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Home » Practice and Policy

PRACTICE & POLICY 

ASCO Issues New End-of-Life Policy Statement and Patient Guide

By CancerNetwork Editors | January 26, 2011

ASCO’s QOPI (Quality Oncology Practice Initiative) analysis recently found that less than half of all cancer patients are enrolled in hospice care before their death and of those who are enrolled, one-third are not enrolled until the last week of their lives. In response to this and other QOPI findings, ASCO published a new policy and guidelines this week, intended to encourage physicians to initiate open dialogue about palliative care and treatment with patients as soon as they are identified as having incurable cancer.

The authors state, “There is a need to change the paradigm for advanced cancer care to include an earlier and more thorough assessment of patients’ options, goals, and preferences, and to tailor the care that we deliver to these individual needs throughout the continuum of care.”

The authors, led by Jeffrey Peppercorn at Duke, state that anticancer therapy should be considered only when it is deemed likely to result in significant clinical benefit, and that the priority throughout the course of the disease should be placed on “enhancing patients’ quality of life.” To this end, the authors cite evidence from a recent randomized trial showing that early palliative care results in improved quality of life and survival when compared with standard disease treatment.

Another important point made in the new policy statement is that now, less than 3% of adult patients with cancer are enrolled in clinical trials, yet willingness to participate is estimated at roughly 50%. The authors state that patients should be encouraged to enroll in clinical trials earlier in their disease, rather than at such a late stage that the expectation of benefit is unrealistic.

Peppercorn and his colleagues cite the following as potential barriers to providing personalized treatment in incurable disease: awareness of the importance of this issue among doctors; a lack of guidelines for discontinuing therapy; the fact that our current reimbursement system favors immediate intervention rather than prolonged discussion between caregiver and patient; and the barriers that prevent incurable cases from participating in clinical trials.

They posit that the steps needed to provide successful personalized treatment include raising awareness of the issue in general  by emphasizing individualized care in medical education and training; prioritizing compensation of oncologists for open discussion of options throughout healthcare reform process; empowering patients; and continuing basic research in advanced cancer care.

The statement was published Monday, January 24th in the Journal of Clinical Oncology; you can read the full-text here: http://jco.ascopubs.org/content/early/2011/01/24/JCO.2010.33.1744.full.pdf+html.

 

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by ronald killips | January 30, 2011 4:56 PM EST

My wifes doctor pulled life support while she was still coming out of sedation. The doctor misconstrued my wifes wishes and thought a "nod" was permission to remove support. The doctor ignored the pharmokenetics of the drug Propofol and did not let  my wife to  fully wake up before she could give a cogent answer. It wasn't the cancer that killed her, it was th pulling of life support that killed her. 

by Herb Skovronek | January 28, 2011 5:47 PM EST

Clinical trials: As Mr Mygrant reports, patient must bear much of the cost.  But of more concern to me is that clinical trials are usually only available as a last ditch effort.  Trials before cancers (e.g., Prostate cancer) reach the hormone resistant, metastatic stage seem to be almost impossible to design to meet govt requirements.  Many drugs seeking clinical trial might fair much better if patients were in better condition at the time.

by John Mygrant | January 28, 2011 4:17 PM EST

My (non-smoking) wife's increasingly severe backache was not a slipped disc--turned out to be metastatic lung cancer with liver and bone mets. Together we investigated a Phase III clinical trial, talked frankly with her oncologist and declined to participate, choosing carboplatin and gemzar for 1 round of 6 cycles.  Very tough time on it, but later we had good time together (though she remained essentially bedridden with spinal mets).  I stayed by her side for 8 months until it progressed into her brain with death following within a month.  But the insurance rules prohibit you from  getting any palliative hospice care while undergoing ANY "treatment"regimen, though her treatments were intended to be palliative--relieve symptoms and slow progression.   I was there in place of hospice; when it was clear that no further treatments would provide any symptom relief, we could finally sign up for hospice.  They were a great help when the going got really tough, but that was the final two weeks.  I suggest to you that part of the issue remains the refusal to recognize some level of palliative "treatment."  As to clinical trials---despite the billions made from the drugs despite very modest effectiveness, you get to pay your own way through clinical trials.  That's a lot to ask of patients and their families.  Let me also say, we had a great Doc, understood the prognosis and the treatment program goals that matched my wife's wishes, used resources wisely and I was able to provide round the clock care (paying for that now, but worth the sacrifice)--- so we got through pretty well.  But there are barriers to making care most helpful, not the least of which is the WALL that is erected between "treatment" and "palliative hospice" care.  Just my observations from the patient/family side.






 
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