Business

June 12, 2009

Aurora Firms Up Its Leadership in Digital Pathology

PORTUGAL JOINS OTHER COUNTRIES AND CHOOSES mScope

MONTREAL, June 5, 2009 – Aurora MSC, the world leader in digital pathology communications, announced today the Hospital Espirito Santo of Évora Portugal has chosen to equip the hospital laboratories with mScope digital pathology clinical software. This is part of an ongoing plan to connect multiple pathology laboratories in the Iberian Peninsula, and the European Community in general, for consultation, continuing education and quality control.

The agreement was made possible through funding provided by the European Commission to assist European hospitals in achieving pathology interconnectivity. The objective is to allow access to state-of-the-art technologies to improve patients’ clinical outcome. This is one more step in a series of initiatives to increase the outreach of hospitals in Portugal and Spain.

Dr. Marcial Garcia Rojo of General Hospital of Spain’s Ciudad Real and chair of the European project Euro-Telepath, Anatomic Telepathology Network, commented "this action by Espirito Santo Hospital is one more step in the elaboration of a trans-Iberian network for pathology collaboration".

"We have chosen mScope Clinical suite to create an online diagnostic center of excellence to improve our quality control and diagnostic capabilities" stated Dr. Luis Gonçalves, Director of Anatomic Pathology of the Espirito Santo Hospital. The agreement covers two applications, one is for tumor panels where specialized pathologists from different centers in Portugal and Spain will regularly come together and look at digital slides using mScope. The other application will be for teleconsultation.

Mr. Pierre Le Fèvre, President and Chief Executive Officer of Aurora MSC stated that: "We are extremely happy to add Dr Gonçalves, a leading specialist in Anatomic Pathology who has been recognized by the European Cervical Cancer Association for his work, as a collaborator and user of digital pathology."

Mr. Le Fèvre pointed out that: "increasingly, a larger number of pathology laboratories throughout the world are using digital pathology to communicate faster and more effectively. These initiatives empower Specialists to work better and ultimately positively impact patient care".

About Aurora MSC

Aurora MSC’s mission is to facilitate and contribute to better patient outcomes. Its medical communications software enables physicians and members of the medical community to realize their full potential by eliminating the learning, diagnostic and collaborative restrictions imposed by time and space. The professionals at Aurora MSC develop and commercialize mScope, a universal web viewer and its collaborative tools to view all medical images anytime, anywhere. mScope is aimed at serving the medical practice (doctors and health professionals) and ultimately the patients. Its digital pathology software has three applications, mScope Education, mScope Clinical, and mScope Universal Viewer. A fourth application is currently in the development phase.

June 11, 2009

Aperio Files Patent Infringement Lawsuit Against Olympus America, Hamamatsu Corporation and Hamamatsu Photonics

VISTA, Calif. - (BUSINESS WIRE) - Aperio Technologies, Inc., (Aperio), a global leader in digital pathology for the healthcare and life sciences industry, announced today that it has filed suit for patent infringement against Olympus America, Inc., Hamamatsu Corporation and Hamamatsu Photonics KK (together, Hamamatsu). The lawsuit, filed in the United States District Court for the District of Delaware, alleges that Hamamatsu's NanoZoomer digital pathology system distributed by Olympus America infringes three United States patents issued to Aperio.

"Aperio has invested significant resources in research and development to create the most technologically advanced slide scanners and software systems available today," said Dirk Soenksen, CEO of Aperio. "Our ultra-fast line-scanning technology has contributed significantly to the creation and growth of the digital pathology market. Additionally, our innovative approaches to image acquisition and processing, including our patented prefocus technology, are poised to unlock a plethora of commercial opportunities. We have an obligation to our shareholders to protect our intellectual property. After years of repeated and unsuccessful attempts to engage Olympus America and Hamamatsu in discussions about our intellectual property, we are taking legal action to defend that property from further infringement."

Aperio's complaint accuses Olympus America and Hamamatsu of infringing three Aperio patents relating to digital pathology. The three patents asserted in the lawsuit are: United States Patent No. 6,917,696 entitled "Fully Automatic Rapid Microscope Slide Scanner," United States Patent No. 7,457,446 entitled "Fully Automatic Rapid Microscope Slide Scanner," and United States Patent No. 7,518,652 entitled "Method and Apparatus for Prefocus in a Linear Array Based Slide Scanner."

Since its inception in 1999, Aperio has built a formidable patent position to protect the valuable inventions resulting from its significant investment in research and development. Aperio's intellectual property portfolio now comprises more than 55 issued or pending patents covering slide scanning, data management, and image viewing and analysis.

