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CRS/HIPEC with Major Organ Resection in Peritoneal Mesothelioma Does not Impact Major Complications or Overall Survival: A Retrospective Cohort Study of the US HIPEC Collaborative.
Roife, David; Powers, Benjamin D; Zaidi, Mohammad Y; Staley, Charles A; Cloyd, Jordan M; Ahmed, Ahmed; Grotz, Travis; Leiting, Jennifer; Fournier, Keith; Lee, Andrew J; Veerapong, Jula; Baumgartner, Joel M; Clarke, Callisia; Patel, Sameer H; Hendrix, Ryan J; Lambert, Laura; Abbott, Daniel E; Pokrzywa, Courtney; Lee, Byrne; Blakely, Andrew; Greer, Jonathan; Johnston, Fabian M; Laskowitz, Danielle; Dessureault, Sophie; Dineen, Sean P.
  • Roife D; Department of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, USA.
  • Powers BD; Department of Oncologic Sciences, University of South Florida, Morsani College of Medicine, Tampa, USA.
  • Zaidi MY; Department of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, USA.
  • Staley CA; Department of Oncologic Sciences, University of South Florida, Morsani College of Medicine, Tampa, USA.
  • Cloyd JM; Division of Surgical Oncology, Winship Cancer Institute, Emory University, Atlanta, USA.
  • Ahmed A; Division of Surgical Oncology, Winship Cancer Institute, Emory University, Atlanta, USA.
  • Grotz T; Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Columbus, USA.
  • Leiting J; Division of Surgical Oncology, Department of Surgery, The Ohio State University Wexner Medical Center, Columbus, USA.
  • Fournier K; Division of Hepatobiliary and Pancreas Surgery, Mayo Clinic, Rochester, USA.
  • Lee AJ; Division of Hepatobiliary and Pancreas Surgery, Mayo Clinic, Rochester, USA.
  • Veerapong J; Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, USA.
  • Baumgartner JM; Department of Surgical Oncology, University of Texas MD Anderson Cancer Center, Houston, USA.
  • Clarke C; Division of Surgical Oncology, Department of Surgery, University of California, San Diego, USA.
  • Patel SH; Division of Surgical Oncology, Department of Surgery, University of California, San Diego, USA.
  • Hendrix RJ; Division of Surgical Oncology, Department of Surgery, Medical College of Wisconsin, Milwaukee, USA.
  • Lambert L; Department of Surgery, University of Cincinnati College of Medicine, Cincinnati, USA.
  • Abbott DE; Division of Surgical Oncology, Department of Surgery, University of Massachusetts Medical School, Worcester, USA.
  • Pokrzywa C; Department of Surgery, Huntsman Cancer Institute, University of Utah, Salt Lake City, USA.
  • Lee B; Division of Surgical Oncology, Department of Surgery, University of Wisconsin, Madison, USA.
  • Blakely A; Division of Surgical Oncology, Department of Surgery, University of Wisconsin, Madison, USA.
  • Greer J; Division of Surgical Oncology, Department of Surgery, City of Hope National Medical Center, Duarte, USA.
  • Johnston FM; Division of Surgical Oncology, Department of Surgery, City of Hope National Medical Center, Duarte, USA.
  • Laskowitz D; Department of Surgery, Johns Hopkins University, Baltimore, MD, USA.
  • Dessureault S; Department of Surgery, Johns Hopkins University, Baltimore, MD, USA.
  • Dineen SP; Department of Gastrointestinal Oncology, Moffitt Cancer Center, Tampa, USA.
Ann Surg Oncol ; 27(13): 4996-5004, 2020 Dec.
Article en En | MEDLINE | ID: mdl-33073341
INTRODUCTION: CRS/HIPEC is thought to confer a survival advantage for patients with malignant peritoneal mesothelioma (MPM). However, the impact of nonperitoneal organ resection is not clearly defined. We evaluated the impact of major organ resection (MOR) on postoperative outcomes and overall survival (OS). PATIENTS AND METHODS: The US HIPEC collaborative database (2000-2017) was reviewed for MPM patients who underwent CRS/HIPEC. MOR was defined as total or partial resection of diaphragm, stomach, spleen, pancreas, small bowel, colon, rectum, kidney, ureter, bladder, and/or uterus. MOR was categorized as 0, 1, or 2+ organs. RESULTS: A total of 174 patients were identified. Median PCI was 16 (3-39). The distribution of patients with MOR-0, MOR-1, and MOR-2+ was 94, 45, and 35 patients, respectively. MOR-1 and MOR-2+ groups had a higher frequency of any complication compared with MOR-0 (57.8%, 74.3%, and 48.9%, respectively, p = 0.035), but Clavien 3/4 complications were similar. Median length of stay was slightly higher in the MOR-1 and MOR-2+ groups (10 and 11 days) compared with the MOR-0 cohort (9 days, p = 0.005). Incomplete cytoreduction, ASA class 4, and male gender were associated with increased mortality on unadjusted analysis; however, their impact on OS was attenuated on multivariable analysis. MOR was not associated with OS based on these data (MOR-1: HR 1.67, 95% CI 0.59-4.74; MOR-2+ : HR 0.77, 95% CI 0.22-2.69). CONCLUSIONS: MOR was not associated with an increase in major complications or worse OS in patients undergoing CRS/HIPEC for MPM and should be considered, if necessary, to achieve complete cytoreduction for MPM patients.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Quimioterapia Intraperitoneal Hipertérmica Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Quimioterapia Intraperitoneal Hipertérmica Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Female / Humans / Male Idioma: En Año: 2020 Tipo del documento: Article