Kimura Hideki, Iizasa Toshihiko, Ishikawa Aki, Shingyouji Masato, Yoshino Mitsuru, Kimura Masaki, Inada Yutaka, Matsubayashi Keiko
Division of Thoracic Diseases, Chiba Cancer Center, Chuo-ku, Chiba City, Chiba, Japan.
Anticancer Res. 2008 Mar-Apr;28(2B):1229-38.
The efficacy and toxicity of adjuvant chemo-immunotherapy using dendritic cells and activated killer cells are not clear in post-surgical primary lung cancer patients.
Pathologically diagnosed N2 lung cancer patients were selected for postsurgical adjuvant chemo-immunotherapy. The activated killer cells and dendritic cells (AKT-DC) obtained from tissue cultures of tumor-draining lymph nodes (TDLN) or from TDLN co-cultured with peripheral blood lymphocytes (TDLN-Pb) were used for the adoptive transfer of immunotherapy. The patients received 4 courses of chemotherapy along with immunotherapy every 2 months for 2 years.
There were 31 N2 patients eligible for the study. Three cases were excluded because of refusal by the patients after 1-2 courses of immunotherapy. For the 28 cases treated, a total of 313 courses of immunotherapy were administered. The main toxicities were fever (78.0%), chill (83.4%), fatigue (23.0%) and nausea (17.0%) on the day of cell transfer. The 2- and 5-year survival rates were 88.9 % (95.9-81.9; 95% confidence interval, C.I.) and 52.9% (76.4-29.4; C.I.).
Adoptive transfer of activated killer cells and dendritic cells from the tumor-draining lymph nodes of primary lung cancer patients is feasible and safe, and a large-scale multi-institutional study is necessary for evaluation of the efficacy of this treatment.
在外科手术后的原发性肺癌患者中,使用树突状细胞和活化杀伤细胞进行辅助化学免疫疗法的疗效和毒性尚不清楚。
选择经病理诊断的N2期肺癌患者进行术后辅助化学免疫治疗。从肿瘤引流淋巴结(TDLN)的组织培养物或与外周血淋巴细胞共培养的TDLN(TDLN-Pb)中获得的活化杀伤细胞和树突状细胞(AKT-DC)用于免疫治疗的过继性转移。患者每2个月接受4个疗程的化疗并同时进行免疫治疗,共持续2年。
有31例N2期患者符合研究条件。3例患者在接受1-2个疗程的免疫治疗后因拒绝而被排除。对于接受治疗的28例患者,共进行了313个疗程的免疫治疗。主要毒性反应为细胞转移当天出现发热(78.0%)、寒战(83.4%)、疲劳(23.0%)和恶心(17.0%)。2年和5年生存率分别为88.9%(95.9 - 81.9;95%置信区间,C.I.)和52.9%(76.4 - 29.4;C.I.)。
原发性肺癌患者肿瘤引流淋巴结来源的活化杀伤细胞和树突状细胞的过继性转移是可行且安全的,需要进行大规模多机构研究以评估该治疗方法的疗效。