Machtay Mitchell, Lee Jason H, Stevenson James P, Shrager Joseph B, Algazy Kenneth M, Treat Joseph, Kaiser Larry R
Department of Radiation Oncology, University of Pennsylvania Medical Center, Philadelphia, PA 19104, USA.
J Thorac Cardiovasc Surg. 2004 Jan;127(1):108-13. doi: 10.1016/j.jtcvs.2003.07.027.
We performed this study to determine the outcomes (pathologic response, survival, local-regional control, and toxicity) in patients treated with neoadjuvant chemoradiotherapy and planned operation for stage IIIA non-small cell lung carcinoma.
Patients treated from 1993 to 2000 with neoadjuvant chemoradiotherapy and a predetermined plan for subsequent surgical resection for stage III non-small cell lung carcinoma were analyzed. All patients underwent pretreatment evaluation at the university's Multidisciplinary Lung Cancer Center. Most patients (87%) had complete mediastinoscopy staging, and all were believed to be poor candidates for up-front operation because of bulky extent of disease. The radiotherapy program used conventional, 2-dimensionally planned treatment to 45 to 54 Gy in 1.8- to 2-Gy fraction size. Concurrent chemotherapy consisted of etoposide/cisplatin or carboplatin/paclitaxel. Study end points included resectability, pathologic response, local-regional control, survival, and toxicity. An exploratory comparison between pathologic response and long-term survival was performed. An exploratory comparison between older chemotherapy (etoposide/cisplatin) and third-generation chemotherapy (carboplatin/paclitaxel) was also performed.
Of 53 patients, 45 (85%) were deemed surgical candidates after induction therapy. Twenty-two (42% of the initial cohort) patients had a major pathologic response to stage 0, I, or II disease. The 5-year actuarial survival was 31%. Major pathologic response was associated with improved survival (48% vs 24%; P =.027). The overall rate of early death potentially related to therapy in this series was 9%; this mostly occurred in patients who underwent right pneumonectomy. There was no difference in efficacy or mortality between etoposide/cisplatin and radiotherapy versus carboplatin/paclitaxel and radiotherapy, although the latter regimen was associated with less grade 3 or higher acute toxicity necessitating interruption or hospitalization during neoadjuvant treatment (P =.02). In-field local control was achieved in 83% of all patients (90% of the patients who underwent resection). Brain metastases as the first site of treatment failure occurred in 23% of all patients.
Neoadjuvant concurrent chemoradiation delivers high resectability, major pathologic response rate, and excellent local-regional control, with encouraging long-term survival considering the patient population studied. Major pathologic response correlates with long-term survival. Neoadjuvant carboplatin/paclitaxel and radiotherapy is an appropriate framework on which to add new therapies.
我们开展这项研究以确定接受新辅助放化疗并计划行手术治疗的IIIA期非小细胞肺癌患者的治疗结果(病理反应、生存率、局部区域控制和毒性)。
分析1993年至2000年期间接受新辅助放化疗及后续III期非小细胞肺癌预定手术切除计划治疗的患者。所有患者均在大学的多学科肺癌中心接受了预处理评估。大多数患者(87%)接受了完整的纵隔镜分期,且由于疾病范围广泛,所有患者均被认为不适合直接进行手术。放疗方案采用常规二维计划治疗,剂量为45至54 Gy,每次分割剂量为1.8至2 Gy。同步化疗包括依托泊苷/顺铂或卡铂/紫杉醇。研究终点包括可切除性、病理反应、局部区域控制、生存率和毒性。对病理反应和长期生存进行了探索性比较。还对较旧的化疗方案(依托泊苷/顺铂)和第三代化疗方案(卡铂/紫杉醇)进行了探索性比较。
53例患者中,45例(85%)在诱导治疗后被认为是手术候选者。22例(占初始队列的42%)患者对0期、I期或II期疾病有主要病理反应。5年精算生存率为31%。主要病理反应与生存率提高相关(48%对24%;P = 0.027)。本系列中可能与治疗相关的早期死亡率为9%;这主要发生在接受右肺切除术的患者中。依托泊苷/顺铂联合放疗与卡铂/紫杉醇联合放疗在疗效或死亡率方面无差异,尽管后一种方案在新辅助治疗期间与3级或更高等级的急性毒性较少相关,这种毒性需要中断治疗或住院治疗(P = 0.02)。83%的所有患者(接受切除的患者中的90%)实现了野内局部控制。23%的所有患者发生脑转移作为首次治疗失败部位。
考虑到所研究的患者群体,新辅助同步放化疗具有高可切除性、主要病理反应率和出色的局部区域控制,长期生存令人鼓舞。主要病理反应与长期生存相关。新辅助卡铂/紫杉醇联合放疗是添加新疗法的合适框架。