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Analysis of key clinical features for achieving complete remission in stage III and IV non-small cell lung cancer patients

BACKGROUND: Although development of immune checkpoint inhibitors and various molecular target agents has extended overall survival time (OS) in advanced non-small cell lung cancer (NSCLC), a complete cure remains rare. We aimed to identify features and treatment modalities of complete remission (CR)...

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Detalles Bibliográficos
Autores principales: Aoki, Takuya, Akiba, Takeshi, Nishiyama, Jun, Tajiri, Sakurako, Hayama, Naoki, Takahashi, Genki, Tanaka, Jun, Sato, Masako, Takiguchi, Hiroto, Tomomatsu, Hiromi, Tomomatsu, Katsuyoshi, Takihara, Takahisa, Niimi, Kyoko, Oguma, Tsuyoshi, Kohno, Mitsutomo, Masuda, Ryota, Urano, Tetsuya, Itoh, Hitoshi, Kajiwara, Hiroshi, Nakamura, Naoya, Kunieda, Etsuo, Matsumae, Mitsunori, Iwazaki, Masayuki, Asano, Koichiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6873580/
https://www.ncbi.nlm.nih.gov/pubmed/31752884
http://dx.doi.org/10.1186/s12931-019-1235-3
Descripción
Sumario:BACKGROUND: Although development of immune checkpoint inhibitors and various molecular target agents has extended overall survival time (OS) in advanced non-small cell lung cancer (NSCLC), a complete cure remains rare. We aimed to identify features and treatment modalities of complete remission (CR) cases in stages III and IV NSCLC by analyzing long-term survivors whose OS exceeded 3 years. METHODS: From our hospital database, 1,699 patients, registered as lung cancer between 1(st) Mar 2004 and 30(th) Apr 2011, were retrospectively examined. Stage III or IV histologically or cytologically confirmed NSCLC patients with chemotherapy initiated during this period were enrolled. A Cox proportion hazards regression model was used. Data collection was closed on 13(th) Feb 2017. RESULTS: There were 164 stage III and 279 stage IV patients, including 37 (22.6%) and 51 (18.3%) long-term survivors and 12 (7.3%) and 5 (1.8%) CR patients, respectively. The long-term survivors were divided into three groups: 3 ≤ OS < 5 years, 5 years ≤ OS with tumor, and 5 years ≤ OS without tumor (CR). The median OS of these groups were 1,405, 2,238, and 2,876 days in stage III and 1,368, 2,503, and 2,643 days in stage IV, respectively. The mean chemotherapy cycle numbers were 16, 20, and 10 in stage III and 24, 25, and 5 in stage IV, respectively. In the stage III CR group, all patients received chemoradiation, all oligometastases were controlled by radiation, and none had brain metastases. Compared with non-CR patients, the stage IV CR patients had smaller primary tumors and fewer metastases, which were independent prognostic factors for OS among long-term survivors. The 80% stage IV CR patients received radiation or surgery for controlling primary tumors, and the surgery rate for oligometastases was high. Pathological findings in the stage IV CR patients revealed that numerous inflammatory cells existed around and inside resected lung and brain tumors, indicating strong immune response. CONCLUSIONS: Multiple line chemotherapies with primary and oligometastatic controls by surgery and/or radiation might achieve cure in certain advanced NSCLC. Cure strategies must be changed according to stage III or IV. This study was retrospectively registered on 16(th) Jun 2019 in UMIN Clinical Trials Registry (number UMIN000037078).