ArcticZymes attending MEDICA in Düsseldorf from 15-18 November

On November 11, 2021 ArcticZymes Technologies reported that participating at the 2021 MEDICA congress in Düsseldorf, Germany from 15-18 November (Press release, Biotec Pharmacon, NOV 11, 2021, View Source [SID1234595259]). Please come and visit us at our stand in Hall 3/ J09 for a discussion around how we can support your company

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Study Shows Guardant360® Liquid Biopsy Test Helps Guide Treatment for Patients with HER2-Driven Metastatic Colorectal Cancer

On November 11, 2021 Guardant Health, Inc. (Nasdaq: GH), a leading precision oncology company, reported that a study published in Nature Medicine reinforces the benefits of using the Guardant360 liquid biopsy test to help guide treatment decisions for patients with HER2-driven metastatic colorectal cancer (mCRC) (Press release, Guardant Health, NOV 11, 2021, View Source [SID1234595292]). Led by the National Cancer Center Hospital East (NCCHE) in Japan, the study demonstrates that the Guardant360 test can select patients for HER2-directed therapy, identify which patients are responding to treatment, as well as identify genetic alterations that predict resistance.

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The Phase 2 TRastuzumab combIned with pertuzUMab for Patients with Her2-positive mCRC (TRIUMPH) study evaluated the efficacy of targeted therapy pertuzumab plus trastuzumab in patients with mCRC harboring HER2 amplification as detected by analysis of circulating tumor DNA (ctDNA) or tissue genotyping. All patients were previously treated with monoclonal antibodies targeting EGFR. Additional exploratory analyses were conducted to evaluate the utility of ctDNA genotyping to predict treatment efficacy, monitor response, and identify the resistance mechanisms.

The study, which follows on last year’s SCRUM-Japan GOZILA study, found that while efficacy of HER2-directed treatment was similar in patients with HER2 amplification detected in tissue or in ctDNA, the ctDNA analysis provided an added benefit of identifying additional alterations that predicted which patients would benefit from HER2-directed therapy. In addition, decreases in ctDNA shortly after treatment initiation corresponded with radiographic response and resistance-related alterations were identified by ctDNA genotyping after disease progression.

"This study demonstrates the clinical utility of the Guardant360 test in helping guide treatment decisions for patients with metastatic colorectal cancer," said Dr. Yoshiaki Nakamura, NCCHE, principal investigator of the TRIUMPH study. "Based on our results, we believe that ctDNA genotyping is beneficial in clinical practice to identify patients who are most likely to benefit from treatment with pertuzumab plus trastuzumab."

"Our Guardant360 blood test consistently demonstrates that it is a critical test in not only determining actionable biomarkers, but helping to guide treatment decisions," said Helmy Eltoukhy, Guardant Health Co-CEO. "This study reinforces the breadth and applicability of our Guardant360 test to help inform clinical decisions for patients with advanced cancer across their treatment journey."

The Guardant360 liquid biopsy test is part of the market leading Guardant360 portfolio that offers oncologists end-to-end testing solutions from treatment selection to treatment response monitoring. The portfolio includes the Guardant360 CDx test, the first FDA-approved liquid biopsy for comprehensive tumor mutation profiling across all solid tumor cancers, and Guardant360 TissueNext to provide oncologists with another option for comprehensive genomic profiling. Also included is Guardant360 Response, the first blood-only liquid biopsy that enables oncologists to view molecular response, or changes in ctDNA levels, from a simple blood draw to get an early indication of whether a patient is responding to treatment. This tool assists oncologists when considering whether to continue, stop, or explore other treatment options for their patients with late-stage or metastatic cancer.

Since it was first introduced, the Guardant360 blood test has become widely accepted for blood-based comprehensive genomic profiling (CGP) with more than 250 peer-reviewed publications including over 60 clinical outcomes studies. It has been trusted by more than 9,000 oncologists with more than 150,000 tests performed to date.

Lunit Presents Studies at SITC 2021, Highlighting the Effectiveness of AI in Predicting Response to Immunotherapy in a Clinical Trial Setting

On November 11, 2021 Lunit reported that it will present three abstracts at the upcoming Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper)’s (SITC) (Free SITC Whitepaper) 36th Annual Meeting being held in Washington D.C. and virtually November 10-14, 2021 (Press release, Lunit, NOV 11, 2021, View Source [SID1234595310]). The abstracts feature the predictive power of the company’s AI biomarker platform ‘Lunit SCOPE IO’, which is also on demonstration during the event in its booth #423, Exhibition Hall E.

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As a leading medical AI provider, Lunit focuses on developing the AI biomarker platform Lunit SCOPE IO, which analyzes cancer patients’ tissue slide images and predicts response to immunotherapy. According to the company, Lunit SCOPE IO analyzes a patient’s cancer tissue slide image by observing the distribution of tumor-infiltrating lymphocytes (TIL), one of the representative immune cells, and accurately classifying the result into three immune phenotypes (3-IP; inflamed, excluded, desert).

Lunit’s AI biomarker platform, Lunit SCOPE IO

In the main study presented at SITC (Free SITC Whitepaper) 2021, Lunit SCOPE IO was applied in a phase I/II clinical trial of a TGF-β inhibitor, MedPacto’s vactosertib, in combination with pembrolizumab to treat metastatic colorectal cancer patients. This clinical trial is significant because the novel treatment regimen targets a subpopulation of colorectal cancer patients known to have a very low overall response rate. The regular lack of response to immune checkpoint inhibitors such as pembrolizumab is expected to be overcome via combination with the TGF-β inhibitor vactosertib, changing the biology of the cancer to be responsive to the combination.

