Concurrent Use of Abemaciclib and Radiotherapy in Metastatic Breast Cancer Patients: A Single-Center Experience.

IF 4.6 Q2 MATERIALS SCIENCE, BIOMATERIALS ACS Applied Bio Materials Pub Date : 2024-06-13 DOI:10.1159/000538847
Edy Ippolito, Francesco Pantano, Sonia Silipigni, Rita Alaimo, Jessica Infante, Elena Onorati, Claudia Talocco, Carlo Greco, Michele Fiore, Marco Donato, Giuseppe Tonini, Rolando Maria D'Angelillo, Sara Ramella
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Abstract

Introduction: There is little evidence regarding the safety and efficacy of the combination of abemaciclib plus radiotherapy (RT). The majority of studies investigated the combination of RT with palbociclib or ribociclib reporting that hematological toxicity is common. Given the unique toxicity profile of abemaciclib with greater gastrointestinal toxicity compared to hematological toxicity, we wanted to evaluate the toxicity of the combination with RT in metastatic breast cancer (BC) patients.

Methods: Patients with histologically proven metastatic or locally advanced BC treated with RT and concurrent abemaciclib were selected. Toxicity was assessed according to the NCI-CTCAE V4.0.

Results: Thirty-two metastatic sites were treated in 19 patients and analyzed. All patients received abemaciclib during the RT course. A total of 68% of patients received a full dose of abemaciclib during RT. Also, 71.9% of patients received a palliative intent (median dose = 30 Gy, range = 8-30 Gy), and 26.3% were treated for 9 oligo-metastatic or oligo-progressive sites of disease with stereotactic body RT (median dose = 30 Gy, range 21-30 Gy, given in 3-5 fractions). Overall, the rate of G3 toxicity was 15.7%. The rate of G3 hematological toxicity was 10.6% (2/19 patients, one G3 neutropenia and one G3 anemia). No patient presented diarrhea, including those treated for RT sites close to the bowel. One patient developed G3 skin toxicity. Pain significantly improved after RT (mean value NRS pre-RT = 3.9, SD = 3.07; mean value NRS after RT = 0.9, SD = 0.46; p < 0.0001).

Conclusion: Abemaciclib and concomitant RT seem well tolerated showing acceptable toxicity.

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在转移性乳腺癌患者中同时使用阿贝昔单抗和放疗:单中心经验。
简介关于阿贝昔单抗(abemaciclib)联合放疗(RT)的安全性和有效性的证据很少。大多数研究都对放疗与Palbociclib或Ribociclib联合用药进行了调查,结果表明血液学毒性很常见。鉴于阿贝昔单抗独特的毒性特征,即胃肠道毒性大于血液学毒性,我们希望对转移性乳腺癌(BC)患者联合 RT 的毒性进行评估:我们选择了经组织学证实的转移性或局部晚期乳腺癌患者,这些患者在接受 RT 治疗的同时还接受了 Abemaciclib 治疗。根据 NCI-CTCAE V4.0 评估毒性:对19名患者的32个转移部位进行了治疗和分析。所有患者都在 RT 疗程中接受了 Abemaciclib 治疗。68%的患者在 RT 期间接受了全剂量的 Abemaciclib。71.9%的患者接受了姑息治疗(中位剂量= 30Gy,范围= 8-30Gy),26.3%的患者对9个少转移或少进展部位的疾病进行了立体定向体放射治疗(SBRT)(中位剂量= 30Gy,范围21-30Gy,分3-5次进行),G3毒性发生率为15.7%。G3级血液毒性发生率为10.6%(2/19例患者,1例G3级中性粒细胞减少,1例G3级贫血)。没有患者出现腹泻,包括在靠近肠道的RT部位接受治疗的患者。一名患者出现了 G3 皮肤毒性。RT 术后疼痛明显改善(RT 术前 NRS 平均值=3.9,SD=3.07;RT 术后 NRS 平均值=0.9,SD=0.46;P=0.05)。
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来源期刊
ACS Applied Bio Materials
ACS Applied Bio Materials Chemistry-Chemistry (all)
CiteScore
9.40
自引率
2.10%
发文量
464
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