EP1170 Development of a risk model for survival and recurrence in patients with vulvar squamous cell carcinoma. (1st November 2019)
- Record Type:
- Journal Article
- Title:
- EP1170 Development of a risk model for survival and recurrence in patients with vulvar squamous cell carcinoma. (1st November 2019)
- Main Title:
- EP1170 Development of a risk model for survival and recurrence in patients with vulvar squamous cell carcinoma
- Authors:
- Kortekaas, KE
Bastiaannet, E
van Doorn, HC
Goddijn, IF
Rogaar, HJ
de Vos van Steenwijk, PJ
Ewing, PC
Creutzberg, CL
Akdeniz, K
Nooij, LS
van der Burg, SH
Bosse, T
van Poelgeest, MIE - Abstract:
- Abstract : Introduction/Background: Increasing evidence points to better prognosis for human papillomavirus (HPV)-positive vulvar squamous cell carcinoma (HPVposVSCC) compared to HPV-negative VSCC (HPVnegVSCC). The aims of this study were to evaluate the clinical significance of HPV and other prognostic factors in a large cohort with VSCC patients and to develop risk models for survival and recurrence. Methodology: Patients with primary VSCC, surgically treated with curative intent between 2000 and 2015 ( n =421) were included. HPV was determined by HPV-PCR and p16 immunohistochemistry. Overall survival (OS), relative survival (RS), and recurrence-free period (RFP) were determined in patients with HPVposVSCC and HPVnegVSCC. A risk model based on prognostic factors with significant impact on OS and RFP was designed to predict risk of death and shorter RFP. Data were internally validated using a bootstrap resampling procedure. Results: Patients with HPVnegVSCC had worse 5-year OS, RS, and RFP than those with HPVposVSCC (52%, 64%, and 46% vs 82%; p =0.001, 90%; p =0.010, and 82%; p <0.001, respectively. Independent prognostic factors for unfavorable OS were FIGO stage III, age ≥70 and tumor-positive resection margins, and for shorter RFP HPV status and age ≥70. Risk models for OS and RFP were developed in which patients were classified into low, intermediate and high-risk categories for death or recurrence (AUC were 0.77 and 0.73 for OS and RFP, respectively). According to thisAbstract : Introduction/Background: Increasing evidence points to better prognosis for human papillomavirus (HPV)-positive vulvar squamous cell carcinoma (HPVposVSCC) compared to HPV-negative VSCC (HPVnegVSCC). The aims of this study were to evaluate the clinical significance of HPV and other prognostic factors in a large cohort with VSCC patients and to develop risk models for survival and recurrence. Methodology: Patients with primary VSCC, surgically treated with curative intent between 2000 and 2015 ( n =421) were included. HPV was determined by HPV-PCR and p16 immunohistochemistry. Overall survival (OS), relative survival (RS), and recurrence-free period (RFP) were determined in patients with HPVposVSCC and HPVnegVSCC. A risk model based on prognostic factors with significant impact on OS and RFP was designed to predict risk of death and shorter RFP. Data were internally validated using a bootstrap resampling procedure. Results: Patients with HPVnegVSCC had worse 5-year OS, RS, and RFP than those with HPVposVSCC (52%, 64%, and 46% vs 82%; p =0.001, 90%; p =0.010, and 82%; p <0.001, respectively. Independent prognostic factors for unfavorable OS were FIGO stage III, age ≥70 and tumor-positive resection margins, and for shorter RFP HPV status and age ≥70. Risk models for OS and RFP were developed in which patients were classified into low, intermediate and high-risk categories for death or recurrence (AUC were 0.77 and 0.73 for OS and RFP, respectively). According to this model, 5-year OS was 89%, for the low, 65% for the intermediate, and 29% for the high-risk groups. In HPVposVSCC, 70% and 100% of patients were classified as low-risk for death and recurrence, respectively, compared to 22% and 21% of HPVnegVSCC patients. Conclusion: The developed risk models contribute to better prediction of survival and recurrence in surgically-treated VSCC patients. They may aid trial design and encourage the selection of high-risk patients potentially benefitting from new therapies or intensified follow-up. Disclosure: Nothing to disclose … (more)
- Is Part Of:
- International journal of gynecological cancer. Volume 29(2019)Supplement 4
- Journal:
- International journal of gynecological cancer
- Issue:
- Volume 29(2019)Supplement 4
- Issue Display:
- Volume 29, Issue 4 (2019)
- Year:
- 2019
- Volume:
- 29
- Issue:
- 4
- Issue Sort Value:
- 2019-0029-0004-0000
- Page Start:
- A606
- Page End:
- A606
- Publication Date:
- 2019-11-01
- Subjects:
- Generative organs, Female -- Cancer -- Periodicals
616.99465 - Journal URLs:
- http://journals.lww.com/ijgc/pages/default.aspx ↗
http://www3.interscience.wiley.com/journal/118544021/toc ↗
https://ijgc.bmj.com/ ↗
http://journals.lww.com ↗ - DOI:
- 10.1136/ijgc-2019-ESGO.1211 ↗
- Languages:
- English
- ISSNs:
- 1048-891X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4542.273500
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 19764.xml