Stafford S L, Kozelsky T F, Garrity J A, Kurtin P J, Leavitt J A, Martenson J A, Habermann T M
Division of Radiation Oncology, Mayo Clinic and Mayo Foundation, Rochester, MN, USA.
Radiother Oncol. 2001 May;59(2):139-44. doi: 10.1016/s0167-8140(00)00328-5.
Orbital non-Hodgkin's lymphomas (NHL) have traditionally been treated with radiation. Forty-eight patients presenting with orbital NHL were treated with radiation and were evaluated for local control, overall survival, cause-specific survival, and complications.
Forty-five patients had low-grade and 3 patients had intermediate-grade histologic findings. Orbit-only disease occurred in 22 patients, the conjunctiva in 16, both in five, and lacrimal gland only in five. Patient age ranged from 35 to 94 years (median, 68). Ann Arbor stages were cIEA (34), cIIEA (six), cIIIEA (two), and cIVEA (six). Radiation doses ranged between 15 and 53.8 Gy (median, 27.5 Gy).
Follow-up ranged from 0.14 to 18.23 years (median, 5.35). Median overall survival and cause-specific survival were 6.5 and 15.5 years, respectively. Patients with clinical stage I or II disease had significantly better overall and cause-specific survival than patients with stage III or IV disease. Ten-year relapse-free survival in 41 patients with stage I or II disease was 66%. However, there was continued downward pressure on relapse-free survival out to 18 years. One local failure occurred. Twenty-five patients sustained acute complications. There were 17 minor and four major late complications. All major late complications occurred with doses more than 35 Gy.
Excellent local control with radiation doses ranging from 15 to 30 Gy is achieved. Patients with stage I or II disease have better overall and cause-specific survival than patients with stage III or IV disease. Late relapse occurs in sites other than the treated orbit, even in patients with early-stage disease. Doses 35 Gy or higher result in significant late complications and are therefore not indicated for patients with low-grade tumors.
眼眶非霍奇金淋巴瘤(NHL)传统上采用放射治疗。48例眼眶NHL患者接受了放射治疗,并对局部控制、总生存率、病因特异性生存率及并发症进行了评估。
45例患者组织学表现为低级别,3例为中级别。仅眼眶病变22例,结膜病变16例,眼眶和结膜均受累5例,仅泪腺受累5例。患者年龄35至94岁(中位数68岁)。Ann Arbor分期为cIEA(34例)、cIIEA(6例)、cIIIEA(2例)和cIVEA(6例)。放射剂量为15至53.8 Gy(中位数27.5 Gy)。
随访时间0.14至18.23年(中位数5.35年)。总生存中位数和病因特异性生存中位数分别为6.5年和15.5年。临床I期或II期疾病患者的总生存率和病因特异性生存率显著高于III期或IV期疾病患者。41例I期或II期疾病患者的10年无复发生存率为66%。然而,直至18年无复发生存率仍持续下降。发生1例局部失败。25例患者出现急性并发症。有17例轻微晚期并发症和4例严重晚期并发症。所有严重晚期并发症均发生于剂量超过35 Gy时。
采用15至30 Gy的放射剂量可实现良好的局部控制。I期或II期疾病患者的总生存率和病因特异性生存率高于III期或IV期疾病患者。即使是早期疾病患者,晚期复发也发生在治疗眼眶以外的部位。35 Gy或更高剂量会导致显著的晚期并发症,因此低级别肿瘤患者不适用。