Issels R D, Bosse D, Abdel-Rahman S, Starck M, Panzer M, Jauch K W, Stiegler H, Berger H, Sauer H, Peter K
Institut für Klinische Hämatologie (GSF), University of Munich, Federal Republic of Germany.
Cancer Chemother Pharmacol. 1993;31 Suppl 2:S233-7.
From November 1990 to September 1991, 23 adults with high-risk, nonmetastatic sarcomas (20 soft-tissue sarcomas and 3 chondrosarcomas) were entered in a pilot protocol (RHT-91) involving regional hyperthermia combined with systemic chemotherapy followed by surgery. Of these patients, 12 had undergone previous surgery and/or radiation, 5 had received previous multidrug chemotherapy, and 6 were previously untreated. A tumor size of > 8 cm and/or an extracompartmental tumor location (11 patients) or local recurrence (12 patients) were defined as high-risk factors in addition to tumor grading (21 patients had grade 2 or 3 sarcomas). Regional hyperthermia was produced by an electromagnetic deep-regional-heating device. For systemic chemotherapy, all patients received etoposide/ifosfamide/doxorubicin (EIA) and mesna, with regional hyperthermia being given only on days 1 and 4 in repeated EIA/regional hyperthermia cycles every 3 weeks. Tumor temperatures (range, 40 degrees-44 degrees C) were measured by invasive thermometry in all patients during each regional hyperthermia treatment. A total of 181 regional hyperthermia treatments were applied within the pelvic region (11 patients) or extremities (12 patients) bearing relatively large tumors (mean volume, 848 cm3). By the cutoff date for this analysis (October 15, 1991), 13 patients had undergone surgery after receiving 2-6 (mean, 3.8) cycles of EIA chemotherapy combined with regional hyperthermia; all tumors except one were resected without disfiguration. In 22 evaluable patients (minimum, 2 EIA plus regional hyperthermia cycles), the clinical response rate was 27%, with 6 patients showing partial responses (PRs). In addition, a pathologic response to preoperative thermochemotherapy was evaluable in 13 patients, with 4 responders (31%) having > 50% histologic necrosis. In all, 3 of the responders (1 PR and 2 patients with > 50% histologic necrosis) relapsed within 3 months of surgical resection. The other 7 responding patients (5 PRs and 2 patients with > 50% histologic necrosis) showed stable disease with local tumor control. The study (RHT-91) is continuing as a multicenter phase II trial (opened on November 19, 1991) in patients with high-risk soft-tissue sarcomas to test the potential of preoperative thermochemotherapy in regard to local control and survival.
1990年11月至1991年9月,23例患有高危、非转移性肉瘤(20例软组织肉瘤和3例软骨肉瘤)的成人患者进入一项试验方案(RHT - 91),该方案包括区域热疗联合全身化疗,随后进行手术。在这些患者中,12例曾接受过手术和/或放疗,5例曾接受过联合化疗,6例此前未接受过治疗。除肿瘤分级外(21例患者为2级或3级肉瘤),肿瘤大小>8 cm和/或肿瘤位于筋膜外(11例患者)或局部复发(12例患者)被定义为高危因素。区域热疗由电磁深部区域加热设备产生。对于全身化疗,所有患者均接受依托泊苷/异环磷酰胺/阿霉素(EIA)和美司钠,区域热疗仅在每3周重复的EIA/区域热疗周期的第1天和第4天进行。在每次区域热疗期间,通过侵入性测温法测量所有患者的肿瘤温度(范围为40摄氏度至44摄氏度)。在盆腔区域(11例患者)或四肢(12例患者)对相对较大的肿瘤(平均体积848 cm³)总共进行了181次区域热疗。截至该分析的截止日期(1991年10月15日),13例患者在接受2 - 6个(平均3.8个)周期的EIA化疗联合区域热疗后接受了手术;除1例肿瘤外,所有肿瘤均在无畸形的情况下被切除。在22例可评估患者(至少接受2个EIA加区域热疗周期)中,临床缓解率为27%,6例患者出现部分缓解(PR)。此外,13例患者可评估术前热化疗的病理反应,4例反应者(31%)组织学坏死>50%。总共有3例反应者(1例PR和2例组织学坏死>50%的患者)在手术切除后3个月内复发。其他7例有反应的患者(5例PR和2例组织学坏死>50%的患者)病情稳定,局部肿瘤得到控制。该研究(RHT - 91)作为一项多中心II期试验(于1991年11月19日开始)仍在继续,针对高危软组织肉瘤患者,以测试术前热化疗在局部控制和生存方面的潜力。