The American Society of Clinical Oncology (ASCO) Annual Meeting 2024 is set to take place from May 31 to June 4 in Chicago, IL, bringing together leading oncologists and researchers from around the world to discuss the latest breakthroughs in cancer treatment and research. Among the highly anticipated sessions are those focusing on colorectal cancer management, cutting-edge cell therapies for solid tumors, and targeting traditionally “undruggable” cancer targets. Team LARVOL will be attending and looks forward to engaging with fellow oncology professionals. Here’s a preview of some key topics that will be highlighted at ASCO 2024.
The American Society of Clinical Oncology (ASCO) Annual Meeting 2024 is set to take place from May 31 to June 4 in Chicago, IL, bringing together leading oncologists and researchers from around the world to discuss the latest breakthroughs in cancer treatment and research. Among the highly anticipated sessions are those focusing on colorectal cancer management, cutting-edge cell therapies for solid tumors, and targeting traditionally “undruggable” cancer targets. Team LARVOL will be attending and looks forward to engaging with fellow oncology professionals. Here’s a preview of some key topics that will be highlighted at ASCO 2024.
One of the highly anticipated sessions, “State of the Art Management of Colorectal Cancer: Treatment Advances and Innovation,” will explore the role of circulating tumor DNA (ctDNA) in colorectal cancer (CRC). Dr. Priyadarshini Pathak from Massachusetts General Hospital will present on how ctDNA is becoming a crucial tool for personalizing adjuvant therapy in early-stage CRC. While ctDNA currently provides prognostic information, ongoing phase 3 trials like the SU2CACT-3 trial are investigating its potential role in guiding adjuvant therapy.This could lead to more precise treatment strategies, enabling escalation or de-escalation of treatment based on ctDNA levels.
Dr. Pathak will discuss how ctDNA testing can identify patients who might benefit from additional therapy post-surgery or those who could avoid unnecessary chemotherapy. She will also address the emotional impact on patients receiving prognostic information from ctDNA testing, emphasizing the importance of managing anxiety related to this information. Looking ahead, ctDNA might even be used for screening asymptomatic individuals for colon cancer, expanding its applications beyond its current scope.
Dr. Cheng Ean Cheefrom the National University Cancer Institute, Singapore, will highlight the significance of molecular characterization and tumor sidedness in metastaticCRC (mCRC). By categorizing CRC into subtypes based on molecular analysis, oncologists can better tailor treatments to individual patients. Dr. Chee will emphasize that understanding the molecular characteristics and primary tumor location (left or right side of the colon) can significantly impact treatment decisions and improve patient outcomes.
Dr. Dustin Deming from the University of Wisconsin will discuss emerging strategies for mCRC treatment, focusing on the evolving use of targeted therapies. He will highlight clinical trials that are investigating the benefits of using targeted therapies earlier in the treatment process. One notable trial is the phase 3BREAKWATER study, which evaluates the combination of the BRAF inhibitor encorafenib and the EGFR inhibitor cetuximab with or without chemotherapy forBRAFV600E mCRC. Additionally, Dr. Deming will explore the potential for retreatment with EGFR inhibitors, as resistance mechanisms may decay over time, allowing for reintroduction of these therapies.
The accelerated approval of lifileucel, a tumor-infiltrating lymphocyte (TIL) therapy, marks a significant milestone in the treatment of advanced melanoma and other solid tumors. Dr. Giao Q. Phan will discuss practical considerations and future enhancements for TIL therapy. Despite its current success, lifileucel’s objective response rate of 31.4% suggests a need for further advancements. Researchers are exploring gene modifications and neoantigen targeting to improve the efficacy of TIL therapy.
Dr. Alison Betof Warner from Stanford Cancer Center will explore next-generation cell-based therapies beyond TIL, including T-cell receptor (TCR) therapy. TCR therapy, which recognizes intracellular antigens, presents a promising alternative toCAR T-cell therapy. Dr. Warner will discuss the development of therapies targeting specific tumor-associated antigens, such as PRAME and NY-ESO-1, which have shown efficacy in clinical trials. Additionally, she will cover strategies to enhance TIL therapy, such as combining TILs with immune checkpoint inhibitors and identifying highly reactive TIL populations.
A joint ASCO/AACR session will focus on the challenges and successes in targeting “undruggable”cancer drivers, with a particular emphasis on KRAS-directed therapy. Dr. Kevan Shokat will share groundbreaking research on KRASG12C inhibitors and their evolution into highly selective drug candidates for various KRAS mutant tumors. This session will underscore the innovative approaches required to develop effective therapies against traditionally resistant cancer targets.
Dr. Susan Galbraith from AstraZeneca will present novel small molecule approaches and enabling technologies that address the druggability challenges of oncology targets. Her discussion will highlight recent advancements in computational chemistry, structural biology, and screening sciences that have facilitated the development of transformative cancer therapies.
Dr. Keith Flaherty from Massachusetts General Hospital will discuss the design and development of mutant-selective inhibitors targeting oncogenes. He will highlight the success of osimertinib, a mutant-selective EGFR inhibitor, and the potential of clinical proteomics to expedite drug discovery and development. Dr. Flaherty will also explore the benefits of utilizing clinical proteomics to identify new compounds, emphasizing its speed and ability to target previously challenging conditions.
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79% had reduction in disease. ORR 31%. Many responses deepen over time.
Toxicity profile was in line with prior TIL/Lifileucel data. No surprises here. Median # doses of IL-2 was 6.
Absolutely agree!… this should be available to our melanoma patients ASAP!… and paves the way for smarter cellular therapies to be designed, studied, and eventually widely disseminated
Just before I start AM clinic at @cityofhopeoc, excited to share results from #COBALT_RCC, a P1 trial of @CRISPRTX#CTX130 in #kidneycancer in the @sitcancer#PressProgram. Will present more on Thurs 5:37p at #SITC22! Thx @neerajaiims@DrBenTran@HaanenJohn#SamerSrour& co-Is! t.co/aDnhG9n92A
@montypal@cityofhopeoc@CRISPRTX@sitcancer@neerajaiims@DrBenTran@HaanenJohn@DrChoueiri@TiansterZhang@tompowles1@brian_rini@AlbigesL@Uromigos@ERPlimackMD@drenriquegrande@PGrivasMDPhD Congrats Monty! Looking forward to hearing about this exciting first-in the field study!
CAR-Ts are coming for #kidneycancer!! Congratulations @montypal and team; can’t wait to see results at #SITC22! t.co/9MrlF2yzBe
Congrats @montypal and team! Great to see CAR T therapy coming to #RCCt.co/ypRHBC89Pt
Another huge step from none other than @montypal!! CAR-Ts in #kidneycancer!Congratulations to the entire team!Looking forward to seeing the results at #SITC22! t.co/HvKeVBPyV7
@montypal you never stop to amaze me! You are brilliant & awesome! Looking forward to hearing more about this trial @sitcancer@OncoAlert@CityofHope_GU@COHMDCareers@neerajaiims@KidneyCancer@KidneyCancerDoc@NazliDizman@ZeynepZengin@LuisMezaco@crisbergerot@PauloBergerott.co/RNzOwxixQm