Department of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Department of Radiation Oncology, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Int J Radiat Oncol Biol Phys. 2015 Nov 1;93(3):677-83. doi: 10.1016/j.ijrobp.2015.07.2267. Epub 2015 Jul 22.
To evaluate the effectiveness of concurrent chemoradiation therapy (CCRT) with 40 Gy followed by consolidation chemotherapy for localized extranodal natural killer (NK)/T-cell lymphoma (ENKTL), nasal type.
From August 2004 to August 2012, 62 patients with newly diagnosed stage IE to IIE ENKTL underwent CCRT followed by consolidation chemotherapy. The median RT dose was 40 Gy. Cisplatin, 30 mg/m(2), was administered weekly during the RT course. Responders to CCRT were encouraged to undergo consolidation chemotherapy. Three different consolidation chemotherapy regimens were used consecutively: VIPD (etoposide, ifosfamide, cisplatin, and dexamethasone); VIDL (etoposide, ifosfamide, and dexamethasone followed by intramuscular injection of l-asparaginase); and MIDLE (methotrexate, etoposide, ifosfamide, mesna, and l-asparaginase).
The median follow-up period was 49 months (range 8-112). After completion of CCRT, 56 patients (90.3%) had a complete response, 4 (6.4%) had a partial response, 1 (1.6%) had stable disease, and 1 patient (1.6%) had progressive disease (PD). Consolidation chemotherapy was recommended to 61 patients, after excluding the patient with PD, but was actually delivered to 58. Of these 58 patients, 56 (96.5%) had a complete response and 2 (3.5%) had PD. During the follow-up period, 17 patients (including 3 with PD) experienced progression. The median interval to progression was 11 months (range 1-61). Local failure developed in 6 patients, of whom, 2 had developed progression outside the RT field. For all patients, the 3-year overall survival, progression-free survival, and local control rates were 83.1%, 77.1%, and 92.4%, respectively. Grade ≥3 nonhematologic toxicity developed in only 3 patients (4.8%).
Excellent clinical outcomes were achieved using CCRT with 40 Gy followed by consolidation chemotherapy. Additional investigation, however, is warranted to confirm our findings.
评估 40Gy 同期放化疗(CCRT)加巩固化疗治疗局限性结外鼻型自然杀伤(NK)/T 细胞淋巴瘤(ENKTL)的疗效。
2004 年 8 月至 2012 年 8 月,62 例初治 IE 至 IIE 期 ENKTL 患者接受 CCRT 加巩固化疗。中位放疗剂量为 40Gy。顺铂,30mg/m2,在放疗过程中每周给予。对 CCRT 有反应的患者鼓励接受巩固化疗。连续使用三种不同的巩固化疗方案:VIPD(依托泊苷、异环磷酰胺、顺铂和地塞米松);VIDL(依托泊苷、异环磷酰胺和地塞米松,随后肌肉注射左旋门冬酰胺酶);和 MIDLE(甲氨蝶呤、依托泊苷、异环磷酰胺、美司钠和左旋门冬酰胺酶)。
中位随访时间为 49 个月(8-112 个月)。CCRT 完成后,56 例(90.3%)患者完全缓解,4 例(6.4%)部分缓解,1 例(1.6%)疾病稳定,1 例(1.6%)疾病进展(PD)。排除 PD 患者后,建议 61 例患者接受巩固化疗,但实际上仅 58 例接受了治疗。在这 58 例患者中,56 例(96.5%)完全缓解,2 例(3.5%)PD。随访期间,17 例患者(包括 3 例 PD)出现进展。中位进展时间为 11 个月(1-61 个月)。6 例患者出现局部复发,其中 2 例在放疗野外出现进展。所有患者的 3 年总生存率、无进展生存率和局部控制率分别为 83.1%、77.1%和 92.4%。仅 3 例(4.8%)患者发生≥3 级非血液学毒性。
采用 40Gy 同期放化疗加巩固化疗治疗局限性结外鼻型 NK/T 细胞淋巴瘤可获得良好的临床疗效。然而,需要进一步的研究来证实我们的发现。