The Effects of Adverse Events and Associated Costs on Value-Based Care for Metastatic Pancreatic Ductal Adenocarcinoma

<b>Background:</b> Rising oncology healthcare costs have led to value-based care reimbursement models that coordinate care and improve quality while reducing overall spending. These models are increasingly important for traditional Medicare and other payers. <b>Objectives:</b> To compare the incidence of adverse events (AEs), AE-associated excess costs, and total cost of care (TCOC) of 3 cohorts receiving first-line treatment for metastatic pancreatic ductal adenocarcinoma (mPDAC). <b>Methods:</b> We conducted a retrospective analysis of administrative claims data from 2018 to 2022 using the Medicare 100% Research Identifiable Files. We examined 3 cohorts receiving mPDAC treatment: FOLFIRINOX (FFX) (oxaliplatin, irinotecan, leucovorin, 5-FU bolus and infusion); modified FFX, (5-FU infusion only); and gemcitabine/nab-paclitaxel (gem/abrax). We compared the incidence of clinically significant AEs, TCOC, components of TCOC, and costs related to AEs/treatment toxicity. <b>Results:</b> Patient AE rates ranged from 6.2% to 51.7%. AEs occurred more frequently in patients receiving FFX with all 4 components. Patients receiving brand name gem/abrax had lower rates of febrile neutropenia (6.2%) and neutropenia (22.2%) than those receiving FFX with no 5-FU bolus (febrile neutropenia, 9.9%; neutropenia, 36.9%) and FFX with all 4 components (febrile neutropenia, 6.9%; neutropenia, 30.4%). Rates of most nonhematologic AEs were higher in patients receiving FFX with all 4 components, with diarrhea occurring in 28.3%, abdominal pain in 31.5%, and nausea/vomiting in 41.5% of patients. TCOC was lower in the gem/abrax cohort: <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mn>6505</mml:mn> <mml:mi>v</mml:mi> <mml:mi>s</mml:mi> <mml:mi>F</mml:mi> <mml:mi>F</mml:mi> <mml:mi>X</mml:mi> <mml:mi>w</mml:mi> <mml:mi>i</mml:mi> <mml:mi>t</mml:mi> <mml:mi>h</mml:mi> <mml:mi>n</mml:mi> <mml:mi>o</mml:mi> <mml:mn>5</mml:mn> <mml:mo>-</mml:mo> <mml:mi>F</mml:mi> <mml:mi>U</mml:mi> <mml:mi>b</mml:mi> <mml:mi>o</mml:mi> <mml:mi>l</mml:mi> <mml:mi>u</mml:mi> <mml:mi>s</mml:mi> <mml:mo>(</mml:mo></mml:math> 6995) and FFX with all 4 components ( <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mn>7142</mml:mn> <mml:mo>)</mml:mo> <mml:mi>p</mml:mi> <mml:mi>e</mml:mi> <mml:mi>r</mml:mi> <mml:mi>a</mml:mi> <mml:mi>d</mml:mi> <mml:mi>m</mml:mi> <mml:mi>i</mml:mi> <mml:mi>n</mml:mi> <mml:mi>i</mml:mi> <mml:mi>s</mml:mi> <mml:mi>t</mml:mi> <mml:mi>r</mml:mi> <mml:mi>a</mml:mi> <mml:mi>t</mml:mi> <mml:mi>i</mml:mi> <mml:mi>o</mml:mi> <mml:mi>n</mml:mi> <mml:mo>.</mml:mo> <mml:mi>T</mml:mi> <mml:mi>h</mml:mi> <mml:mi>e</mml:mi> <mml:mi>d</mml:mi> <mml:mi>e</mml:mi> <mml:mi>v</mml:mi> <mml:mi>e</mml:mi> <mml:mi>l</mml:mi> <mml:mi>o</mml:mi> <mml:mi>p</mml:mi> <mml:mi>m</mml:mi> <mml:mi>e</mml:mi> <mml:mi>n</mml:mi> <mml:mi>t</mml:mi> <mml:mi>o</mml:mi> <mml:mi>f</mml:mi> <mml:mi>a</mml:mi> <mml:mi>n</mml:mi> <mml:mi>y</mml:mi> <mml:mi>s</mml:mi> <mml:mi>t</mml:mi> <mml:mi>u</mml:mi> <mml:mi>d</mml:mi> <mml:mi>i</mml:mi> <mml:mi>e</mml:mi> <mml:mi>d</mml:mi> <mml:mi>h</mml:mi> <mml:mi>e</mml:mi> <mml:mi>m</mml:mi> <mml:mi>a</mml:mi> <mml:mi>t</mml:mi> <mml:mi>o</mml:mi> <mml:mi>l</mml:mi> <mml:mi>o</mml:mi> <mml:mi>g</mml:mi> <mml:mi>i</mml:mi> <mml:mi>c</mml:mi> <mml:mi>A</mml:mi> <mml:mi>E</mml:mi> <mml:mi>w</mml:mi> <mml:mi>a</mml:mi> <mml:mi>s</mml:mi> <mml:mi>a</mml:mi> <mml:mi>s</mml:mi> <mml:mi>s</mml:mi> <mml:mi>o</mml:mi> <mml:mi>c</mml:mi> <mml:mi>i</mml:mi> <mml:mi>a</mml:mi> <mml:mi>t</mml:mi> <mml:mi>e</mml:mi> <mml:mi>d</mml:mi> <mml:mi>w</mml:mi> <mml:mi>i</mml:mi> <mml:mi>t</mml:mi> <mml:mi>h</mml:mi> <mml:mi>a</mml:mi> <mml:mi>m</mml:mi> <mml:mi>e</mml:mi> <mml:mi>a</mml:mi> <mml:mi>n</mml:mi> <mml:mi>e</mml:mi> <mml:mi>x</mml:mi> <mml:mi>c</mml:mi> <mml:mi>e</mml:mi> <mml:mi>s</mml:mi> <mml:mi>s</mml:mi> <mml:mi>c</mml:mi> <mml:mi>o</mml:mi> <mml:mi>s</mml:mi> <mml:mi>t</mml:mi> <mml:mi>o</mml:mi> <mml:mi>f</mml:mi></mml:math> 5993 per administration, while the development of any studied nonhematological AE was associated with a mean per-administration excess cost of $3665. <b>Discussion:</b> Treatment decisions intended to minimize chemotherapy costs may lead to suboptimal decisions if the goal is to reduce TCOC. Our research suggests FFX is more costly than gem/abrax (TCOC per administration). Patients receiving gem/abrax were older and had higher baseline Charlson Comorbidity Index scores; however, other factors may be important in driving cost differences. <b>Conclusions:</b> Irrespective of drug cost, chemotherapy leading to a significant increase in AEs is associated with higher TCOC.

