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NCRI关于CHOP联合奥法妥木单抗用于初诊Richter综合征诱导和维持治疗的II期研究。

NCRI phase II study of CHOP in combination with ofatumumab in induction and maintenance in newly diagnosed Richter syndrome.

作者信息

Eyre Toby A, Clifford Ruth, Bloor Adrian, Boyle Lucy, Roberts Corran, Cabes Maite, Collins Graham P, Devereux Stephen, Follows George, Fox Christopher P, Gribben John, Hillmen Peter, Hatton Chris S, Littlewood Tim J, McCarthy Helen, Murray Jim, Pettitt Andrew R, Soilleux Elizabeth, Stamatopoulos Basile, Love Sharon B, Wotherspoon Andrew, Schuh Anna

机构信息

Department of Haematology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.

NIHR BRC Oxford Molecular Diagnostic Centre, Oxford University Hospitals NHS Foundation Trust, John Radcliffe Hospital, Oxford, UK.

出版信息

Br J Haematol. 2016 Oct;175(1):43-54. doi: 10.1111/bjh.14177. Epub 2016 Jul 5.

Abstract

Richter syndrome (RS) is associated with chemotherapy resistance and a poor historical median overall survival (OS) of 8-10 months. We conducted a phase II trial of standard CHOP-21 (cyclophosphamide, doxorubicin, vincristine, prednisolone every 21 d) with ofatumumab induction (Cycle 1: 300 mg day 1, 1000 mg day 8, 1000 mg day 15; Cycles 2-6: 1000 mg day 1) (CHOP-O) followed by 12 months ofatumumab maintenance (1000 mg given 8-weekly for up to six cycles). Forty-three patients were recruited of whom 37 were evaluable. Seventy-three per cent were aged >60 years. Over half of the patients received a fludarabine and cyclophosphamide-based regimen as prior CLL treatment. The overall response rate was 46% (complete response 27%, partial response 19%) at six cycles. The median progression-free survival was 6·2 months (95% confidence interval [CI] 4·9-14·0 months) and median OS was 11·4 months (95% CI 6·4-25·6 months). Treatment-naïve and TP53-intact patients had improved outcomes. Fifteen episodes of neutropenic fever and 46 non-neutropenic infections were observed. There were no treatment-related deaths. Seven patients received platinum-containing salvage at progression, with only one patient obtaining an adequate response to proceed to allogeneic transplantation. CHOP-O with ofatumumab maintenance provides minimal benefit beyond CHOP plus rutuximab. Standard immunochemotherapy for RS remains wholly inadequate for unselected RS. Multinational trials incorporating novel agents are urgently needed.

摘要

里氏综合征(RS)与化疗耐药相关,既往中位总生存期(OS)较差,为8 - 10个月。我们开展了一项II期试验,采用标准的CHOP - 21方案(环磷酰胺、阿霉素、长春新碱、泼尼松龙,每21天一次)联合奥法木单抗诱导治疗(第1周期:第1天300mg,第8天1000mg,第15天1000mg;第2 - 6周期:第1天1000mg)(CHOP - O),随后进行12个月的奥法木单抗维持治疗(每8周1000mg,最多6个周期)。招募了43例患者,其中37例可评估。73%的患者年龄>60岁。超过一半的患者之前接受过基于氟达拉滨和环磷酰胺的方案治疗慢性淋巴细胞白血病(CLL)。6个周期时的总缓解率为46%(完全缓解27%,部分缓解19%)。中位无进展生存期为6.2个月(95%置信区间[CI] 4.9 - 14.0个月),中位OS为11.4个月(95% CI 6.4 - 25.6个月)。初治且TP53基因完整的患者预后较好。观察到15例中性粒细胞减少性发热和46例非中性粒细胞减少性感染。无治疗相关死亡。7例患者在疾病进展时接受了含铂挽救治疗,只有1例患者获得了足够的缓解以进行异基因移植。CHOP - O联合奥法木单抗维持治疗相较于CHOP加利妥昔单抗仅提供了极小的益处。对于未选择的RS患者,标准免疫化疗仍然完全不足。迫切需要纳入新型药物的多国试验。

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