ASH Clinical News ACN_4.1_FULL_ISSUE_DIGITAL | Page 54

On Location ASH Annual Meeting Continued from page 47 stable disease (SD; n=25); at the first tumor assessment (1 month post-infusion), 23 patients with either PR or SD subsequently achieved CR up to 15 months, without ad- ditional therapy. The median time to conversion from PR to CR was 64 days (range = 49-424 days). Median duration of CR had not been reached by data cutoff, with three of seven patients (43%) in ongoing CR at 24 months. Median progression-free survival was 5.8 months (range = 3.3 months – not reached), while the median overall survival (OS) was not reached (range = 12.0 months – not reached). “Patients who are in remission at six months tend to stay in remission,” Dr. Neelapu said, adding that, while the median OS was not reached, “there is a plateauing of the OS curve at the 16-month timepoint.” The investigators also reviewed baseline and post- progression biopsies for 12 evaluable patients, shedding some light on why certain patients’ disease fails to respond to treatment. About one-third of patients experienced CD19 antigen loss at the time of disease progression, and 80 percent of patients evaluable for PD-L1 at the time of disease progression had PD-L1–positive disease (see TABLE 3 ). “Loss of CD19 and gain of PD-L1 expression in tumors are identified as possible mechanisms of resistance following axicabtagene ciloleucel treatment,” the authors noted. The safety profile was consistent with previously reported studies of axicabtagene ciloleucel, Dr. Neelapu added. In earlier analysis of ZUMA-1, four patients died within two months after CAR T-cell infusion, two of which were deemed related to study treatment and two attributable to unrelated adverse events (AEs). In this longer-term follow-up, no new treatment- related deaths were observed. Nearly all patients experienced at least one grade ≥3 T:7” POMALYST ® (pomalidomide) capsules, for oral use 2.2 Dose Adjustments for Toxicities The following is a Brief Summary; refer to full Prescribing Information for complete product information. Table 1: Dose Modification Instructions for POMALYST for Hematologic Toxicities WARNING: EMBRYO-FETAL TOXICITY and VENOUS AND ARTERIAL THROMBOEMBOLISM Embryo-Fetal Toxicity • POMALYST is contraindicated in pregnancy. POMALYST is a thalidomide analogue. Thalidomide is a known human teratogen that causes severe birth defects or embryo-fetal death. In females of reproductive potential, obtain 2 negative pregnancy tests before starting POMALYST treatment. • Females of reproductive potential must use 2 forms of contraception or continuously abstain from heterosexual sex during and for 4 weeks after stopping POMALYST treatment [see Contraindications (4), Warnings and Precautions (5.1), and Use in Specific Populations (8.1, 8.3)]. POMALYST is only available through a restricted distribution program called POMALYST REMS [see Warnings and Precautions (5.2)]. Venous and Arterial Thromboembolism • Deep venous thrombosis (DVT), pulmonary embolism (PE), myocardial infarction, and stroke occur in patients with multiple myeloma treated with POMALYST. Prophylactic antithrombotic measures were employed in clinical trials. Thromboprophylaxis is recommended, and the choice of regimen should be based on assessment of the patient’s underlying risk factors [see Warnings and Precautions (5.3)]. 2 DOSAGE AND ADMINISTRATION 2.1 Multiple Myeloma Females of reproductive potential must have negative pregnancy testing and use contraception methods before initiating POMALYST [see Warnings and Precautions (5.1) and Use in Specific Populations (8.3)]. The recommended starting dose of POMALYST is 4 mg once daily orally on Days 1-21 of repeated 28-day cycles until disease progression. POMALYST should be given in combination with dexamethasone. POMALYST may be taken with water. Inform patients not to break, chew, or open the capsules. POMALYST may be taken with or without food. Dose Modification • Interrupt POMALYST treatment, follow CBC weekly • Resume POMALYST treatment at 3 mg daily • For each subsequent • Interrupt POMALYST drop <500 per mcL treatment • Return to more than or • Resume POMALYST equal to 500 per mcL treatment at 1 mg less than the previous dose Thrombocytopenia • Platelets <25,000 per mcL • Platelets return to >50,000 per mcL • Interrupt POMALYST treatment, follow CBC weekly • Resume POMALYST treatment at 3 mg daily • For each subsequent • Interrupt POMALYST drop <25,000 per mcL treatment • Resume POMALYST • Return to more than or equal to 50,000 per treatment at 1 mg less than previous dose mcL ANC, absolute neutrophil count To initiate a new cycle of POMALYST, the neutrophil count must be at least 500 per mcL and the platelet count must be at least 50,000 per mcL. If toxicities occur after dose reductions to 1 mg, then discontinue POMALYST. Permanently discontinue POMALYST for