Ó Springer Science+Business Media Dordrecht 2015 Abstract Black rot is the most widespread and Himjyoti x BR-207) and (Pusa Sharad x BR-207) were devastating disease in Brassica oleracea crops. The evaluated. Segregation ratios obtained were compared objective of this work was to identify new sources of by Chi square test at 5 % probability. The F1 resistance to races 1 and 4 of Xcc in 46 B. oleracea generations were resistant and segregation ratio of accessions and to understand genetics of resistance. resistant and susceptible plants indicated 3(R):1(S) in Most of the accessions were susceptible to both the F2 and 1(R):2 (Seg):1(S) in F3 which suggested that races, except accessions BR-207, BR-1, BR-202-2 and resistance to Xcc race 1 in BR-207 is governed by a AL-15 of botrytis group to Xcc race 1. The partial single dominant gene. The information obtained in this resistant plants were observed in some accessions BR- study could be valuable for black rot resistance 202-2 (90 % plants) and AL-27 (10 % plants) of breeding and in planning a systematic breeding botrytis, DJ8012 (20 % plants) of capitata, 005426 programme to incorporate the black rot resistance (10 % plants) of italica. All the accessions were into the susceptible cultivars. -
Guidelines on Paediatric Urology S
Guidelines on Paediatric Urology S. Tekgül (Chair), H.S. Dogan, E. Erdem (Guidelines Associate), P. Hoebeke, R. Ko˘cvara, J.M. Nijman (Vice-chair), C. Radmayr, M.S. Silay (Guidelines Associate), R. Stein, S. Undre (Guidelines Associate) European Society for Paediatric Urology © European Association of Urology 2015 TABLE OF CONTENTS PAGE 1. INTRODUCTION 7 1.1 Aim 7 1.2 Publication history 7 2. METHODS 8 3. THE GUIDELINE 8 3A PHIMOSIS 8 3A.1 Epidemiology, aetiology and pathophysiology 8 3A.2 Classification systems 8 3A.3 Diagnostic evaluation 8 3A.4 Disease management 8 3A.5 Follow-up 9 3A.6 Conclusions and recommendations on phimosis 9 3B CRYPTORCHIDISM 9 3B.1 Epidemiology, aetiology and pathophysiology 9 3B.2 Classification systems 9 3B.3 Diagnostic evaluation 10 3B.4 Disease management 10 3B.4.1 Medical therapy 10 3B.4.2 Surgery 10 3B.5 Follow-up 11 3B.6 Recommendations for cryptorchidism 11 3C HYDROCELE 12 3C.1 Epidemiology, aetiology and pathophysiology 12 3C.2 Diagnostic evaluation 12 3C.3 Disease management 12 3C.4 Recommendations for the management of hydrocele 12 3D ACUTE SCROTUM IN CHILDREN 13 3D.1 Epidemiology, aetiology and pathophysiology 13 3D.2 Diagnostic evaluation 13 3D.3 Disease management 14 3D.3.1 Epididymitis 14 3D.3.2 Testicular torsion 14 3D.3.3 Surgical treatment 14 3D.4 Follow-up 14 3D.4.1 Fertility 14 3D.4.2 Subfertility 14 3D.4.3 Androgen levels 15 3D.4.4 Testicular cancer 15 3D.5 Recommendations for the treatment of acute scrotum in children 15 3E HYPOSPADIAS 15 3E.1 Epidemiology, aetiology and pathophysiology -
35°C—47°C Today D
Community Community Bazm-e-Sadaf Chaliyar Doha International’s observes P7evening for Urdu P16 World lovers is attended Environment Day by Doha-based in association writers and with embassy of poets. India. Sunday, June 10, 2018 Ramadan 25, 1439 AH DOHA 35°C—47°C TODAY PUZZLES 12 & 13 LIFESTYLE/HOROSCOPE 14 Incredible journey Bollywood yesteryear star COVER Kajol on her journey and STORY the latest ventures. P4-5 2 GULF TIMES Sunday, June 10, 2018 COMMUNITY ROUND & ABOUT PRAYER TIME Fajr 3.14am Shorooq (sunrise) 4.43am Zuhr (noon) 11.33am Asr (afternoon) 2.56pm Maghreb (sunset) 6.27pm Isha (night) 7.57pm USEFUL NUMBERS Kaala lead role, while Nana Patekar, Samuthirakani, Easwari Rao DIRECTION: Pa. Ranjith portray the supporting roles. Music is composed by Santhosh CAST: Rajinikanth, Huma Qureshi, Nana Patekar Narayanan. Kaala who runs away from Tirunelveli in his SYNOPSIS: Kaala is an upcoming Indian Tamil political childhood, moves to Mumbai where he becomes a powerful gangster movie written and directed by Pa Ranjith and don living in the slums of Dharavi. produced by Dhanush. The fi lm stars Rajinikanth in the THEATRES: The Mall, Royal Plaza, Landmark Emergency 999 Worldwide Emergency Number 112 Kahramaa – Electricity and Water 991 Local Directory 180 International Calls Enquires 150 Hamad International Airport 40106666 Labor Department 44508111, 44406537 Mowasalat Taxi 44588888 Qatar Airways 44496000 Hamad Medical Corporation 44392222, 44393333 Qatar General Electricity and Water Corporation 44845555, 44845464 Primary Health Care Corporation 44593333 44593363 Qatar Assistive Technology Centre 44594050 Qatar News Agency 44450205 44450333 Q-Post – General Postal Corporation 44464444 Humanitarian Services Offi ce (Single window facility for the repatriation of bodies) Ministry of Interior 40253371, 40253372, 40253369 Ministry of Health 40253370, 40253364 Hamad Medical Corporation 40253368, 40253365 Qatar Airways 40253374 Jurassic World: Fallen Kingdom destruction of the Jurassic World theme soon encounter terrifying new breeds DIRECTION: J. -
Updates in Assessment of the Breast After Neoadjuvant Treatment