Aperio has retained Quinn Emanuel Urquhart Oliver & Hedges, LLP, the premier business litigation firm in the United States, as counsel in this action.

June 03, 2009

Mayo Clinic Finds New Pathology Tests Double Sensitivity to Detect Bile Duct and Pancreatic Cancers

Pancreatic cancer and bile duct cancer are difficult to diagnose and often fatal because they are discovered in the advanced stages of the disease. Researchers have developed new tests that double the ability to detect bile duct and pancreatic cancers, according to a Mayo Clinic study published in the June issue of Gastroenterology.

    -- Additional audio and video resources, including excerpts from an interview with Dr. Lewis Roberts describing the research, are available on the Mayo Clinic News Blog, password: fish059.

Pancreatobiliary tumors such as bile duct cancer (cholangiocarcinoma) and pancreatic cancer often present as strictures, or a narrowing of the duct that can either be caused by benign inflammation or cancer. Physicians insert an endoscope down the throat and into the bile duct and pancreas region to examine possible tumors; however, the narrowness of the bile duct makes it difficult to distinguish benign and malignant strictures.

In this study, 498 patients with pancreatobiliary duct narrowing underwent an endoscopic procedure, and cell brushings were taken. Brushings were then analyzed by routine cytology, digital image analysis and fluorescence in situ hybridization (FISH) to determine the various tests' effectiveness and sensitivity in detecting and diagnosing cancer. While traditional cytology analysis relies on identifying abnormally shaped cells, the FISH test detects malignant cells using colored probes visible with a fluorescence microscope. Since cancer cells have an abnormal amount of DNA, by FISH these cells show extra copies of the probes compared to normal cells. The Mayo research team found that the combination of cytology and FISH raised the detection rate of bile duct and pancreatic cancer from 20 percent to 43 percent. "Bile duct and pancreatic cancers are very difficult to diagnose," says Lewis Roberts, M.B.Ch.B., Ph.D., Mayo Clinic gastroenterologist and the study's senior author.

"We were very pleased to see that the combination of FISH and cytology significantly improved our chances of diagnosing patients reliably. The earlier we can diagnose a patient, the better the types of treatment we can offer and the more likely they are to have long-term survival after treatment."

Treatments for bile duct cancer vary with the size of the tumor and how far it has advanced. These tumors usually grow slowly and spread gradually. In many cases, bile duct cancers are diagnosed at later stages. Current treatments include surgery, liver transplantation, chemotherapy, radiation therapy, photodynamic therapyand biliary drainage with plastic or metal stents. If the cancer cannot be completely removed by surgery but has not spread outside the liver, chemotherapy and radiation followed by liver transplantation may be an option. Mayo Clinic is one of the few medical facilities that offers a liver transplant protocol for early-stage bile duct cancer patients.

Bile duct cancer is rare and is most common in people aged 50 to 70. Approximately 5,000 cases of bile duct cancer are diagnosed in the United States each year, and the incidence of bile duct cancer is on the rise. Between 35,000 and 40,000 cases of pancreatic cancer are diagnosed per year in the United States.

Dr. K. Halling and Mayo Clinic have a financial interest in technology used in this research. Dr. Halling and Mayo Clinic have received annual royalties greater than the federal threshold for significant financial interest from the licensing to Abbott Molecular of other technology related to this research.

Mayo Clinic's Division of Gastroenterology and Hepatology has been ranked #1 in the U.S. News & World Report Honor Roll of Top Hospitals since the rankings began 19 years ago.

Other members of the Mayo research team included Emily Barr Fritcher; Benjamin Kipp, Ph.D.; Kevin Halling, M.D., Ph.D.; Trynda Oberg; Sandra Bryant; Robert Tarrell; Gregory Gores, M.D.; Michael Levy, M.D.; Amy Clayton, M.D.; and Thomas Sebo, M.D., Ph.D.

June 02, 2009

Olympus America Inc. Continues to Broaden its Virtual Microscopy Patent Portfolio

CENTER VALLEY, Pa., June 2, 2009 - Olympus America Inc. (“Olympus”) announced today that The United States Patent and Trademark Office has issued Patent No. 7,542,596, “Method & Apparatus for Internet, Intranet and Local Viewing of Virtual Microscope Slides.”  This patent further broadens the scope of the Olympus portfolio in the field of virtual microscopy. 
 
The patent claims methods for the transmission of virtual microscope image data and allows for the quick and efficient viewing of these large image files over the Internet or an intranet. The patent also relates to methods for multiple users to simultaneously view and discuss images over the Internet or an intranet.   
 
