Pralatrexate, a novel class of antifol with high affinity for the reduced folate carrier-type 1, produces marked complete and durable remissions in a diversity of chemotherapy refractory cases of T-cell lymphoma

Br J Haematol. 2007 Nov;139(3):425-8. doi: 10.1111/j.1365-2141.2007.06658.x.

Abstract

T-cell lymphomas (TCLs) are characterised by poor responses to therapy with brief durations of remissions. An early phase study of pralatrexate has demonstrated dramatic activity in patients with relapsed/refractory disease. Of the first 20 lymphoma patients treated, 16 had B-cell lymphoma and four had refractory aggressive TCL. All four patients with TCL achieved a complete remission. Patients with B-cell lymphoma achieved stable disease at best. For each TCL patient, the response was more durable than their best response with chemotherapy. This early experience is the first to document this unique activity of pralatrexate in TCL.

Publication types

  • Clinical Trial, Phase I
  • Clinical Trial, Phase II

MeSH terms

  • Adult
  • Aged
  • Aminopterin / analogs & derivatives*
  • Aminopterin / metabolism
  • Aminopterin / therapeutic use
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / therapeutic use*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Female
  • Folic Acid Antagonists / metabolism
  • Folic Acid Antagonists / therapeutic use*
  • Humans
  • Lymphoma, B-Cell / drug therapy
  • Lymphoma, T-Cell / diagnostic imaging
  • Lymphoma, T-Cell / drug therapy*
  • Male
  • Membrane Transport Proteins / metabolism
  • Middle Aged
  • Positron-Emission Tomography
  • Treatment Failure
  • Treatment Outcome

Substances

  • 10-propargyl-10-deazaaminopterin
  • Antineoplastic Agents
  • Folic Acid Antagonists
  • Membrane Transport Proteins
  • SLC19A2 protein, human
  • Aminopterin