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Showing posts with label clinical trials. Show all posts
Showing posts with label clinical trials. Show all posts

Wednesday, April 11, 2012

Faults seen in cancer study funding | Reuters



Faults seen in cancer study funding | Reuters

NEW YORK | Wed Apr 11, 2012 11:08am EDT
 
(Reuters Health) - It's well-known that clinical trials of cancer treatments often can't cover their costs. But a new study suggests that government-funded trials could take at least one cue from those backed by drug companies.

In 2010, the Institute of Medicine (IOM) released a report saying that the U.S. system for conducting cancer clinical trials was approaching a "state of crisis" (see Reuters story of April 10, 2010).
The IOM -- an expert panel with federal support -- said the National Cancer Institute's Clinical Trials Cooperative Group program was inefficient, bogged down by red tape and underfunded.

The NCI program includes a number of collaborative groups -- academic cancer centers, researchers and community doctors that work together to conduct trials on cancer treatment. Altogether, the program involves more than 3,100 institutions in the U.S., Canada and Europe.

In the new study, researchers at one Canadian cancer center focused specifically on the timing of cancer clinical trial funding.
With cooperative group trials, funding typically comes as a "modest payment up front" for each patient enrolled, explained lead researcher Dr. Hsien-Yeang Seow of McMaster University and the Juravinski Cancer Center in Hamilton, Ontario.

Trials done by the drug industry, on the other hand, dole out money over time, as patients hit certain "milestones" -- like during treatment, and as they come back for follow-up visits after treatment ends.


Seow's team looked at 97 clinical trials done at its center in recent years. Two-thirds of those studies were cooperative group trials, including some with NCI funding, while the rest were industry-sponsored.
Those included early- and late-stage trials of treatments for cancers including breast, lung and stomach cancer.


The researchers found that the cooperative group trials quickly began to lose money after the initial stages because the funds were all spent early on. That leaves nothing for study patients' follow-up, which can last for years.

The industry trials, in contrast, had more money going in than out at multiple time points -- though any net income typically disappeared during longer term follow-up.

What's more, Seow's team found, its center had fallen into a pattern of starting new clinical trials in order to pay for patients' follow-up in the older, ongoing trials.
Seow likened it to a "Ponzi scheme" -- albeit an unintentional and legal variant.
"In order to stay afloat," Seow explained in an interview, "we have to start new trials and recruit new patients."

The money from that new-patient accrual then goes to "pay down the deficit" of earlier trials. "Obviously, that's not sustainable," Seow said.
One way to help with the larger issue of sustaining cooperative group trials could be to switch from "up front" payment, according to Seow.
The author of an editorial published with the study in the Journal of Clinical Oncology agrees. "Perhaps it is time to consider more closely following the pharmaceutical industry model of progress payments," writes Dr. David M. Dilts, of the Knight Cancer Institute in Portland, Oregon.
That, he adds, could help stop the "robbing Peter to pay Paul" habit of using new trials to fund old ones.

FUNDING GAP
An alternative for individual cancer centers would be to take part in fewer and fewer cooperative group trials, and more industry-funded ones.

A recent survey of centers in the NCI cooperative program suggested that is happening: one-third said they were going to limit their participation in NCI-funded trials in the future.

But non-industry trials are vital, Seow pointed out. Drug company studies may bring us the "next blockbuster drug," he noted, but the cooperative group trials help answer the bigger questions of how to improve cancer patients' overall care.
This new analysis, Seow said, looks at just one aspect of the larger, complicated issue.

The 2010 report from the IOM recommended an overhaul of the NCI cooperative group program. Many of its suggestions focused on efficiency: the process of simply designing a trial, for example, is lengthy and cumbersome -- taking an average of two years to complete.
It also called for more funding. The NCI's payment-per-patient has not changed in a decade, standing at about $2,000. But the actual cost is thought to be closer to $6,000, Dilts points out in his editorial.
The NCI has said it plans to boost that reimbursement to $4,000, at least to "high performance" centers that enroll a large number of patients in clinical trials.