Olympus currently holds over 40 issued patents and published patent applications worldwide in the field of virtual microscopy. This patent portfolio broadly covers many of the fundamental aspects for the creation, storage, transmission, and remote viewing of virtual microscope slide images.  Olympus strives to continually research and develop new and innovative technologies to further advance this important and rapidly growing market. 


About Olympus Scientific Equipment Group
Olympus America Scientific Equipment Group provides innovative microscope imaging solutions for researchers, doctors, clinicians and educators. Olympus microscope systems offer unsurpassed optics, superior construction and system versatility to meet the ever-changing needs of microscopists, paving the way for future advances in life science.
About Olympus


Olympus is a precision technology leader, creating innovative opto-digital solutions in healthcare, life science and consumer electronics products. 

Olympus works collaboratively with its customers and its affiliates worldwide to leverage R&D investment in precision technology and manufacturing processes across diverse business lines. These include:

  • Gastrointestinal endoscopes, accessories, and minimally invasive surgical products;
  • Advanced clinical and research microscopes;
  • Lab automation systems, chemistry-immuno and blood bank analyzers and reagents;
  • Digital cameras and voice recorders.
Olympus serves healthcare and commercial laboratory markets with integrated product solutions and financial, educational and consulting services that help customers to efficiently, reliably and more easily achieve exceptional results. Olympus develops breakthrough technologies with revolutionary product design and functionality for the consumer and professional photography markets, and also is the leader in gastrointestinal endoscopy and clinical and educational microscopes. For more information, visit www.olympusamerica.com.

May 29, 2009

Bruker and Carl Zeiss Announce Collaboration to Advance Molecular Histology

Integration of MIRAX Virtual Slide Scanner from Carl Zeiss into Bruker’s MALDI Molecular Imager™ Enables Non-Targeted Molecular Histology -- Combined Solution to be Introduced at German Pathology Society (DGP) Meeting in June 2009

BREMEN, Germany & JENA, Germany--(BUSINESS WIRE)--Bruker Daltonik GmbH and Carl Zeiss MicroImaging GmbH today announced the integration of the MIRAX Virtual Slide Scanner from Carl Zeiss into Bruker’s MALDI Molecular Imager. The goal of the Bruker–Carl Zeiss collaboration is to advance molecular histology research by providing an integrated solution (for research use only) for biological tissue research and pathology that adds non-targeted molecular information and ‘molecular contrast’ to histology.

The MALDI Molecular Imager is a molecular imaging system based on matrix-assisted laser desorption ionization (MALDI) time-of-flight (TOF) mass spectrometry directly from tissue sections. It allows histology researchers to measure spatially resolved peptide, protein and lipid profiles in tissue sections. MALDI imaging is a non-targeted, broadly applicable molecular imaging approach without the need for any antibody or nucleotide probe. Tissue-type specific molecular signatures (e.g. from tumors) can be generated and used for biomarker discovery and molecular histology.

A major bottleneck in the interpretation of MALDI imaging data in pathology research has been the interpretation of results in a histological context. Until now, this has required repeated switching between evaluated MALDI molecular images and microscope views. The integration of Carl Zeiss’ MIRAX Slide Scanner results into the MALDI Molecular Imager solution allows the direct overlay of the full microscopic image with the full molecular and spectral information in one convenient visualization software tool, enabling true untargeted molecular histology.

Dr. Sören-Oliver Deininger, MALDI Imaging Product Specialist at Bruker Daltonics, explained: “Bruker has been the market and commercial technology leader in MALDI imaging for several years. Proprietary technologies such as the smartbeam™ laser for best spectra quality at highest speed and best spatial resolution, as well as the Bruker ImagePrep™ for easy and reproducible sample preparation, have turned MALDI imaging into a mainstream research application. Now, the full integration of the MIRAX virtual slides allows tissue and pathology researchers for the first time to evaluate their results directly in the histological context with the full spatial resolution of optical microscopy and the molecular information from MALDI imaging.

“This integrated molecular histology solution will significantly accelerate clinical pathology research, particularly in oncology, where the untargeted molecular information is expected to reveal additional subtle changes in tissue that cannot be distinguished by traditional histology methods today.”

“The integration of the MIRAX Virtual Slide Scanner into the MALDI Molecular Imager solution is a very good example of how the combination of two innovative technologies can create new benefits for biomedical research. With two technology leaders working together, we believe that we have a strong foundation for a novel, breakthrough histology solution. We look forward to working closely together with Bruker,” said Dr. Richard Ankerhold, business unit manager from Carl Zeiss.

