Current Treatment Options in Oncology
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1534-6277, 1527-2729

2021 ◽  
Vol 22 (12) ◽  
Author(s):  
Aurora Leibold ◽  
Katyayani Papatla ◽  
Kristen P. Zeligs ◽  
Stephanie V. Blank
Keyword(s):  

2021 ◽  
Vol 22 (12) ◽  
Author(s):  
Amy A. Case ◽  
Justin Kullgren ◽  
Sidra Anwar ◽  
Sandra Pedraza ◽  
Mellar P. Davis
Keyword(s):  

2021 ◽  
Vol 22 (12) ◽  
Author(s):  
Olivia Craig ◽  
Carolina Salazar ◽  
Kylie L. Gorringe

2021 ◽  
Vol 22 (12) ◽  
Author(s):  
Joseph B. Meleca MD ◽  
Emily Zhang MD ◽  
Michael A. Fritz MD ◽  
Peter J Ciolek MD
Keyword(s):  

2021 ◽  
Vol 22 (12) ◽  
Author(s):  
Javier Ros ◽  
Iosune Baraibar ◽  
Giulia Martini ◽  
Francesc Salvà ◽  
Nadia Saoudi ◽  
...  

2021 ◽  
Vol 22 (12) ◽  
Author(s):  
Alessia Pellerino ◽  
Francesco Bruno ◽  
Roberta Rudà ◽  
Riccardo Soffietti

2021 ◽  
Vol 22 (12) ◽  
Author(s):  
Daniel A. Cehic ◽  
Aaron L. Sverdlov ◽  
Bogda Koczwara ◽  
Jon Emery ◽  
Doan T. M. Ngo ◽  
...  
Keyword(s):  

2021 ◽  
Vol 22 (11) ◽  
Author(s):  
Thomas J. Ettrich ◽  
Thomas Seufferlein

Opinion statementPancreatic cancer is mainly diagnosed at an advanced, often metastatic stage and still has a poor prognosis. Over the last decades, chemotherapy of metastatic pancreatic cancer (mPDAC) has proven to be superior to a mere supportive treatment with respect to both survival and quality of life. Recently, even sequential treatment of mPDAC could be established. Options for first-line treatment are combination chemotherapy regimens such as FOLFIRINOX and gemcitabine plus nab-paclitaxel when the performance status of the patient is good. For patients with poorer performance status, gemcitabine single-agent treatment is a valid option. Recently, the PARP inhibitor olaparib has been demonstrated to improve progression-free survival when used as a maintenance treatment in the subgroup of patients with mPDAC and a BRCA1/-2 germ line mutation having received at least 16 weeks of platinum-based chemotherapy. This group of patients also benefits from platinum-based chemotherapy combinations. Therefore, the BRCA1/-2 stats should be examined early in patients with mPDAC even when the occurrence of these mutations is only about 5% in the general Caucasian population. After the failure of first-line treatment, patients should be offered a second-line treatment if their ECOG permits further treatment. Here, the combination of 5-FU/FA plus nanoliposomal irinotecan has shown to be superior to 5-FU/FA alone with respect to overall survival. Immune checkpoint inhibitors like PD1/PD-L1 mAbs are particularly efficacious in tumors with high microsatellite instability (MSI-h). Limited data in mPDACs shows that only a part of the already small subgroup of MSI-H mPDACs (frequency about 1%) appears to benefit substantially from a checkpoint inhibitor treatment. The identification of further subgroups, e.g., tumors with DNA damage repair deficiency, gene fusions, as well as novel approaches such as tumor-organoid-informed treatment decisions, may further improve therapeutic efficacy.


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