In an email to Reuters Health, a spokesperson for the organization said it recognizes the need for more funding going to individual study sites.
But centers may still end up spending the money up front, Dilts notes -- especially with today's trend of doing expensive genetic testing of patients. That's done because researchers are increasingly trying to develop treatments that are "personalized" to patients' genetic makeup.
So there still may be no money left over for years of patient follow-up.
Another option, Seow said, is to finally close some of the long-running "mega-trials" that are no longer generating useful information.
But the wider problem will ultimately need multiple solutions, according to Seow.
"There have been remarkable breakthroughs in cancer therapies," he said. "But there's a state of crisis in clinical trials right now, and there are many reasons for it."

SOURCE: bit.ly/GSkEGD Journal of Clinical Oncology, online March 26, 2012.

ME-344/NV-128 - Marshall Edwards - Trials Open for Broad-Acting Oncology Candidate - Chemotherapy Advisor



Trials Open for Broad-Acting Oncology Candidate - Chemotherapy Advisor


close
cer Care Costs Seem to Be Worth It
Read More >>
(ChemotherapyAdvisor) – San Diego-based pharmaceutical company Marshall Edwards, Inc., announced today that it has received approval from the U.S. Food and Drug Administration (FDA) for its Investigational New Drug (IND) application for ME-344, the company's lead mitochondrial inhibitor. A Phase 1 clinical trial of intravenous ME-344 in patients with solid refractory tumors is currently being initiated.
Data from a preclinical study of NV-128, the metabolic precursor of ME-344, demonstrated its ability to induce mitochondrial instability, ultimately leading to cell death in otherwise chemotherapy-resistant ovarian cancer stem cells.....

Tuesday, April 10, 2012

abstract: A systematic review evaluating the relationship between progression free survival and post progression survival in advanced ovarian cancer



 Blogger's Note:
this is and has been an ongoing issue in clinical trials as most use still use overall survival (OS) (as per this paper and others)  as the endpoint as opposed to progression free survival; it is a technical debate having wide implications for ovarian cancer treatments/patients, without access to the full text paper and based on the abstract alone,  one outstanding issue would be the impact of QOL/side effects/number of prior treatments, so in plain english as an example - clinical trial x includes standard treatment vs other, no more than eg. 3 prior chemos would be a component of the clinical trial - therefore - what was/is the mix of patients in the trial - all of which impact survival ratios irrespective of PFS/OS; opinions as usual are welcome
                                      ~~~~~~~~~~~~~~~~~

A systematic review evaluating the relationship between progression free survival and post progression survival in advanced ovarian cancer:




Objective 
Although overall survival is the ultimate goal of cancer therapy, many clinical and health economic decisions are taken when only progression free survival (PFS) data are available. This study evaluates the relationship between PFS and post progression survival (i.e. the time between disease progression and death) to estimate how many months a new drug for ovarian cancer might add to overall survival if the number of months the drug added to PFS (relative to a standard drug) was already known.

Methods 
A literature search was conducted over Medline for randomised controlled trials published between January 1990 and July 2010 that evaluated the effect of a drug treatment in comparison to alternative drug treatment in patients with either advanced stage primary or recurrent ovarian cancer.
A systematic review of progression free and post progression survival (PPS) was performed. The relationship between PFS and PPS was evaluated by a graphical method and standard statistical tests.

Results
Thirty-seven trials involving 15,850 patients met the inclusion criteria. The review found that increases in median PFS generally lead to little change in post-progression survival. Percentage gains in PFS are generally associated with no percentage gains or with very slight percentage gains or losses in post-progression survival

Conclusion
If the effect of a new drug treatment for ovarian cancer is to extend median PFS by x months, then it is reasonable to estimate that the treatment will also extend median overall survival by x months. This information will be useful for individual and collective decision making.

