-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
-
Cosmetic Ingredient
- Water Treatment Chemical
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
In January 2020, the U.
In January 2020, the U.
immunity
Eligible patients were assigned to the following neoadjuvant chemoimmunotherapy (NACI): original cohort 1 arm (durvalumab 1500 mg q3w + tremelimumab 75 mg q3w + paclitaxel 175 mg/㎡ + carboplatin AUC 5 [ 3 cycles]) or expansion cohort 2 (durvalumab 1500 mg q3w + tremelimumab 300 mg [1 dose] + original chemotherapy), with cohort 2 starting after completion of cohort 1
During treatment, immunological changes in the tumor microenvironment (TME) were explored by performing a series of biopsies
The results of the interim analysis, published last year, showed: A total of 23 patients were included in the study, with a median age of 60 years.
Published this time are 45 patients, as follows: group 1 (n=23) and group 2 (n=22)
After neoadjuvant immunotherapy combined with chemotherapy, immunohistochemical results showed that stromal tumor-infiltrating lymphocytes (P=0.
These data now highlight the clinical activity and manageable toxicity of durvalumab and tremelimumab added to neoadjuvant chemotherapy in advanced epithelial ovarian cancer
leave a message here