Peer-influenced content. Sources you trust. No registration required. This is HCN.

Hematology AdvisorRegimen May Eliminate Need for Transplant in Low-Risk Hodgkin Lymphoma

The 3-year event free survival rate was 86.9%, and the 3-year progression-free survival rate was 95%.

A recent phase 2 trial has revealed a promising treatment option for young patients with low-risk, relapsed classical Hodgkin lymphoma. The regimen, involving nivolumab and brentuximab vedotin, followed by consolidative involved-site radiotherapy (ISRT), could potentially eliminate the need for high-dose therapy and transplant.

HCN Medical Memo
This regimen presents a less invasive and potentially more effective treatment option for young patients with low-risk, relapsed classical Hodgkin lymphoma. It’s important to consider this approach when treating such patients, as it could eliminate the need for high-dose therapy and transplant, reducing both physical and psychological stress on our patients.

Key Points

  • The trial, known as CheckMate 744, was presented at the 2023 ASTRO Annual Meeting.
  • The low-risk cohort of the trial included 28 patients with classical Hodgkin lymphoma, aged between 6 and 27 years.
  • After 4 cycles of induction, the complete metabolic response (CMR) rate was 82.1%, and the overall response rate (ORR) was 96.4%.
  • At any time before ISRT, the CMR rate was 92.9%, and the ORR was 100%.
  • The 3-year event-free survival rate was 86.9%, and the 3-year progression-free survival rate was 95%.
  • No patients have had to go on to get high-dose therapy and transplant.

“The findings suggest that children, adolescents, and young adults with low-risk relapsed classic Hodgkin lymphoma can be salvaged with low-toxicity chemoimmunotherapy and involved-site radiation and may not require high-dose therapy and transplant for cure.”
– Bradford S. Hoppe, MD of the Mayo Clinic in Jacksonville, Florida


More on Hodgkin Lymphoma (HL)

The Healthcare Communications Network is owned and operated by IQVIA Inc.

Click below to leave this site and continue to IQVIA’s Privacy Choices form