Reyngold Marsha, Schoenfeld Joshua D, O'Reilly Eileen M, Varghese Anna M, White Charlie, Zinovoy Melissa, Romesser Paul B, Wu Abraham J, Hajj Carla, Cuaron John J, Khalil Danny N, Park Wungki, Lu Wei, Zhang Zhigang, Yu Kenneth H, Diaz Luis A, Crane Christopher H
Department of Radiation Oncology, Memorial Sloan Kettering Cancer Center, New York, New York.
David M. Rubenstein Center for Pancreatic Cancer Research, New York, New York.
JAMA Oncol. 2025 Apr 10. doi: 10.1001/jamaoncol.2025.0460.
Surgical resection of pancreatic ductal adenocarcinoma (PDAC) modestly improves long-term survival due to the competing risk of metastatic disease. However, postoperative morbidity often interferes with administration of systemic therapy and may be unacceptable to some patients. Ablative radiation therapy (A-RT) has emerged as an effective noninvasive local treatment in many tumor types and may provide an alternative to surgery in select patients with resectable PDAC.
To estimate the efficacy of A-RT in technically resectable PDAC.
DESIGN, SETTING, AND PARTICIPANTS: This cohort study of consecutive patients with histologically confirmed, radiographically resectable T1-2N0-1M0 PDAC treated with A-RT at Memorial Sloan Kettering Cancer Center between June 2016 and December 2022 were included from a prospectively maintained database. Patients were not eligible for surgery because of noncancer-related comorbidities. Data were frozen for analysis in December 2023, which took place between March and November 2024.
All patients received A-RT exceeding 97.5-Gy biologically effective dose with daily computed tomography or magnetic resonance imaging guidance, motion management, and daily or selective adaptation of the dose distribution.
The primary outcome was overall survival (OS). Secondary outcomes included biochemical and radiographic objective response rate, cumulative incidence of local progression, progression-free survival, and distant metastasis-free survival.
Of 25 patients with radiographically resectable PDAC who received A-RT, 13 (52%) were male, and the median (IQR) age at time of A-RT was 80 (74-87) years. A total of 20 patients (80%) had a Karnofsky Performance Status score of 80 or lower. A total of 15 tumors (60%) were T2, and 4 (16%) were node positive. A total of 17 patients (68%) received induction chemotherapy for a median (range) of 2.9 (1.0-6.1) months. Radiation therapy regimens delivered with conventional linear accelerators included 75 Gy in 25 fractions among 13 patients, 67.5 Gy in 15 fractions among 9 patients, 50 Gy in 5 fractions among 2 patients (magnetic resonance imaging-guided linear accelerator), and 60 Gy in 10 for 1 patient. OS, local progression, and distant metastasis-free survival at 2 years were 43.7% (95% CI, 27.4%-69.5%), 20.8% (95% CI, 7.3%-39.0%), and 20.0% (95% CI, 9.1%-43.8%), respectively. Grade 3 acute and late gastrointestinal tract toxic effects were noted in 3 and 1 patients, respectively, with no grade 4 or higher events.
In this cohort study, A-RT in patients with technically resectable PDAC led to effective local tumor control and favorable OS despite advanced age, poor Karnofsky Performance Status score, and conservative use of chemotherapy in the cohort studied. These data support a prospective study of A-RT for the management of resectable PDAC.
由于转移性疾病这一竞争风险,手术切除胰腺导管腺癌(PDAC)只能适度提高长期生存率。然而,术后发病率常常会干扰全身治疗的实施,并且对一些患者来说可能难以接受。消融性放射治疗(A-RT)已成为许多肿瘤类型中一种有效的非侵入性局部治疗方法,对于部分可切除的PDAC患者,它可能是手术的替代选择。
评估A-RT在技术上可切除的PDAC中的疗效。
设计、设置和参与者:这项队列研究纳入了2016年6月至2022年12月期间在纪念斯隆凯特琳癌症中心接受A-RT治疗的连续患者,这些患者经组织学确诊、影像学上可切除的T1-2N0-1M0 PDAC,数据来自一个前瞻性维护的数据库。患者因非癌症相关合并症而不符合手术条件。数据于2023年12月冻结用于分析,分析在2024年3月至11月期间进行。
所有患者均接受超过97.5 Gy生物等效剂量的A-RT,采用每日计算机断层扫描或磁共振成像引导、运动管理以及每日或选择性调整剂量分布。
主要结局是总生存期(OS)。次要结局包括生化和影像学客观缓解率、局部进展累积发生率、无进展生存期以及无远处转移生存期。
在25例接受A-RT的影像学上可切除的PDAC患者中,13例(52%)为男性,A-RT时的中位(IQR)年龄为80(74 - 87)岁。共有20例患者(80%)卡氏功能状态评分≤80分。共有15个肿瘤(60%)为T2期,4个(16%)有淋巴结转移。共有17例患者(68%)接受了诱导化疗,中位(范围)化疗时间为2.9(1.0 - 6.1)个月。使用传统直线加速器的放射治疗方案包括:13例患者25次分割给予75 Gy,9例患者15次分割给予67.5 Gy,2例患者(磁共振成像引导直线加速器)5次分割给予50 Gy,1例患者10次分割给予60 Gy。2年时的OS、局部进展和无远处转移生存期分别为43.7%(95%CI,27.4% - 69.5%)、20.8%(95%CI,7.3% - 39.0%)和20.0%(95%CI,9.1% - 43.8%)。分别有3例和1例患者出现3级急性和晚期胃肠道毒性反应,无4级或更高级别的事件。
在这项队列研究中,对于技术上可切除的PDAC患者,A-RT尽管研究队列中患者年龄较大、卡氏功能状态评分较差且化疗使用保守,但仍能实现有效的局部肿瘤控制和良好的OS。这些数据支持对A-RT用于可切除PDAC治疗进行前瞻性研究。