IOM Cancer Report

The Institute of Medicine this week released “Delivering High-Quality Cancer Care: Charting a New Course for a System in Crisis.” [full report; briefing slides]

The report lays out the cancer care continuum in this way.

ScreenHunter_02 Sep. 12 11.06

Two of the reasons the IOM describes cancer care as being “in crisis” is the degree to which they say that the current system is not patient centered and evidence based. When searching for value in cancer care or health care generally, you are really asking whether a given course of treatment improves quality of life, extends life and how much it costs. If you can answer these three questions, then you have a chance of asking (and maybe answering) the question of “is this worth it?” The “is it worth it?” question is relevant at both an individual, but also at a system and payer level (for Medicare in particular, given that 8 in 10 decedents in the U.S. are insured by Medicare and the fact that cancer disproportionately affects older persons, which is a bit of a tautology since it is the second leading cause of death in the U.S.).

The key in trying to join “patient centeredness” with the “evidence base” at the patient level are the items in the purple box (care planning, palliative care, imagining and responding to sequelae of symptoms and burden to patients and caregivers, etc). This is one place those three questions should be asked, discussed and answered over and over, since this is where the choices that patients have in treating cancer (say if covered by Medicare) get banged out into an actual treatment trajectory.

The choices that are offered to patients are also important, and Medicare has the legal/regulatory authority to make coverage decisions and truncate choices, but of course this is politically very difficult.

Our team here at Duke will hopefully be publishing the results of a study we have just completed in which patients with cancer and their caregivers identify what treatment options are most important if a serious resource constraint were imposed in Medicare, as it provides some insight, both into how conversations that are inherent in the purple arrow above can be structured, as well as how policy at the Medicare-level might be altered.

About Don Taylor
Professor of Public Policy at Duke University (with appointments in Business, Nursing, Community and Family Medicine, and the Duke Clinical Research Institute). I am one of the founding faculty of the Margolis Center for Health Policy, and currently serve as Chair of Duke's University Priorities Committee (UPC). My research focuses on improving care for persons who are dying, and I am co-PI of a CMMI award in Community Based Palliative Care. I teach both undergrads and grad students at Duke. On twitter @donaldhtaylorjr

One Response to IOM Cancer Report

  1. Hospice is no longer a place but, rather, a philosophy of care that offers spiritual,mental, emotional, physical, and medical support to those facing one of life’s greatest journeys. It is a compassionate approach that allows those faced with a life-threatening illness to maintain dignity and control over their lives and to spend quality time with their family and friends in the comfort of their own homes whether that is in a private residence, skilled nursing facility, or assisted living facility. The goal is not to cure, but to provide comfort and maintain the highest possible quality of life for as long as possible.

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