CAR T Cells Highly Successful in ALL

Wayne Kuznar
Published: Monday, Oct 09, 2017

David Maloney, MD, PhD
David Maloney, MD, PhD
Defined composition chimeric antigen receptor (CAR) T cells directed against CD19 have potent anti-tumor activity in B cell malignancies, including acute lymphocytic leukemia (ALL). The experience with CD19 CAR T cells in ALL was addressed by David Maloney, MD, PhD, at the NCCN 12th Annual Congress: Hematologic Malignancies in San Francisco.

“A CAR is essentially using an antibody to redirect the T cell to attack whatever the antigen that the antibody is specific for,” said Maloney, member of the Clinical Research Division, Fred Hutchinson Cancer Research Center in Seattle. “The second-generation CARs is where all the action is.” They are usually directed against CD19, CD20, or CD22 (Maloney focused his talk on CARs directed against CD19). The target is key in the success of these treatments.

“They’re linked to a transmembrane domain of the T cell receptor and have a signaling domain from either CD28 or 4-1BB,” he said. “This greatly improves the recognition and the killing of tumor cells and has led to the explosion of these new therapies.”

His group at Fred Hutchinson has treated >200 patients with relapsed/refractory B-cell malignancies.1 In a preclinical model, the combination of CD8-derived CAR T cells and CD4-derived CAR T cells provided optimal potency. They were able to make CAR T cells in 100% of patients. In the 36 patients with heavily pretreated ALL, the CAR T cell product was manufactured to the target dose for all patients, and 33 of 36 (92%) had products formulated in the defined composition. Outpatient delivery of lymphodepletion and CAR T-cell infusion was possible in 26 of the 36 (72%).

The rate of complete response (CR) was 94% and the molecular CR rate by high resolution flow cytometry was also 94%.“Even in patients with massive extramedullary disease, most of these patients [6 of 7] will achieve a complete remission,” he said.

Two lessons learned from the protocol is that higher doses of CAR T cells of defined composition result in an earlier and higher peak of CAR T cell proliferation in blood and the peak of CAR T cell expansion is greater in patients with higher bone marrow tumor burden.2 Also, adding fludarabine to cyclophosphamide improves CAR T cell persistence, translating into improved rates of disease-free survival (DFS) and overall survival (OS).

Serious toxicity (ie, neurotoxicity and requirement for admission to the intensive care unit) occurs mainly in patients with high tumor burden and robust CAR T cell expansion. “People who get into real trouble could have toxicity very early on,” said Maloney. Levels of interferon-gamma, interleukin-6, ferritin, and C-reactive protein are higher in patients who experience toxicity, but are noted after the fact, he said. A predictive biomarker of serious toxicity that may allow early intervention is serum cytokine level on day 1 after CAR T cell infusion.

“We do risk-adaptive dosing of CAR T cell dosing,” he said. The more marrow blasts you have, the fewer CAR T cells we give. We actually give more T cells to less disease. This has led to a reduced incidence of toxicity.”

The main toxicities are cytokine release syndrome (CRS) and neurotoxicity. CRS responds rapidly to tocilizumab (Actemra) and dexamethasone. “Patients can have fevers of 105 and be hypothermic within hours,” he said. Neurotoxicity presents later (onset often 2 to 4 days after CRS), often manifests as word finding difficulties, and can progress to coma. It may be associated with cerebral edema or seizures. It is generally reversible. Whether treatments aimed at treating CRS can prevent neurotoxicity is not clear.

The Memorial Sloan Kettering Cancer Center experience with CAR T 19-28zeta in patients with adult ALL is similar to that at Fred Hutchinson.3 The CR rate in the 31 patients with >5% marrow blasts was 77% and in those with <5% marrow blasts the CR rate was 95%.

Among the first 50 patients enrolled in the ELIANA phase 2 trial of tisagenlecleucel (Kymriah), in which pediatric patients were studied, the CR/CRi rate was 82% at 3 months after the first infusion.4 Six-month OS was 89% and the 6-month DFS was 60%. There were two deaths in the first 30 days after infusion, one from ALL and one from cerebral hemorrhage. The rate of CRS was 79%, occurring at a median of 3 days. Based on these data, tisagenlecleucel was approved in August 2017 for use in patients up to 25 years old.

Monoclonal antibodies

Maloney also described recent findings with the monoclonal antibodies rituximab (Rituxan), inotuzumab ozogamicin (Besponsa), and blinatumomab (Blincyto).

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