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Publication Details

Journal
Journal of health economics and outcomes research
Published
2024-12-18
DOI
https://doi.org/10.36469/001c.124367
Primary Topic
Pancreatic and Hepatic Oncology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

The Effects of Adverse Events and Associated Costs on Value-Based Care for Metastatic Pancreatic Ductal Adenocarcinoma

Jared Hirsch, George Kim, Prachi Bhatt, Gabriela Dieguez et al.
Journal of health economics and outcomes research
Pancreatic and Hepatic Oncology Research
article

The Effects of Adverse Events and Associated Costs on Value-Based Care for Metastatic Pancreatic Ductal Adenocarcinoma

Jared Hirsch, George Kim, Prachi Bhatt, Gabriela Dieguez, Paul Cockrum
article en

Abstract

<b>Background:</b> Rising oncology healthcare costs have led to value-based care reimbursement models that coordinate care and improve quality while reducing overall spending. These models are increasingly important for traditional Medicare and other payers. <b>Objectives:</b> To compare the incidence of adverse events (AEs), AE-associated excess costs, and total cost of care (TCOC) of 3 cohorts receiving first-line treatment for metastatic pancreatic ductal adenocarcinoma (mPDAC). <b>Methods:</b> We conducted a retrospective analysis of administrative claims data from 2018 to 2022 using the Medicare 100% Research Identifiable Files. We examined 3 cohorts receiving mPDAC treatment: FOLFIRINOX (FFX) (oxaliplatin, irinotecan, leucovorin, 5-FU bolus and infusion); modified FFX, (5-FU infusion only); and gemcitabine/nab-paclitaxel (gem/abrax). We compared the incidence of clinically significant AEs, TCOC, components of TCOC, and costs related to AEs/treatment toxicity. <b>Results:</b> Patient AE rates ranged from 6.2% to 51.7%. AEs occurred more frequently in patients receiving FFX with all 4 components. Patients receiving brand name gem/abrax had lower rates of febrile neutropenia (6.2%) and neutropenia (22.2%) than those receiving FFX with no 5-FU bolus (febrile neutropenia, 9.9%; neutropenia, 36.9%) and FFX with all 4 components (febrile neutropenia, 6.9%; neutropenia, 30.4%). Rates of most nonhematologic AEs were higher in patients receiving FFX with all 4 components, with diarrhea occurring in 28.3%, abdominal pain in 31.5%, and nausea/vomiting in 41.5% of patients. TCOC was lower in the gem/abrax cohort: <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mn>6505</mml:mn> <mml:mi>v</mml:mi> <mml:mi>s</mml:mi> <mml:mi>F</mml:mi> <mml:mi>F</mml:mi> <mml:mi>X</mml:mi> <mml:mi>w</mml:mi> <mml:mi>i</mml:mi> <mml:mi>t</mml:mi> <mml:mi>h</mml:mi> <mml:mi>n</mml:mi> <mml:mi>o</mml:mi> <mml:mn>5</mml:mn> <mml:mo>-</mml:mo> <mml:mi>F</mml:mi> <mml:mi>U</mml:mi> <mml:mi>b</mml:mi> <mml:mi>o</mml:mi> <mml:mi>l</mml:mi> <mml:mi>u</mml:mi> <mml:mi>s</mml:mi> <mml:mo>(</mml:mo></mml:math> 