Langer C J, Curran W J, Keller S M, Catalano R, Fowler W, Blankstein K, Litwin S, Bagchi P, Nash S, Comis R
Department of Medical Oncology, Fox Chase Cancer Center (FCCC), Philadelphia, PA 19111.
Int J Radiat Oncol Biol Phys. 1993 Jun 15;26(3):469-78. doi: 10.1016/0360-3016(93)90965-x.
To assess the response rate, median and long-term survival of patients (pts) with locally advanced, initially inoperable non-small cell lung cancer (NSCLC) treated on a phase II study of radical thoracic radiotherapy (TRT) and concurrent radiosensitizing chemotherapy.
From 3/87 to 7/90, 41 previously untreated patients at Fox Chase Cancer Center with locally advanced non-small cell lung cancer, 24 with bulky clinical Stage IIIA, and 17 with IIIB disease, received concurrent thoracic radiotherapy (60 Gy/2.0 Gy/d in 6 weeks) and 2 cycles of infusional 5FU (640-800 mg/m2/24 hrs x 5 d); cisplatin (20 mg/m2 qd x 5); and etoposide (50 mg/m2 d 1, 2, 5) administered days 1 and 28 of TRT.
Forty of 41 were evaluable. Response rate was 90%, with radiographic CR in 20%. Thirteen pts (33%) underwent thoracotomy and complete resection with clinical downstaging in 10, including three pathologic CR's. Overall median survival was 14 months and 2-year survival was 38% with no difference between CS IIIA and IIIB pts (p = 0.2224). At median potential follow-up of 42 months, 8/40 pts. (20%) are alive and progression-free, including 4 of 13 resected pts. The chief toxicity was esophagitis, occurring in 32 pts. (80%), Grade 3-4 in 21 (52%), with 13 (33%) requiring hospitalization and 7 (18%) needing TPN. Grade 3-4 granulocytopenia was noted in 20 pts. (50%) with ten episodes of fever mandating intravenous antibiotics. Cardiac ischemia was documented in 2 (5%). Of 13 thoracotomy pts, six underwent lobectomy without perioperative mortality; 3 of 7 pneumonectomy pts died post-operatively, two from broncopleural fistula, and one from ARDS.
This aggressive regimen produced a 2-year survival (38%) comparable to the best arm of cancer and leukemia groups B study 8433, which administered radical thoracic radiotherapy after protoadjuvant vinblastine and cisplatin in similar and earlier stage non-small cell lung cancer patients. Toxicity, particularly esophagitis, was severe, but of short duration. An unacceptably high complication rate was seen following pneumonectomy, but not lobectomy.
评估在一项局部晚期、初始不可切除的非小细胞肺癌(NSCLC)的II期根治性胸部放疗(TRT)和同步放射增敏化疗研究中患者的缓解率、中位生存期和长期生存率。
从1987年3月至1990年7月,福克斯蔡斯癌症中心的41例先前未接受过治疗的局部晚期非小细胞肺癌患者,其中24例为大块临床IIIA期,17例为IIIB期,接受同步胸部放疗(6周内60 Gy,2.0 Gy/天)以及2个周期的5-氟尿嘧啶静脉输注(640 - 800 mg/m²/24小时×5天);顺铂(20 mg/m²,每日1次,共5天);依托泊苷(50 mg/m²,第1、2、5天),在TRT的第1天和第28天给药。
41例患者中有40例可评估。缓解率为90%,影像学完全缓解率为20%。13例患者(33%)接受了开胸手术并完全切除,10例实现了临床分期降期,其中3例为病理完全缓解。总体中位生存期为14个月,2年生存率为38%,IIIA期和IIIB期患者之间无差异(p = 0.2224)。中位潜在随访42个月时,40例患者中有8例(20%)存活且无疾病进展,其中13例接受手术切除的患者中有4例。主要毒性为食管炎,32例患者(80%)发生,3 - 4级食管炎21例(52%),13例(33%)需要住院治疗,7例(18%)需要全胃肠外营养(TPN)。20例患者(50%)出现3 - 4级粒细胞减少,10次发热发作需要静脉使用抗生素。2例(5%)记录有心脏缺血。13例接受开胸手术的患者中,6例行肺叶切除术,无围手术期死亡;7例行全肺切除术的患者中有3例术后死亡,2例死于支气管胸膜瘘,1例死于急性呼吸窘迫综合征(ARDS)。
这种积极的治疗方案产生了2年生存率(38%),与癌症和白血病B组研究8433的最佳治疗组相当,该研究在类似的早期非小细胞肺癌患者中使用长春碱和顺铂进行原辅助化疗后给予根治性胸部放疗。毒性,尤其是食管炎,较为严重,但持续时间较短。全肺切除术后出现了不可接受地高并发症发生率,但肺叶切除术并非如此。