Monday, April 09, 2012

Blogger's Opinion: repost (2011) : Proteomic biomarkers in combination with CA 125 for detection of epithelial ovarian cancer using prediagnostic serum samples from the Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial - Moore - 2011 - Cancer - Wiley Online Library



Blogger's Note/Opinion:  
efforts to improve on the existing CA125 biomarkers remain elusive, as we speak;  this may be confirmed by the multitude of research studies/meta-analsyes (known issues); we, as patients/survivors, all have examples which are contrary, or exceptions,  to what is presently known and therefore the issue of 'personalized medicine'; biomarker banking (tissues from surgery for research) is an important key element for those diagnosed so that we may move forward beyond the standard CA125 (as one example); on the bonus side - research is moving forward at a greatly accelerated pace (molecular/proteomics...) but the research is still in the phase/s of being brought to the 'clinic',  meaning what actually works for our ovarian cancer women pre-present-post diagnosis; it is a common philosophy in ovarian cancer research that due to our low numbers (relative to other cancers) that we must have global research (not least of which is to mention global economics); as patients you can make a difference by ensuring that the clinical studies which you enroll will make a difference in these efforts as opposed to small isolated studies - specifically those that continue to regurgitate past studies which do not move forward beyond the existing eg. psychosocial aspects of prophlactic surgery


Proteomic biomarkers in combination with CA 125 for detection of epithelial ovarian cancer using prediagnostic serum samples from the Prostate, Lung, Colorectal, and Ovarian (PLCO) Cancer Screening Trial - Moore - 2011 - Cancer

RESULTS (abstract):

"CA 125 levels were elevated (≥35 U/mL) in 61.5% of 65 patients who had CA 125 data available from samples that were collected <12 months before cancer diagnosis; however, levels of the additional 7 biomarkers were not different between cases and the 3 control groups individually or combined. Two panels that combined CA 125 and the 7 biomarkers failed to improve the sensitivity of CA 125 alone."

DISCUSSION

 ".....Although a marginally better performance was observed for the identification of cases at least 6 months before diagnosis using an all-site multimarker panel (which included CA 125, HE4, tumor-associated glycoprotein 72 [CA 72-4], substance P-like immunoreactivity, andĪ²2M) were observed compared with CA 125 alone, the increase was not statistically significant.21 In addition to the current study, 5 additional panels were evaluated, none of which improved on the results with CA 125 alone.8 Considering the failure of multiple biomarkers to improve upon CA 125 in prediagnostic samples, new approaches are badly needed for biomarker discovery. One weakness of the current study is that we were unable to evaluate markers in nonwhite populations because of a very small number of nonwhite cases in the PLCO trial. The results of this combined effort will likely reshape our approach to biomarker discovery and validation. In addition to searching for protein analytes, autoantibodies also may be sought. Finally, previous studies have had limited success in identifying and evaluated autoantibodies of human proteins expressed in bacteria or insect cells. Recent advances in expressing human proteins in human cells could allow the identification of new epitopes that are selective for altered tertiary structure and glycosylation status of selected protein targets."

Saturday, April 07, 2012

abstract: Assumptions of Expected Benefits in Randomized Phase III Trials Evaluating Systemic Treatments for Cancer



Blogger's Note: also reference related commentary: " Why Do Phase III Clinical Trials in Oncology Fail so Often?


                 ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Assumptions of Expected Benefits in Randomized Phase III Trials Evaluating Systemic Treatments for Cancer

open access: Why Do Phase III Clinical Trials in Oncology Fail so Often?



Why Do Phase III Clinical Trials in Oncology Fail so Often?

 "Achieving success in the development of a cancer drug continues to be challenging. Given the increasing costs (1) and the small number of drugs that gain regulatory approval (2), it is crucial to understand these failures. In this issue of the Journal, Gan et al. (3) reviewed 235 recently published phase III randomized clinical trials (RCTs). They report that 62% of the trials did not achieve results with statistical significance. Trying to explain the high failure rate, they note the actual magnitude of benefit achieved in a clinical trial (designated B) is nearly always less than what was predicted at the time the trial was designed (designated Ī“) and conclude, “investigators consistently make overly-optimistic assumptions regarding treatment benefits when designing RCTs.”
But really should we be surprised that phase III trials, the venue for detecting “small” differences, so often disappoint? Almost by definition, phase III studies are designed to detect small differences (4,5). The problem is that small has given way to “marginal” as outcomes have fallen below our already modest expectations. And who or what is to blame? Are investigators really overly optimistic regarding experimental therapies and, as the authors suggest, responsible for the large number of negative studies? Although we agree that optimism regarding clinical benefit may lead to an underpowered trial, we disagree that optimistic investigators are those we should blame. We would ask, how do Gan et al. (3) define optimism? Where do they place the line between an optimistic and a realistic expectation?.........

