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Poster display session

521P - A randomized, phase II study comparing irinotecan versus amrubicin as maintenance therapy after first-line induction therapy for extensive disease small cell lung cancer (HOT1401/NJLCG1401)

Date

23 Nov 2019

Session

Poster display session

Topics

Tumour Site

Small Cell Lung Cancer

Presenters

Keisuke Baba

Citation

Annals of Oncology (2019) 30 (suppl_9): ix157-ix181. 10.1093/annonc/mdz437

Authors

K. Baba1, H. Tanaka2, Y. Fujita3, A. Nakamura4, E. Kikuchi5, Y. Kawai6, T. Harada7, N. Watanabe8, H. Yokouchi9, K. Usui10, R. Saito11, H. Watanabe12, T. Masuda13, T. Fukuhara14, K. Kudo15, R. Honda16, S. Oizimi17, M. Maemondo18, A. Inoue19, N. Morikawa18

Author affiliations

  • 1 Department Of Respiratory Medicine, Aomori Prefectural Central Hospital, 030-8553 - Hirosaki/JP
  • 2 Department Of Respiratory Medicine, Hirosaki University, 036-8562 - Hirosaki/JP
  • 3 3. department Of Respiratory Medicine, National Hospital Organization Asahikawa Medical Center, 070-8644 - Asahikawa/JP
  • 4 Respiratory Medicine, Sendai Kousei Hospital, 980-0873 - Sendai/JP
  • 5 5. first Department Of Medicine, Hokkaido University Hospital, 0608648 - Sapporo/JP
  • 6 6. department Of Respiratory Medicine, Oji General Hospital, 0538506 - Tomakomai/JP
  • 7 Department Of Respiratory Medicine, JCHO Hokkaido Hospital, 062-8618 - Sapporo/JP
  • 8 8. department Of Respiratory Medicine, Sunagawa City Medical Center, Sunagawa/JP
  • 9 9. department Of Pulmonary Medicine, Fukushima Medical University School of Medicine, Fukushim/JP
  • 10 11. division Of Respirology, NTT Medical Center Tokyo, Tokyo/JP
  • 11 12. department Of Respiratory Medicine, Tohoku University School of Medicine, Sendai/JP
  • 12 13. department Of Respiratory Medicine, Saka General Hospital, Sendai/JP
  • 13 14. department Of Respiratory Medicine, Gunma University, Maebashi/JP
  • 14 15. department Of Respiratory Medicine, Miyagi Cancer Center, Sendai/JP
  • 15 16. department Of Medical Oncology And Department Of Respiratory Medicine, National Hospital Organization Osaka Minami Medical Center, Osaka/JP
  • 16 17. department Of Respiratory Medicine, Asahi General Hospital, Chiba/JP
  • 17 10. department Of Respiratory Medicine, National Hospital Organization Hokkaido Cancer Center, