Meta-Analysis Showing DecisionDx-Melanoma Test as Independent, Significant Predictor of Recurrence and Metastatic Risk Presented during Late-Breaking Research Session at the 2019 AAD Annual Meeting

On March 4, 2019 Castle Biosciences, Inc., a skin cancer diagnostics company providing personalized genomic information to improve cancer management decisions, reported three presentations at the 2019 American Academy of Dermatology (AAD) Annual Meeting held in Washington, DC from March 1-5 (Press release, Castle Biosciences, MAR 4, 2019, View Source [SID1234533938]).

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A meta-analysis of four DecisionDx-Melanoma studies including 1,479 patients titled, "Meta-Analysis of the Prognostic 31-Gene Expression Profile Test in 1479 Melanoma Cases," was presented during the Late-Breaking Research: Basic Science/Cutaneous Oncology/Pathology session. The study demonstrates that the DecisionDx-Melanoma test is an independent, significant predictor of recurrence and metastatic risk in a meta-analysis of four study cohorts.

DecisionDx-Melanoma Meta-Analysis

Multiple published archival and prospective studies have described the prognostic capability, performance and clinical utility of the DecisionDx-Melanoma test to assess recurrence risk and inform patient management decisions on sentinel lymph node recommendations, follow up, surveillance imaging, and referrals for patients with cutaneous melanoma.

This meta-analysis was performed to evaluate the cumulative prognostic effect of the test across multiple cohorts with a focus on differences in recurrence and distant metastasis between patients with a Class 1A (lowest risk) and Class 2B (highest risk) test result. Three published studies and one newly reported cohort including a total of 1,479 non-overlapping patients with Stage I-III melanoma were included in the analysis.

Key Study Findings:

The meta-analysis demonstrates that the DecisionDx-Melanoma test accurately identifies cutaneous melanoma patients who are at greater risk of metastasis with an effect that is consistent across multiple studies reaching the highest Strength of Recommendation Taxonomy (SORT) level for a prognostic biomarker (Level 1A evidence).
The DecisionDx-Melanoma test was found to be a consistent, independent and significant predictor of recurrence and metastatic risk in a meta-analysis of four study cohorts.
The DecisionDx-Melanoma risk assessment is independent from other clinical factors (age, Breslow tumor thickness, ulceration and node status).
Patients with Class 2B tumors are 2.83 times more likely to experience a recurrence than patients with Class 1A tumors (p<0.0001). Likewise, patients with Class 2B tumors are 2.75 times more likely to experience a distant metastasis than patients with Class 1A tumors (p<0.0001).
Despite differences in populations and study design, heterogeneity among the four studies was not significant.
"This study is important because it demonstrates the strong and consistent effect of the DecisionDx-Melanoma test as a significant, independent predictor of recurrence and metastasis in patients with Stage I-III melanoma," said lead author Bradley Greenhaw, M.D., Dermatology Center of North Mississippi, Tupelo, Mississippi. "Across these four unique study cohorts, this meta-analysis shows that the highest level of evidence supports the use of the DecisionDx-Melanoma gene expression profile test to inform patient management decisions."

The SORT system is used by the AAD and other organizations to evaluate the quality, quantity and consistency of evidence supporting tests such as DecisionDx-Melanoma. The SORT scale evaluates both the quality of the evidence (Level 1, 2 or 3) and strength of the recommendation (A, B or C). Using SORT ranking, a systematic review or meta-analysis of good quality studies or a prospective study with good follow-up represents the highest level of evidence (Level 1), and recommendations based on consistent, good quality evidence are deemed strongest (Strength of Recommendation: A).

Additional Castle Biosciences Data

DecisionDx-Melanoma Value in Stage IB-IIA Melanoma

A second study titled, "Improved Risk Assessment through Incorporation of a Prognostic 31-gene Expression Profile Test for AJCC Stage IB-IIA Cutaneous Melanoma," (Abstract 10597), which highlights the test’s accuracy in patients with Stage IB-IIA melanoma was presented as a poster at the AAD 2019 Annual Meeting.

Risk assessment is critical for guiding patient care decisions and treatment of cutaneous melanoma, especially for patients with Stage IB-IIA cutaneous melanoma who are considered for sentinel lymph node biopsy and adjuvant clinical trials. This study of 214 patients with Stage IB-IIA cutaneous melanoma from a previously published multicenter cohort with long-term outcomes assessed the use of AJCC staging combined with results from the DecisionDx-Melanoma test to improve recurrence risk prediction.

