Table I.
Bortezomib was administered after obatoclax.
If dose-limiting toxicity (DLT) was attributable to myelosuppression and peripheral neuropathy, the dose level was repeated with bortezomib dose reduced to 1.0 mg/m2. Dose escalation of obatoclax was permitted to continue if DLT did not recur at the reduced bortezomib dose. A second dose reduction of bortezomib to 0.75 mg/m2 was permitted if peripheral neuropathy persisted after initial dose reduction.