Please use this identifier to cite or link to this item: https://observatorio.fm.usp.br/handle/OPI/32462
Full metadata record
DC FieldValueLanguage
dc.contributorSistema FMUSP-HC: Faculdade de Medicina da Universidade de São Paulo (FMUSP) e Hospital das Clínicas da FMUSP
dc.contributor.authorV, Carlos E. C. Abreu
dc.contributor.authorMORAES, Fabio Y.
dc.contributor.authorMIRANDA, Fabiana A.
dc.contributor.authorSIQUEIRA, Gabriela S. M.
dc.contributor.authorGADIA, Rafael
dc.contributor.authorHADDAD, Cecilia K.
dc.contributor.authorCARVALHO, Heloisa A.
dc.date.accessioned2019-06-26T17:29:01Z-
dc.date.available2019-06-26T17:29:01Z-
dc.date.issued2018
dc.identifier.citationJOURNAL OF GLOBAL ONCOLOGY, v.4, 2018
dc.identifier.issn2378-9506
dc.identifier.urihttps://observatorio.fm.usp.br/handle/OPI/32462-
dc.description.abstractPurpose Stereotactic body radiation therapy (SBRT) has emerged as a treatment option for patients with non-small-cell lung cancer (NSCLC). We report the clinical outcomes and toxicity for patients with inoperable primary NSCLC treated with SBRT. Methods Between 2007 and 2015, 102 consecutive lung lesions were treated with SBRT at our center, of which 59 primary NSCLC lesions (from 54 patients with inoperable disease) were retrospectively reviewed (43 lesions were excluded because of metastases or because there was no biopsy specimen). We report infield local control (LC) per SBRT target, regional or distant failure-free survival, and overall survival (OS) per patient, using Kaplan-Meier estimates. Serious toxicity was retrospectively scored using Common Terminology Criteria for Adverse Events, version 4. Results Most of the 54 patients were men (n = 41; 76%), median age was 75 years; stage IA (n = 36; 66%) and adenocarcinoma (n = 43; 80%) were the most common stage and histologic diagnosis, respectively. Five patients had two lung lesions. A median of three fractions (range, 3 to 5 fractions) and a total median dose of 54 Gy (range, 45 to 60 Gy) per lesion were prescribed. The median follow-up was 17.8 months (range, 4 to 56.4 months). The 2-year rates of LC, regional or distant failure-free survival, and OS were 89.1% (95% CI, 72.2% to 96%), 79% (95% CI, 59.8% to 89.8%), and 80% (95% CI, 64% to 89.8%), respectively. Grade 3 to 4 toxicities were observed in two patients (3%): grade 3 pneumonitis (n = 1) and grade 4 skin toxicity (n = 1). Conclusion SBRT results in high rates of 2-year LC, regional or distant failure-free survival, and OS with low rates of severe toxicity in patients with inoperable primary NSCLC disease. (C) 2018 by American Society of Clinical Oncologyeng
dc.language.isoeng
dc.publisherAMER SOC CLINICAL ONCOLOGYeng
dc.relation.ispartofJournal of Global Oncology
dc.rightsopenAccesseng
dc.subject.otherhypofractionated radiotherapyeng
dc.subject.otherablative radiotherapyeng
dc.subject.othersurvivaleng
dc.subject.othertoxicityeng
dc.subject.otheroutcomeseng
dc.subject.othertumorseng
dc.titleStereotactic Body Radiation Therapy for Biopsy-Proven Primary Non-Small-Cell Lung Cancer: Experience of Patients With Inoperable Cancer at a Single Brazilian Institutioneng
dc.typearticleeng
dc.rights.holderCopyright AMER SOC CLINICAL ONCOLOGYeng
dc.identifier.doi10.1200/JGO.18.00020
dc.identifier.pmid30085881
dc.subject.wosOncologyeng
dc.type.categoryoriginal articleeng
dc.type.versionpublishedVersioneng
hcfmusp.author.externalV, Carlos E. C. Abreu:Hosp Sfrio Libanes, Sao Paulo, SP, Brazil
hcfmusp.author.externalMORAES, Fabio Y.:Hosp Sfrio Libanes, Sao Paulo, SP, Brazil; Univ Toronto, Toronto, ON, Canada; Univ Hlth Network, Princess Margaret Canc Ctr, Toronto, ON, Canada
