120 Factors associated with extended survival for patients with platinum-resistant ovarian cancer (PROC) treated with modified vaccinia oncolytic virotherapy (VOV). (18th September 2019)
- Record Type:
- Journal Article
- Title:
- 120 Factors associated with extended survival for patients with platinum-resistant ovarian cancer (PROC) treated with modified vaccinia oncolytic virotherapy (VOV). (18th September 2019)
- Main Title:
- 120 Factors associated with extended survival for patients with platinum-resistant ovarian cancer (PROC) treated with modified vaccinia oncolytic virotherapy (VOV)
- Authors:
- Manyam, M
Stephens, A
Kennard, J
Fitzsimmons, C
Kendrick, J
McKenzie, N
LeBlanc, J
Smith, J
Ahmad, S
Holloway, R - Abstract:
- Abstract : Objectives: VIRO-15 phase IB trial (NCT02759588 ) enrolled 11 patients with PROC, extensive tumor burden, and median 5 prior lines of therapy. We aimed to retrospectively determine factors that predict clinical benefit from VOV monotherapy in PROC. Methods: Patients received a modified VOV (GL-ONC1, Genelux Corp.) intra-peritoneally on two consecutive days. Four patients had apparent clinical benefit with >5 mos progression-free survival (PFS) following virotherapy (A). Seven (B) patients had <5 mo PFS. Comparative analyses included: measures of immune-competence with neutralizing antibody (NA) titers, virus-encoded glucuronidase activity (GA), tumor response by RECIST 1.1, Prognostic Nutritional Index (PNI), circulating tumor cells (CTCs), number of prior platinum and total therapies. Mann-Whitney test, t- test, z- test were used to evaluate differences between the groups. Results: Following GL-ONC1, the PFS was 10.9±5.1 and 2.4±1.1 mos for A vs B ( p < 0.05). Mean OS for A was 21.7±8.2 mos vs 3.6±1.5 mos for B ( p <0.05). Three A pts are alive, and one with stable disease died at 8-mos from pulmonary embolism. Factors that predicted clinical benefit were: i) PNI [mean 49.0±5.7 vs 42.1±4.3 ( p <0.05)], ii) Week-5 CA125 values < Week-2 [4/4 vs 0/7 ( p <0.01)], iii) absence of CTC [3/4 vs 1/7 pts ( p <0.05)]. Conclusions: Factors associated with clinical benefit post GL-ONC1 monotherapy in PROC include higher PNI, absence of CTCs, and Week-5 CA125 less than Week-2Abstract : Objectives: VIRO-15 phase IB trial (NCT02759588 ) enrolled 11 patients with PROC, extensive tumor burden, and median 5 prior lines of therapy. We aimed to retrospectively determine factors that predict clinical benefit from VOV monotherapy in PROC. Methods: Patients received a modified VOV (GL-ONC1, Genelux Corp.) intra-peritoneally on two consecutive days. Four patients had apparent clinical benefit with >5 mos progression-free survival (PFS) following virotherapy (A). Seven (B) patients had <5 mo PFS. Comparative analyses included: measures of immune-competence with neutralizing antibody (NA) titers, virus-encoded glucuronidase activity (GA), tumor response by RECIST 1.1, Prognostic Nutritional Index (PNI), circulating tumor cells (CTCs), number of prior platinum and total therapies. Mann-Whitney test, t- test, z- test were used to evaluate differences between the groups. Results: Following GL-ONC1, the PFS was 10.9±5.1 and 2.4±1.1 mos for A vs B ( p < 0.05). Mean OS for A was 21.7±8.2 mos vs 3.6±1.5 mos for B ( p <0.05). Three A pts are alive, and one with stable disease died at 8-mos from pulmonary embolism. Factors that predicted clinical benefit were: i) PNI [mean 49.0±5.7 vs 42.1±4.3 ( p <0.05)], ii) Week-5 CA125 values < Week-2 [4/4 vs 0/7 ( p <0.01)], iii) absence of CTC [3/4 vs 1/7 pts ( p <0.05)]. Conclusions: Factors associated with clinical benefit post GL-ONC1 monotherapy in PROC include higher PNI, absence of CTCs, and Week-5 CA125 less than Week-2 levels. In the absence of these factors, cytotoxic therapy should be considered by Week-6 following GL-ONC1. Three patients are currently alive at 22.8–28.2 mos, following additional therapies. … (more)
- Is Part Of:
- International journal of gynecological cancer. Volume 29(2019)Supplement 3
- Journal:
- International journal of gynecological cancer
- Issue:
- Volume 29(2019)Supplement 3
- Issue Display:
- Volume 29, Issue 3 (2019)
- Year:
- 2019
- Volume:
- 29
- Issue:
- 3
- Issue Sort Value:
- 2019-0029-0003-0000
- Page Start:
- A58
- Page End:
- A58
- Publication Date:
- 2019-09-18
- 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-IGCS.120 ↗
- 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:
- 19726.xml