Friday, March 30, 2012

Medpage SGO news: :Combo Promising for Resistant Ovarian Cancer - in Meeting Coverage, SGO from MedPage Today



Medical News:Combo Promising for Resistant Ovarian Cancer - in Meeting Coverage, SGO from MedPage Today

"....The between-group difference increased to 4 months in the subgroup of patients whose lesions had imaging-confirmed folate-receptor expression.
Overall survival did not differ between the groups, due in part to an unusually prolonged survival in the control arm, R. Wendel Naumann, MD, said here at the Society of Gynecologic Oncology meeting.
"This is the first clinical trial that has shown a benefit in progression-free survival over standardized therapy in a randomized trial in patients with platinum-resistant ovarian cancer, and we think it's pretty exciting," said Naumann, of Carolinas Medical Center in Charlotte, N.C.
"We know that EC20 scanning identifies patients who will benefit most from the combination of pegylated liposomal doxorubicin and vintafolide, as well as those who will not benefit. It appears that patients in whom all lesions are folate-receptor positive benefit the most from this combination."
A phase III randomized trial of PLD plus vintafolide has already begun, he added.............



Action Points


  • This study was published as an abstract and presented at a conference. These data and conclusions should be considered to be preliminary until published in a peer-reviewed journal.
  • Note that a compound which binds with high affinity to the folate receptor, which is expressed on the majority of epithelial ovarian cancers, and releases a cytotoxic component significantly increased progression-free survival in this phase two study.

Tuesday, March 27, 2012

March 27th: Medscape article - Olaparib for Ovarian Cancer, No Longer in Development



Olaparib for Ovarian Cancer, No Longer in Development

open access: ecancer - Phase 0 clinical trials: towards a more complete ethics critique



Phase 0 clinical trials: towards a more complete ethics critique

Summary
In efforts to modernise the entire drug-development process, making it more efficient, less costly, and ultimately of real benefit to patients, The Federal Drug Administration (FDA) authorised the use of exploratory IND or early Phase I (Phase 0) studies. Quite different in structure from Phase I, II, and III studies, the Phase 0 construct understandably poses a set of ethical problems not seen in the other research phases and so far not adequately addressed by ethicists. In an effort to deal with this deficiency, this paper proposes an ethics critique, based not on the usual concept of benefit, but on the means–end relation, and placed within an ethic of science derived from the practice of science.

To date, the ethics analysis of Phase 0 clinical trials has remained incomplete [13]. Focusing, for the most part, on the Phase 0 construct itself, the analysis has neglected the larger economic context in relation to which Phase 0 trials must be understood for any complete analysis.......

"The Ethics of the Phase 0 Construct
It is clear from the way the Phase 0 construct is described in both the Critical Path Initiative and the Guidance that the FDA is promoting it as a means to achieve an end, namely, solving the “pipeline problem”. If so, then an ethics assessment of the construct should start by asking whether the end justifies the means in moral terms.......

medical news: Improved clinical quality leads to decline in quality of patients' experiences



Improved clinical quality leads to decline in quality of patients' experiences

....."Clinical quality is about doing things correctly - strict guidelines, standardization and checklists, for example - so when you consider experiential quality is about customizing health-care delivery to an individual patient's needs, there is a tension there," said Aravind Chandrasekaran, assistant professor of management sciences at Ohio State and lead author of the study.
How might this tension play out?......

