Perez C A, Grigsby P W, Chao K S, Mutch D G, Lockett M A
Radiation Oncology Center, Mallinckrodt Institute of Radiology, St. Louis, MO 63108, USA.
Int J Radiat Oncol Biol Phys. 1998 May 1;41(2):307-17. doi: 10.1016/s0360-3016(98)00067-4.
To assess the impact of tumor size and extent, and dose of irradiation on pelvic tumor control, incidence of distant metastases, and disease-free survival in carcinoma of the uterine cervix.
Records were reviewed of 1499 patients (Stages IA-IVA) treated with definitive irradiation (combination of external beam plus two intracavitary insertions to deliver doses of 65-95 Gy to point A, depending on stage and tumor volume). Follow-up was obtained in 98% of patients (median 11 years, minimum 3 years, maximum 30 years). The relationship between outcome and tumor size was analyzed in each stage. Pelvic tumor control was correlated with total doses to point A and to the lateral pelvic wall.
The 10-year actuarial pelvic failure rate in Stage IB was 5% for tumors <2 cm, 15% for 2.1-5 cm, and 35% for tumors >5 cm (p = 0.01); in Stage IIA, the rates were 0%, 28%, and 25%, respectively (p = 0.12). Stage IIB unilateral or bilateral nonbulky tumors <5 cm had a 23% pelvic failure rate compared with 34% for unilateral or bilateral bulky tumors >5 cm (p = 0.13). In Stage IIB, pelvic failures were 18% with medial parametrial involvement only, compared with 28% when tumor extended into the lateral parametrium (p = 0.05). In Stage III, unilateral parametrial involvement was associated with a 32% pelvic failure rate versus 50% for bilateral extension (p < 0.01). Ten-year disease-free survival rates were 90% for IB tumors <2 cm, 76% for 2.1-4 cm, 61% for 4.1-5 cm, and 47% for >5 cm (p = 0.01); in Stage IIA, the rates were 93%, 63%, 39%, and 59%, respectively (p < or = 0.01). Patients with Stage IIB medial parametrial involvement had better 10-year disease-free survival (67%) than those with lateral parametrial extension (56%) (p = 0.02). Stage III patients with unilateral tumor extension had a 48% 10-year disease-free survival rate compared with 32% for bilateral parametrial involvement (p < or = 0.01). The presence of endometrial extension or tumor only in the endometrial curettings had no significant impact on pelvic failure. However, in patients with Stage IB disease, the incidence of distant metastases was 31% with positive curettings, 15% with negative curettings, and 22% with admixture (p < or = 0.01). In Stage IIA, the corresponding values were 51%, 33%, and 18% (p = 0.05). The 10-year disease-free survival rates in Stage IB were 67% with positive curettings, 81% for negative curettings, and 77% for admixture (p = 0.02); in Stage IIA, the rates were 45%, 66%, and 67%, respectively (p = 0.14). Because this is not a prospective Phase II dose-escalation study, the correlation of doses of irradiation with pelvic tumor control in the various stages and tumor size groups is not consistent. Nevertheless, with Stage IB and IIA tumors <2 cm in diameter, the pelvic failure rate was under 10% with doses of 70-80 Gy to point A, whereas for larger lesions even doses of 85-90 Gy resulted in 25% to 37% pelvic failure rates. In Stage IIB with doses of 70 Gy to point A, the pelvic failure rate was about 50% compared with about 20% in nonbulky and 30% in bulky tumors with doses > 80 Gy. In Stage III unilateral lesions, the pelvic failure rate was about 50% with < or =70 Gy to point A versus 35% with higher doses, and in bilateral or bulky tumors it was 60% with doses <70 Gy and 50% with higher doses.
