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Roche launches new highly-sensitive test to more easily diagnose patients who may have B-cell lymphoma

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Roche has launched the VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail assay, the first clinically approved highly-sensitive in-situ hybridisation (ISH) test to diagnose B-cell lymphoma. This test helps distinguish B-cell cancers from normal immune responses, providing diagnostic certainty for healthcare providers. B-cell lymphoma accounts for about 85% of non-Hodgkin lymphoma (NHL) cases, the tenth most common cancer globally. This CE Mark-approved test can identify over 60 B-cell lymphoma subtypes and plasma cell neoplasms using a single tissue slide, reducing the need for fresh tissue samples and additional biopsies. The assay is part of Roche’s extensive hematopathology portfolio.

Positive
  • Launch of the first clinically approved highly-sensitive ISH test for B-cell lymphoma.
  • Ability to differentiate B-cell cancer from a normal immune response.
  • Can assess over 60 B-cell lymphoma subtypes and plasma cell neoplasms.
  • Reduces the need for additional patient biopsies.
  • Part of Roche's industry-leading hematopathology portfolio including over 65 biomarkers.
Negative
  • None.
  • The VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail assay is the first clinically approved in-situ hybridisation (ISH) test with the sensitivity to assess the full spectrum of B-cell lymphoma subtypes.1,2
  • The test helps differentiate a B-cell cancer from a normal, reactive immune response, providing diagnostic certainty for healthcare providers and their patients.
  • B-cell lymphoma accounts for approximately 85 percent of non-Hodgkin lymphoma (NHL) cases, which is the tenth most common cancer worldwide.3

Basel, 20 June 2024 - Roche (SIX: RO, ROG; OTCQX: RHHBY) announced today the launch of the first clinically approved, highly-sensitive in-situ hybridisation (ISH) test, the VENTANA® Kappa and Lambda Dual ISH mRNA Probe Cocktail assay, in countries accepting the CE Mark. The test is designed to help pathologists differentiate a B-cell malignancy from a normal, reactive response to an infection.4

B-cell lymphoma is a type of cancer that typically develops in the lymphatic system. It accounts for approximately 85 percent of non-Hodgkin lymphoma (NHL) cases. NHL is the tenth most common cancer worldwide and each year more than 250,000 people die from this disease.3 In the early stages of NHL, patients may experience symptoms like swelling of the lymph nodes, fever, fatigue, loss of appetite or a red rash.

“It’s important to be able to provide patients with a definitive diagnosis as symptoms of lymphoma can appear similar to the body’s normal reactive response to an infection,” said Matt Sause, CEO of Roche Diagnostics. “This highly sensitive assay offers diagnostic certainty for patients with suspected B-cell lymphoma.”

With increased sensitivity, the new test enables assessment across the more than 60 B-cell lymphoma subtypes and plasma cell neoplasms on a single tissue slide. The test can assess small biopsies and formalin-fixed tissue, reducing the need for a fresh tissue sample, which may not be available especially if lymphoma was not originally suspected. These test properties preserve tissue, may result in fewer additional patient biopsies and make interpretation quicker and easier for the pathologist, helping create a faster diagnosis and access to treatment for patients.

This first-of-its-kind assay is a significant addition to Roche’s industry-leading hematopathology portfolio, which includes more than 65 biomarkers.

About the VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail
VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail is intended for the qualitative detection of Kappa mRNA and Lambda mRNA in formalin-fixed, paraffin-embedded (FFPE) human bone marrow and lymphoid tissue stained on a BenchMark IHC/ISH instrument using chromogenic in-situ hybridisation (ISH) and visualised using light microscopy. VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail is intended as an aid in the identification of B-cell lymphomas and plasma cell neoplasms. The results of the assay should be interpreted by a qualified pathologist in conjunction with histological examination, relevant clinical information, and proper controls. This product is intended for in vitro diagnostic (IVD) use.4

About Roche
Founded in 1896 in Basel, Switzerland, as one of the first industrial manufacturers of branded medicines, Roche has grown into the world’s largest biotechnology company and the global leader in in-vitro diagnostics. The company pursues scientific excellence to discover and develop medicines and diagnostics for improving and saving the lives of people around the world. We are a pioneer in personalised healthcare and want to further transform how healthcare is delivered to have an even greater impact. To provide the best care for each person we partner with many stakeholders and combine our strengths in Diagnostics and Pharma with data insights from the clinical practice.

In recognising our endeavour to pursue a long-term perspective in all we do, Roche has been named one of the most sustainable companies in the pharmaceuticals industry by the Dow Jones Sustainability Indices for the fifteenth consecutive year. This distinction also reflects our efforts to improve access to healthcare together with local partners in every country we work.

Genentech, in the United States, is a wholly owned member of the Roche Group. Roche is the majority shareholder in Chugai Pharmaceutical, Japan.

For more information, please visit www.roche.com.

All trademarks used or mentioned in this release are protected by law.

References
[1] Rimsza LM, et al. Kappa and lambda light chain mRNA in situ hybridization compared to flow cytometry and immunohistochemistry in B cell lymphomas. Diagn Pathol. 2014;9:144.
[2] F. Hoffmann-La Roche Ltd. Conjoint Market Research. [Survey; Cited 2024 April 4]. Data on File.
[3] Global Cancer Observatory. Non-Hodgkin Lymphoma Fact Sheet [Internet; Cited 11 April 2024]. Available from: https://gco.iarc.who.int/media/globocan/factsheets/cancers/34-non-hodgkin-lymphoma-fact-sheet.pdf
[4] F. Hoffmann-La Roche Ltd. VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail. [Method Sheet; cited 2024 April 16]. Data on file.
 

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FAQ

What is the VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail assay?

It is the first clinically approved highly-sensitive in-situ hybridisation (ISH) test for diagnosing B-cell lymphoma.

When was the VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail assay launched?

It was launched on 20 June 2024.

What is the significance of the VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail assay?

The test helps differentiate B-cell cancers from normal immune responses, reducing the need for additional biopsies and providing diagnostic certainty.

What percentage of non-Hodgkin lymphoma cases does B-cell lymphoma account for?

B-cell lymphoma accounts for approximately 85% of non-Hodgkin lymphoma (NHL) cases.

What are the benefits of the VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail assay?

The test can assess over 60 B-cell lymphoma subtypes and plasma cell neoplasms, preserving tissue and reducing the need for additional biopsies.

Where is the VENTANA Kappa and Lambda Dual ISH mRNA Probe Cocktail assay approved?

It is approved in countries accepting the CE Mark.

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