New adjuvant therapy for pancreatic cancer comes out

Share This Post

In a recent interview, Dr. Afsaneh Barzi, assistant professor of clinical medicine at the University of Southern California Norris Comprehensive Cancer Center, told you about existing and emerging new adjuvant therapies for patients with non-metastatic pancreatic cancer.

Gemcitabine is given to patients with pancreatic cancer as a standard practice to assess response. However, Barzi said that the patient’s response to gemcitabine was very poor and that many patients were unable to undergo surgery. The LAPACT trial investigated the combination therapy of gemcitabine and nab-paclitaxel (Abraxane). Tests show that 36% of pancreatic cancer patients respond to treatment, and about 15% of pancreatic cancer patients can receive surgical treatment.

In addition, a meta-analysis of the FOLFIRINOX study of patients with locally advanced pancreatic cancer showed that approximately 28% of pancreatic cancer patients were able to undergo surgery. Barzi explained that as chemotherapy becomes more effective, the likelihood of resection increases. Therefore, the patient’s resection should be evaluated accordingly. Barzi concluded that although most patients may still not be eligible for surgery, it is still worth evaluating patients to find patients who can undergo surgery after neoadjuvant therapy.

https://www.onclive.com/conference-coverage/soss-gi-usc-2018/dr-barzi-on-available-and-emerging-neoadjuvant-approaches-in-pancreatic-cancer

Subscribe To Our Newsletter

Get updates and never miss a blog from Cancerfax

More To Explore

Targeting FGFR4 and CD276 with CAR T-cells demonstrates a strong antitumor impact against children rhabdomyosarcoma
CAR T-Cell therapy

Targeting FGFR4 and CD276 with CAR T-cells demonstrates a strong antitumor impact against children rhabdomyosarcoma

Chimeric antigen receptor (CAR) T-cells that specifically target Fibroblast Growth Factor Receptor 4 (FGFR4), a surface tyrosine receptor that is extensively expressed in rhabdomyosarcoma (RMS), are now undergoing clinical research. However, the effectiveness of these CAR T-cells may be hindered by tumor heterogeneity and inadequate activation. In this study, we present a method to enhance the co-stimulatory and targeting characteristics of a FGFR4 CAR through an optimization process. We substituted the hinge and transmembrane domain of CD8 as well as the 4-1BB co-stimulatory domain with the corresponding domains of CD28. The CARs produced exhibit heightened anti-tumor efficacy in multiple RMS xenograft models, with the exception of the RMS559 cell line, which is known for its aggressive nature.

Need help? Our team is ready to assist you.

We wish a speedy recovery of your dear and near one.

Start chat
We Are Online! Chat With Us!
Scan the code
Hello,

Welcome to CancerFax !

CancerFax is a pioneering platform dedicated to connecting individuals facing advanced-stage cancer with groundbreaking cell therapies like CAR T-Cell therapy, Gene therapy, TIL therapy, and clinical trials worldwide.

Let us know what we can do for you.

1) CAR T-Cell therapy
2) Gene therapy
3) Gamma-Delta T Cell therapy
4) TIL therapy
5) NK Cell therapy