Dr. Axel Walch, a pathologist at the Helmholtz Centre in Munich, and a user of both the MALDI Molecular Imager and the MIRAX slide scanner, commented: “The protein expression observed in MALDI Imaging data cannot be fully understood without the underlying histological information: the correlation of the MALDI image with a micrometer-resolution microscopic image is therefore mandatory for MALDI Imaging in clinical research. The Zeiss Mirax Scanner has the true advantage of online scalable high lateral resolution that can zoom in quickly to any tissue sections investigated by MALDI. Merging both techniques, Bruker MALDI Imaging and MIRAX virtual microscopy, leads to synergistic effects with outstanding benefits for clinical research. It truly completes the superior Bruker product line for imaging comprising of sample preparation, high performance MALDI mass spectrometry and highly sophisticated software for data interpretation.”

For further product information, please visit www.bdal.com/molecular-histology.

ABOUT BRUKER DALTONICS: For more information about Bruker Daltonics and Bruker Corporation (NASDAQ: BRKR), please visit www.bdal.com or www.bruker.com.

Photos/Multimedia Gallery Available: http://tinyurl.com/n82766

Source: Bruker Daltonik (press release)

May 13, 2009

CMS rejects Medicare coverage for virtual colonoscopy

In the past I have blogged about virtual colonoscopy and concern over how in the future this may diminish the number of colon biopsies done to be reviewed.  Others have argued this might actually increase the number of colonoscopies performed and subsequent biopsies, citing a number of reasons, including more people getting at least virtual colonoscopy when age appropriate rather than putting off the more invasive procedure or not getting one at all.  Yesterday CMS rejected the latest proposal to pay for this sevice claiming it wasn't ready for "prime time", as the radiology community has felt. 

So, for the time being it looks like this is not an immediate threat to GI pathologists (if you believe as I do), although I can see the arguments for reimbursement and how this technology may cost costs and save lives. Gastroenterologists are safe from the CT scan as well for now.

As the digital pathology community advances the technology, garners FDA clearances for clinical use and promotes reimbursement for these services, I wonder how CMS will address the issue. 

CPT codes are in place for image assisted IHC interpretation, providing a driver to use the technology with appropriate validation perhaps but will scanned archives, image-linked or enhanced reports, image repositories for data mining or content based image retrieval or enterprise wide PACS image uploads be"compensated".  I think there will be some opportunities to have these services paid for to pathologists and laboratories but will require a tremendous amount of validation of the technologies and will not likely occur for many years to come, particularly if virtual colonoscopy is any indicator.


By Eric Barnes
AuntMinnie.com staff writer
May 12, 2009

The U.S. Centers for Medicare and Medicaid Services (CMS) today rejected a proposal to pay for virtual colonoscopy (also known as CT colonography or CTC) for routine colon cancer screening of Medicare patients in the U.S., saying that VC, while promising for detecting colorectal polyps and cancer, is "not yet ready for widespread screening use."

"The evidence is inadequate to conclude that CT colonography is an appropriate colorectal cancer screening test under §1861(pp)(1) of the Social Security Act. CT colonography for colorectal cancer screening remains noncovered," the May 12 memo states.

The decision comes as a blow to advocates of CTC, who held out hope that the agency would reverse its proposed February 11 decision to deny reimbursement for screening CTC based on the body of evidence presented to it since the analysis of CTC as a screening tool began last year.

Advocates for virtual colonoscopy were quick to criticize the decision.

"The news is obviously disappointing, but not unexpected, given the inseparable politics and purse strings involved," said Dr. Perry Pickhardt, associate professor of radiology at the University of Wisconsin in Madison. "In the end, CTC will ultimately prevail as a highly effective screening test -- it's simply too good to hold down for much longer."

Dr. James Thrall, chair of the American College of Radiology Board of Chancellors, was even more emphatic.

“Make no mistake: If it stands, this CMS decision not to pay for CT colonography will cost lives. More than 140,000 Americans are diagnosed with colorectal cancer each year. Nearly 50,000 of them die due to late detection. How can CMS ignore the fact that people are dying because they do not want to have the tests that are currently covered?” Thrall said in a statement to the American College of Radiology.

“For CMS to turn its back to a technology that can attract more patients to be screened and save countless lives is deeply concerning," he continued. "CMS should reverse this determination immediately, or Congress should step in and vote to mandate coverage of CTC."

"The decision is understandable in these tough economic times," said Dr. Judy Yee, professor and vice chair of radiology and biomedical imaging at the University of California, San Francisco. "The decision is unacceptable when considering the large body of scientific evidence clearly documenting that CTC has been proven to be as effective as colonoscopy for the detection of clinically significant polyps in adults."

