Irradiated Bone Marrow Volume is Associated With Hematologic Toxicity in Patients With Multiple Myeloma.

Samuel C Zhang, Sungjin Kim, Jennifer Steers, Bradley Stiehl, Katrina D Silos, Giana Grigsby, Maria Oorloff, Taman Upadhaya, Robert A Vescio, David R Oveisi, Behrooz Hakimian, Katelyn M Atkins, Leslie K Ballas
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Abstract

Purpose: Palliative radiation therapy (RT) is effective for multiple myeloma (MM) but may cause cytopenia. Bone marrow volume receiving 10 Gy (BMV10Gy) has been associated with hematologic toxicity (HT) in cervical cancer, but no studies have investigated this in MM. We hypothesized that absolute BMV10Gy is associated with acute HT in MM patients receiving palliative RT.

Materials and methods: This single institution retrospective analysis evaluated 125 MM patients who received palliative RT between 2007 and 2023 and had ≥2 weeks of follow-up laboratory data. Laboratory values were recorded pre-RT, post-RT, and at nadir within 90 days of completing RT. Clinical HT was defined as new transfusion/growth factor, admission for HT, and/or systemic therapy pause/discontinuation. BM was defined as a bone volume within the RT field. BMV5-40Gy (cubic centimeter [cm3]) was recorded for each treatment. Logistic regressions were performed with clinical HT as the primary endpoint.

Results: Around 105 (84%) patients received concurrent systemic therapy. Median BMV10Gy was 266 cm3 (IQR, 157-501 cm3). Median RT equivalent dose in 2 Gy fractions was 26 Gy (IQR, 23-33 Gy). On univariable analysis, BMV5Gy, BMV10Gy, and BMV15Gy were significantly associated with clinical HT (P = .014, P = .018, P = .050, respectively), while RT equivalent dose in 2 Gy fractions dose was not (P = .997). On multivariable analysis, BMV10Gy was significantly associated with clinical HT (P = .049) after adjusting for dose, number of lesions treated, lesion location (spine, pelvis, limb, and soft tissue), and systemic therapy class. Disease course (number of prior systemic therapies) was significantly associated with clinical HT on univariable and multivariable analysis, with late relapsed/refractory patients (≥3 prior systemic therapies) having 9.6 higher odds of clinical HT compared to newly diagnosed patients (P < .001).

Conclusions: To our knowledge, this is the first study to associate the volume of irradiated BM with acute HT in MM. In addition to BMV5-15Gy, number of prior relapses and systemic therapy lines were significantly associated with HT. Disease history should be evaluated, and RT field volumes were minimized for patients with poor bone marrow reserve (eg, late relapsed/refractory disease).

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辐照骨髓量与多发性骨髓瘤患者的血液学毒性有关。
目的/目标:姑息放疗(RT)对多发性骨髓瘤(MM)有效,但可能导致细胞减少。接受 10Gy 的骨髓量(BMV10Gy)与宫颈癌的血液毒性(HT)有关,但在 MM 中还没有相关研究。我们假设,在接受姑息性 RT 的 MM 患者中,BMV10Gy 的绝对值与急性 HT 有关:这项单一机构的回顾性分析评估了2007-2023年间接受姑息性RT且随访实验室数据≥2周的125名MM患者。记录了RT前、RT后以及完成RT后90天内的实验室值。临床 HT 定义为新输血/生长因子、因血液学毒性入院和/或系统治疗暂停/中止。BM定义为RT区域内的骨量。记录每次治疗的 BMV5-40Gy (cc)。以临床 HT 为主要终点进行逻辑回归:105名(84%)患者同时接受了系统治疗。中位 BMV10Gy 为 266cc(IQR 157-501cc)。中位 RT EqD2 为 26Gy(IQR 23-33Gy)。在单变量分析中,BMV5Gy、BMV10Gy 和 BMV15Gy 与临床 HT 显著相关(分别为 p=0.014、p=0.018、p=0.050),而 RT EqD2 剂量与之无关(p=0.997)。多变量分析显示,在调整剂量、治疗病灶数量、病灶位置(脊柱、骨盆、四肢、软组织)和系统治疗等级后,BMV10Gy 与临床 HT 显著相关(p=0.049)。在单变量和多变量分析中,病程(既往接受过系统治疗的次数)与临床HT显著相关,晚期复发/难治性患者(既往接受过≥3次系统治疗)与新诊断的患者相比,临床HT的几率要高出9.6(P结论:据我们所知,这是第一项将辐照后的骨髓体积与 MM 急性 HT 相关联的研究。除了 BM V5-15Gy 外,既往复发次数和系统治疗次数也与 HT 显著相关。对于骨髓储备较差的患者(如晚期复发/难治性疾病),应评估疾病史并尽量减少RT野的体积。
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来源期刊
CiteScore
11.00
自引率
7.10%
发文量
2538
审稿时长
6.6 weeks
期刊介绍: International Journal of Radiation Oncology • Biology • Physics (IJROBP), known in the field as the Red Journal, publishes original laboratory and clinical investigations related to radiation oncology, radiation biology, medical physics, and both education and health policy as it relates to the field. This journal has a particular interest in original contributions of the following types: prospective clinical trials, outcomes research, and large database interrogation. In addition, it seeks reports of high-impact innovations in single or combined modality treatment, tumor sensitization, normal tissue protection (including both precision avoidance and pharmacologic means), brachytherapy, particle irradiation, and cancer imaging. Technical advances related to dosimetry and conformal radiation treatment planning are of interest, as are basic science studies investigating tumor physiology and the molecular biology underlying cancer and normal tissue radiation response.
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