Morphotek®, Inc. Announces Completion of Enrollment in the FAR-131 Trial for Relapsed Ovarian Cancer



Morphotek®, Inc. Announces Completion of Enrollment in the FAR-131 Trial for Relapsed... -- EXTON, Pa., March 27, 2012 /PRNewswire/ --

Clinical Study Seeks to Evaluate Farletuzumab in Combination with Standard of Care in First-Relapse Patients with Platinum-Sensitive Ovarian Cancer

EXTON, Pa., March 27, 2012 /PRNewswire/ -- Morphotek®, Inc., a subsidiary of Eisai Inc., announced today it has completed enrollment of the FAR-131 clinical trial. The study is a pivotal Phase 3 randomized trial of farletuzumab in first-relapsed patients with platinum-sensitive ovarian cancer. Farletuzumab is a humanized monoclonal antibody that targets folate receptor alpha (FRA), which is expressed on the majority of non-mucinous epithelial ovarian cancers as well as a subset of other carcinomas.
The trial is designed as a three-armed, randomized, double-blinded, controlled study in patients with platinum-sensitive ovarian cancer who relapse after first-line treatment with standard of care. FAR-131 tests the ability of farletuzumab at two different dosages in combination with second-line standard-of-care (carboplatin or cisplatin plus paclitaxel or docetaxel) for patients with platinum-sensitive disease to improve progression-free survival as compared to those treated with standard-of-care and placebo. Secondary endpoints include improvements in overall survival, objective tumor responses and the number of patients exhibiting longer second remission periods as compared to their primary remission.

FAR-131 was initiated in March 2009, and has reached its randomization target of 1080 patients at clinical sites in 30 countries located in North America, South America, Europe, Asia, Australia and the Middle East.

Farletuzumab is a monoclonal antibody that binds to and blocks the function of FRA, a cell surface protein on tumor cells that confers a growth advantage to tumorigenic ovarian cells in vitro. FRA has been demonstrated by several independent studies to be expressed on a variety of cancer types. The antibody also is being tested in a randomized Phase 2 study to assess its effect in patients with FRA+ non-small-cell lung adenocarcinoma in combination with standard of care in first-line therapy.

Further information on the clinical study can be found at www.clinicaltrials.gov, study number NCT00849667.

Found 1 study with search of: NCT00849667

 




Active, not recruiting Efficacy and Safety of MORAb-003 in Subjects With Platinum-sensitive Ovarian Cancer in First Relapse
Condition: Ovarian Cancer
Interventions: Drug: MORAb-003 (farletuzumab);   Drug: 0.9% Saline

abstract: Funding Oncology Clinical Trials: Are Cooperative Group Trials Sustainable?



Funding Oncology Clinical Trials: Are Cooperative Group Trials Sustainable?

Conclusion
The negative trough in the lifetime net income of a cooperative group trial occurs because follow-up costs are typically not funded or are underfunded. CTDs accrue more patients in new trials to offset that deficit. The CTD uses revenue from accrual to existing trials to cross-subsidize past trials in follow-up. As the number of patients on follow-up increases, the fiscal deficit grows larger each year, perpetuating the cycle. 


JCO (pdf) Comment - Robbing Peter to Pay Paul: Financing Clinical Trial Follow-Up





 Robbing Peter to Pay Paul: Financing Clinical Trial Follow-Up

David M. Dilts, Oregon Health and Science University, Knight Cancer Institute, Portland, OR
See accompanying article doi: 10.1200/JCO.2011.37.2698

"....With this total-cost knowledge, sites should be able to
do a better job of selecting trials that match their scientific interests,
their patient populations, and their fiscal necessities, and stop cross subsidizing old trials with new trials—in essence, stop robbing Peter to
pay Paul."

Tuesday, March 20, 2012

Dr Maurie Markman: Clinical Oncology News - A Provocative Intersection: Rare cancers, “approved” anti-neoplastics and preclinical models



Clinical Oncology News - A Provocative Intersection: Rare cancers, “approved” anti-neoplastics and preclinical models

"Preclinical results describing a novel approach to the treatment of an uncommon malignant condition raise a provocative question: How, in the current increasingly rigid “guideline-based” era of cancer management, can such observations ever leave the realm of the laboratory to be examined in the clinic? And can a rational approach to this highly relevant dilemma be devised?
Primary mucinous tumors comprise a very small proportion (<5%) of morphologic subtypes found in patients with advanced epithelial ovarian cancer......."

