The role of radiotherapy in patients with refractory Hodgkin's lymphoma after treatment with brentuximab vedotin and/or immune checkpoint inhibitors

Ruizhi Zhao , Han Shao , Guiqing Shi , Yanyan Qiu , Tianlan Tang , Yuping Lin , Silin Chen , Cheng Huang , Siqin Liao , Jinhua Chen , Haiying Fu , Jianzhi Liu , Benhua Xu , Tingbo Liu , Yujing Zhang , Yong Yang
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Abstract

Background

Approximately 10%–30% of patients with Hodgkin's lymphoma (HL) experience relapse or refractory (R/R) disease after first-line standard therapy. Brentuximab vedotin (BV) and immune checkpoint inhibitors (ICIs) have important roles in the salvage treatment of R/R HL. However, subsequent treatment for HL refractory to BV and/or ICI treatment is challenging.

Methods

We retrospectively analyzed patients in two institutions who had R/R HL, experienced BV or ICI treatment failure, and received radiotherapy (RT) thereafter. The overall response rate (ORR), duration of response (DOR), progression-free survival (PFS), and overall survival (OS) were analyzed.

Results

Overall, 19 patients were enrolled. First-line systemic therapy comprised doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD, 84.2%); AVD plus ICIs (10.5%); and bleomycin, etoposide, doxorubicin, cyclophosphamide, vincristine, procarbazine, and prednisone (BEACOPP, 5.3%). After first-line therapy, 15 (78.9%) and four patients (21.1%) had refractory disease and relapsed, respectively. After R/R HL diagnosis, six (31.6%), two (10.5%), and 11 (57.9%) patients received BV and ICIs concurrently, BV monotherapy, and ICI monotherapy, respectively. All patients received intensity-modulated RT (n = 12, 63.2%) or volumetric modulated arc therapy (VMAT; n = 7, 36.8%). The ORR as well as the complete response (CR) rate was 100%; the median DOR to RT was 17.2 months (range, 7.9–46.7 months). Two patients showed progression outside the radiation field; one patient had extensive in-field, out-of-field, nodal, and extranodal relapse. With a median follow-up time of 16.2 months (range, 9.2–23.2 months), the 1-year PFS and OS were 84.4% and 100%, respectively. PFS was associated with extranodal involvement (P = 0.019) and gross tumor volume (P = 0.044). All patients tolerated RT well without adverse events of grade ≥ 3.

Conclusion

RT is effective and safe for treating HL refractory to BV or ICIs and has the potential to be part of a comprehensive strategy for HL.

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放疗在接受布仑妥昔单抗韦多汀和/或免疫检查点抑制剂治疗后的难治性霍奇金淋巴瘤患者中的作用
背景约有10%-30%的霍奇金淋巴瘤(HL)患者在接受一线标准治疗后复发或难治(R/R)。布伦妥昔单抗维多汀(BV)和免疫检查点抑制剂(ICIs)在R/R HL的挽救治疗中发挥着重要作用。方法我们回顾性分析了两家机构的R/R HL患者,这些患者经历了BV或ICI治疗失败,之后接受了放疗(RT)。我们分析了总反应率(ORR)、反应持续时间(DOR)、无进展生存期(PFS)和总生存期(OS)。一线系统治疗包括多柔比星、博来霉素、长春新碱和达卡巴嗪(ABVD,84.2%);AVD加ICIs(10.5%);博来霉素、依托泊苷、多柔比星、环磷酰胺、长春新碱、丙卡巴嗪和泼尼松(BEACOPP,5.3%)。经过一线治疗后,分别有 15 名(78.9%)和 4 名(21.1%)患者出现难治性疾病和复发。R/R HL确诊后,分别有6名(31.6%)、2名(10.5%)和11名(57.9%)患者同时接受了BV和ICI治疗、BV单药治疗和ICI单药治疗。所有患者都接受了强度调控 RT(12 人,63.2%)或容积调控弧治疗(VMAT;7 人,36.8%)。ORR和完全缓解(CR)率均为100%;RT的中位延迟时间为17.2个月(范围为7.9-46.7个月)。两名患者在放射野外出现进展;一名患者出现广泛的放射野内、放射野外、结节和结节外复发。中位随访时间为16.2个月(9.2-23.2个月),1年的PFS和OS分别为84.4%和100%。PFS与结节外受累(P = 0.019)和肿瘤总体积(P = 0.044)有关。所有患者对RT的耐受性良好,未出现≥3级的不良反应。结论RT治疗BV或ICIs难治性HL有效且安全,有望成为HL综合治疗策略的一部分。
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14.20
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0.00%
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审稿时长
70 days
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