Updates in Assessment of The Breast After Neoadjuvant Treatment Laila Khazai 3/3/18 AJCC, 8th Edition AJCC • Pathologic Prognostic Stage is not applicable for patients who receive neoadjuvant therapy. • Pathologic staging includes all data used for clinical staging, plus data from surgical resection. • Information recorded should include: – Clinical Prognostic Stage. – The category information for either clinical (ycT and ycN) response to therapy if surgery is not performed, or pathologic (ypT and ypN) if surgery is performed. – Degree of response (complete, partial, none). AJCC • Post -treatment size should be estimated based on the best combination of imaging, gross, and microscopic histological findings. • The ypT is determined by measuring the largest single focus of residual invasive tumor, with a modifier (m) indicating multiple foci of residual tumor. • This measurement does not include areas of fibrosis within the tumor bed. • When the only residual cancer intravascular or intralymphatic (LVI), the yPT0 category is assigned, but it is not classified as complete pathologic response. A formal system (i.e. RCB, Miller-Payne, Chevalier, …) may be offered in the report. Otherwise, description of the distance over which tumor foci extend, the number of tumor foci present, or the number of tumor slides/blocks in which tumor appears might be offered. AJCC • The ypN categories are the same as those used for pN. • Only the largest contiguous focus of residual tumor is used for classification (treatment associated fibrosis is not included). • Inclusion of additional information such as distance over which tumor foci extend and the number of tumor foci present, may assist the clinician in estimating the extent of residual disease. -
The Updated AJCC/TNM Staging System (8Th Edition) for Oral Tongue Cancer
166 Editorial The updated AJCC/TNM staging system (8th edition) for oral tongue cancer Kyubo Kim, Dong Jin Lee Department of Otorhinolaryngology-Head and Neck Surgery, Hallym University College of Medicine, Seoul, South Korea Correspondence to: Dong Jin Lee, MD, PhD. 1 Singil-ro, Yeongdeungpo-gu, Seoul 150-950, South Korea. Email: [email protected]. Comment on: Almangush A, Mäkitie AA, Mäkinen LK, et al. Small oral tongue cancers (≤ 4 cm in diameter) with clinically negative neck: from the 7th to the 8th edition of the American Joint Committee on Cancer. Virchows Arch 2018;473:481-7. Submitted Dec 22, 2018. Accepted for publication Dec 28, 2018. doi: 10.21037/tcr.2019.01.02 View this article at: http://dx.doi.org/10.21037/tcr.2019.01.02 An increasing amount of literature shows solid evidence that updated classification system and the applicability of DOI as the depth of invasion (DOI) of oral cavity squamous cell a predictor of clinical behavior for early-stage OTSCC. carcinoma is an independent predictor for occult metastasis, The AJCC 8th edition employs a cut-off value of 5 mm recurrence, and survival (1-3). Furthermore, the DOI of the DOI for upstaging from stage T1 to T2 and 10 mm for primary tumor has been a major criterion when deciding to upstaging to T3. This may be questionable as it has been perform elective neck dissection on oral cavity squamous shown that an invasion depth of more than 4 mm increases cell carcinoma patients since as early as the mid-1990s (4). the risk of locoregional metastasis and is associated with a A cut-off value of 4 mm has conventionally been used poor prognosis (9-11), but with the new staging system, a when determining the need for elective neck dissection, large number of invasive tumors in which the DOI is less based on a study by Kligerman et al. -
Endocrine Surgery Goals and Objectives
Lenox Hill Hospital Department of Surgery Endocrine Surgery Goals and Objectives Medical Knowledge and Patient Care: Residents must demonstrate knowledge and application of the pathophysiology and epidemiology of the diseases listed below for this rotation, with the pertinent clinical and laboratory findings, differential diagnosis and therapeutic options including preventive measures, and procedural knowledge. They must show that they are able to gather accurate and relevant information using medical interviewing, physical examination, appropriate diagnostic workup, and use of information technology. They must be able to synthesize and apply information in the clinical setting to make informed recommendations about preventive, diagnostic and therapeutic options, based on clinical judgement, scientific evidence, and patient preferences. They should be able to prescribe, perform, and interpret surgical procedures listed below for this rotation. All Residents are expected to understand: 1. Normal physiology and anatomy of the thyroid glands. 2. Normal physiology and anatomy of the parathyroid glands. 3. Normal physiology and anatomy of the adrenal glands 4. Normal physiology of the pancreatic neuroendocrine cells. 5. Normal physiology of the pituitary gland. Disease-Based Learning Objectives: Hyperfunctioning Thyroid and Hypothyroid State: 1. Physiology of Grave’s disease and toxic goiter. 2. Management of a patient in hyperthyroid storm. 3. Medical and surgical treatment options for hyperthyroidism. 4. Physiology of Hashimoto’s thyroiditis and hypothyroidism. Thyroid Neoplasm: 1. Workup of a cold thyroid nodule. 2. Surgical management of papillary, follicular, medullary, and anaplastic thyroid carcinoma. 3. Adjuvant therapy for thyroid neoplasms. 4. Postoperative medical management and long-term follow-up of thyroid cancer. Hyperparathyroidism: 1. Diagnosis and work-up of hypercalcemia and primary, secondary, and tertiary hyperparathyroidism.