High Response Rate Seen With Concurrent Ibrutinib Plus CAR T-Cell Therapy in High-Risk CLL

Jordan Gauthier, MD, MSc

Jordan Gauthier, MD, MSc

Significant activity was observed when ibrutinib (Imbruvica) was administered concurrently with CD19-directed CAR T-cell therapy compared with separately in patients with high-risk relapsed/refractory chronic lymphocytic leukemia (CLL) who had progressed on or were intolerant of ibrutinib. Data presented at the 15th International Conference on Malignant Lymphoma show a high response rate with this concurrent treatment. 

Results showed that high rates of response by 2018 International Workshop Group CLL criteria were seen in 18 evaluable patients at 4 weeks after CD19-targeted CAR T-cell therapy and concurrent ibrutinib. The objective response rate (ORR) was 83%, which included 4 (22%) complete responses in the marrow (CRi) and 11 (61%) partial responses (PR). In patients who did not receive concurrent ibrutinib, the ORR was 65%.

No patients had stable disease and 3 (17%) patients had disease progression. Regarding the marrow response, no detectable disease was detected by flow cytometry in 13 (72%) patients or by IGH sequencing in 11 (61%) patients.

Lead study author Jordan S. Gauthier MD, MSc, a senior fellow in the Clinical Research Division at Fred Hutchinson Cancer Research Center, discussed the unmet need for treatments in patients with high-risk CLL due to a complex karyotype (CKT) or ibrutinib failure; this subgroup demonstrates decreased survival.

"We previously reported that CD19 CAR T cells could lead to durable responses in relapsed/refractory CLL in patients who had previously failed ibrutinib therapy," he explained. "However, preclinical studies showed that ibrutinib might improve CAR T-cell antitumor efficacy and reduce cytokine release syndrome (CRS)."

Therefore, Gauthier and colleagues explored the safety and efficacy of CD19-directed CAR T cells with concurrent ibrutinib administration in a pilot cohort of a phase I/II trial (NCT01865617). The cohort comprised 19 patients with high-risk relapsed/refractory CLL. The patients were required to be beyond first remission and to have received or been ineligible for chemoimmunotherapy containing a purine analogue and a CD20-targeted antibody, plus no response to or progression on ibrutinib.

Among the baseline demographics, Gauthier highlighted that 89% of patients had high-risk cytogenetics, including del(17p) in 74%, and a CKT in 74% of patients. The median number of prior therapies was 5 (range, 1-10), which included venetoclax (Venclexta) in 58% and idelalisib (Zydelig) in 21% of patients, and 10% had shown ibrutinib intolerance. Overall, the median age was 65 years (range, 40-71), 63% of patients were male, and all patients had an ECOG performance status of 0 or 1. All patients had failed treatment with ibrutinib prior to study entry.

In the concurrent ibrutinib cohort, patients received concurrent administration of ibrutinib at 420 mg daily at least 2 weeks before leukapheresis and continuously though leukapheresis and lymphodepletion, as well as with infusion of a defined composition of 2 x 105 or 2 x 106/kg CD4+ and CD8+ CD19-directed CAR T cells subsequent to lymphodepletion chemotherapy. Ibrutinib was continued for 3 months after CAR T-cell infusion.

Most patients (68%) in this cohort tolerated ibrutinib and continued with treatment as planned. However, 7 patients discontinued ibrutinib or required dose reductions due to disease progression, thrombocytopenia, intravascular coagulation during CRS, or microembolic stroke, which each occurred in one patient, and CAR T-cell—related toxicity in 2 patients. One patient died 4 days after infusion.

At a median follow-up of 12 months (range 4-17), durable responses were observed in the patients showing response by day 28; the 1-year OS rate was 72% (P= .002) and 1-year PFS rate was 46% (P<.001). In patients achieving minimal residual disease (MRD) by IgH sequencing on day 28, the 1-year OS and PFS rates were 86% (P= .02) and 59%(P= .02), respectively.

The study also contained a cohort of 24 patients with high-risk relapsed/refractory CLL and detectable disease after initial ibrutinib treatment who received an infusion of up to 2 x 106 CAR T cells but no ibrutinib. A retrospective comparison of the 2 cohorts indicated that the rates of any grade CRS (74% vs 92%) severe CRS (0% vs 25%), and grade &ge;3 cytotoxicity (26% vs 29%) favored the concurrent ibrutinib cohort over the no-ibrutinib arm.

"All grade 1 through 4 CRS and neurotoxicity events were reversible," he said.

One patient in each cohort died; in the concurrent ibrutinib arm, the death occurred on day 4 in a patient with cardiac history and grade 2 CRS on the day of death. In the no-ibrutinib arm, the death was due to CRS and neurotoxicity on day 11.

"Close cardiac monitoring using telemetry might be considered in patients developing CRS due to the potential risk of cardiac arrhythmia," he advised. "Despite robust CAR T-cell expansion the levels of cytokines associated with severe CRS were lower in the concurrent ibrutinib cohort."

For the comparison between the concurrent and no ibrutinib arms and MCP-1 (P= .0176), soluble IL-2 receptor alpha (P= .001), and IL-6 (P= .27).

Further comparison of the concurrent and no ibrutinib cohorts showed high rates of response at 4 weeks post CAR T-cell infusion (83% vs 65%), marrow response by flow cytometry (72% vs 74%), marrow response by IGH sequencing (85% vs 50%), nodal CR/PR (71% vs 64%), and PET CR/PR by Lugano criteria (80% vs 69%), respectively.

"CD19 CAR T cells with concurrent ibrutinib leads to high response rates without severe CRS in ibrutinib-refractory CLL," commented Gauthier. "Concurrent administration of ibrutinib is feasible in most patients, and provides high rates of MRD-negative responses."

The therapy is now being prospectively explored in the phase I/II TRANSCEND-CLL 17004 trial (NCT03331198).

Reference:

Gauthier J. Durable responses after CD19-targeted CAR-T cell immunotherapy with concurrent ibrutinib for CLL after prior ibrutinib failure. Presented at: 15th International Conference on Malignant Lymphoma; June 18-22, 2019; Lugano, Switzerland. Abstract 120.