hcfmusp.author.externalMIRANDA, Fabiana A.:Hosp Sfrio Libanes, Sao Paulo, SP, Brazil
hcfmusp.author.externalSIQUEIRA, Gabriela S. M.:Hosp Sfrio Libanes, Sao Paulo, SP, Brazil
hcfmusp.author.externalGADIA, Rafael:Hosp Sfrio Libanes, Sao Paulo, SP, Brazil
hcfmusp.author.externalHADDAD, Cecilia K.:Hosp Sfrio Libanes, Sao Paulo, SP, Brazil
hcfmusp.description.volume4
hcfmusp.origemWOS
hcfmusp.origem.idWOS:000462457700001
hcfmusp.origem.id2-s2.0-85060558783
hcfmusp.publisher.cityALEXANDRIAeng
hcfmusp.publisher.countryUSAeng
hcfmusp.relation.referenceBezjak A, 2016, INT J RADIAT ONCOL, V96, pS8, DOI 10.1016/j.ijrobp.2016.06.035eng
hcfmusp.relation.referenceAbreu CECV, 2015, J BRAS PNEUMOL, V41, P376, DOI 10.1590/S1806-37132015000000034eng
hcfmusp.relation.referencede Moraes FY, 2016, CLINICS, V71, P101, DOI 10.6061/clinics/2016(02)09eng
hcfmusp.relation.referenceFakiris AJ, 2009, INT J RADIAT ONCOL, V75, P677, DOI 10.1016/j.ijrobp.2008.11.042eng
hcfmusp.relation.referenceKelly P, 2010, INT J RADIAT ONCOL, V78, P1387, DOI 10.1016/j.ijrobp.2009.09.070eng
hcfmusp.relation.referenceKoshy M, 2015, INT J RADIAT ONCOL, V91, P344, DOI 10.1016/j.ijrobp.2014.10.002eng
hcfmusp.relation.referenceLackey A, 2013, SEMIN INTERVENT RAD, V30, P133, DOI 10.1055/s-0033-1342954eng
hcfmusp.relation.referenceNagata Y, 2005, INT J RADIAT ONCOL, V63, P1427, DOI 10.1016/j.ijrobp.2005.05.034eng
hcfmusp.relation.referenceNanda RH, 2015, CANCER-AM CANCER SOC, V121, P4222, DOI 10.1002/cncr.29640eng
hcfmusp.relation.referenceNaruke T, 2001, ANN THORAC SURG, V71, P1759, DOI 10.1016/S0003-4975(00)02609-6eng
hcfmusp.relation.referenceNyman J, 2006, LUNG CANCER-J IASLC, V51, P97, DOI 10.1016/j.lungcan.2005.08.011eng
hcfmusp.relation.referenceOnishi H, 2007, J THORAC ONCOL, V2, pS94, DOI 10.1097/JTO.0b013e318074de34eng
hcfmusp.relation.referencePotters L, 2010, INT J RADIAT ONCOL, V76, P326, DOI 10.1016/j.ijrobp.2009.09.042eng
hcfmusp.relation.referenceSenthi S, 2013, RADIOTHER ONCOL, V106, P276, DOI 10.1016/j.radonc.2013.01.004eng
hcfmusp.relation.referenceSiegel RL, 2017, CA-CANCER J CLIN, V67, P7, DOI 10.3322/caac.21387eng
hcfmusp.relation.referenceSobin LH, 2011, TNM CLASSIFICATION Meng
hcfmusp.relation.referenceSun B, 2017, CANCER-AM CANCER SOC, V123, P3031, DOI 10.1002/cncr.30693eng
hcfmusp.relation.referenceTimmerman R, 2006, J CLIN ONCOL, V24, P4833, DOI 10.1200/JCO.2006.07.5937eng
hcfmusp.relation.referenceTimmerman R, 2010, JAMA-J AM MED ASSOC, V303, P1070, DOI 10.1001/jama.2010.261eng
hcfmusp.relation.referenceU. S. Department of Health and Human Services, 2010, COMMON TERMINOLOGY Ceng
hcfmusp.relation.referenceUeki N, 2015, J THORAC ONCOL, V10, P116, DOI 10.1097/JTO.0000000000000359eng
hcfmusp.relation.referenceUematsu M, 2001, INT J RADIAT ONCOL, V51, P666, DOI 10.1016/S0360-3016(01)01703-5eng
hcfmusp.relation.referenceZhang J, 2011, INT J RADIAT ONCOL, V81, pE305, DOI 10.1016/j.ijrobp.2011.04.034eng
hcfmusp.relation.referenceZimmermann FB, 2006, ACTA ONCOL, V45, P796, DOI 10.1080/02841860600913210eng
dc.description.indexMEDLINEeng
hcfmusp.citation.scopus3-
hcfmusp.scopus.lastupdate2024-03-29-
Appears in Collections:

Artigos e Materiais de Revistas Científicas - FM/MDR
Departamento de Radiologia - FM/MDR

Artigos e Materiais de Revistas Científicas - HC/InRad
Instituto de Radiologia - HC/InRad

Artigos e Materiais de Revistas Científicas - ODS/03
ODS/03 - Saúde e bem-estar


Files in This Item:
File Description SizeFormat 
art_V_Stereotactic_Body_Radiation_Therapy_for_BiopsyProven_Primary_NonSmallCell_2018.PDFpublishedVersion (English)768.74 kBAdobe PDFThumbnail
View/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.