Randomized phase III study of irinotecan/cisplatin (IP) versus etoposide/cisplatin (EP) for completely resected high-grade neuroendocrine carcinoma (HGNEC) of the lung: JCOG1205/1206.

Authors

null

Hirotsugu Kenmotsu

Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan

Hirotsugu Kenmotsu , Seiji Niho , Masahiro Tsuboi , Masashi Wakabayashi , Genichiro Ishii , Kazuo Nakagawa , Haruko Daga , Hiroshi Tanaka , Haruhiro Saito , Keiju Aokage , Toshiaki Takahashi , Toshi Menju , Takashi Kasai , Ichiro Yoshino , Koichi Minato , Morihito Okada , Hiroshi Katayama , Hisao Asamura , Yuichiro Ohe , Shun-ichi Watanabe

Organizations

Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka, Japan, National Cancer Center Hospital East, Kashiwa, Japan, Department of Thoracic Surgery and Oncology, National Cancer Center Hospital East, Chiba, Japan, Clinical Research Support Office, National Cancer Center Hospital East, Kashiwa, Japan, Exploratory Oncology Research & Clinical Trial Center, National Cancer Center, Kashiwa, Japan, Department of Thoracic Surgery, National Cancer Center Hospital, Tokyo, Japan, Department of Medical Oncology, Osaka City General Hospital, Osaka, Japan, Department of Respiratory Medicine, Niigata Cancer Center Hospital, Niigata, Japan, Department of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan, National Cancer Center Hospital East, Chiba, Japan, Department of Thoracic Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan, Department of Respiratory Medicine, Tochigi Cancer Center, Utsunomiya, Japan, Department of General Thoracic Surgery, Chiba University Graduate School of Medicine, Chiba, Japan, Division of Respiratory Medicine, Gunma Prefectural Cancer Center, Ota, Japan, Hiroshima University Hospital, Department of Surgical Oncology, Hiroshima, Japan, Japan Clinical Oncology Group Data Center/Operations Office, National Cancer Center Hospital, Tokyo, Japan, Keio University School of Medicine, Tokyo, Japan, National Cancer Center Hospital, Tokyo, Japan, Division of Thoracic Surgery, National Cancer Center Hospital, Tokyo, Japan

Research Funding

Other
the Japan Agency for Medical Research and Development

Background: In the WHO classification, small cell lung cancer (SCLC) and large cell neuroendocrine carcinoma (LCNEC) are considered as high-grade neuroendocrine carcinoma (HGNEC) of the lung. Although there were no randomized trials evaluating adjuvant chemotherapy for patients (pts) with resected HGNEC, EP was considered to be a standard regimen for this population. A phase III study showed the superiority of IP to EP in pts with extensive stage SCLC (JCOG9511). Methods: Pts with completely resected HGNEC were randomized in a 1:1 ratio to receive either etoposide (100 mg/m2, days 1-3)/cisplatin (80 mg/m2, day 1) or irinotecan (60 mg/m2, days 1, 8, 15)/cisplatin (60 mg/m2, day 1), using the minimization method according to sex, pathologic stage, histology and institution. The primary endpoint was changed from overall survival (OS) to relapse-free survival (RFS) during the study period. We assumed a 3-year RFS of 59% of EP arm and 72% of IP arm (hazard ratio (HR) of 0.623). Planned sample size was 220 in total to give a power of 80% with a one-sided alpha of 5%, an accrual period of 6 years and a follow-up period of 3 years. Results: Between April 2013 and October 2018, 221 pts with a median age of 66 years, pathological stage I (54%), SCLC (53%), were randomly assigned to the EP arm (n = 111) or the IP arm (n = 110). In the second interim analysis, the predictive probability that IP would be superior to EP at the time of the primary analysis was 15.9%, which led to early termination of the trial. With a median follow-up of 24.1 months, 3-year RFS was 65.4% versus 69.0% with HR of 1.076 (95% CI, 0.666-1.738; log-rank test, one-sided P= 0.619). In the subgroup analyses of histology, 3-year RFS in SCLC was 65.2% versus 66.5% with HR of 1.029 (95% CI, 0.544-1.944), and 3-year RFS in LCNEC was 66.5% versus 72.0% with HR of 1.072 (95% CI, 0.517-2.222). Overall survival at 3 years was 84.1% versus 79.0% with HR of 1.539 (95% CI, 0.760-3.117). Proportions of treatment completion were 87.4% (EP) and 72.7% (IP). Incidences (EP/IP) of grade 3 or 4 febrile neutropenia (20.2/3.7%) or neutropenia (97.2/35.8%) were more common in EP. Grade 3 or 4 diarrhea (0.9/8.3%) or anorexia (6.4/11.1%) were more common in IP. One treatment-related death due to tracheal bleeding was observed in IP. Conclusions: This study failed to show the superiority of IP to EP in RFS for pts with completely resected HGNEC. EP is still a standard treatment for this population. Clinical trial information: UMIN000010298.

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Abstract Details

Meeting

2020 ASCO Virtual Scientific Program

Session Type

Oral Abstract Session

Session Title

Lung Cancer—Non-Small Cell Local-Regional/Small Cell/Other Thoracic Cancers

Track

Lung Cancer

Sub Track

Small Cell Lung Cancer

Clinical Trial Registration Number

UMIN000010298

Citation

J Clin Oncol 38: 2020 (suppl; abstr 9006)

DOI

10.1200/JCO.2020.38.15_suppl.9006

Abstract #

9006

Abstract Disclosures