Hurwitz Mark D, Kaplan Irving D, Hansen Jorgen L, Prokopios-Davos Savina, Topulos George P, Wishnow Kenneth, Manola Judith, Bornstein Bruce A, Hynynen Kullervo
Department of Radiation Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Int J Radiat Oncol Biol Phys. 2002 Jul 15;53(4):913-8. doi: 10.1016/s0360-3016(02)02809-2.
Although hyperthermia has been used for more than two decades in the treatment of pelvic tumors, little is known about the potential impact of heat on rectal toxicity when combined with other treatment modalities. Because rectal toxicity is a concern with radiation and may be exacerbated by hyperthermia, definition of the association of thermal dose parameters with rectal toxicity is important. In this report, we correlate rectal toxicity with thermal dose parameters for patients treated with hyperthermia and radiation for prostate cancer.
Thirty patients with T2b-T3b disease (1992 American Joint Committee On Cancer criteria) enrolled in a Phase II study of external beam radiation +/- androgen-suppressive therapy with two transrectal ultrasound hyperthermia treatments were assessed for rectal toxicity. Prostatic and anterior rectal wall temperatures were monitored for all treatments. Rectal wall temperatures were limited to 40 degrees C in 19 patients, 41 degrees C in 3 patients, and 42 degrees C in 8 patients. Logistic regression was used to estimate the log hazard of developing National Cancer Institute Common Toxicity Criteria Grade 2 toxicity based on temperature parameters. The following were calculated: hazard ratios, 95% confidence intervals, p values for statistical significance of each parameter, and proportion of variability explained for each parameter.
Gastrointestinal toxicity was limited to Grade 2. The rate of acute Grade 2 proctitis was greater for patients with an allowable rectal wall temperature of >40 degrees C. In this group, 7 of 11 patients experienced acute Grade 2 proctitis, as opposed to 3 of 19 patients in the group with rectal wall temperatures limited to 40 degrees C (p = 0.004). Preliminary assessment of long-term toxicity revealed no differences in toxicity. Hazard ratios for acute Grade 2 proctitis for allowable rectal wall temperature, average rectal wall Tmax, and average prostate Tmax were 9.33 (p = 0.01), 3.66 (p = 0.03), and 2.29 (p = 0.08), respectively. A model combining these three parameters explained 48.6% of the variability among groups.
Rectal toxicity correlates with maximum allowable rectal wall temperature, average rectal wall Tmax, and average prostate Tmax for patients undergoing transrectal ultrasound hyperthermia combined with radiation for treatment of advanced clinically localized prostate cancer. Further definition of this association of thermal dose parameters with rectal toxicity in treatment of pelvic malignancies with hyperthermia should advance the goal of delivering thermal therapy in an effective yet safe manner.
尽管热疗已用于盆腔肿瘤治疗二十多年,但对于热疗与其他治疗方式联合应用时对直肠毒性的潜在影响知之甚少。由于直肠毒性是放疗时需要关注的问题,且热疗可能会使其加重,因此明确热剂量参数与直肠毒性之间的关联很重要。在本报告中,我们将接受热疗和放疗的前列腺癌患者的直肠毒性与热剂量参数进行了关联分析。
30例患有T2b - T3b期疾病(按照1992年美国癌症联合委员会标准)的患者参加了一项II期研究,该研究采用外照射放疗±雄激素抑制治疗,并进行两次经直肠超声热疗,对这些患者的直肠毒性进行了评估。所有治疗过程中均监测前列腺和直肠前壁温度。19例患者的直肠壁温度限制在40℃,3例患者限制在41℃,8例患者限制在42℃。采用逻辑回归分析,根据温度参数估计发生美国国立癌症研究所常见毒性标准2级毒性的对数风险。计算了以下指标:风险比、95%置信区间、各参数统计学显著性的p值以及各参数可解释的变异比例。
胃肠道毒性仅限于2级。直肠壁允许温度>40℃的患者急性2级直肠炎发生率更高。在该组中,11例患者中有7例发生急性2级直肠炎,而直肠壁温度限制在40℃的19例患者中有3例发生(p = 0.004)。对长期毒性的初步评估显示毒性无差异。直肠壁允许温度、直肠壁平均Tmax和前列腺平均Tmax发生急性2级直肠炎的风险比分别为9.33(p = 0.01)、3.66(p = 0.03)和2.29(p = 0.08)。结合这三个参数的模型解释了组间48.6%的变异。
对于接受经直肠超声热疗联合放疗治疗晚期临床局限性前列腺癌的患者,直肠毒性与直肠壁最大允许温度、直肠壁平均Tmax和前列腺平均Tmax相关。在热疗治疗盆腔恶性肿瘤中,进一步明确这种热剂量参数与直肠毒性的关联,应有助于实现以有效且安全的方式进行热疗的目标。