While CMS states that the evidence is insufficient to conclude that CTC improves health outcomes, "the same can be stated for other colorectal cancer screening tests that are currently covered by CMS," Yee told AuntMinnie.com in an e-mail. "We know that colorectal cancer is preventable. We know that a very large percentage of the American public remains unscreened for colorectal cancer. A positive decision from CMS could have helped to change this."

Dr. Abraham Dachman, professor and chair of radiology at the University of Chicago, told AuntMinnie.com that VC utilization is inseparable from efforts to cut healthcare costs.

"CTC experts strongly believe that current data support use of screening CTC in the Medicare aged population as do a large bipartisan group of members of Congress who signed a letter urging CMS to approve coverage of CTC for screening," Dachman wrote in an e-mail. "Even as the nation discusses ways to reign in the cost of healthcare, CTC screening makes sense. Use of CTC for colorectal cancer screening is consistent with President Obama's push for prevention and use of new technology to benefit patients. The public and the medical community at large should work to get this decision reversed."

Radiologists should work to publish data focused on individuals ages 65 and older, he said, and third-party payors should encourage CTC use as radiologists continue to attend courses to ensure that CTC providers continue to offer high-quality services.

"The public and the medical community at large should work to get this decision reversed," Dachman wrote. ... I am confident that CTC will eventually achieve full reimbursement status."

Urgency of screening

Colorectal cancer is the third most commonly diagnosed cancer and the second most common cause of cancer deaths in the U.S. The U.S. Centers for Disease Control and Prevention (CDC) estimates that as many as 60% of deaths caused by colorectal cancer could be prevented if all Americans older than 50 years of age underwent regular screening.

The issue is particularly critical for older patients. Of the approximately 75 million Americans older than 50 who are eligible for colorectal cancer screening, fewer than 50% present for screening due to myriad factors that include, for some, a fear of invasive examination with a colonoscope, which virtual colonoscopy avoids.

Yet patient surveys also suggest that it is the purgative bowel preparation, generally required for virtual colonoscopy and always needed for conventional optical colonoscopy, that patients most dislike about colorectal cancer screening.

Some adults eligible for screening refuse to be examined with optical colonoscopy or cannot undergo the procedure due to contraindications. Virtual colonoscopy advocates believe that Medicare access to VC would improve screening compliance and reduce the death toll from colorectal cancer. Because 90% of colon cancers are diagnosed in people older than 50, they note, colorectal cancer screening is critical for Medicare recipients, who are denied the noninvasive screening option as a result of today's decision.

Private insurance more promising

Although national Medicare coverage may be off the table for now, VC has fared better among private payors. Twenty-six states already mandate that patients with private healthcare coverage are ensured access to virtual colonoscopy. Many regions also cover virtual colonoscopy exams under Medicare local coverage decisions.

Based on early results of the multicenter ACRIN 6664 trial that found equivalent sensitivities for virtual and optical colonoscopy exams, the American Cancer Society (ACS) added CTC to its five-year colon screening guidelines in March 2008.

Other ACS-approved screening exams include optical colonoscopy (every 10 years), flexible sigmoidoscopy (every five years), double contrast barium enema (every five years), annual guaiac fecal occult blood testing (gFOBT), annual fecal immunochemical testing (FIT), and stool DNA testing.

Of these, only virtual colonoscopy remains ineligible for Medicare reimbursement following today's decision. In addition to many physicians and public health advocates, Medicare coverage for CTC is supported by the American College of Radiology, the American Gastroenterological Association, and the U.S. Multisociety Task Force on Colorectal Cancer.

Detractors argue that the evidence remains insufficient to recommend VC screening as a cost-effective alternative to colonoscopy.

In March, the U.S. House of Representatives passed Congressional Resolution 60, calling for increased support for colorectal cancer screening for Americans ages 50 and older. Forty-two representatives also signed a letter to CMS expressing their concerns with CMS' proposed denial of coverage for routine screening with CTC.

The lobbying group CTC Coalition, which includes the Colon Cancer Alliance, the American College of Radiology, and the Medical Imaging and Technology Alliance, argued that Medicare coverage for VC screening would break down barriers to screening for the populations most at risk of the disease.

Observers of all persuasions have complained that a protracted tug-of-war between radiology and gastroenterology interests is more about who will make a living from colorectal cancer screening than the adequacy of CTC. For now, at least, the gastroenterology interests appear to have the upper hand.

Related Reading

Pressure builds on CMS to pay for VC, April 2, 2009

CMS rejects case for virtual colonoscopy reimbursement, February 12, 2009

MedCAC panel members question VC's effectiveness, November 25, 2008

CMS announces VC evidence meeting, September 26, 2008

April 30, 2009

Genetix announces further expansion into digital pathology market through acquisition of SlidePath

Earlier today Genetix announced acquisition of SlidePath - see abbreviated press release below (underline mine).

