Cost-Effectiveness of PET Directed Versus Combined Modality Therapy for Early-Stage Favorable Hodgkin's Lymphoma

Clin Lymphoma Myeloma Leuk. 2022 Nov;22(11):e992-e999. doi: 10.1016/j.clml.2022.07.005. Epub 2022 Jul 17.

Abstract

Introduction: The standard of care for early-stage Hodgkin Lymphoma (HL) is combined modality therapy (CMT) consisting of chemotherapy and involved site radiation therapy (ISRT). Recent treatment de-escalation trials have assessed the impact of omitting radiation with the use of positron emission tomography (PET) and have suggested a detriment in progression free survival (PFS) for patients who do not receive radiation therapy (RT) but similar overall survival. The purpose of this study was to compare the cost-effectiveness of PET-directed therapy versus standard of care CMT.

Methods: This study used a cost-effectiveness Markov model simulating 5 year outcomes for 1 million patients with early-stage HL treated with either PET-directed therapy consisting of 2 cycles of ABVD chemotherapy ± ISRT or CMT consisting of 2 cycles of ABVD + ISRT. Patients progressed to no evidence of disease, progression of disease (PD), or death. Patients with PD underwent salvage therapy with high dose chemotherapy and stem cell transplant (HDC-SCT). The primary outcome measured was the incremental cost-effectiveness ratio. Deterministic sensitivity analyses were performed.

Results: We found that PET-directed therapy and CMT strategies were associated with costs of $47,362 and $41,167, respectively. The CMT strategy was equally as effective as the PET-directed therapy strategy with QALYs of 3.4. On 1-way sensitivity analyses, the model was most sensitive to CMT and HDC-SCT costs. Two-way sensitivity analyses showed the model was sensitive to the relative costs of these treatments.

Conclusion: For patients with early-stage HL, CMT is the cost-effective strategy as compared with PET-directed therapy.

Keywords: Cost-effectiveness analysis; Early Stage Hodgkin's lymphoma; Markov Model; PET directed therapy; Radiation therapy.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Bleomycin / therapeutic use
  • Combined Modality Therapy
  • Cost-Benefit Analysis
  • Dacarbazine / therapeutic use
  • Disease-Free Survival
  • Doxorubicin / therapeutic use
  • Hodgkin Disease* / pathology
  • Humans
  • Positron-Emission Tomography
  • Vinblastine / therapeutic use

Substances

  • Vinblastine
  • Dacarbazine
  • Bleomycin
  • Doxorubicin