The role of surgery in platinum-resistant ovarian cancer: A call to the scientific community

Author(s):  
Marco Petrillo ◽  
Giulio Sozzi ◽  
Margherita Dessole ◽  
Giampiero Capobianco ◽  
Salvatore Dessole ◽  
...  
2021 ◽  
Vol 22 (24) ◽  
pp. 13650
Author(s):  
Carolina Maria Sassu ◽  
Innocenza Palaia ◽  
Serena Maria Boccia ◽  
Giuseppe Caruso ◽  
Giorgia Perniola ◽  
...  

Ovarian cancer (OC) is the second most common cause of death in women with gynecological cancer. Considering the poor prognosis, particularly in the case of platinum-resistant (PtR) disease, a huge effort was made to define new biomarkers able to help physicians in approaching and treating these challenging patients. Currently, most data can be obtained from tumor biopsy samples, but this is not always available and implies a surgical procedure. On the other hand, circulating biomarkers are detected with non-invasive methods, although this might require expensive techniques. Given the fervent hope in their value, here we focused on the most studied circulating biomarkers that could play a role in PtR OC.


2019 ◽  
Vol 23 (6) ◽  
pp. 4005-4018 ◽  
Author(s):  
Jiang Yang ◽  
Hui Xing ◽  
Danhua Lu ◽  
Jun Wang ◽  
Bingshu Li ◽  
...  

Biomedicines ◽  
2021 ◽  
Vol 9 (1) ◽  
pp. 55
Author(s):  
Francesco Plotti ◽  
Corrado Terranova ◽  
Federica Guzzo ◽  
Carlo De Cicco Nardone ◽  
Daniela Luvero ◽  
...  

Even though 80% of patients with High-Grade Serous Ovarian Cancer respond to standard first-line chemotherapy, a majority of them could relapse in the following five years due to a resistance to platinum. Human Epididymis protein 4 (HE4) is one of the most promising markers in predicting platinum therapy response. This pilot study aims to evaluate the potential role of HE4 value in predicting chemotherapy response in BRCA mutated patients and in BRCA wild-type (non-mutated) ones. We selected 69 patients, affected by High-Grade Serous Ovarian Cancer, and optimally debulked and submitted to standard chemotherapy protocols. HE4 was dosed during every chemotherapy course. Patients were classified as platinum-resistant and platinum-sensitive. According to BRCA mutation test, patients were further divided into BRCA wild-type (53 patients), and BRCA mutated (16 patients). 35 patients out of 69 (52%) were platinum-sensitive (recurrence > 12 months), while 33 patients (48%) were platinum-resistant (recurrence < 12 months). Thus, in the total population, HE4 performed as a marker of chemosensitivity with a sensibility of 79% and a specificity of 97%. In the BRCA WT group, 23 patients out of 53 (43%) were platinum-sensitive, while 30 patients out of 53 (57%) were platinum-resistant. In the BRCA WT group, HE4 performed as a predictive marker of chemosensitivity with a sensibility of 80% and a specificity of 100%. In the BRCA mutated group, 13 patients out of 16 (82%) were platinum-sensitive, while 3 patients (18%) were platinum-resistant. In the BRCA mutated group, HE4 performed as a predictive marker of chemosensitivity in all patients. The ability to detect platinum-resistant patients before tumor relapse probably could open new therapeutic scenarios.


Cancer ◽  
2006 ◽  
Vol 107 (3) ◽  
pp. 536-543 ◽  
Author(s):  
Rodney P. Rocconi ◽  
Ashley S. Case ◽  
J. Michael Straughn ◽  
Jacob M. Estes ◽  
Edward E. Partridge

2011 ◽  
Vol 29 (15_suppl) ◽  
pp. 5047-5047 ◽  
Author(s):  
A. A. Garcia ◽  
I. B. Vergote ◽  
J. P. Micha ◽  
C. H. Pippitt ◽  
G. G. Rao ◽  
...  

2019 ◽  
Vol 49 (8) ◽  
pp. 789-792 ◽  
Author(s):  
Jung-Yun Lee ◽  
Ju Yeon Yi ◽  
Hyun-Soo Kim ◽  
June Lim ◽  
Sunghoon Kim ◽  
...  

Abstract A pilot study of biomarker-driven targeted therapy in patients with platinum-resistant recurrent ovarian cancer has been started in Korea. Archival tumor samples were tested for HRD and PD-L1 status. Treatment arms will be allocated according to the test results. For HRD+ patients, we tested the synergistic effects of olaparib and other agents; treatment arms will randomly be allocated. (Arm 1: olaparib and cediranib; Arm 2: olaparib and durvalumab). For HRD- patients, we tested the role of biomarker-driven immunotherapy according to PD-L1 expression (Arm 3: durvalumab and chemotherapy in patients with high PD-L1 expression; Arm 4: durvalumab, tremelimumab, and chemotherapy in patients with low PD-L1 expression). Sixty-eight patients will be included from three Korean institutions within 1 year. The primary endpoint is the response rate according to RECIST 1.1 (6 months after treatment initiation). This trial has been registered with clinicaltrials.gov, and the registration number is NCT03699449.


2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Hong Zhao ◽  
Rong Li ◽  
Xiaoyan Wang ◽  
Xin Lu ◽  
Min Hu ◽  
...  

This article has been retracted. Please see the Retraction Notice for more detail: https://doi.org/10.1186/s13048-021-00785-1.


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