I think this is positive for the digital pathology market in several ways.  First, it brings the Genetix Group increasingly into the clinical space with their cell imaging and analysis technologies having largely been based with pharma and research in the past.  Secondly, I think this acquisition helps to show increasing validation for digital pathology and the digital pathology marketplace.  I also like the fact that European-based companies have an increasing footprint along with US and Japanese-based companies that offer digital pathology technologies for clinical use.

Genetix announces further expansion into digital pathology market through acquisition of SlidePath

Genetix Group plc (“Genetix”) (AIM: GTX), the cell imaging and analysis group, today announces that it has signed a definitive agreement to acquire all of the issued share capital of SlidePath Limited (“SlidePath”), further strengthening its position in the fast growing digital pathology market.

The acquisition is in line with Genetix’ strategy to accelerate and strengthen its presence in the growing digital pathology market and is a natural progression following on from the 2006 acquisition of Applied Imaging. SlidePath’s competencies in cell imaging analysis software are aligned to Genetix’ core skills in imaging and image analysis which enables Genetix to build a stronger platform to offer a broader mix of products for the digital pathology market.  SlidePath’s expertise in web enabled viewing, information management and computer aided image analysis solutions will enhance Genetix’ product offerings through added functionality in its current markets of drug discovery and diagnostics and by leveraging Genetix’ sales and customer support infrastructure worldwide and deep customer relationships with diagnostics and pharmaceutical companies to expand the reach for new markets and new customers for SlidePath products.

SlidePath was founded in 2004 by Dr Donal O’Shea and Dr Sean Costello. The company has 25 employees and more than 60 customers in 10 countries, including the UK, US, Ireland, Germany, France and Australia.

 

Over the two years ended 31 December 2008 SlidePath has grown its reported revenues at a compound annual growth rate of 61%.  SlidePath has a strong product offering allowing the analysis, management and web enabled image viewing of tissue and cellular samples for the growing digital pathology market. Digital pathology is the computer enabled management and interpretation of pathology information generated from slides. The market has multiple applications, ranging from clinical laboratories, clinical trials, drug discovery and academia. Digital slides overcome problems associated with glass sides including damage and deterioration and allow samples to be viewed, archived and re-examined remotely.

The founders of SlidePath, the Chief Executive Officer, Dr Donal O’Shea, and Head of Customer Relations, Dr Sean Costello will remain with and continue to lead the business.

Commenting on the acquisition, Charles de Rohan, Chief Executive of Genetix said, “This transaction brings together two companies with highly complementary core skills that will greatly strengthen our competitive position in the growing digital pathology market. Combining Genetix’ global infrastructure with SlidePath’s leading-edge products and technologies will allow us to offer compelling new products and enhance our existing product ranges. We are impressed by the skill and expertise of SlidePath’s employees and believe that this investment will further solidify Genetix’ position in this exciting growth market as well as enhancing shareholder value.”

                         

Dr Donal O’Shea, Chief Executive of SlidePath said, “We are excited to be joining forces with Genetix, a company which has an excellent track record in product innovation and has built a high quality customer base and global infrastructure. The combined company will have many synergistic opportunities, a stronger market position and capital structure to be able to execute on its strategic growth initiatives. We believe this is an excellent fit”

                         

About Genetix Group plc

Headquartered in New Milton, UK, with offices in the UK, US, Germany and Japan, and quoted on the AIM (GTX: AIM), Genetix provides scientists and clinicians with unrivalled solutions for imaging and intelligent image analysis in the life science and diagnostic markets.

In life sciences, the company’s systems set industry standards for accurate selection of microbial colonies, and for screening and selection of mammalian secretory cell lines. Other systems evaluate the response of cells to potential therapeutic agents and quantify tissue biomarkers.

In diagnostics, Genetix holds a leading position in genetic testing with thousands of the company’s platforms used in laboratories worldwide.

Through its expertise in robotics, cell and molecular biology, image analysis and interpretation, supported by a strong IP portfolio, Genetix is committed to the continual development of innovative solutions.

 

April 28, 2009

Another innovation from Aperio - Press release

Global Digital Pathology Leader Further Expands Its Patents Portfolio Enabling New Forms of Image Query

Vista, CA – April 28, 2009 – Aperio Technologies, Inc., (Aperio), a global leader in digital pathology for the healthcare and life sciences industry, announced today that the United States Patent and Trademark Office has issued the company patent No. 7,502,519, covering systems and methods for image pattern recognition using vector quantization (VQ). This is Aperio’s second patent on the use of VQ for pattern recognition applications.

