Alpha-blockers adverse events: Analysis of real-life data from Eudra-Vigilance

2021 ◽  
Vol 79 ◽  
pp. S49
Author(s):  
C. De Nunzio ◽  
A. Nacchia ◽  
R. Lombardo ◽  
A. Franco ◽  
G. Tema ◽  
...  
2021 ◽  
Vol 79 ◽  
pp. S21-S22
Author(s):  
C. De Nunzio ◽  
A. Nacchia ◽  
R. Lombardo ◽  
A. Franco ◽  
G. Tema ◽  
...  

2019 ◽  
Vol 12 (1) ◽  
pp. 100007 ◽  
Author(s):  
Giorgio Walter Canonica ◽  
Giorgio Lorenzo Colombo ◽  
Giacomo Matteo Bruno ◽  
Sergio Di Matteo ◽  
Chiara Martinotti ◽  
...  

2021 ◽  
Vol 32 ◽  
pp. S19
Author(s):  
A. Franco ◽  
C. De Nunzio ◽  
A. Nacchia ◽  
R. Lombardo ◽  
G. Tema ◽  
...  

2021 ◽  
Vol 39 (15_suppl) ◽  
pp. 5560-5560
Author(s):  
Bente Vilming ◽  
Jørgen Fallås-Dahl ◽  
Anne-Gry Bentzen ◽  
Vibeke Anett Ingebrigtsen ◽  
Elisabeth Berge Nilsen ◽  
...  

5560 Background: PARP (poly adenosine diphosphate [ADP]–ribose polymerase) inhibitors are the new standard for maintenance treatment in platinum sensitive recurrent ovarian cancer (PSROC), independent of germline (g-BRCA) or somatic BRCA mutation status. Real-life data after the introduction of new anti-neoplastic agents are needed to evaluate whether the benefit observed in phase III trials can be translated into clinical practice. The aim of this study was to provide real-life data on efficacy and safety of niraparib in non-gBRCA PSROC. Methods: This retrospective multi-center cohort study included patients with PSROC who were enrolled in a national individual patient access program in Norway. Efficacy and safety data were collected from the patients´ electronic medical records. The primary outcome was time from start of niraparib treatment to first subsequent treatment (TFST). Secondary endpoints included prevalence of dose interruption and -reduction, as well as adverse events. Results: The study included 106 patients with median age of 64 years (range 38-81). After median follow up of 15.3 months (95% CI 12.1-18.5), 71 patients (67%) had progressed, 64 (60%) had started a new line of treatment, and 25 (24%) had died. 25 (24%) patients were still receiving niraparib. Median duration of niraparib treatment was 7.6 months (0.4 to 27.3 months). Median TFST was 11.7 months (95% CI 9.2 -14.2). Patients with elevated CA125 after chemotherapy prior to start of niraparib had shorter progression-free survival (PFS) compared to patients with complete serological response (6.5 months (95% CI 5.7 – 7.3) vs 12 months (95% CI 6.2 – 17.9, (p < 0.001)). Grade 3-4 hematologic and non-hematologic events occurred in 25% and 17% of the patients, respectively. The most common grade 3/4 hematologic events were anemia (15%), thrombocytopenia (11%) and neutropenia (8%). Adverse events led to dose interruption in 38% and dose reduction in 44% of the patients. Patients with individualized dosing based on baseline weight and platelet counts had fewer dose reductions (p < 0.001) and -interruptions (p = 0.042) than patients whose dose was not adjusted to those baseline values. Conclusions: In a real-life setting, niraparib maintenance treatment in patients with non-gBRCA PSROC showed efficacy comparable with the published phase III data and an acceptable safety profile. Individualized dosing at start of treatment minimized adverse events. The prolonged PFS in patients with CA125 normalization after last chemotherapy, suggests that these patients in particular benefit from maintenance treatment but warrants confirmation in a larger sample.[Table: see text]


2021 ◽  
Vol 73 (3) ◽  
Author(s):  
Giorgia TEMA ◽  
Riccardo LOMBARDO ◽  
Olivia VOGLINO ◽  
Angela SICA ◽  
Valeria BALDASSARRI ◽  
...  

2021 ◽  
Vol 79 ◽  
pp. S47-S48
Author(s):  
C. De Nunzio ◽  
A. Nacchia ◽  
R. Lombardo ◽  
A. Franco ◽  
G. Tema ◽  
...  

Cancers ◽  
2021 ◽  
Vol 13 (19) ◽  
pp. 4928
Author(s):  
Jean-Matthieu L’Orphelin ◽  
Emilie Varey ◽  
Amir Khammari ◽  
Brigitte Dreno ◽  
Anne Dompmartin

Background: For several decades, PD-1 has been a target in malignant melanoma (MM). PD-1 inhibitors (nivolumab, pembrolizumab) and anti-CTLA-4 (CD152) (ipilimumab) have revolutionized cancer therapy. PD-1 and CTLA-4 inhibition leads to prolonged lymphocyte effects, which explains the cytotoxicity underlying immune-reaction-based adverse events (irAEs). Most irAEs occur in the first cycle of treatment at a median of 40 days. IrAEs of any grade have been observed in 68.2% of patients, with 10% of patients experiencing severe grade III/IV irAEs. Data on late-onset irAEs are lacking. Methods: Data on patients with advanced melanoma (N = 1862) from March 2016 to March 2021 were obtained from the RicMel database, a French national multicentric biobank dedicated to the follow-up of MM patients. Patients who received anti-PD-1 therapy or a combination therapy and experienced grade III-IV irAEs were selected and analyzed at 7 months, one year and two years after treatment was initiated. Results: Superficial spreading melanoma (SSM) and previous oncological drug administration before immunotherapy are significant risk factors for late-onset irAEs over 2 years after beginning immunotherapy in the univariate and multivariate analysis. The other parameters—sex, mutational status, association of immunotherapy (PD-1i and CTLA-4i) and overall response—were not significantly associated with late-onset irAEs. In our real-life data study, the median onset time of grade III-IV irAES was 128 days after the initiation of immune checkpoint inhibitors (ICI) therapy. Conclusions: Our study, using real-life data, suggests that patients with SSM and those who have received previous oncological treatments are more likely to experience late-onset grade III-IV irAES. Further multicentric studies with wider recruitment of patients should be performed to confirm our findings, potentially leading to changes in the recommended treatment for carefully monitored at-risk patients.


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