On my desks at home and at work, I keep copies of a 2012 internal medicine text written by several esteemed professors from my medical school. It is not there to remind me what they got right, but rather, to remind me how, in retrospect, so much of what we took as indisputable knowledge is now plainly wrong. As Joshua Y. Yang, MD, notes, few of his fellow medical students appreciated the prescience of their professor’s first-year prediction that, “Ninety percent of what you will learn over the next 4 years will be wrong in a couple of decades from now.”
This misalignment is especially true in the domain of cancer care. From the perspective of
someone practicing oncology in the late 1990s, there was no way to accurately predict how radically oncology and hematology would be transformed in the subsequent 2 decades by advances in genomic diagnostics/risk stratifi cation, targeted therapeutics, immuno-oncologic drugs, and gene-modifi ed therapeutics. My 2012 textbook serves as a reminder to remain humble and embrace a broader perspective when making sweeping pronouncements about the future of cancer care.
Instead, we must embrace this hyperdynamic period of innovation with the perspective that the
best way to create a system path that ensures these discoveries are delivered sustainably, equitably,
and effectively may only become clear in time through the persistence of those who are passionately engaged in bringing care to patients and families. There are more than 8000 new medications in development; up to 75% may represent new therapeutic classes. The failure to embrace this dizzying pace of change will exacerbate care disparities, produce more misaligned payment systems, and erect more barriers to life-saving, life-transforming care.
In 1984, CMS created the Prospective Payment System. Inasmuch as this represented an advance
from prior payment systems, it now seems antiquated in light of the dramatic advances in cancer
care. In 1984, 5-year relative cancer survival rates were only 52.74%. Since then, cancer survival rates
have risen by the greatest increments ever, fueled by the impact of novel targeted therapeutics and
immuno-oncological agents. Our payment systems have not kept up. CMS’ slow response in creating a payment model for chimeric antigen receptor T cells should not set the precedent for how our systems adapt to this era.. The profound differentiation of cancer care from other care types needs to be more effectively integrated into payment design models, lest existing care disparities grow in the face of misaligned models for payment.
Neither systemic inertia nor the quest for a “perfect” model of care payment should paralyze
the pace of progress, nor should it result in patients and families encountering additional barriers to
life-saving access in their respective cancer journeys. In this issue of Evidence-Based Oncology™,
we look forward, humbly, toward how our systems may more effectively evolve to become more patient-centered, more effective, more innovative, and more sustainable.
As we move forward through this unprecedented period in cancer care innovations, the quest for
grand strategies and elegant systems should not be our principal goals. The growing disparities in care access coupled with a growing portfolio of therapeutics require that we act now to ensure that patients, oncologist, and health systems can move with unfettered speed in bringing hope to those whose lives have been affected by a cancer diagnosis.
As long as we keep this as our truth north and continue to push past the systemic imperfections
and incorrect assumptions that stand in our way, the connected dots of a robust care delivery system will become increasingly clear in time. The first step is to humbly embrace this level of uncertainty—and to then move with speed.
Addressing Cancer Care Challenges to Achieve Optimal Outcomes
September 23rd 2024Linda Bosserman, MD, PhD, FASCO, FACP, of City of Hope, highlights challenges in cancer care, focusing on improving access to accurate diagnoses and treatments, promoting patient-centered approaches, and fostering collaboration to achieve better outcomes.
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Daratumumab and Hyaluronidase-fihj–Based Quadruplet Regimen Approved in MM
July 31st 2024Daratumumab/hyaluronidase-fihj plus bortezomib, lenalidomide, and dexamethasone is now approved by the FDA to treat newly diagnosed multiple myeloma (MM) in patients eligible for autologous stem cell transplant.
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The Importance of Treatment Sequencing in Mantle Cell Lymphoma
July 16th 2024We recently spoke with Tycel Phillips, MD, associate professor, Division of Lymphoma, Department of Hematology & Hematopoietic Cell Transplantation, City of Hope, about his team’s interim analysis of their dose-escalation study of glofitamab against relapsed/refractory B-cell non-Hodgkin lymphoma.
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The Tremendous Complexity of Treating RRMM
June 27th 2024In this interview from our coverage of the European Hematology Association 2024 Congress, Joseph Mikhael, MD, MEd, FRCPC, FACP, International Myeloma Foundation, discusses the complex principles that underlie treating multiple myeloma (MM) in the US.
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