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The 3-year follow-up results from the phase III TRANSFORM trial (NCT03575351) were presented at the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting by Kamdar.1 This trial investigated lisocabtagene maraleucel (liso-cel) vs standard of care (SOC) with salvage chemotherapy followed by autologous stem cell transplantation (auto-SCT) as second-line treatment for patients with relapsed or refractory (R/R) large B-cell lymphoma (LBCL) (N = 184).1
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Key learnings: |
After a median follow-up of 33.9 months, median event-free survival (EFS) was longer in the liso-cel arm vs SOC arm (29.5 months vs 2.4 months), and the 36-month EFS rate was higher in patients treated with liso-cel vs SOC (45.8% vs 19.1%). |
The best overall response rate was higher following treatment with liso-cel vs SOC (87% vs 49%), with complete response rates of 74% vs 43%. |
Median progression-free survival (PFS) was not reached in the liso-cel arm and was 6.2 months in the SOC arm, and the 36-month PFS rate was higher with liso-cel vs SOC (50.9% vs 26.5%). |
Median overall survival (OS) was not reached in either arm, and the 36-month OS rate was higher with liso-cel vs SOC (62.8% vs 51.8%). |
Median duration of response (DoR) was not reached in the liso-cel arm and was 9.1 months in the SOC arm, and the 24-month DoR rate was higher following liso-cel treatment vs SOC (60.5% vs 43.5%). |
Grade 1–3 cytokine release syndrome and neurological events were low in the liso-cel arm, with no Grade 4–5 events, and patients needed minimal use of tocilizumab and steroids to manage these, with no prophylactic use. |
The 3-year follow-up data from the TRANSFORM trial demonstrate the sustained efficacy of liso-cel vs SOC and further support the use of liso-cel as a second-line treatment for patients with primary refractory or early relapsed LBCL. |
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