Gustavo Werutsky

Dr. Gustavo Werutsky


Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 April 2012 in The Lancet Oncology
Verified
Journal Article
Closed access
SLSaskia Litière
Saskia Litière
GWGustavo Werutsky
Gustavo Werutsky
IFIan S Fentiman
Ian S Fentiman
EREmiel Rutgers
Emiel Rutgers
MCMarie-Rose Christiaens
Marie-Rose Christiaens
HBHarry Bartelink
Harry Bartelink

10 May 2021 in Journal of Clinical Oncology
Verified
Journal Article
Closed access
SLSibylle Loibl
Sibylle Loibl
FMFrederik Marmé
Frederik Marmé
MMMiguel Martin
Miguel Martin
MUMichael Untch
Michael Untch
HBHervé Bonnefoi
Hervé Bonnefoi
GMGunter von Minckwitz
Gunter von Minckwitz
PURPOSE: About one third of patients with hormone receptor–positive, human epidermal growth factor receptor 2–negative breast cancer who have residual invasive disease after neoadjuvant chemotherapy (NACT) will relapse. Thus, additional therapy is needed. Palbociclib is a cyclin-dependent kinase 4 and 6 inhibitor demonstrating efficacy in the metastatic setting. PATIENTS AND METHODS: PENELOPE-B ( NCT01864746 ) is a double-blind, placebo‐controlled, phase III study in women with hormone receptor–positive, human epidermal growth factor receptor 2–negative primary breast cancer without a pathological complete response after taxane‐containing NACT and at high risk of relapse (clinical pathological staging-estrogen receptor grading score ≥ 3 or 2 and ypN+). Patients were randomly assigned (1:1) to receive 13 cycles of palbociclib 125 mg once daily or placebo on days 1-21 in a 28-day cycle in addition to endocrine therapy (ET). Primary end point is invasive disease-free survival (iDFS). Final analysis was planned after 290 iDFS events with a two-sided efficacy boundary P < .0463 because of two interim analyses. RESULTS: One thousand two hundred fifty patients were randomly assigned. The median age was 49.0 years (range, 19-79), and the majority were ypN+ with Ki-67 ≤ 15%; 59.4% of patients had a clinical pathological staging-estrogen receptor grading score ≥ 3. 50.1% received aromatase inhibitor, and 33% of premenopausal women received a luteinizing hormone releasing hormone analog in addition to either tamoxifen or an aromatase inhibitor. After a median follow-up of 42.8 months (92% complete), 308 events were confirmed. Palbociclib did not improve iDFS versus placebo added to ET-stratified hazard ratio, 0.93 (95% repeated CI, 0.74 to 1.17) and two-sided weighted log-rank test (Cui, Hung, and Wang) P = .525. There was no difference among the subgroups. Most common related serious adverse events were infections and vascular disorders in 113 (9.1%) patients with no difference between the treatment arms. Eight fatal serious adverse events (two palbociclib and six placebo) were reported. CONCLUSION: Palbociclib for 1 year in addition to ET did not improve iDFS in women with residual invasive disease after NACT.

1 February 2018 in Jornal Brasileiro de Pneumologia
Verified
Journal Article
Open access
PDF file
LALuiz Henrique Araujo
Luiz Henrique Araujo
CBClarissa Baldotto
Clarissa Baldotto
GJGilberto de Castro Jr
Gilberto de Castro Jr
AKArtur Katz
Artur Katz
CFCarlos Gil Ferreira
Carlos Gil Ferreira
CBCarlos Barrios
Carlos Barrios
Lung cancer is one of the most incident types of cancer and a leading cause of cancer mortality in Brazil. We reviewed the current status of lung cancer by searching relevant data on prevention, diagnosis, and treatment in the country. This review highlights several issues that need to be addressed, including smoking control, patient lack of awareness, late diagnosis, and disparities in the access to cancer health care facilities in Brazil. We propose strategies to help overcome these limitations and challenge health care providers, as well as the society and governmental representatives, to work together and to take a step forward in fighting lung cancer.

3 November 2011 in European Journal of Cancer
Verified
Journal Article
Closed access
PDF file
EREmiel Rutgers
Emiel Rutgers
MPMartine J. Piccart-Gebhart
Martine J. Piccart-Gebhart
JBJan Bogaerts
Jan Bogaerts
SDSuzette Delaloge
Suzette Delaloge
LVLaura Van ‘T Veer
Laura Van ‘T Veer
FCFatima Cardoso
Fatima Cardoso

1 November 2021 in The Lancet Oncology
Verified
Journal Article
Closed access
GWGustavo Werutsky
Gustavo Werutsky
CBCarlos H Barrios
Carlos H Barrios
ACAndres F Cardona
Andres F Cardona
AAAndré Albergaria
André Albergaria
AVAlfonso Valencia
Alfonso Valencia
ECEduardo Cazap
Eduardo Cazap

1 January 2010 in International Journal of Surgery
Verified
Journal Article
Closed access
SFSheila S. Ferreira
Sheila S. Ferreira
GWGustavo Werutsky
Gustavo Werutsky
MTMarcelo Garcia Toneto
Marcelo Garcia Toneto
JAJarcedy Machado Alves
Jarcedy Machado Alves
CPChristina Duarte Piantá
Christina Duarte Piantá
BGBernardo Garicochea
Bernardo Garicochea
Gastrointestinal stromal tumors (GISTs) are rare mesenchymal neoplasm affecting the gastrointestinal tract. The incidental occurrence of mesenchymal tumors and other primary tumors has not been well described in literature. The aim of this study was to evaluate the clinical and pathologic features of GIST occurring synchronously with other primary tumors. Forty-three patients with diagnosis of GIST treated surgically with curative intent at our institution from 1998 to 2006 were included. The patient clinical data and pathological reports were reviewed. Of the 43 patients, there were 6 (14%) cases of synchronous GIST and other primary tumors discovered as coincidental findings. The synchronous GISTs analyzed were located in the stomach (50%) and small intestine (50%), size ranging from 0.7 to 7.6 cm (median 3.35 cm). Five (83%) of the concurrent primary tumors were from gastrointestinal origin and only one (17%) patient presented with concurrent breast cancer and GIST. The synchronous GISTs immunofenotype shows positivity for CD117 and CD34 (100%), smooth-muscle actin (SMA) (67%), S100 (50%) and desmin (33%). Whereas staining for cytokeratin AE1/AE3 and PDGF were all negative. According to GIST risk category for aggressive behavior three were classified as very low, one intermediate and two high. The synchronous occurrence of GISTs and other primary neoplasm is not an uncommon entity and usually they are discovery incidentally. Epithelial tumors of the gastrointestinal tract are the most associated with concomitant GISTs. Further studies are required to clarify the molecular and genetic mechanisms of carcinogenesis and progression associating GIST and synchronous tumors.