Key Study Findings:

Using AJCC staging alone, patients with Stage IB melanoma have an estimated 5-year melanoma specific survival (MSS) rate of 97%. Among these patients, those with a Class 1A (lowest risk) DecisionDx-Melanoma test result had an MSS rate of 98.6%, a risk equivalent to AJCC Stage IA. However, patients in this group who had a Class 2B (highest risk) test result had an 87.5% 5-year MSS rate. These risk estimates are lower than AJCC Stage IIIA disease.
Patients with Stage IIA cutaneous melanoma had an estimated 5-year MSS rate of 94% using AJCC staging alone. Patients in that group who had a Class 1A DecisionDx-Melanoma test result had an MSS rate of >99% (equivalent to Stage IA). Patients with a Class 2B test result had a 5-year MSS rate of 85.7%, similar to risk estimates for AJCC Stage IIIB.
As a group, Stage IB-IIA patients with a Class 1A result had significantly higher MSS, DMFS and RFS rates of 98.8%, 92.0% and 87.4% than those for patients with a Class 2B result (86.7%, 69.4% and 52%; p<0.01).
"Accurate risk assessment is important for clinical decision-making, especially for patients with Stage IB and IIA cutaneous melanoma who may be candidates for sentinel lymph node biopsy and adjuvant therapy clinical trials," commented study co-author Darrell S. Rigel, M.D., M.S., Clinical Professor at New York University School of Medicine. "These results show that use of the DecisionDx-Melanoma test further stratified patients into lower and higher risk groups following AJCC staging, supporting its value in developing individualized patient management plans and potentially future adjuvant therapy trials."

Update on cSCC Test Development

An update on the development of a cutaneous squamous cell carcinoma (cSCC) test was also presented at the AAD 2019 meeting as a poster (with oral discussion) titled, "Microarray Analysis to Identify Genes Associated with a High-Risk of Metastasis in Cutaneous Squamous Cell Carcinoma Tumors," (Abstract 10630). Many patients with cSCC will have a favorable prognosis, but a substantial number of them will experience metastasis or develop recurrences and die from their disease. The goal of this development program is to identify and validate a test that improves upon existing staging systems by identifying patients who have a relatively high risk for recurrence and enable more informed clinical management decisions.

As part of a larger archival development study, microarray analysis was performed on 80 recurrent and non-recurrent cases to identify novel genes associated with disease outcomes. Predictive modeling was performed to select and prioritize genes based on preliminary accuracy metrics for recurrence prediction. A subset of selected genes demonstrated positive correlation between microarray and qPCR analysis, suggesting feasibility in a clinical assay. Gene expression from microarray-identified targets will now be analyzed together with targets previously identified from the literature in order to optimize a prognostic signature.

Collaborative site recruitment and clinical trial activities for the cSCC test development program are actively continuing.

About DecisionDx-Melanoma

DecisionDx-Melanoma is a gene expression profile test that uses an individual patient’s tumor biology to predict individual risk of cutaneous melanoma metastasis or recurrence, as well as sentinel lymph node positivity, independent of traditional staging factors and has been studied in over 2,900 patients. Using tissue from the primary melanoma, the test measures the expression of 31 genes. The test has been validated in three multicenter studies that have included 690 patients and have demonstrated consistent results. Performance has also been confirmed in five prospective studies including over 780 patients. The consistent high performance and accuracy demonstrated in these studies, which combined have included over 1,470 patients, provides confidence in disease management plans that incorporate DecisionDx-Melanoma test results.

Prediction of the likelihood of sentinel lymph node positivity has also been validated in two prospective multicenter studies that included over 1,400 patients. Impact on patient management plans for one of every two patients tested has been demonstrated in multicenter and single-center studies. More information about the test and disease can be found at www.SkinMelanoma.com.

About Cutaneous Squamous Cell Carcinoma

Cutaneous squamous cell carcinoma (cSCC), a non-melanoma skin cancer, is one of the most common cancers. Approximately 200,000 patients are diagnosed with cSCC with high-risk features. Most patients have a favorable prognosis, but a subset of patients will develop metastasis and up to 15,000 patients each year die from their disease. As current staging parameters have a low positive predictive value, many more patients are considered high risk than actually develop metastatic disease. Conversely, many patients that develop metastatic disease are misidentified as low risk. This leads to over and undertreatment of a substantial number of cSCC patients. To address this clinical need, Castle Biosciences is developing a gene expression profile test to improve upon current staging systems and identify patients with cSCC at high risk for metastasis or recurrence, enabling more informed clinical decisions regarding adjuvant therapy and other management options.

SpringWorks Therapeutics to Present at the Cowen and Company 39th Annual Health Care Conference

On March 4, 2019 SpringWorks Therapeutics, a clinical-stage biopharmaceutical company focused on developing life-changing medicines for patients with severe rare diseases and cancer, reported that Saqib Islam, Chief Executive Officer, will present at the Cowen and Company 39th Annual Health Care Conference in Boston on Tuesday, March 12, 2019, at 3:30 p.m. Eastern Standard Time (Press release, SpringWorks Therapeutics, MAR 4, 2019, View Source [SID1234533937]).

