Hallqvist Andreas, Rylander Hillevi, Björk-Eriksson Thomas, Nyman Jan
Department of Oncology, Sahlgrenska University Hospital, Gothenburg, Sweden.
Acta Oncol. 2007;46(7):969-74. doi: 10.1080/02841860701316065.
Addition of thoracic radiation therapy (TRT) to chemotherapy (CHT) can increase overall survival in patients with small cell lung cancer limited-disease (SCLC-LD). Accelerated fractionation and early concurrent platinum-based CHT, in combination with prophylactic cranial irradiation, represent up-front treatment for this group of patients. Optimised and tailored local and systemic treatment is important. These concepts were applied when a new regional treatment programme was designed at Sahlgrenska University Hospital in 1997. The planned treatment consisted of six courses of CHT (carboplatin/etoposide) + TRT +/- prophylactic cranial irradiation (PCI). Standard TRT was prescribed at 1.5 Gy BID to a total of 60 Gy during 4 weeks, starting concomitantly with the second or third course of CHT. However, patients with large tumour burdens, poor general condition and/or poor lung function received 45 Gy, 1.5 Gy BID, during 3 weeks. PCI in 15 fractions to a total dose of 30 Gy was administered to all patients with complete remission (CR) and "good" partial remission (PR) at response evaluation. Eighty consecutive patients were treated between January 1998 and December 2004. Forty-six patients were given 60 Gy and 34 patients 45 Gy. Acute toxicity occurred as esophagitis grade III (RTOG/EORTC) in 16% and as pneumonitis grade I-II in 10%. There were no differences in toxicity between the two groups. Three- and five-year overall survival was 25% and 16%, respectively. Medica survival was 20.8 months with no significant difference between the two groups. In conclusion, TRT with a total dose of 60 to 45 Gy is feasible with comparable toxicity and no difference in local control or survival. Distant metastasis is the main cause of death in this disease; the future challenge is thus further improvement of the systemic therapy combines with optimised local TRT.
在局限期小细胞肺癌(SCLC-LD)患者的化疗(CHT)中加入胸部放射治疗(TRT)可提高总生存率。加速分割和早期同步铂类CHT,联合预防性颅脑照射,是这类患者的前期治疗方案。优化和定制局部及全身治疗很重要。1997年在萨尔格伦斯卡大学医院设计新的区域治疗方案时应用了这些理念。计划的治疗包括六个疗程的CHT(卡铂/依托泊苷)+TRT+/-预防性颅脑照射(PCI)。标准TRT规定为每日两次,每次1.5 Gy,共60 Gy,在4周内完成,与第二或第三个疗程的CHT同时开始。然而,肿瘤负荷大、一般状况差和/或肺功能差的患者在3周内接受45 Gy,每日两次,每次1.5 Gy。对所有在疗效评估时达到完全缓解(CR)和“良好”部分缓解(PR)的患者给予15次分割、总剂量30 Gy的PCI。1998年1月至2004年12月期间连续治疗了80例患者。46例患者接受60 Gy,34例患者接受45 Gy。急性毒性反应表现为16%的患者出现III级食管炎(RTOG/EORTC),10%的患者出现I-II级肺炎。两组之间的毒性反应无差异。三年和五年总生存率分别为25%和16%。中位生存期为20.8个月,两组之间无显著差异。总之,总剂量为60至45 Gy的TRT是可行的,毒性相当,局部控制或生存率无差异。远处转移是该疾病死亡的主要原因;因此,未来面临的挑战是进一步改善全身治疗并结合优化的局部TRT。