Ibrutinib


Ibrutinib, sold under the brand name Imbruvica among others, is a small molecule drug that binds permanently to a protein, Bruton's tyrosine kinase, that is important in B cells. It is used to treat B cell cancers like mantle cell lymphoma, chronic lymphocytic leukemia, and Waldenström's macroglobulinemia.

Medical uses

Ibrutinib is used to treat chronic lymphocytic leukemia, Waldenström's macroglobulinemia, and as a second-line treatment for mantle cell lymphoma, marginal zone lymphoma, and chronic graft vs host disease.
In the United States ibrutinib is indicated for the treatment of adults with mantle cell lymphoma who have received at least one prior therapy, adults with chronic lymphocytic leukemia /small lymphocytic lymphoma with or without 17p deletion, adults with Waldenström's macroglobulinemia, adults with marginal zone lymphoma who require systemic therapy and have received at least one prior anti-CD20-based therapy, adults with chronic graft versus host disease after failure of one or more lines of systemic therapy.
It is a first line treatment in those with CLL who require treatment and are newly diagnosed. It may also be used in CLL that relapses.

Resistance

Both primary and secondary resistance has been reported in various lymphomas, including CLL and MCL. Resistance may arise due to mutations that impair the affinity of ibrutinib for BTK, or due to alterations in pathways downstream of BTK and may confer BCR signaling independence in resistant clones.

Adverse effects

Very common adverse effects include pneumonia, upper respiratory tract infection, sinusitis, skin infection, low neutrophil count, low platelet counts, headache, bleeding, bruising, diarrhea, vomiting, inflammation of mouth and lips, nausea, constipation, rash, joint pain, muscle spasms, musculoskeletal pain, fever, and edema.
Common adverse effects include sepsis, urinary tract infection, non-melanoma skin cancer, low leukocyte count, low lymphocyte count, interstitial lung disease, tumor lysis syndrome, high uric acid levels, dizziness, blurred vision, atrial fibrillation, subdural hematoma, nosebleeds, small bruises from broken blood vessels, high blood pressure, hives, and skin redness or blushing.

Pharmacology

Ibrutinib oral bioavailability is 3.9% in a fasting state, 8.4% in a fed state, and 15.9% after consumption of grapefruit juice.

Mechanism

Ibrutinib has been reported to reduce chronic lymphocytic leukemia cell chemotaxis towards the chemokines CXCL12 and CXCL13, and inhibit cellular adhesion following stimulation at the B-cell receptor. Additionally, ibrutinib down-modulates the expression of CD20 by targeting the CXCR4/SDF1 axis.
Together, these data are consistent with a mechanistic model whereby ibrutinib blocks BCR signaling, which drives cells into apoptosis and/or disrupts cell migration and adherence to protective tumour microenvironments.
In preclinical studies on chronic lymphocytic leukemia cells, ibrutinib has been reported to promote apoptosis, inhibit proliferation, and also prevent CLL cells from responding to survival stimuli provided by the microenvironment. This also leads to a reduction of MCL1 levels in malignant B cells. Treatment of activated CLL cells with ibrutinib resulted in inhibition of BTK tyrosine phosphorylation and also effectively abrogated downstream survival pathways activated by this kinase including ERK1/2, PI3K, and NF-κB. Additionally, ibrutinib inhibited proliferation of CLL cells in vitro, effectively blocking survival signals provided externally to CLL cells from the microenvironment including soluble factors, fibronectin engagement and stromal cell contact.
In early clinical studies, the activity of ibrutinib has been described to include a rapid reduction in lymphadenopathy accompanied by a transient lymphocytosis, suggesting that the drug might have direct effects on cell homing or migration to factors in tissue microenvironments.

History

Ibrutinib was created by scientists at Celera Genomics as a tool compound for studying BTK function; it covalently binds its target which is ideal for a reagent but generally not considered ideal for drugs.
In 2006, in the course of acquiring an HDAC-focused program from Celera after its own initial discovery program had failed, Pharmacyclics also picked up Celera's small molecule BTK inhibitor discovery program for $2M in cash and $1M in stock and named the tool compound PCI-32765. In 2011 after the drug had completed Phase II trials, Johnson & Johnson and Pharmacyclics agreed to co-develop the drug, and J&J paid Pharmacyclics $150 million upfront and $825 million in milestones. Pharmacyclics was acquired by AbbVie in May 2015, and Abbvie projected global sales of US$1 billion in 2016 and $5 billion in 2020.
It was approved by the US Food and Drug Administration on November 13, 2013, for the treatment of mantle cell lymphoma. On February 12, 2014, the FDA expanded the approved use of ibrutinib to chronic lymphocytic leukemia. It was approved for Waldenström's macroglobulinemia in 2015.
In March 2015, Pharmacyclics and AbbVie agreed that Abbvie would acquire Pharmacyclics for $21 billion; the deal was completed that May.
In March 2016, a new indication for ibrutinib was approved in the United States for patients with chronic lymphocytic leukemia.
In May 2016, a new indication for ibrutinib was approved in the United States for chronic lymphocytic leukemia and small lymphocytic lymphoma.
In January 2017, a new indication for ibrutinib was approved in the United States for the treatment of adults with relapsed/refractory marginal zone lymphoma who require systemic therapy and have received at least one prior anti-CD20-based therapy.
In August 2017, the FDA approved a new indication for ibrutinib to treat graft-versus-host disease. It was the first drug approved by the FDA for this condition.
In February 2018, a tablet formulation of ibrutinib was approved for use in the United States.
In August 2018, ibrutinib in combination with rituximab was approved in the United States for the treatment of adults with Waldenström's macroglobulinemia, a rare and incurable type of non-Hodgkin's lymphoma.
In January 2019, ibrutinib in combination with obinutuzumab was approved for the treatment of adults with previously untreated chronic lymphocytic leukemia/small lymphocytic lymphoma.
In April 2020, the FDA expanded the indication of ibrutinib to include its combination with rituximab for the initial treatment of adults with chronic lymphocytic leukemia or small lymphocytic lymphoma. Approval was based on the E1912 trial, a 2:1 randomized, multicenter, open-label, actively controlled trial of ibrutinib with rituximab compared to fludarabine, cyclophosphamide, and rituximab in 529 adult subjects 70 years or younger with previously untreated CLL or SLL requiring systemic therapy.

Cost

The typical cost of ibrutinib in the United States is about $148,000 a year. Preliminary PK/PD focused research found that people could potentially be put on lower and less expensive regimen of ibrutinib without losing efficiency; however, no data showing efficiency of lower doses has been published.
Janssen Pharmaceutica and Pharmacyclics introduced a new single dose tablet formulation with a flat pricing structure in the first half of 2018 and discontinue the capsule formulation. This caused an outcry as it was perceived to triple in the cost of the drug to the average patient. Patients receiving the FDA approved and recommended doses would have seen either no price change or a price decrease with the tablet pricing structure.
Janssen Pharmaceutica and Pharmacyclics have since reversed the decision to discontinue the capsule formulation with the drug currently available in both capsule and tablet forms.
Ibrutinib was added to the Australian Pharmaceutical Benefits Scheme in 2018.
Generic ibrutinib was added to the Indian Pharmaceutical Benefits Scheme in 2020.

Brand names

In Bangladesh it is available under the brandname Ibrutix by Beacon Pharmaceuticals.