Friday, March 06, 2020

Johns Hopkins researchers make progress in the development of noninvasive urine test for prostate cancer

Researchers at the Johns Hopkins Kimmel Cancer Center have made significant progress toward development of a simple, noninvasive liquid biopsy test that detects prostate cancer from RNA and other specific metabolic chemicals in the urine.

A description of their findings appears in the Feb. 28 issue of the journal Scientific Reports.

The investigators emphasize that this is a proof-of-principle study for the urine test, and it must be validated in additional, larger studies before it is ready for clinical use.

The researchers used RNA deep-sequencing and mass spectrometry to identify a previously unknown profile of RNAs and dietary byproducts, known as metabolites, among 126 patients and healthy, normal people. The cohort included 64 patients with prostate cancer, 31 with benign prostatic hyperplasia and prostatitis diseases, and 31 healthy people with none of these conditions. RNA alone was not sufficient to positively identify the cancer, but addition of a group of disease-specific metabolites provided separation of cancer from other diseases and healthy people.


"A simple and noninvasive urine test for prostate cancer would be a significant step forward in diagnosis. Tissue biopsies are invasive and notoriously difficult because they often miss cancer cells, and existing tests, such as PSA (prostate-specific antigen) elevation, are not very helpful in identifying cancer," says Ranjan Perera, Ph.D., the study's senior author. Perera is also the director of the Center for RNA Biology at Johns Hopkins All Children's Hospital, a senior scientist at the Johns Hopkins All Children's Cancer & Blood Disorders Institute and the Johns Hopkins All Children's Institute for Fundamental Biomedical Research, and an associate professor of oncology at the Johns Hopkins University School of Medicine and Johns Hopkins Kimmel Cancer Center member.

We discovered cancer-specific changes in urinary RNAs and metabolites that -- if confirmed in a larger, separate group of patients -- will allow us to develop a urinary test for prostate cancer in the future."  Bongyong Lee, Ph.D., study's first author and a senior scientist at the Cancer & Blood Disorders Institute.


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Monday, February 10, 2020

Liquid biopsy independently associated with melanoma relapse, study shows

A study at The University of Texas MD Anderson Cancer Center showed that circulating tumor cells (CTCs), a form of liquid biopsy, was independently associated with melanoma relapse, suggesting CTC assessment may be useful in identifying patients at risk for relapse who could benefit from more aggressive therapy following primary treatment.

Results from the study were published in Clinical Cancer Research, a journal of the American Association for Cancer Research. Although CTCs can be detected in melanoma patients, there is limited data regarding their significance in stage III (node-positive) disease. This prospective study was based on earlier research that found CTCs in a significant number of breast cancer patients, which was associated with relapse, independent of other existing methods for determining prognosis.

Our findings are significant, given that there is a need for blood-based biomarkers to guide clinical decision making for stage III melanoma patients. There currently are no blood tests available to help doctors accurately tell which patients are likely to relapse, and should be given therapy, and which are low risk, and could be observed."     Anthony Lucci, M.D., professor of Breast Surgical Oncology and Surgical Oncology, and study lead.


The researchers assessed CTCs during the patient's first clinic visit, and relapse-free survival was compared between patients with one or more CTCs, versus those with no CTCs. CTCs were observed in 90 out of 243 patients enrolled in the study.

"Our analysis demonstrated that CTC detection was significantly associated with a decrease in relapse-free survival at six months, and persisted at a 54-month longer-term follow-up," said Lucci. "The data from this study provides support for the future pursuit of liquid biopsy techniques to help identify patients most likely to benefit from adjuvant systemic therapy."

Lucci added that this is vital given that there currently is no clear consensus on when to recommend immunotherapy for node-positive melanoma patients. Despite the development of new targeted and immune therapies to treat melanoma, many patients either do not respond to these therapies or develop resistance to therapy within six to eight months. Because such therapies also can have side effects, avoiding treatment in patients at low risk for relapse may prevent overtreatment.


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Saturday, July 13, 2019

CellMax Life partners with CORE Diagnostics to introduce cancer screening tests

Aimed at reducing cancer mortality in India through better cancer risk assessment and screening, Indias leading clinical laboratory CORE Diagnostics has joined hands with Silicon Valley-based CellMax Life to introduce a genetic cancer risk test and ctDNA-based liquid biopsy throughout the country.

CellMax-DNA Genetic Cancer Risk Test is a simple saliva DNA test to identify hereditary cancer risk. The test examines 98 genes across 25 hereditary cancers — currently the broadest gene panel on the market, while priced to be affordable to the largest possible number of families, the company said.

CellMax-LBx Liquid Biopsy is a non-invasive ctDNA blood test to improve cancer treatment management, monitor treatment response, and screen for recurrence “ in real time.

This test analyses a comprehensive profile of 73 genes from circulating tumour DNA (ctDNA). Circulating tumour DNA are small DNA fragments shed by the tumour. Tumour genes may mutate over time, either as the cancer grows, or the treatment suppresses the cancer.

“CellMax Life has made tremendous advances in precision analysis of key oncology biomarkers for cancer risk assessment and screening. This enables CORE to make these compelling personalized cancer tests available across India, said its Founder.

CellMax Life is bringing early, non-invasive DNA cancer detection via affordable, accessible, accurate cancer saliva and blood tests, said Atul Sharan, President and CEO of CellMax Life in India.

The rate of survival of cancer victims remains dismal in India. According to estimates, less than 30 per cent of people diagnosed with cancer in India survive for more than five years after their diagnosis”an indication that cancer is not diagnosed until later stages, when it becomes difficult to treat them effectively.

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