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May 31, 2026Medicine1 citationsOpen Access

Romiplostim-N01 for cancer therapy-induced thrombocytopenia: A propensity score-matched cohort study

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TYTing YuZXZhiman XiongYSYongfeng Su

Key Points

  • This research aims to assess the effectiveness of romiplostim-N01 compared to standard therapies for cancer therapy-induced thrombocytopenia (CTIT).
  • Retrospective cohort study with 92 matched patients having grade ≥2 CTIT.
  • Comparison of treatment-marked responders and platelet count elevation between romiplostim-N01 and rhIL-11/rhTPO groups.
  • Utilization of propensity score matching and multivariate logistic regression for treatment effect estimation.
  • The 7-day marked response rate for romiplostim-N01 was 58.7%, while for rhIL-11/rhTPO it was 28.3%, P < .05.
  • 14-day overall response rates were both 89.1%, P > .05, showing no significant difference.
  • Chemotherapy delays were shorter in the romiplostim-N01 group (5.5 days versus 9.5 days, P < .001).

Abstract

Cancer therapy-induced thrombocytopenia (CTIT) is a common complication in patients with solid tumors during their cancer treatment. The sole therapeutic agents approved for this indication are recombinant human interleukin-11 (rhIL-11) or recombinant human thrombopoietin (rhTPO). Romiplostim-N01 is a novel thrombopoietic agent launched in China in 2024, which has demonstrated preliminary therapeutic efficacy in the management of CTIT. This retrospective study compared romiplostim-N01 with rhIL-11 or rhTPO for CTIT management. Ninety-two matched consecutive patients with grade ≥2 CTIT (platelet PLT count .05). The median duration of chemotherapy delay was significantly shorter in the romiplostim-N01 group compared with the rhIL-11/rhTPO group (5.5 vs 9.5 days, P < .001). Multivariate regression analysis confirmed that romiplostim-N01 was independently associated with an elevation in PLT count. These findings position romiplostim-N01 as a favorable alternative to rhIL-11 or rhTPO in CTIT, given its enhanced early PLT response and reduced risk of chemotherapy disruption.

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Cite This Study

Yu et al. (2026) studied this question.

synapsesocial.com/papers/6a1bd1745783ba022b6fd0bchttps://doi.org/10.1097/md.0000000000048855
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