Clinical stage and size of tumor are critical factors in prognosis, therapy efficacy, and evaluation of results in carcinoma of the uterine cervix. The doses to point A suggest that for lesions <2 cm, doses of 75 Gy result in < or =10% pelvic failures, whereas in more extensive lesions, even with doses of 85 Gy, the pelvic failure rate is about 30%; and in Stage IIB-III tumors, doses of 85 Gy result in 35-50% pelvic failures. Refinements in brachytherapy techniques and/or use of agents to selectively sensitize the tumors to irradiation will be necessary to improve the present results in invasive carcinoma of t
评估肿瘤大小、范围及照射剂量对子宫颈癌盆腔肿瘤控制、远处转移发生率及无病生存率的影响。
回顾性分析1499例(IA - IVA期)接受根治性放疗患者的记录(外照射联合两次腔内照射,根据分期和肿瘤体积向A点给予65 - 95 Gy剂量)。98%的患者获得随访(中位随访时间11年,最短3年,最长30年)。分析各分期中结局与肿瘤大小的关系。盆腔肿瘤控制情况与A点及盆腔侧壁的总剂量相关。
IB期肿瘤<2 cm者10年精算盆腔失败率为5%,2.1 - 5 cm者为15%,>5 cm者为35%(p = 0.01);IIA期相应比例分别为0%、28%和25%(p = 0.12)。IIB期单侧或双侧<5 cm非巨大肿瘤盆腔失败率为23%,而单侧或双侧>5 cm巨大肿瘤为34%(p = 0.13)。IIB期仅累及宫旁内侧者盆腔失败率为18%,肿瘤延伸至宫旁外侧者为28%(p = 0.05)。III期单侧宫旁受累盆腔失败率为32%,双侧受累为50%(p < 0.01)。IB期肿瘤<2 cm者10年无病生存率为90%,2.1 - 4 cm者为76%,4.1 - 5 cm者为61%,>5 cm者为47%(p = 0.01);IIA期相应比例分别为93%、63%、39%和59%(p ≤ 0.01)。IIB期宫旁内侧受累患者10年无病生存率(67%)高于宫旁外侧延伸者(56%)(p = 0.02)。III期单侧肿瘤延伸患者10年无病生存率为48%,双侧宫旁受累者为32%(p ≤ 0.01)。子宫内膜受累或仅在子宫内膜刮出物中发现肿瘤对盆腔失败无显著影响。然而,IB期患者中,刮宫阳性者远处转移发生率为31%,阴性者为15%,混合情况者为22%(p ≤ 0.01)。IIA期相应数值分别为51%、33%和18%(p = 0.05)。IB期刮宫阳性者10年无病生存率为67%,阴性者为81%,混合情况者为77%(p = 0.02);IIA期相应比例分别为45%、66%和67%(p = 0.14)。由于这不是一项前瞻性II期剂量递增研究,各分期和肿瘤大小组中照射剂量与盆腔肿瘤控制的相关性并不一致。尽管如此,对于直径<2 cm的IB期和IIA期肿瘤,A点给予70 - 80 Gy剂量时盆腔失败率低于10%,而对于较大病变,即使给予85 - 90 Gy剂量,盆腔失败率仍为25%至37%。IIB期A点给予70 Gy剂量时,盆腔失败率约为50%,而剂量>80 Gy时,非巨大肿瘤约为20%,巨大肿瘤约为30%。III期单侧病变,A点给予≤70 Gy剂量时盆腔失败率约为50%,较高剂量时为35%;双侧或巨大肿瘤,剂量<70 Gy时为60%,较高剂量时为50%。
临床分期和肿瘤大小是子宫颈癌预后、治疗效果及结果评估的关键因素。A点剂量提示,对于<2 cm的病变,75 Gy剂量可使盆腔失败率≤10%,而对于范围更广的病变,即使给予85 Gy剂量,盆腔失败率仍约为30%;对于IIB - III期肿瘤,85 Gy剂量可导致35 - 50%的盆腔失败率。为改善目前浸润性宫颈癌的治疗效果,需要改进近距离放疗技术和/或使用药物使肿瘤对放疗产生选择性增敏作用。