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立体定向体部放疗和立体定向体部质子治疗高危、不可手术、早期非小细胞肺癌的 2 期研究。

Phase 2 Study of Stereotactic Body Radiation Therapy and Stereotactic Body Proton Therapy for High-Risk, Medically Inoperable, Early-Stage Non-Small Cell Lung Cancer.

机构信息

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas; Division of Therapeutic Radiation and Oncology, Department of Radiology, King Chulalongkorn Memorial Hospital, Chulalongkorn University, Bangkok, Thailand.

Department of Radiation Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.

出版信息

Int J Radiat Oncol Biol Phys. 2018 Jul 1;101(3):558-563. doi: 10.1016/j.ijrobp.2018.02.022. Epub 2018 Mar 2.

Abstract

PURPOSE

To report the feasibility of conducting a randomized study to compare the toxicity and efficacy of stereotactic body radiation therapy (SBRT) versus stereotactic body proton therapy (SBPT) for high-risk, medically inoperable, early-stage non-small cell lung cancer (NSCLC).

PATIENTS AND METHODS

Patients with medically inoperable NSCLC with high-risk features (centrally located or <5 cm T3 tumor or isolated lung parenchymal recurrences) were randomly assigned to SBRT or SBPT. Radiation dose was 50 Gy(relative biological effectiveness [RBE]) in 4 12.5-Gy(RBE) fractions prescribed to the planning target volume. Stereotactic body radiation therapy was given using 3-dimensional conformal radiation therapy or intensity modulated radiation therapy, and SBPT was given using passive scattering. Consistency in patient setup was ensured with on-board cone beam computed tomography for the SBRT group and with orthogonal X rays for the SBPT group.

RESULTS

The study closed early owing to poor accrual, largely because of insurance coverage and lack of volumetric imaging in the SBPT group. Ultimately, 21 patients were enrolled, and 19 patients who received 50 Gy in 4 fractions were included for analysis (9 SBRT, 10 SBPT). At a median follow-up time of 32 months, median overall survival time was 28 months in the SBRT group and not reached in the SBPT group. Three-year overall survival was 27.8% and 90%, 3-year local control was 87.5% (8 of 9) and 90.0% (9 of 10), and 3-year regional control was 47.6% (5 of 9) and 90% (9 of 10) in the SBRT and SBPT groups, respectively. One patient in the SBPT group developed grade 3 skin fibrosis. No patients experienced grade 4/5 toxicity.

CONCLUSION

Poor accrual, due to lack of volumetric imaging and insurance coverage for proton therapy, led to early closure of the trial and precluded accurate assessment of efficacy and toxicity. Comparable maturity of 2 radiation therapy modalities, particularly on-board imaging, and better insurance coverage for SBPT should be considered for future studies.

摘要

目的

报告一项比较立体定向体部放射治疗(SBRT)与立体定向体部质子治疗(SBPT)治疗高危、不可手术、早期非小细胞肺癌(NSCLC)的毒性和疗效的随机研究的可行性。

患者和方法

我们将患有不可手术 NSCLC 且具有高危特征(中央或<5 cm T3 肿瘤或孤立性肺实质复发)的患者随机分配至 SBRT 或 SBPT 组。处方剂量为 50 Gy(相对生物效应[RBE]),共 4 次,每次 12.5 Gy(RBE),适形放疗或调强放疗用于 SBRT,而被动散射则用于 SBPT。SBRT 组采用机载锥形束 CT 确保患者摆位一致,SBPT 组采用正交 X 射线。

结果

由于保险覆盖范围和 SBPT 组缺乏容积成像,该研究因入组人数少而提前关闭。最终,共入组 21 例患者,19 例患者接受 4 次 50 Gy 治疗,其中 9 例接受 SBRT,10 例接受 SBPT。中位随访时间为 32 个月,SBRT 组的中位总生存时间为 28 个月,SBPT 组未达到。SBRT 和 SBPT 组的 3 年总生存率分别为 27.8%和 90%,3 年局部控制率分别为 87.5%(9/9)和 90.0%(9/10),3 年区域控制率分别为 47.6%(5/9)和 90%(9/10)。SBPT 组有 1 例患者出现 3 级皮肤纤维化。没有患者发生 4/5 级毒性。

结论

由于缺乏容积成像和质子治疗的保险覆盖范围,入组人数少导致试验提前关闭,无法准确评估疗效和毒性。对于未来的研究,应考虑立体定向放射治疗方式(特别是机载成像)的成熟度相当,并为 SBPT 提供更好的保险覆盖范围。

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