Abstract
Background
ITP is an autoimmune disorder characterized by isolated thrombocytopenia in the absence of other causes. Although the pathogenetic mechanisms may vary between cases, in common is the accelerated peripheral destruction of platelets due to a failure of self-tolerance and a complex interplay between autoantibodies, autoreactive T cells, antigen-presenting cells and the reticuloendothelial system. Conventional therapies such as glucocorticoids and rituximab target only one or some of these players in autoimmunity.
Aims
To demonstrate the safety and efficacy of a triple therapy approach to targeting all three major agents for autoimmunity in ITP: B-cells, T-cells and antigen-presenting cells. Simultaneous suppression of these three cell lines may benefit responders with prolonged relapse free survival without the burden of significant additional toxicity.
Methods
A total of 26 patients with ITP were enrolled into two separate sites with three separate triple therapy protocols (TT4, R1 and R2). Eligibility criteria, definitions and toxicity are as per IWG criteria and CTCAE 4.02.
Results
25/26 patients completed treatment as planned. Three required salvage glucocorticoids/IVIG during the first four weeks of therapy. One patient additionally required splenectomy and completed triple therapy.
There was only one therapy-related Grade III-IV ASE in all of the treatment protocols: hypertension in a patient with a prior history. All therapy-related Grade I-II ASE listed with numbers of patients affected: hirsuitism and dyspepsia 4; headache, insomnia, nausea and tremor 2; hypertension, blurred vision, diarrhea, peripheral oedema, myalgia, parasthesiae, gum hypertrophy, cramps, chills and mood swings 1.
There were no therapy-related SAE although five patients required hospital admission: three during treatment phase (social 1, bleeding due to thrombocytopenia 2) and two over 12 months following therapy (atrial fibrillation with prior history and acute renal failure due to non-steroidal anti-inflammatory drugs). One male patient aged 85 was diagnosed with prostate cancer 18 months following treatment with TT4 and has been successfully treated. Other therapy-unrelated AE included renal colic, gum bleeding, easy bruising, back pain and menorrhagia.
Conclusions
We report on the efficacy, safety and tolerability of a triple therapy approach to treating adult ITP. Notwithstanding the bias of non-random patient selection, we targeted B-cells, T-cells and antigen-presenting cells without the introduction of serious adverse events over the median follow-up period of 15.8 months across all arms. Overall, the 6 month response rate of 75% appears to be maintained beyond 12 months. Ongoing studies are required to confirm the safety of triple therapy approach to ITP. Although the median 7 days time to response seen in triple therapy compares favourably with other regimens, three patients required salvage therapy while awaiting their final doses of rituximab highlighting the need to further optimise sequential dosing strategies in future studies.
Disclosures:
No relevant conflicts of interest to declare.
Abortive Proliferation of Rare T Cells Induced by Direct or Indirect Antigen Presentation by Rare B Cells In Vivo