According to the study, among the group of patients categorized as high "immune-excluded" by Lunit SCOPE IO, 25% responded to treatment, compared to no response among the group of patients categorized as low "immune-excluded" by Lunit SCOPE IO.

"These results demonstrate that the AI-powered analysis of the immune cells surrounding the cancer is highly predictive of response to immunotherapy, and adds significant evidence to the usefulness of applying this technology in clinical practice to identify the right target patient population," explained Chan-Young Ock, Chief Medical Officer of Lunit.

"This study is also significant because the usefulness of Lunit SCOPE has been successfully demonstrated for combination immunotherapy, in addition to its usefulness for predicting response to monotherapy of immune checkpoint inhibitors, as previously demonstrated in ASCO (Free ASCO Whitepaper) 2019, 2020, 2021 and ESMO (Free ESMO Whitepaper) 2021," added Ock.

In the other two studies, the molecular mechanisms that are associated with Lunit SCOPE IO’s prediction of response to immunotherapy have been demonstrated. According to the studies, the "immune excluded" subpopulation categorized by Lunit SCOPE IO is linked to the APOBEC signature and subclonal tumor heterogeneity, as well as oncogenic PI3K/Akt/mTOR pathway, adding biological plausibility to why Lunit SCOPE IO is highly predictive of response to immunotherapy.

"Over the years we have been validating the predictive power of our AI biomarker through multiple studies and we are excited to present meaningful results at SITC (Free SITC Whitepaper) showing its further potential," said Brandon Suh, CEO of Lunit. "With the official launch of Lunit SCOPE IO for research use approaching within a few months, we hope our AI will contribute to offering optimized treatment to solid tumor cancer patients."

Lunit at SITC (Free SITC Whitepaper) 2021

Exhibition booth: #423, Exhibition Hall E (floor plan)

Poster Title: Spatial analysis of tumor-infiltrating lymphocytes correlates with the response of metastatic colorectal cancer patients treated with vactosertibin combination with pembrolizumab
Abstract number: 823
Session Date/Time: Nov. 12, 7:00 a.m. – 8:30 p.m. ET (on-site) and Nov. 12, 7:00 a.m. ET (ePoster)

Poster Title: Artificial intelligence powered spatial analysis of tumor infiltrating lymphocytes reveals Immune excluded phenotype related to APOBEC signature and clonal evolution of cancer
Abstract number: 830
Session Date/Time: Nov. 13, 7:00 a.m. – 8:30 p.m. ET (on-site) and Nov. 12, 7:00 a.m. ET (ePoster)

Poster Title: Comparison of PI3K/AKT/mTOR Pathway Profiles Amongst Three Immune Phenotypes Classified by Artificial Intelligence-Powered H&E Analyzer in Non-Small Cell Lung Cancer
Abstract number: 921
Session Date/Time: Nov. 12, 7:00 a.m. – 8:30 p.m. ET (on-site) and Nov. 12, 7:00 a.m. ET (ePoster)

CytomX Therapeutics to Present at Upcoming November Investor Conferences

On November 11, 2021 CytomX Therapeutics, Inc. (Nasdaq: CTMX), a leader in the field of conditionally activated therapeutics, reported that Sean McCarthy, D.Phil., president, chief executive officer, and chairman, will participate in virtual fireside chats at the following investor conferences in November (Press release, CytomX Therapeutics, NOV 11, 2021, View Source [SID1234595242]).

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12th Annual Jefferies Global Healthcare Conference
Date: Thursday, November 18, 2021

33rd Annual Piper Sandler Virtual Healthcare Conference
Date: Tuesday, November 30, 2021

The Jefferies fireside chat will be made available at 3:00 a.m. ET (8:00 a.m. GMT) on Thursday, November 18, 2021 on the Events and Presentations page of CytomX’s website at www.cytomx.com. The Piper Sandler fireside chat will be made available at 10:00 a.m. ET on Monday, November 22, 2021. Archived replays of both fireside chats will be available on the CytomX website for 30 days following the event. In addition, management will be available for one-on-one meetings with investors who are registered to attend the conferences.

Heron Therapeutics to Present at Upcoming Investor Conferences

On November 11, 2021 Heron Therapeutics, Inc. (Nasdaq: HRTX), a commercial-stage biotechnology company focused on improving the lives of patients by developing best-in-class treatments to address some of the most important unmet patient needs, reported that Heron management will present and host one-on-one meetings at the following investor conferences (Press release, Heron Therapeutics, NOV 11, 2021, View Source [SID1234595260]).

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Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

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Jefferies London Healthcare Conference: November 18-19, 2021

Fireside chat will be available on-demand for attendees during the virtual portion of the meeting beginning on Thursday, November 18, 2021.
A webcast of the fireside chat will be available on the Company’s website at www.herontx.com in the Investor Resources section.
4th Annual Evercore ISI HealthCONx Conference: November 30 – December 2, 2021

Fireside chat on Wednesday, December 1, 2021 at 2:40 pm ET.
A live webcast of the fireside chat will be available on the Company’s website at www.herontx.com in the Investor Resources section.