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E-Poster Display

1611P - Healthcare resource utilization (HCRU) and costs in patients (pts) with advanced cancer treated with immune checkpoint inhibitors (ICIs) who experienced select immune-related adverse events (irAEs)

Date

17 Sep 2020

Session

E-Poster Display

Topics

Bioethical Principles and GCP

Tumour Site

Presenters

Saby George

Citation

Annals of Oncology (2020) 31 (suppl_4): S903-S913. 10.1016/annonc/annonc287

Authors

S. George1, Y. Zheng2, E.J. Bell3, N.M. Engel-Nitz3, J.C. White3, L.S. Lal4, R. Kim5, S. Krulewicz6, J. Smith7, F.X. Liu2

Author affiliations

  • 1 Department Of Medicine, Roswell Park Comprehensive Cancer Center, 14263 - Buffalo/US
  • 2 Us Health Economics And Outcomes Research, North America Medical Affairs, EMD Serono Inc., 02370 - Rockland/US
  • 3 Health Economics Outcomes Research, Optum, 55344 - Eden Prairie/US
  • 4 Life Sciences, Optum, 77459 - Missouri City/US
  • 5 Health Economics & Outcomes Research, Pfizer Inc., 10017 - New York/US
  • 6 Health Economics & Outcomes Research, Pfizer Inc., 19426 - Collegeville/US
  • 7 Medical Affairs, EMD Serono Inc., 02370 - Rockland/US

Resources

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Abstract 1611P

Background

Historically, adverse event (AE)-related hospitalizations were reported in >50% of pts on chemotherapy, while limited data exist for pts on ICIs. We examined real-world HCRU and costs for pts with urothelial carcinoma (UC), renal cell carcinoma (RCC), non-small cell lung cancer (NSCLC), or Merkel cell carcinoma (MCC) treated with PD-L1/PD-1 ICIs who experienced irAEs.

Methods

This retrospective cohort study used Optum's claims database to identify US commercial and Medicare Advantage health plan members with UC, RCC, MCC, or NSCLC treated with ICIs between 01 Sep 14 and 30 Apr 19. Twenty-one irAEs were chosen a priori based on ASCO guidelines. Pts were followed up for newly occurring irAEs, based on ICD codes from claims, from ICI initiation to earliest date of following: 6 months after initial line of ICI therapy ended, start of new treatment, death, disenrollment, or 30 Apr 19. irAE-related HCRU and costs were calculated in the same time period. HCRU and costs were considered irAE related if an ICD code for an irAE was present in field 1 or 2 on the claim. Descriptive analyses used per-patient-per-month (PPPM) measures and the Kaplan-Meier method.

Results

Among pts treated with ICI monotherapy with irAEs (N=955; 71 y, 54% male, 69% with treatment before ICI), the top HCRU for irAEs was ambulatory visits (0.23 PPPM), followed by inpatient stays (0.09 PPPM; Table). Mean irAE-related medical costs were $2,359 PPPM, driven by the cost of inpatient stays. 34% of all pts who experienced an irAE had an irAE-related inpatient stay within 12 mo after ICI initiation.

Conclusions

Inpatient stays were the driver for irAE-related costs; approximately one-third of pts with an irAE ultimately required an inpatient stay within a year of initiating ICIs. These study findings help elucidate the economic burden associated with the management of ICI irAEs. Table: 1611P

irAE-related HCRU and costs among ICI pts with an irAE

All Patients N=955 UC n=90 RCC n=127 NSCLC n=722 MCC n=16
HCRU, mean ± SD, visits PPPM
Ambulatory 0.23 ± 0.57 0.30 ± 1.14 0.21 ± 0.28 0.23 ± 0.50 0.28 ± 0.27
Emergency department 0.03 ± 0.14 0.06 ± 0.22 0.03 ± 0.11 0.03 ± 0.13 0.03 ± 0.06
Inpatient stay 0.09 ± 0.23 0.16 ± 0.43 0.08 ± 0.16 0.09 ± 0.20 0.02 ± 0.05
Medical costs PPPM, mean ± SD, US $ 2,359 ± 7,496 4,195 ± 12,699 2,066 ± 4,339 2,221 ± 7,113 563 ± 1,219
Ambulatory 201 ± 1,150 116 ± 389 422 ± 2,118 176 ± 968 42 ± 69
Emergency department 11 ± 70 22 ± 113 7 ± 25 11 ± 69 11 ± 33
Inpatient stay 2,120 ± 7,190 3,831 ± 11,009 1,636 ± 3,955 2,029 ± 7,085 468 ± 1,101

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

EMD Serono, Inc.; a business of Merck KGaA, Darmstadt, Germany; Pfizer, Inc.

Funding

EMD Serono, Inc.; a business of Merck KGaA, Darmstadt, Germany, Germany; Pfizer, Inc.

Disclosure

S. George: Advisory/Consultancy, Research grant/Funding (institution): Bayer; BMS; Research grant/Funding (institution): Agensys; Advisory/Consultancy: Exelixis; Genentech; Sanofi/ Genzyme; Advisory/Consultancy, Research grant/Funding (institution): Corvus; Advisory/Consultancy, Research grant/Funding (institution): Pfizer; Merck; Eisai; EMD Serono. Y. Zheng: Full/Part-time employment: EMD Serono Research & Development Institute, Inc. E.J. Bell: Research grant/Funding (self): Novartis; Sandoz; Incyte; EMD Serono Research & Development Institute, Inc.; Celgene; AstraZeneca; Full/Part-time employment: Optum. N.M. Engel-Nitz: Research grant/Funding (institution): EMD Serono Research & Development Institute, Inc.; Exact Sciences; Alexion; AstraZeneca; GlaxoSmithKline; Eli Lilly; Genentech; UnitedHealth Care; Shareholder/Stockholder/Stock options, Full/Part-time employment: UnitedHealth Group. J.C. White: Research grant/Funding (institution): EMD Serono Research & Development Institute, Inc.; Research grant/Funding (institution): Optum; Full/Part-time employment: Optum. L.S. Lal: Full/Part-time employment: Optum. R. Kim: Full/Part-time employment: Pfizer Inc. S. Krulewicz: Full/Part-time employment: Pfizer Inc. J. Smith: Leadership role, Research grant/Funding (self), Travel/Accommodation/Expenses, Shareholder/Stockholder/Stock options, Full/Part-time employment: EMD Serono Research & Development Institute, Inc. F.X. Liu: Full/Part-time employment: EMD Serono Research & Development Institute, Inc.

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