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Uterine serous carcinoma.
Bogani, Giorgio; Ray-Coquard, Isabelle; Concin, Nicole; Ngoi, Natalie Y L; Morice, Philippe; Enomoto, Takayuki; Takehara, Kazuhiro; Denys, Hannelore; Nout, Remi A; Lorusso, Domenica; Vaughan, Michelle M; Bini, Marta; Takano, Masashi; Provencher, Diane; Indini, Alice; Sagae, Satoru; Wimberger, Pauline; Póka, Robert; Segev, Yakir; Kim, Se Ik; Candido Dos Reis, Francisco J; Lopez, Salvatore; Mariani, Andrea; Leitao, Mario M; Raspagliesi, Francesco; Panici, Pieluigi Benedetti; Di Donato, Violante; Muzii, Ludovico; Colombo, Nicoletta; Scambia, Giovanni; Pignata, Sandro; Monk, Bradley J.
Afiliação
  • Bogani G; Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy. Electronic address: giorgiobogani@yahoo.it.
  • Ray-Coquard I; Centre Leon Bérard, Hesper lab. EA 7425 Université Claude Bernard Lyon Est, Lyon, France.
  • Concin N; Department of Gynecology and Obstetrics, Innsbruck Medical University, Innsbruck, Austria; Department of Gynecology and Gynecological Oncology, Evangelische Kliniken Essen-Mitte, Essen, Germany.
  • Ngoi NYL; National University Cancer Institute, Singapore, Singapore.
  • Morice P; Gystave Roussy Cancer Campus, Villejuif, France.
  • Enomoto T; Department of Obstetrics and Gynecology, Niigata University Graduate School of Medical and Dental Sciences, Japan.
  • Takehara K; Department of Gynecologic Oncology, National Hospital Organization Shikoku Cancer Center, Japan.
  • Denys H; Medical Oncology, Department of Internal Medicine and Pediatrics, Ghent University Hospital, Ghent, Belgium.
  • Nout RA; Erasmus MC Cancer Institute, University Medical Center Rotterdam, the Netherlands.
  • Lorusso D; Fondazione Policlinico Universitario A Gemelli IRCCS, Rome, Italy.
  • Vaughan MM; Medical Oncology, Canterbury Regional Cancer and Haematology Service, Christchurch, New Zealand.
  • Bini M; Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
  • Takano M; Department of Obstetrics and Gynecology, National Defense Medical College, Tokorozawa, Saitama, Japan.
  • Provencher D; Centre hospitalier de l'Université de Montréal (CHUM), Institut du cancer de Montréal, Montréal, Canada.
  • Indini A; Medical Oncology Unit, IRCCS Foundation Ca' Granda Maggiore Hospital Policlinic, Milan, Italy.
  • Sagae S; Gynecologic Oncology Unit, Hokkaido Ohno Memorial Hospital, Sapporo, Japan.
  • Wimberger P; Department of Gynecology and Obstetrics, Carl-Gustav-Carus University, TU Dresden, Dresden, Germany on behalf of the AGO-Ovar, Germany.
  • Póka R; Institute of Obstetrics and Gynecology, Clinical Center, University of Debrecen, Debrecen, Hungary.
  • Segev Y; Carmel Medical Center, Affiliated to the Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel.
  • Kim SI; Department of Obstetrics and Gynecology, Seoul National University College of Medicine, Seoul 03080, Republic of Korea.
  • Candido Dos Reis FJ; Department of Gynecology and Obstetrics, Ribeirao Preto Medical School, University of Sao Paulo, Brazil.
  • Lopez S; Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
  • Mariani A; Department of Obstetrics and Gynecology, Mayo Clinic, Rochester, MN, USA.
  • Leitao MM; Gynecology Service, Department of Surgery, Memorial Sloan Kettering Cancer Center, New York, NY, United States of America; Joan & Sanford I. Weill Medical College of Cornell University, New York, NY, United States of America.
  • Raspagliesi F; Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milan, Italy.
  • Panici PB; Department of Maternal and Child Health and Urological Sciences, Sapienza University, Policlinico Umberto I, Rome, Italy.
  • Di Donato V; Department of Maternal and Child Health and Urological Sciences, Sapienza University, Policlinico Umberto I, Rome, Italy.
  • Muzii L; Department of Maternal and Child Health and Urological Sciences, Sapienza University, Policlinico Umberto I, Rome, Italy.
  • Colombo N; Gynecologic Oncology Program, European Institute of Oncology, IRCCS, Milan and University of Milan-Bicocca, Milan, Italy.
  • Scambia G; Fondazione Policlinico Universitario A Gemelli IRCCS, Rome, Italy.
  • Pignata S; Department of Urology and Gynecology, Istituto Nazionale Tumori IRCCS Fondazione G. Pascale Napoli, Italy.
  • Monk BJ; Arizona Oncology (US Oncology Network), University of Arizona, Creighton University, Phoenix, USA.
Gynecol Oncol ; 162(1): 226-234, 2021 07.
Article em En | MEDLINE | ID: mdl-33934848
ABSTRACT
Serous endometrial cancer represents a relative rare entity accounting for about 10% of all diagnosed endometrial cancer, but it is responsible for 40% of endometrial cancer-related deaths. Patients with serous endometrial cancer are often diagnosed at earlier disease stage, but remain at higher risk of recurrence and poorer prognosis when compared stage-for-stage with endometrioid subtype endometrial cancer. Serous endometrial cancers are characterized by marked nuclear atypia and abnormal p53 staining in immunohistochemistry. The mainstay of treatment for newly diagnosed serous endometrial cancer includes a multi-modal therapy with surgery, chemotherapy and/or radiotherapy. Unfortunately, despite these efforts, survival outcomes still remain poor. Recently, The Cancer Genome Atlas (TCGA) Research Network classified all endometrial cancer types into four categories, of which, serous endometrial cancer mostly is found within the "copy number high" group. This group is characterized by the increased cell cycle deregulation (e.g., CCNE1, MYC, PPP2R1A, PIKCA, ERBB2 and CDKN2A) and TP53 mutations (90%). To date, the combination of pembrolizumab and lenvatinib is an effective treatment modality in second-line therapy, with a response rate of 50% in advanced/recurrent serous endometrial cancer. Owing to the unfavorable outcomes of serous endometrial cancer, clinical trials are a priority. At present, ongoing studies are testing novel combinations of various targeted and immunotherapeutic agents in newly diagnosed and advanced/recurrent endometrial cancer - an important strategy for serous endometrial cancer, whereby tumors are usually p53+ and pMMR, making response to PD-1 inhibitor monotherapy unlikely. Here, the rare tumor working group (including members from the European Society of Gynecologic Oncology (ESGO), Gynecologic Cancer Intergroup (GCIG), and Japanese Gynecologic Oncology Group (JGOG)), performed a narrative review reporting on the current landscape of serous endometrial cancer and focusing on standard and emerging therapeutic options for patients affected by this difficult disease.
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias Uterinas / Cistadenocarcinoma Seroso Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Female / Humans Idioma: En Revista: Gynecol Oncol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Neoplasias Uterinas / Cistadenocarcinoma Seroso Tipo de estudo: Clinical_trials / Prognostic_studies Limite: Female / Humans Idioma: En Revista: Gynecol Oncol Ano de publicação: 2021 Tipo de documento: Article