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Efficacy and safety of subcutaneous mosunetuzumab plus polatuzumab vedotin in patients with relapsed/refractory large B-cell lymphoma: Japan subgroup analysis of the phase III SUNMO trial

Oncologia
Imagem de arquivo, ilustrativa — não é do estudo. Células em divisão (mitose), em microscopia de fluorescência. ZEISS Microscopy · CC BY 2.0 · Wikimedia Commons

Ensaio clínico randomizadoNível 2 · Nova evidênciaInternational journal of clinical oncology15 jun 20260 citações

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Resumo original em inglês

O que aconteceu

Novel, accessible treatment options, are needed for patients with relapsed/refractory (R/R) large B-cell lymphoma (LBCL). Mosunetuzumab, a T-cell-engaging bispecific antibody, plus polatuzumab vedotin, an antibody-drug conjugate, (Mosun-Pola), represents a novel fixed-duration outpatient therapy. The phase III SUNMO study (NCT05171647) demonstrated superior efficacy of Mosun-Pola versus rituximab plus gemcitabine-oxaliplatin (R-GemOx) in patients with R/R LBCL, with a manageable safety profile. We report outcomes of a Japan subgroup analysis of the SUNMO study.

Patients were randomized 2:1 to receive Mosun-Pola or R-GemOx. Dual primary endpoints were centrally assessed overall response rate and progression-free survival (PFS).

ClinicalTrials.gov, NCT05171647.

O que encontraram

At data cutoff (February 17, 2025), of 208 patients randomized (Mosun-Pola, n = 138; R-GemOx, n = 70), 16 were enrolled from Japan (Mosun-Pola, n = 9; R-GemOx, n = 7). All patients receiving Mosun-Pola achieved a response (100% [n = 9]) versus 57.1% (n = 4/7) for those receiving R-GemOx. PFS was significantly prolonged with Mosun-Pola; median PFS of 16.2 months versus 3.8 months with R-GemOx (hazard ratio: 0.42; 95% confidence interval: 0.07-2.63). In the safety-evaluable population (Mosun-Pola, n = 9; R-GemOx, n = 7), overall incidence of adverse events was similar between the Japan subgroup and the overall population across both treatment arms. Cytokine release syndrome occurred in 5 patients who received Mosun-Pola; all events were grade 1, and all resolved. No incidence of immune effector cell-associated neurotoxicity syndrome was reported.

Por que isso importa

Mosun-Pola demonstrated promising efficacy and manageable safety in patients with R/R LBCL enrolled from Japan, which was comparable with the overall population, supporting Mosun-Pola as a potential new treatment option in this patient population.

Resumo publicado sob licença CC BY. A tradução para o português ainda não chegou a este estudo.

O estudo original

Efficacy and safety of subcutaneous mosunetuzumab plus polatuzumab vedotin in patients with relapsed/refractory large B-cell lymphoma: Japan subgroup analysis of the phase III SUNMO trial

Dai Maruyama, Hideki Goto, Takahiro Kumode, Keiko Aizawa, Noriko Fukuhara, Jason R Westin, Won Seog Kim, Chiemi Mori, Tatsuki Imaizumi, Koji Kato

Descritores MeSH

  • Neoplasm Recurrence, Local
  • Antibodies, Monoclonal
  • Lymphoma, Large B-Cell, Diffuse
  • Antibodies, Bispecific
  • Immunoconjugates
  • Antineoplastic Combined Chemotherapy Protocols
  • Female
  • Humans
  • Japan
  • Male

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