As pathology labs, hospitals, biopharma companies and educational institutions increasingly adopt digital pathology, they generate vast libraries of digital slides that play a critical role in disease management, medical research, and education. These libraries have historically been indexed for access with text-based labels such as tissue type, patient age, or primary diagnosis.

Now, Aperio’s VQ technology enables content-based image retrieval (CBIR) to allow pathologists and researchers to search libraries of digital slides using image data, and to efficiently retrieve similar images from a large image archive. The ability to search image archives using image regions of interest in addition to text-based searches represents a significant advancement in image query.

“Vector quantization is a breakthrough technology providing a novel way to perform content-based image retrieval,” said Dirk Soenksen, CEO of Aperio. “The image pattern recognition technology covered by this patent is unique in that it does not rely on prior knowledge of image-based features, but involves statistical comparisons to imagery data that exhibit characteristics of interest.”

In addition to providing an efficient way to search large libraries of digital slides for image regions that match a given image, vector quantization also allows searching for exceptions, such as regions of an image which are different from previously characterized images.

March 31, 2009

Executive War College to hold Digital Pathology Symposium

From Dark Daily:

Pathologists Soon to say Sayonara to Glass Slides!

March 26, 2009

Digital Pathology Imaging: Coming Soon to a Pathology Group near You!

Will pathologists soon say "sayonara" to glass slides? Plenty of smart money already bets the answer to that question is "yes"! Every pathologist in the United States and abroad should be watching developments in whole slide imaging and digital pathology systems. That's because digital pathology imaging is a trend with momentum-and it also has the potential to be disruptive, although probably not in the short term.

One powerful sign that digital imaging in pathology is ready to go mainstream is the take-up of digital imaging solutions and digital pathology systems by leading pathology laboratories in the United States and developed countries across the globe. These are academic and tertiary center pathology labs, along with major private pathology companies. As the pathology profession's first-movers and early adopters, it is these laboratories which set the pace for the entire profession. Their acceptance and growing use of digital imaging and digital pathology systems can be taken as evidence that the current generation of imaging and informatics technologies perform adequately.

However, there is another powerful force propelling digital imaging forward in anatomic pathology. It is the emergence of molecular assays which incorporate digital images and use either computer-aided diagnosis (CAD) or pattern recognition software to help the pathologist make a precise diagnosis. By design, these molecular tests require the pathologist to work from a digital image of the specimen. At The Dark Report's  second annual Molecular Summit on the Integration of In Vivo and In Vitro Diagnostics, conducted last February in Philadelphia, examples of these types of emerging assays were abundant.

Thus, the movement to adopt digital imaging and digital pathology systems is propelled forward by three discrete forces:

*One, acceptance and adoption of digital imaging and digital pathology by larger pathology laboratories, with the goal of assisting pathologists' work flow, improving pathologist productivity and quality, and having digital images available to share with other clinicians and to populate an electronic patient record.

*Two, as the foundation for emerging molecular assays and tests, where a digital image of the processed specimen is then assessed by computer-aided diagnosis or pattern recognition software that helps the pathologist make an accurate diagnosis.

*Three, the major vendors of anatomic pathology laboratory information systems (LIS) have already written interfaces that allow the leading digital imaging and digital pathology systems to integrate with their pathology LIS products. These pathology LIS vendors recognize that digital pathology images are now "prime time" for their larger pathology customers.

And don't forget! Last year, General Electric  and the University of Pittsburgh Medical Center  (UPMC) formed a joint venture. Each ponied up $20 million to create Omnyx, LLC, which is developing whole-slide imaging and a fully digital pathology system. At the press conference announcing the formation of Omnyx last spring, GE officials stated that they expect the market for whole slide imaging and digital pathology systems to be $2 billion.

These are important reasons why every pathology practice should be tracking the profession's uptake of digital imaging and digital pathology systems. It is no longer a question of whether or not a group should acquire digital imaging capability. Digital imaging technology is now robust-and some digital systems are affordable even for two- and three-pathologist groups! Rather, today's question is "when" a pathology group will make the investment in capital and time to acquire and use digital imaging and/or a fully digital pathology system.

That is why the upcoming Executive War College on Laboratory and Pathology Management  has organized a special, one-day workshop on Thursday, April 30, in New Orleans, titled: "Saying Sayonara to Glass Slides! Everything You Need to Know about Digital Imaging and Digital Pathology Systems." At one place and in one day, you'll hear case studies from pathology groups already using digital imaging and listen to one of the leading pathology LIS vendors discuss issues and opportunities when interfacing the pathology LIS with either or both digital imaging and digital pathology systems.

