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多中心 II 期研究:序贯 Brentuximab Vedotin 与多柔比星、长春碱和达卡巴嗪化疗治疗未经治疗的老年经典型霍奇金淋巴瘤患者。

Multicenter Phase II Study of Sequential Brentuximab Vedotin and Doxorubicin, Vinblastine, and Dacarbazine Chemotherapy for Older Patients With Untreated Classical Hodgkin Lymphoma.

机构信息

Andrew M. Evens, Rutgers Cancer Institute of New Jersey, New Brunswick, NJ; Ranjana H. Advani, Stanford University, Stanford, CA; Irene B. Helenowski, Borko D. Jovanovic, Jane N. Winter, and Leo I. Gordon, Northwestern University Feinberg School of Medicine; Jane N. Winter and Leo I. Gordon, Robert H. Lurie Comprehensive Cancer Center; Sonali M. Smith, University of Chicago, Chicago, IL; Michelle Fanale, University of Texas MD Anderson Cancer Center, Houston, TX; Gregory R. Bociek, University of Nebraska, Omaha, NE; Andreas K. Klein, Tufts Medical Center, Boston, MA; and Paul A. Hamlin, Memorial Sloan Kettering Cancer Center, New York, NY.

出版信息

J Clin Oncol. 2018 Oct 20;36(30):3015-3022. doi: 10.1200/JCO.2018.79.0139. Epub 2018 Sep 4.

Abstract

PURPOSE

To improve the curability of older patients with newly diagnosed Hodgkin lymphoma.

PATIENTS AND METHODS

We conducted a multicenter phase II study that administered brentuximab vedotin (Bv) sequentially before and after standard doxorubicin, vinblastine, and dacarbazine (AVD) for untreated patients with Hodgkin lymphoma age 60 years or older. After two lead-in doses of single-agent Bv (1.8 mg/kg once every 3 weeks), patients received six cycles of AVD chemotherapy followed by four consolidative doses of Bv in responding patients.

RESULTS

Patient characteristics included median age of 69 years (range, 60 to 88 years), 63% male, median Eastern Cooperative Oncology Group performance status 1, 81% stage III to IV disease, 60% International Prognostic Score 3 to 7, median Cumulative Illness Rating Scale-Geriatric comorbidity score of 7 (52% grade 3 to 4); and 12% had loss of instrumental activities of daily living at diagnosis. Thirty-seven (77%) of 48 patients completed six cycles of AVD, and 35 patients (73%) received at least one Bv consolidation. Overall response and complete remission rates after initial Bv lead-in dose were 18 (82%) of 22 and 8 (36%) of 22, respectively, and 40 (95%) of 42 and 34 (90%) of 42, respectively, after six cycles of AVD among 42 response-evaluable patients. Twenty (42%) of 48 patients experienced a grade 3 to 4 adverse event, most commonly neutropenia (44%), febrile neutropenia and pneumonia (8%), or diarrhea (6%); 33% had grade 2 peripheral neuropathy, which was reversible in a majority of patients. By intent-to-treat, the 2-year event-free survival, progression-free survival, and overall survival rates were 80%, 84%, and 93%, respectively. Furthermore, 2-year progression-free survival rates for patients with a Cumulative Illness Rating Scale-Geriatric comorbidity score of ≥ 10 versus < 10 were 45% versus 100%, respectively ( < .001), and with baseline loss versus no loss of instrumental activities of daily living were 25% versus 94% ( < .001), respectively, the latter persisting on multivariable analyses.

CONCLUSION

Altogether, sequential Bv-AVD was well tolerated and was associated with robust outcomes. Furthermore, geriatric-based measures were strongly associated with patient survival.

摘要

目的

提高新诊断霍奇金淋巴瘤老年患者的治愈率。

患者和方法

我们进行了一项多中心 2 期研究,对年龄 60 岁及以上未经治疗的霍奇金淋巴瘤患者,在标准多柔比星、长春碱和达卡巴嗪(AVD)之前和之后序贯给予 Brentuximab vedotin(Bv)。在接受两剂单药 Bv(1.8mg/kg,每 3 周一次)后,患者接受六周期 AVD 化疗,然后在有反应的患者中接受四剂 Bv 巩固治疗。

结果

患者特征包括中位年龄 69 岁(范围,60-88 岁)、63%为男性、中位东部肿瘤协作组体能状态 1、81%为 III 期至 IV 期疾病、60%为国际预后评分 3-7、中位累积疾病评分-老年合并症评分 7(52%为 3-4 级);12%的患者在诊断时存在工具性日常生活活动丧失。48 例患者中,37 例(77%)完成了六周期 AVD,35 例(73%)接受了至少一次 Bv 巩固治疗。在 42 例可评估反应的患者中,在接受两剂单药 Bv 后,初次 Bv 先导剂量后的总缓解率和完全缓解率分别为 18(82%)和 8(36%),在接受六周期 AVD 后分别为 40(95%)和 34(90%)。在 48 例患者中,有 20 例(42%)发生了 3-4 级不良事件,最常见的是中性粒细胞减少症(44%)、发热性中性粒细胞减少症和肺炎(8%)或腹泻(6%);33%的患者出现 2 级周围神经病,多数患者可逆。意向治疗分析的 2 年无事件生存率、无进展生存率和总生存率分别为 80%、84%和 93%。此外,累积疾病评分-老年合并症评分≥10 与<10 的患者 2 年无进展生存率分别为 45%与 100%(<0.001),基线有工具性日常生活活动丧失与无丧失的患者 2 年无进展生存率分别为 25%与 94%(<0.001),后者在多变量分析中仍然存在。

结论

总的来说,序贯 Bv-AVD 耐受良好,与显著的疗效相关。此外,基于老年人的措施与患者生存密切相关。

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