Prosnitz Robert G, Yao Bin, Farrell Catherine L, Clough Robert, Brizel David M
Department of Radiation Oncology, Box 3085, Duke University Medical Center, Durham, NC 27710, USA.
Int J Radiat Oncol Biol Phys. 2005 Mar 15;61(4):1087-95. doi: 10.1016/j.ijrobp.2004.07.710.
Pretreatment anemia is an adverse prognostic variable in squamous cell head-and-neck cancer (HNC) patients treated with radiotherapy (RT) alone. Tumor hypoxia is an adverse parameter for treatment with RT alone or with RT and concurrent chemotherapy (CCT). Tumor hypoxia is more prevalent in patients who present with pretreatment hemoglobin (Hgb) concentrations less than 13 g/dL. RT/CCT improves survival over RT alone in advanced HNC, and its use is becoming more widespread. This study was performed to evaluate whether pretreatment Hgb less than 13 g/dL was correlated with treatment outcome in patients with advanced HNC treated with a uniform regimen of RT/CCT.
The study population consisted of patients with AJCC Stage III or IV, M0 HNC who were treated with 70 to 72.5 Gy accelerated hyperfractionated RT (1.25 Gy b.i.d.) and CCT consisting of 2 cycles of CDDP (12-20 mg/m(2)/d x 5 days) and continuous infusion 5-FU (600 mg/m(2)/d x 5 days) during Week 1 and Week 6. A planned break in RT occurred during Week 4. These patients were enrolled on the experimental arm of a prospective randomized trial that compared this regimen to hyperfractionated irradiation alone from 1990 to 1996. RT/CCT was delivered as standard therapy from 1996 to 2000. The primary endpoint was failure-free survival (FFS). Secondary endpoints included local-regional control and overall survival.
One hundred and fifty-nine patients were treated from 1990 to 2000. The median (25-75%) pretreatment Hgb was 13.6 (12.2-13.5) g/dL. Hgb was 13 g/dL or higher in 105 patients and less than 13 g/dL in 54 patients. Primary tumor sites included oropharynx (43%), hypopharynx/larynx (36%), oral cavity (9%), and nasopharynx (6%). Seventy-eight percent of the patients with Hgb 13 g/dL or higher and 92% of the patients with Hgb less than 13 g/dL had a primary tumor stage of T3 or T4 (p = 0.01). Node-positive disease was present in 74 of 105 (70%) of patients with Hgb 13 g/dL or higher patients and in 36/54 (67%) of patients with Hgb less than 13 g/dL patients. Median follow-up of surviving patients was 42 months (range, 4-128 months). Five-year FFS was 75% for patients with Hgb 13 g/dL or higher vs. 50% for patients with Hgb less than 13 g/dL had a (p < 0.01). A total of 49 failures occurred in both patient cohorts. The median (25-75%) decrease in Hgb during RT/CCT was 2.2 (1.3-3.1) g/dL, both in patients who failed and in those who remained disease-free.
Pretreatment Hgb less than 13 g/dL is correlated with adverse outcomes in advanced HNC patients treated with RT/CCT. Whether anemia actually causes poor outcomes remains unknown. The therapeutic effect of anemia correction is being evaluated in prospective trials.
在单纯接受放疗(RT)的头颈部鳞状细胞癌(HNC)患者中,治疗前贫血是一个不良预后变量。肿瘤缺氧是单纯放疗或放疗联合同步化疗(CCT)治疗的一个不良参数。肿瘤缺氧在治疗前血红蛋白(Hgb)浓度低于13 g/dL的患者中更为普遍。在晚期HNC中,RT/CCT比单纯RT能提高生存率,且其应用越来越广泛。本研究旨在评估治疗前Hgb低于13 g/dL是否与接受统一RT/CCT方案治疗的晚期HNC患者的治疗结果相关。
研究人群包括美国癌症联合委员会(AJCC)III期或IV期、M0的HNC患者,他们接受70至72.5 Gy的加速超分割放疗(每次1.25 Gy,每日2次)以及CCT,CCT包括在第1周和第6周进行2个周期的顺铂(CDDP,12 - 20 mg/m²/d×5天)和顺铂持续输注5-氟尿嘧啶(5-FU,600 mg/m²/d×5天)。放疗在第4周计划中断。这些患者被纳入一项前瞻性随机试验的试验组,该试验在1990年至1996年期间将此方案与单纯超分割放疗进行比较。1996年至2000年期间,RT/CCT作为标准治疗方案。主要终点是无失败生存(FFS)。次要终点包括局部区域控制和总生存。
1990年至2000年期间共治疗了159例患者。治疗前Hgb的中位数(25%-75%)为13.6(12.2 - 13.5)g/dL。105例患者的Hgb为13 g/dL或更高,54例患者的Hgb低于13 g/dL。原发肿瘤部位包括口咽(43%)丶下咽/喉(36%)丶口腔(9%)和鼻咽(6%)。Hgb为13 g/dL或更高的患者中78%以及Hgb低于13 g/dL的患者中92%的原发肿瘤分期为T3或T4(p = 0.01)。105例Hgb为13 g/dL或更高的患者中有74例(占70%)以及54例Hgb低于13 g/dL的患者中有36例(占67%)存在淋巴结阳性疾病。存活患者的中位随访时间为42个月(范围4 - 128个月)。Hgb为13 g/dL或更高的患者5年FFS为75%,而Hgb低于13 g/dL的患者为50%(p < 0.01)。两个患者队列中总共发生了49次失败。在接受RT/CCT治疗期间,失败患者和无疾病患者的Hgb中位数(25%-75%)下降均为2.2(1.3 - 3.1)g/dL。
治疗前Hgb低于13 g/dL与接受RT/CCT治疗的晚期HNC患者的不良结局相关。贫血是否真的导致不良结局尚不清楚。前瞻性试验正在评估纠正贫血的治疗效果。