Dose-Response Relationships Between Radiation Exposure, Bone Marrow Function as Measured by 18F-Fluorothymidine Positron Emission Tomography, and Lymphocyte Counts During Chemoradiation for Non-Small Cell Lung Cancer.

IF 6.4 1区 医学 Q1 ONCOLOGY International Journal of Radiation Oncology Biology Physics Pub Date : 2025-02-01 Epub Date: 2024-09-02 DOI:10.1016/j.ijrobp.2024.08.035
Michael P MacManus, Elizabeth Prins, Jing Xie, Tim Akhurst, Rodney J Hicks, Jason Callahan, Fiona Hegi-Johnson, Nicholas Hardcastle, Sarah Everitt
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Abstract

Purpose: 18F-fluorothymidine (FLT) positron emission tomography (PET) enables sensitive imaging of bone marrow (BM) proliferation. Sequential FLT-PET/computed tomography scans before and during chemoradiation therapy (CRT) for non-small cell lung cancer were repurposed to investigate the dose-response effects of radiation on BM proliferation.

Methods and materials: Twenty-six non-small cell lung cancer patients underwent platinum-based CRT to 60 Gy in 30 fractions with FLT-PET/computed tomography scans at baseline, week 2 (20 Gy), and week 4 (40 Gy). FLT uptake in BM was isolated using Medical Image Merge software. Weeks 2 and 4 FLT-PET BM scans were fused with contemporaneous radiation isodose distributions. Relationships between radiation dose and FLT BM uptake (highest standardized uptake values within the volume and visual parameters) were analyzed using generalized linear and restricted cubic spline models. Percentage volumes of total BM without appreciable FLT uptake ("ablated") on weeks 2 and 4 FLT-PET scans were calculated by comparisons with baseline scans.

Results: Thoracic FLT uptake was ablated in BM regions exposed to cumulative radiation doses ≥3 Gy by week 2. In all cases, BM FLT's highest standardized uptake values within the volume declined rapidly as the radiation dose increased. BM proliferation significantly decreased by >95% after ≥3 to 4 Gy at 2 weeks and ≥4 to 5 Gy at 4 weeks. The ablated BM volume increased from week 2 to week 4 as BM in the penumbra accumulated radiation dose. The median percentage of total BM ablated was 13.1% (range, 5.6%-20.3%) at 2 weeks and 15.7% (range, 9.2%-24.1%) at 4 weeks. Mean lymphocyte counts fell from a baseline of 2.01 × 109/L to 0.77 at week 2 and 0.60 at week 4. Lymphocyte decline strongly correlated with the percentage of total BM ablated by week 4 (y = -46 to 1.64x; R2adj = 0.34; P = .001).

Conclusions: BM ablation associated with low-dose radiation exposure during CRT correlated significantly with lower week 4 lymphocyte counts. BM is a potential organ at risk, and reducing the BM volume exposed to ≥3 Gy may help preserve lymphocytes, which is essential for effective adjuvant immunotherapy.

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非小细胞肺癌化疗期间辐射量、18F-FLT PET 测量的骨髓功能和淋巴细胞计数之间的剂量反应关系。
目的:18F-氟胸苷(FLT)-PET能够对骨髓(BM)增殖进行敏感成像。我们将非小细胞肺癌(NSCLC)化疗(CRT)前和化疗期间的FLT-PET/CT顺序扫描重新用于研究辐射对骨髓增殖的剂量反应效应:26名NSCLC患者接受了30次60Gy的铂类CRT,并在基线、第2周(20Gy)和第4周(40Gy)进行了FLT-PET/CT扫描。使用医学影像合并软件分离出骨髓中的 FLT 摄取。第 2 周和第 4 周的 FLT-PET BM 扫描与同期辐射等剂量分布相融合。使用广义线性模型和限制性三次样条模型分析了辐射剂量与 FLT 基底吸收(SUVmax 和视觉参数)之间的关系。通过与基线扫描进行比较,计算出第2周和第4周FLT-PET扫描中无明显FLT摄取("消融")的总基质体积百分比:结果:第2周时,在累积辐射剂量≥3Gy的骨髓区域,胸腔FLT摄取被消融。在所有病例中,随着辐射剂量的增加,BM FLT SUVmax迅速下降。在2周时接受≥3-4Gy辐射和4周时接受≥4-5Gy辐射后,骨髓增殖明显减少95%以上。从第2周到第4周,随着半影内的骨髓累积辐射剂量,被消融的骨髓体积有所增加。在第 2 周和第 4 周,消融的全血细胞的中位百分比分别为 13.1%(范围 5.6-20.3)和 15.7%(范围 9.2-24.1)。平均淋巴细胞计数从基线的 2.01×109/L 降至第 2 周的 0.77 和第 4 周的 0.60。淋巴细胞的下降与第4周时消融的全部基质细胞的百分比密切相关(y=-46 -1.64 x, R2adj = 0.34, p=0.001):结论:CRT期间的低剂量放射照射导致的骨髓组织消融与第4周淋巴细胞计数的降低有显著相关性。骨髓是潜在的高危器官,减少暴露于≥3Gy射线的骨髓体积可能有助于保留有效辅助免疫疗法所必需的淋巴细胞。
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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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