Prognosis after local recurrence in vulvar cancer: A subset analysis of the AGO-CaRE-1 study.

2016 ◽  
Vol 34 (15_suppl) ◽  
pp. 5595-5595
Author(s):  
Linn Lena Woelber ◽  
Christine Eulenburg ◽  
Jens Kosse ◽  
Petra Neuser ◽  
Christoph Heiss ◽  
...  
Author(s):  
Linn Woelber ◽  
Katharina Prieske ◽  
Christine zu Eulenburg ◽  
Stefanie Corradini ◽  
Cordula Petersen ◽  
...  

2019 ◽  
Vol 154 (3) ◽  
pp. 571-576 ◽  
Author(s):  
Linn Woelber ◽  
Christine Eulenburg ◽  
Jens Kosse ◽  
Petra Neuser ◽  
Christoph Heiss ◽  
...  

2008 ◽  
Vol 279 (2) ◽  
pp. 239-241 ◽  
Author(s):  
Tayfun Gungor ◽  
Adnan Simsek ◽  
Umit Bilge ◽  
Leyla Mollamahmutoglu

2008 ◽  
Vol 7 (5) ◽  
pp. 375-380 ◽  
Author(s):  
Charles Kunos ◽  
Vivian von Gruenigen ◽  
Steven Waggoner ◽  
James Brindle ◽  
Yuxia Zhang ◽  
...  

Limited options exist for patients experiencing a local recurrence of vulvar malignancies after surgery and pelvic radiation. These recurrences often are associated with cancer-related skin desquamation and poor clinical outcomes. A new radiotherapeutic treatment modality for the previously irradiated patient is cyberknife radiosurgery, which uses a linear accelerator mounted on an industrial robotic arm to allow non-coplanar radiation therapy delivery with sub-millimeter precision. This study describes the first reported use of cyberknife radiosurgery for the treatment of recurrent vulvar cancer in three women.


2020 ◽  
Author(s):  
L Woelber ◽  
M Bommert ◽  
P Harter ◽  
K Prieske ◽  
C zu Eulenburg ◽  
...  

2019 ◽  
Vol 30 (3) ◽  
pp. 402-405
Author(s):  
Diana Zach ◽  
Paivi Kannisto ◽  
Katja Stenström Bohlin ◽  
Louise Moberg ◽  
Preben Kjölhede

BackgroundIn squamous cell vulvar cancer, sentinel node biopsy is accepted as standard treatment in well-defined patient groups and has reduced surgical morbidity considerably. Currently, due to the lack of evidence, it cannot be offered to patients with tumors of 4 cm diameter or greater or with multifocal tumors, or in local recurrences.Primary objectiveThis study is primarily a pilot and feasibility trial, aiming to evaluate if the prerequisites concerning detection rate and negative predictive value are satisfactory before the implementation of a multinational trial.Study hypothesisSentinel node biopsy has an acceptable negative predictive value and detection rate in the study cohort.Trial designThis study is planned as a prospective, national, multicenter interventional trial. Participating patients will undergo a sentinel node biopsy in addition to an inguinofemoral lymphadenectomy.Inclusion and exclusion criteriaInclusion criteria: for women in group 1, a primary tumor ≥4 cm in diameter; in group 2, a multifocal primary tumor; in group 3, a local recurrence without previous inguinofemoral lymphadenectomy or radiation to the groins; in group 4, a local recurrence, with previous inguinofemoral lymphadenectomy and/or radiation to the groins.Primary endpointThe primary endpoints are the detection rate and the negative predictive value of the sentinel node procedure.Sample sizeIn each of the four study arms, recruitment of 20–30 patients is planned.Estimated dates for completing recruitment and presenting resultsRecruitment will take place between November 2019 and October 2021. Results will be available in December 2021.Trial registrationThe trial is registered at “ClinicalTrials.gov” (ID: NCT04147780).


2014 ◽  
Vol 32 (15_suppl) ◽  
pp. 5608-5608
Author(s):  
Linn Lena Woelber ◽  
Jalid Sehouli ◽  
Anika Habermann ◽  
Peter Hillemanns ◽  
Petra Neuser ◽  
...  

2016 ◽  
Vol 26 (9) ◽  
pp. 1699-1705 ◽  
Author(s):  
Divya Natesan ◽  
Matthew Susko ◽  
Laura Havrilesky ◽  
Junzo Chino

ObjectivesThis study aimed to evaluate clinical outcomes after chemoradiation (CRT) for the definitive (nonsurgical) treatment of vulvar cancer.Materials and MethodsWomen with vulvar cancer treated with definitive CRT at a single academic institution between 1994 and 2015 were retrospectively identified. Overall survival (OS), freedom from local recurrence, freedom from distant recurrence, and late toxicities were estimated using the Kaplan–Meier method at 3 years after radiotherapy completion. Univariate Cox regression models were used to estimate the effects of risk factors on these clinical end points. Acute and late toxicities were assessed according to the Common Terminology Criteria for Adverse Events v. 4.0.ResultsTwenty-five women met criteria for inclusion. At 3 years, OS was 71% (95% confidence interval [CI], 49%–93%), freedom from local recurrence was 65% (95% CI, 43%–87%), and freedom from distant recurrence was 78% (95% CI, 59%–97%). Older age was significantly associated with decreased OS (hazard rate, 1.069/y; 95% CI, 1.005–1.124; P = 0.035) and local recurrence (hazard rate, 1.077/y; 95% CI, 1.009–1.150; P = 0.026). Larger size of the primary was borderline associated with distant recurrence (P = 0.057). Skin changes were the most common late toxicity, with a 3-year rate of late G3 skin toxicity of 45% (95% CI, 20%–69%). The rate of lymphedema at 3 years was 25% (95% CI, 5%–44%).ConclusionsDefinitive CRT for advanced vulvar cancer was an effective and well-tolerated approach for women with unresectable disease. Further work is needed to more appropriately select women who will benefit most from a nonsurgical approach.


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