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Axicabtagene Ciloleucel in Combination with Atezolizumab in Patients with Refractory Diffuse Large B-Cell Lymphoma: The Phase 1/2 ZUMA-6 Trial.

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Clinical cancer research : an official journal of the American Association for Cancer Research 📖 저널 OA 53.1% 2022: 3/4 OA 2023: 6/8 OA 2024: 8/14 OA 2025: 57/92 OA 2026: 78/165 OA 2022~2026 2026 Vol.32(5) p. 894-904
Retraction 확인
출처

PICO 자동 추출 (휴리스틱, conf 3/4)

유사 논문
P · Population 대상 환자/모집단
34 patients received axi-cel plus atezolizumab in ZUMA-6.
I · Intervention 중재 / 시술
a single axi-cel infusion (2 × 106 cells/kg), followed by atezolizumab 1,200 mg i
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Safety and efficacy of this combination were consistent with axi-cel monotherapy. Correlative analyses could inform with regard to which patients with LBCL may benefit from axi-cel and immune checkpoint inhibitor combinations.

Jacobson CA, Westin JR, Miklos DB, Herrera AF, Ritz J, Rodig S, Arihara Y, Cao S, Sun J, Mao D, Adhikary S, Neumann F, Grechko N, Locke FL

📝 환자 설명용 한 줄

[PURPOSE] Chimeric antigen receptor (CAR) T-cell therapies have improved outcomes in patients with relapsed/refractory large B-cell lymphoma (LBCL).

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↓ .bib ↓ .ris
APA Jacobson CA, Westin JR, et al. (2026). Axicabtagene Ciloleucel in Combination with Atezolizumab in Patients with Refractory Diffuse Large B-Cell Lymphoma: The Phase 1/2 ZUMA-6 Trial.. Clinical cancer research : an official journal of the American Association for Cancer Research, 32(5), 894-904. https://doi.org/10.1158/1078-0432.CCR-25-0602
MLA Jacobson CA, et al.. "Axicabtagene Ciloleucel in Combination with Atezolizumab in Patients with Refractory Diffuse Large B-Cell Lymphoma: The Phase 1/2 ZUMA-6 Trial.." Clinical cancer research : an official journal of the American Association for Cancer Research, vol. 32, no. 5, 2026, pp. 894-904.
PMID 41231109 ↗

Abstract

[PURPOSE] Chimeric antigen receptor (CAR) T-cell therapies have improved outcomes in patients with relapsed/refractory large B-cell lymphoma (LBCL). However, up to two thirds of these patients do not maintain long-term responses. The phase 1/2 ZUMA-6 study investigated the feasibility of combining the CD19-directed CAR T-cell therapy axicabtagene ciloleucel (axi-cel) with the PD-L1 inhibitor atezolizumab as a potential approach to increase treatment efficacy while maintaining acceptable safety.

[PATIENTS AND METHODS] Patients with refractory diffuse LBCL received a single axi-cel infusion (2 × 106 cells/kg), followed by atezolizumab 1,200 mg i.v. every 21 days for four cycles. Primary endpoints were dose-limiting toxicities (phase 1) and complete response rate (phase 2). Other efficacy and safety outcomes and pharmacokinetics/pharmacodynamics were assessed.

[RESULTS] Overall, 34 patients received axi-cel plus atezolizumab in ZUMA-6. The median follow-up for the final analysis was 56.9 months. In phase 1, one patient experienced dose-limiting toxicities (grade 4 neutropenia and thrombocytopenia). Thirty patients (88%) experienced grade ≥3 treatment-emergent adverse events. Three (9%) and 11 (32%) patients experienced grade ≥3 cytokine release syndrome and neurologic events, respectively. In the final analysis, 15 patients (54%) had a complete response. The median progression-free survival and overall survival were 9 and 32.2 months, respectively. Peak CAR T-cell and cytokine profiles were comparable with those previously reported for axi-cel monotherapy (ZUMA-1).

[CONCLUSIONS] Axi-cel plus atezolizumab had a manageable safety profile, with no new safety signals. Safety and efficacy of this combination were consistent with axi-cel monotherapy. Correlative analyses could inform with regard to which patients with LBCL may benefit from axi-cel and immune checkpoint inhibitor combinations.

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