"....One might even argue that the outcome of such individual non-investigative experiences be posted in an easily identified, well-organized, condition-specific online database (with absolutely no accompanying patient-specific identifiers), so the oncology community would be aware of any clinically beneficial effects observed if colleagues had previously attempted to employ this novel approach in an individual patient with a metastatic mucinous ovarian cancer.....

Sunday, March 18, 2012

Faculty of Health Science - News - New Blood Test for Early Cancer Detection Developed by Ben-Gurion University of the Negev Researchers



Faculty of Health Science - News - Cancer_detection


New Blood Test for Early Cancer Detection Developed by Ben-Gurion University of the Negev Researchers



90 Percent Detection Rate in Clinical Tests for Multiple Types of Cancers
A simple blood test is being developed by researchers at Ben-Gurion University of the Negev (BGU) and Soroka University Medical Center in Beer-Sheva, Israel that may provide early detection of many types of cancer.
Prof. Joseph Kapelushnik of BGU’s Faculty of Health Sciences and his team developed a device that illuminates cancer cells with less than a teaspoon of blood. The test uses infrared light to detect miniscule changes in the blood of a person who has a cancerous growth somewhere, even before the disease has spread. Various molecules released into the bloodstream cause it to absorb infrared light slightly differently compared to that of healthy people.  
In the latest clinical trial with 200 patients and a control group, the test identified specific cancers in 90 percent of the patients and found other types of cancer, as well.  The researchers are focused on detection of common cancers, such as lung and ovarian cancer. 
Doctors believe that it is critical to increase cancer detection in early stages to prevent the need for long, difficult and costly treatments in more advanced stages.
“This is still research in the early stages of clinical trials,” clarifies Prof. Joseph Kapelushnik, who is also head of the Department of Pediatric Hemato-Oncology at Soroka hospital. 
“But the purpose is to develop an efficient, cheap and simple method to detect as many types of cancers as possible. We want to be able to detect cancer while a patient is still feeling good, before it has a chance to metastasize, meaning fewer treatments, less suffering and many more lives saved.”
More clinical trials will be conducted in the next 18 months.
Publish date: 26/02/2012

Saturday, March 17, 2012

abstract: Patient Selection for Oncology Phase I Trials: A Multi-Institutional Study of Prognostic Factors [Phase I and Clinical Pharmacology]



Patient Selection for Oncology Phase I Trials: A Multi-Institutional Study of Prognostic Factors [Phase I and Clinical Pharmacology]:

Purpose
The appropriate selection of patients for early clinical trials presents a major challenge. Previous analyses focusing on this problem were limited by small size and by interpractice heterogeneity. This study aims to define prognostic factors to guide risk-benefit assessments by using a large patient database from multiple phase I trials.

Patients and Methods
Data were collected from 2,182 eligible patients treated in phase I trials between 2005 and 2007 in 14 European institutions. We derived and validated independent prognostic factors for 90-day mortality by using multivariate logistic regression analysis.

Results
The 90-day mortality was 16.5% with a drug-related death rate of 0.4%. Trial discontinuation within 3 weeks occurred in 14% of patients primarily because of disease progression. Eight different prognostic variables for 90-day mortality were validated: performance status (PS), albumin, lactate dehydrogenase, alkaline phosphatase, number of metastatic sites, clinical tumor growth rate, lymphocytes, and WBC. Two different models of prognostic scores for 90-day mortality were generated by using these factors, including or excluding PS; both achieved specificities of more than 85% and sensitivities of approximately 50% when using a score cutoff of 5 or higher. These models were not superior to the previously published Royal Marsden Hospital score in their ability to predict 90-day mortality.

Conclusion
Patient selection using any of these prognostic scores will reduce non–drug-related 90-day mortality among patients enrolled in phase I trials by 50%. However, this can be achieved only by an overall reduction in recruitment to phase I studies of 20%, more than half of whom would in fact have survived beyond 90 days.