Predictors of response to immune checkpoint inhibition in a real world gynecologic cancer population

Prognostic factors for immune checkpoint inhibitor (CPI) response in gynecologic cancer are limited. This retrospective study aimed to identify prognostic factors associated with improved overall response rate (ORR) and progression free survival (PFS) in gynecologic cancer patients receiving at leas...

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Váldodahkkit: Michelle L. Kuznicki (Dahkki), Carrie Bennett (Dahkki), Meng Yao (Dahkki), Amy Joehlin-Price (Dahkki), Peter G. Rose (Dahkki), Haider Mahdi (Dahkki)
Materiálatiipa: Girji
Almmustuhtton: Elsevier, 2020-11-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Michelle L. Kuznicki  |e author 
700 1 0 |a Carrie Bennett  |e author 
700 1 0 |a Meng Yao  |e author 
700 1 0 |a Amy Joehlin-Price  |e author 
700 1 0 |a Peter G. Rose  |e author 
700 1 0 |a Haider Mahdi  |e author 
245 0 0 |a Predictors of response to immune checkpoint inhibition in a real world gynecologic cancer population 
260 |b Elsevier,   |c 2020-11-01T00:00:00Z. 
500 |a 2352-5789 
500 |a 10.1016/j.gore.2020.100671 
520 |a Prognostic factors for immune checkpoint inhibitor (CPI) response in gynecologic cancer are limited. This retrospective study aimed to identify prognostic factors associated with improved overall response rate (ORR) and progression free survival (PFS) in gynecologic cancer patients receiving at least two cycles of CPI. PFS was compared by univariate cox regressions. Univariate and multivariable analyses were used for prognostic factors of PFS and ORR. 72 patients were identified (20 ovarian, 36 endometrial, 13 cervix, 1 vaginal, 2 others). Immune related adverse events (IRAE) occurred in 40.3% of patients (29/72). IRAE was associated with higher ORR (44.8% IRAE vs 20.9% no IRAE, OR 3.1, p = 0.024), improved PFS (12.9 m IRAE vs 4.7 m no IRAE, HR 0.43, p = 0.004) and improved OS (22.9 m IRAE vs 12.2 m no IRAE, HR 0.47, p = 0.021). Additionally, Clear cell histology had superior ORR compared to MSI stable endometrial and ovarian cancers (ORR 57.1% vs 11.8%, OR 10.0, p = 0.032). Responders more often had ARIDIA mutation, PI3K/PTEN alteration and less often had a P53 mutation. In a subset of six MSI-H, recurrent, chemo-naive endometrial cancer ORR was 83.3%. Overall, we found favorable outcomes after CPI for clear cell tumors and patients who developed IRAE. Additionally, first-line systemic therapy with CPI in recurrent MSI-H endometrial cancer had encouraging ORR with durable responses. 
546 |a EN 
690 |a Checkpoint inhibition 
690 |a Gynecologic cancer 
690 |a Immune toxicity 
690 |a Clear cell histology 
690 |a Recurrent endometrial cancer 
690 |a Gynecology and obstetrics 
690 |a RG1-991 
690 |a Neoplasms. Tumors. Oncology. Including cancer and carcinogens 
690 |a RC254-282 
655 7 |a article  |2 local 
786 0 |n Gynecologic Oncology Reports, Vol 34, Iss , Pp 100671- (2020) 
787 0 |n http://www.sciencedirect.com/science/article/pii/S2352578920301375 
787 0 |n https://doaj.org/toc/2352-5789 
856 4 1 |u https://doaj.org/article/d47f0383948d44cfa6684e5bfebdf536  |z Connect to this object online.