Conference Coverage

Some MCL patients can safely stop venetoclax-ibrutinib, study suggests


 

REPORTING FROM ASH 2019

Treatment status

Five patients are still receiving treatment with ibrutinib and venetoclax, and one patient is receiving only venetoclax. One patient went off study treatment due to a diagnosis of myelodysplastic syndrome, but that patient’s MCL is still in CR.

Five patients were able to stop treatment after achieving MRD-negative CR and were placed under “stringent surveillance,” Dr. Handunnetti said.

One of the five patients who stopped treatment progressed at 7 months and died. The remaining four patients are still alive and in CR at 6 months, 13 months, 17 months, and 18 months off treatment.

Safety update

Within the first 56 weeks of treatment, 15 patients required dose adjustments. Twelve patients required an adjustment to ibrutinib, seven to venetoclax, and four to both drugs. After 56 weeks, there were no dose adjustments.

Two patients developed therapy-related myelodysplastic syndrome. One patient had previously received FCR (fludarabine, cyclophosphamide, and rituximab) and BR (bendamustine and rituximab). The other patient had received R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone).

This investigator-initiated trial was funded by Janssen and Abbvie. Dr. Handunnetti reported relationships with Abbvie and Gilead.

SOURCE: Handunnetti S et al. ASH 2019. Abstract 756.

Pages

Recommended Reading

Staging PET/CT better defines extent of mantle cell lymphoma
MDedge Hematology and Oncology
Follow-up shows favorable results with acalabrutinib in MCL
MDedge Hematology and Oncology
ASCO to award $50,000 young investigator grant to study MCL
MDedge Hematology and Oncology
Survival ‘excellent’ after rituximab-bendamustine induction in transplant-eligible MCL
MDedge Hematology and Oncology
FDA approves Brukinsa for relapsed, refractory MCL
MDedge Hematology and Oncology
Acalabrutinib may outperform other targeted therapies in MCL
MDedge Hematology and Oncology
SOX11 shows value as diagnostic marker in MCL
MDedge Hematology and Oncology
The clinical impact of new approvals in sickle cell, MCL
MDedge Hematology and Oncology
Orelabrutinib could be ‘preferred’ BTK inhibitor for MCL
MDedge Hematology and Oncology
KTE-X19 produces highest response rate in MCL subgroup
MDedge Hematology and Oncology