Best of all, we've assembled six of the leading companies in digital pathology to introduce you to their products and discuss how they help improve the productivity of pathologists and the precision of diagnoses. Expected to participate, in alphabetical order, are Aperio Technologies, Inc. ; BioImagene, Inc. ; DMetrix, Inc. ; Milestone Medical, Inc. ; SlidePath, Inc. ; and Applied Spectral Imaging, Inc.  (invited). There will also be a special two-hour exhibition where you can meet these vendors and explore the capabilities of their products and systems.

For every pathology group practice and laboratory, this "Saying Sayonara to Glass Slides" event is the perfect opportunity! At one time, gathered in one place, you can learn from users like you, hear from the pathology IT vendors, and see the products and people from all the major companies in this fast-moving field.

Is your group thinking about investing in digital imaging or a digital pathology system? Then this is your "must attend" opportunity! Kick the tires of the major vendors. Meet the important players in this field. Learn from pathology groups already using these solutions. Best of all, there is still time to take advantage of the early bird discount on registration. Use this registration and agenda link to guarantee your place at this vital event and benefit from the early-bird discount!

Related Information:

Convergence of In Vivo Imaging and Digitized Pathology Is Under Way
 

Recent article entitled "Digital Pathology is Growing Despite Fears"
 

Dark Report: Momentum Continues for Digital Pathology
 

Brand new! Just released is a full color program agenda PDF. (or paste this URL into your browser: http://www.executivewarcollege.com/PDFs/09brochure.pdf )

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THE DARK REPORT
21806 Briarcliff Dr.
Spicewood, TX 78669

It is the first time all these major players in digital imaging and digital pathology systems have assembled in one place at one time, specifically to discuss the advances in this field. It is your perfect opportunity to gather all the information you need to develop your pathology group's strategy.

March 12, 2009

Observations from USCAP 2009 - From A to Z

Attended the USCAP meeting in Boston over the weekend.  On Saturday attended the DICOM Working Group 26 (WG 26) meeting.  A copy of the document discussed is available here. This was my first DICOM WG 26 meeting (as an observer) and my sense is they are close to getting the document into a DICOM format within a year with some assistance in the actual writing of the document in DICOM format.  The committee has certainly made great strides.  Will provide updates as more information gets released following the meeting.

On Sunday gave a talk about digital pathology at an evening seminar hosted by BioImagene along with Jared Schwartz, MD, PhD, CAP President, Mahul Amin MD, Chairman of Pathology and Laboratory Medicine at Cedars Sinai & Ajit Singh PhD, CEO of BioImagene. 

Spoke briefly on use of pathology images in our hospital PACS, image analysis and what I am calling Pathology 2.0 - that is the use of Web 2.0 technology in the surgical pathology practice.  Blogging aside, gave several examples of using the tools of technology of Web 2.0 to harness collective intelligence in simple terms where anyone can participate, share, exchange and collaborate.

People have already moved on to Web 3.0 where anyone can innovate but that is for another post...

The meeting was well attended in record number this year with over 4,000 registrants.  I saw several excellent scientific sessions and posters with continued focus on molecular pathogenesis and less direct observation or correlation with immunohistochemistry. 

My sense of the attendance at the meeting with a large number of housestaff is a reflection of travel budgets.  I think budgets for meetings and conferences are being scaled back (including at my institution) and if given a meeting to attend, this is it. 

On the exhibit floor there were many notable products and services displayed among just over 100 vendors.  Here is a short review (in alpabetical order) of some of my observations:

Aperio showed me a demo of their SecondSlide sharing service for pathology and their application for referring and consulting pathologists to share whole slide images.

BioImagene released several new products including a family of scanners on the heels of a recent flurry of activity and press releases.  Their booth showcased several new applications including PathXchange, an online professional networking portal for pathologists worldwide.  This is another example of Web 2.0 and of course joined the community - look for my cases soon. I did not get a chance to see PathSearch, their product in collaboration with Visuvi for content based image retrieval (CBIR).

Clarient continues to bring to market innovative products and services in cancer diagnostics.

DMetrix did not exhibit at the meeting.  You can still check out their comments on other vendors over at their blog, Virchow's Pixel (great name - why didn't I think of that?)

Quest Diagnostics showcased their virtual IHC service, InScape (video link).

Lastly, SlidePath demonstrated their products for use in the clinical space, including their Digital Slide Server which is compliant with Aperio Scanscope, Hamamatsu Nanozoomer and Zeiss Mirax digital slides.

Clearly digital pathology vendors have increased their footprint at this meeting with the largest showing to date and I expect this to continue for some time at other similar clinically-oriented pathology meetings. 

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