Mehta V K, Fisher G A, Ford J M, Poen J C, Vierra M A, Oberhelman H A, Bastidas A J
Department of Radiation Oncology, Stanford University Medical Center, 300 Pasteur Dr, Stanford, CA 94305, USA.
Arch Surg. 2001 Jan;136(1):65-9. doi: 10.1001/archsurg.136.1.65.
Adjuvant chemoradiotherapy decreases the risk of local recurrence in patients with adenocarcinoma of the ampulla of Vater and high-risk features. Adjuvant chemoradiotherapy for this population can be administered safely and without much morbidity.
Controlled, prospective, single-arm study.
Tertiary care referral hospital.
From June 1995 to March 1999, 12 patients (7 men and 5 women; median age, 66 years; age range, 38-78 years) with "unfavorable" ampullary carcinoma were treated with adjuvant chemoradiotherapy. All patients underwent pancreaticoduodenectomy, and all pathologic findings were confirmed at Stanford University Medical Center, Stanford, Calif. Unfavorable features were defined as involved lymph nodes (n = 10), involved surgical margins (n = 1), poorly differentiated histological features (n = 3), tumor size greater than 2 cm (n = 6), or the presence of neurovascular invasion (n = 4).
Four to 6 weeks after undergoing pylorus-preserving pancreaticoduodenectomy with regional lymphadenectomy, patients began adjuvant chemoradiotherapy consisting of concurrent radiotherapy (45 Gy) and fluorouracil by protracted venous infusion (225-250 mg/m(2) per day, 7 days per week) for 5 weeks.
Local recurrence, distant recurrence, overall survival rate, and treatment-related toxic effects.
All patients completed the prescribed treatment course. Toxic effects were assessed twice a week during treatment and graded according to the National Cancer Institute Common Toxicity Criteria Scale. One patient required a treatment interruption of 1 week for grade III nausea/vomiting. No grade IV or V toxic effects were observed. At median follow-up of 24 months (range, 13-50 months), 8 of 12 patients were alive and disease free. One patient was alive but had disease recurrence. Three patients died of this disease (liver metastases). Actuarial overall survival at 2 years was 89%, and median survival was 34 months. One surviving patient developed a local recurrence and a lung lesion. Actuarial overall survival and median survival were better than in a parallel cohort with resected high-risk pancreatic cancer (n = 26) treated with the same adjuvant chemoradiotherapy regimen (median survival, 34 vs 14 months; P<.004).
Adjuvant chemoradiotherapy for carcinoma of the ampulla of Vater is well tolerated and might improve control of this disease in patients with unfavorable features.
辅助放化疗可降低壶腹腺癌伴高危特征患者的局部复发风险。对该人群进行辅助放化疗可安全实施,且并发症较少。
对照、前瞻性、单臂研究。
三级医疗转诊医院。
1995年6月至1999年3月,12例(7例男性和5例女性;中位年龄66岁;年龄范围38 - 78岁)患有“预后不良”壶腹癌的患者接受了辅助放化疗。所有患者均接受了胰十二指肠切除术,所有病理结果均在加利福尼亚州斯坦福市的斯坦福大学医学中心得到证实。预后不良特征定义为有淋巴结转移(n = 10)、手术切缘受累(n = 1)、组织学分化差(n = 3)、肿瘤大小大于2 cm(n = 6)或存在神经血管侵犯(n = 4)。
在接受保留幽门的胰十二指肠切除术及区域淋巴结清扫术后4至6周,患者开始辅助放化疗,包括同步放疗(45 Gy)和持续静脉输注氟尿嘧啶(每天225 - 250 mg/m²,每周7天),持续5周。
局部复发、远处复发、总生存率及治疗相关毒性反应。
所有患者均完成了规定的治疗疗程。治疗期间每周对毒性反应评估两次,并根据美国国立癌症研究所通用毒性标准量表进行分级。1例患者因Ⅲ级恶心/呕吐需要中断治疗1周。未观察到Ⅳ级或Ⅴ级毒性反应。中位随访24个月(范围13 - 50个月),12例患者中有8例存活且无疾病复发。1例患者存活但有疾病复发。3例患者死于该疾病(肝转移)。2年精算总生存率为89%,中位生存期为34个月。1例存活患者出现局部复发和肺部病变。与接受相同辅助放化疗方案的同期高危胰腺癌切除患者队列(n = 26)相比,精算总生存率和中位生存期更好(中位生存期,34对14个月;P <.004)。
壶腹腺癌的辅助放化疗耐受性良好,可能改善预后不良特征患者对该疾病的控制。