6995) and FFX with all 4 components ( <mml:math xmlns:mml="http://www.w3.org/1998/Math/MathML"><mml:mn>7142</mml:mn> <mml:mo>)</mml:mo> <mml:mi>p</mml:mi> <mml:mi>e</mml:mi> <mml:mi>r</mml:mi> <mml:mi>a</mml:mi> <mml:mi>d</mml:mi> <mml:mi>m</mml:mi> <mml:mi>i</mml:mi> <mml:mi>n</mml:mi> <mml:mi>i</mml:mi> <mml:mi>s</mml:mi> <mml:mi>t</mml:mi> <mml:mi>r</mml:mi> <mml:mi>a</mml:mi> <mml:mi>t</mml:mi> <mml:mi>i</mml:mi> <mml:mi>o</mml:mi> <mml:mi>n</mml:mi> <mml:mo>.</mml:mo> <mml:mi>T</mml:mi> <mml:mi>h</mml:mi> <mml:mi>e</mml:mi> <mml:mi>d</mml:mi> <mml:mi>e</mml:mi> <mml:mi>v</mml:mi> <mml:mi>e</mml:mi> <mml:mi>l</mml:mi> <mml:mi>o</mml:mi> <mml:mi>p</mml:mi> <mml:mi>m</mml:mi> <mml:mi>e</mml:mi> <mml:mi>n</mml:mi> <mml:mi>t</mml:mi> <mml:mi>o</mml:mi> <mml:mi>f</mml:mi> <mml:mi>a</mml:mi> <mml:mi>n</mml:mi> <mml:mi>y</mml:mi> <mml:mi>s</mml:mi> <mml:mi>t</mml:mi> <mml:mi>u</mml:mi> <mml:mi>d</mml:mi> <mml:mi>i</mml:mi> <mml:mi>e</mml:mi> <mml:mi>d</mml:mi> <mml:mi>h</mml:mi> <mml:mi>e</mml:mi> <mml:mi>m</mml:mi> <mml:mi>a</mml:mi> <mml:mi>t</mml:mi> <mml:mi>o</mml:mi> <mml:mi>l</mml:mi> <mml:mi>o</mml:mi> <mml:mi>g</mml:mi> <mml:mi>i</mml:mi> <mml:mi>c</mml:mi> <mml:mi>A</mml:mi> <mml:mi>E</mml:mi> <mml:mi>w</mml:mi> <mml:mi>a</mml:mi> <mml:mi>s</mml:mi> <mml:mi>a</mml:mi> <mml:mi>s</mml:mi> <mml:mi>s</mml:mi> <mml:mi>o</mml:mi> <mml:mi>c</mml:mi> <mml:mi>i</mml:mi> <mml:mi>a</mml:mi> <mml:mi>t</mml:mi> <mml:mi>e</mml:mi> <mml:mi>d</mml:mi> <mml:mi>w</mml:mi> <mml:mi>i</mml:mi> <mml:mi>t</mml:mi> <mml:mi>h</mml:mi> <mml:mi>a</mml:mi> <mml:mi>m</mml:mi> <mml:mi>e</mml:mi> <mml:mi>a</mml:mi> <mml:mi>n</mml:mi> <mml:mi>e</mml:mi> <mml:mi>x</mml:mi> <mml:mi>c</mml:mi> <mml:mi>e</mml:mi> <mml:mi>s</mml:mi> <mml:mi>s</mml:mi> <mml:mi>c</mml:mi> <mml:mi>o</mml:mi> <mml:mi>s</mml:mi> <mml:mi>t</mml:mi> <mml:mi>o</mml:mi> <mml:mi>f</mml:mi></mml:math> 5993 per administration, while the development of any studied nonhematological AE was associated with a mean per-administration excess cost of $3665. <b>Discussion:</b> Treatment decisions intended to minimize chemotherapy costs may lead to suboptimal decisions if the goal is to reduce TCOC. Our research suggests FFX is more costly than gem/abrax (TCOC per administration). Patients receiving gem/abrax were older and had higher baseline Charlson Comorbidity Index scores; however, other factors may be important in driving cost differences. <b>Conclusions:</b> Irrespective of drug cost, chemotherapy leading to a significant increase in AEs is associated with higher TCOC.

Journal of health economics and outcomes researchVol. 11(2)
George Washington University (US), Ipsen (United States) (US), Milliman (United States) (US)
Ipsen Biopharmaceuticals
Openalex Percentile: Top 59%
Pancreatic and Hepatic Oncology Research
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