三氧化二砷和α干扰素在复发/难治性成人t细胞白血病/淋巴瘤患者中的II期试验。

Olivier Hermine, Hervé Dombret, Joel Poupon, Bertrand Arnulf, Francois Lefrère, Phillippe Rousselot, Gandhi Damaj, Richard Delarue, Jean Paul Fermand, Jean Claude Brouet, Laurent Degos, Bruno Varet, Hugues de Thé, Ali Bazarbachi
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引用次数: 129

摘要

人类t细胞嗜淋巴病毒1型相关的成人t细胞白血病/淋巴瘤由于其对化疗的内在耐药性而预后非常差。虽然齐多夫定(AZT)和干扰素(IFN)能产生一些反应并改善ATL预后,但需要其他治疗方法。三氧化二砷与干扰素协同作用诱导ATL白血病细胞生长阻滞和凋亡。这些结果促使我们在7例复发/难治性ATL(4例急性和3例淋巴瘤)患者中启动了a /IFN联合治疗的II期试验。4例患者表现出明确的初始反应(1例完全缓解,3例部分缓解)。然而,由于毒性(3例)或后续进展(4例),治疗在中位22天后停止。6名患者最终死于疾病进展(5名患者)或感染(1名患者),但其余患者在32个月时仍然存活且无疾病。药代动力学研究表明,最大砷血浓度(中位数0.46微米)是缓慢达到的(8-15天)。总之,砷/IFN治疗是可行的,并且在预后非常差的ATL患者中显示出抗白血病的效果,尽管有明显的毒性。未来的研究应评估砷治疗的最佳时机:一线使用干扰素/AZT或诱导后维持。
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Phase II trial of arsenic trioxide and alpha interferon in patients with relapsed/refractory adult T-cell leukemia/lymphoma.

Human T-cell lymphotropic virus type 1 associated adult T-cell leukemia/lymphoma carries a very poor prognosis due to its intrinsic resistance to chemotherapy. Although zidovudine (AZT) and alpha-interferon (IFN) yield some responses and improve ATL prognosis, alternative therapies are needed. Arsenic trioxide (As) dramatically synergizes with IFN to induce growth arrest and apoptosis of ATL leukemia cells in vitro. These results prompted us to initiate a phase II trial of As/IFN combination in seven patients with relapsed/refractory ATL (four acute and three lymphoma). Four patients exhibited a clear initial response (one complete remission and three partial remissions). Yet, the treatment was discontinued after a median of 22 days because of toxicity (three patients) or subsequent progression (four patients). Six patients eventually died from progressive disease (five patients) or infection (one patient), but the remaining patient is still alive and disease free at 32 months. Pharmacokinetic studies showed that maximum arsenic blood levels (median 0.46 microM) were slowly achieved (8-15 days). In conclusion, arsenic/IFN treatment is feasible and exhibits an anti-leukemia effect in very poor prognosis ATL patients despite a significant toxicity. Future studies should assess the best timing for arsenic therapy: frontline with IFN/AZT or as maintenance after induction.

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