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Savara to Present at the 39th Annual Cowen and Company Healthcare Conference

On March 4, 2019 Savara Inc. (NASDAQ: SVRA), an orphan lung disease company, reported that the company’s Chief Executive Officer, Rob Neville, will present at the 39th Annual Cowen and Company Healthcare Conference on Monday, March 11, 2019 at 2:10 p.m. Eastern Time in Salon B of the Boston Marriott Copley Place in Boston (Press release, Savara, MAY 4, 2019, View Source [SID1234533936]).

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Interested parties can access a live audio webcast on the Investors page of the Savara website at www.savarapharma.com/investors/events/. Please connect to the company’s website at least 15 minutes prior to the start of the presentation to ensure sufficient time for any software download that may be required for the webcast. An archived presentation will be available on Savara’s website for 30 days.

CohBar to Announce 2018 Fourth Quarter Financial Results and Host Conference Call on March 18, 2019

On March 4, 2019 CohBar, Inc. (NASDAQ: CWBR), a clinical stage biotechnology company developing mitochondria based therapeutics (MBTs) to treat age-related diseases, reported that the company will release its fourth quarter 2018 financial results after the market closes on Monday, March 18, 2019 (Press release, CohBar, MAR 4, 2019, View Source [SID1234533935]). Management will host a conference call with a slide presentation at 5:00 p.m. ET (2:00 p.m. PT) on the same day to provide an update on the company’s business.

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Details for the Conference Call and Slide Presentation:

Date: March 18, 2019
Time: 5:00 p.m. ET (2:00 p.m. PT)

Conference Audio

Dial-in U.S. and Canada: (800) 289-0438
Dial-in International: (323) 794-2423
Conference ID No.: 8144256
Slide Presentation

Go to www.webex.com, click on the ‘Join’ button and enter meeting number 923 629 679 and Password CWBR, or
Go to www.cohbar.com and click on Q4 2018 Shareholder Presentation at top of homepage.
We kindly request that you please call into the conference audio and log into WebEx approximately 10 minutes prior to the start time so that we can begin promptly.

An audio replay of the call will be available beginning at 8:00 p.m. Eastern Time on March 18, 2019, through 11:59 p.m. Eastern Time on April 8, 2019. To access the recording please dial (844) 512-2921 in the U.S. and Canada, or (412) 317-6671 internationally, and reference Conference ID# 8144256. The audio replay along with the slide presentation will also be available on the homepage at www.cohbar.com from March 18, 2019 through April 8, 2019.

NantKwest Signs Worldwide License Agreement with ProMab Biotechnologies to Exclusively Develop Select Next Generation Targeted Natural Killer Cell Therapeutics

On March 4, 2019 NantKwest, Inc.(Nasdaq:NK), a leading clinical-stage Natural Killer (NK) cell based therapeutics company, and ProMab Biotechnologies reported the establishment of a worldwide license to a B-Cell Maturation Antigen (BCMA) targeted antibody sequence for multiple myeloma along with an option for up to five undisclosed targeting sequences for exclusive use in the development of chimeric antigen receptor (CAR) based NK cell therapies (Press release, NantKwest, MAR 4, 2019, https://ir.nantkwest.com/news-releases/news-release-details/nantkwest-signs-worldwide-license-agreement-promab?field_nir_news_date_value[min]=2019 [SID1234533934]).

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"We are pleased to announce this collaboration with ProMab Biotechnologies, marking another milestone for NantKwest in the development of targeted, next generation, NK cell therapeutics against multiple myeloma and other cancers," said Dr. Patrick Soon-Shiong, CEO of NantKwest. "With an estimated five-year survival rate of around 49% and accounting for 10% of all hematological malignancies, patients with multiple myeloma are in critical need for more effective treatment options. We believe, NantKwest’s CAR-based NK cell therapy may represent a much needed new treatment option for these patients. We eagerly anticipate growing our relationship with ProMab and accelerate the development of these new and innovative, next-generation off-the shelf, CAR-based NK cell therapies."

"ProMab’s strategic focus is on the development of monoclonal antibodies and their application in cell therapy through the integration of next generation sequencing, bioinformatics, high-throughput screening technologies, and novel in vitro in vivo validation tools. This new partnership allows NantKwest to leverage the breadth of our monoclonal antibody generation and validation platform, our human antibody library screening capabilities, together with NantKwest’s strong NK cell engineering, manufacturing, and clinical expertise," said John Wu, President and CEO of ProMab Biotechnologies. "We look forward to working together with the NantKwest team to more rapidly bring new NK cell therapeutics into the clinic."

Multiple Myeloma

Multiple myeloma is a debilitating blood cancer that while treatable is usually considered incurable, resulting in over 100,000 deaths annually on a worldwide basis. Representing a significant unmet medical need, without treatment, survival is typically less than one year. Even with treatment, which typically involves the use of chemotherapy, steroids, targeted therapy, and in some cases, stem cell transplant, survival often can only be extended to 4 to 5 years. The BCMA protein is important in B cell development and preferentially expressed in mature B lymphocytes. BCMA protein is also believed to be involved in the development of multiple myeloma and other blood cancers and is an important target for drug development.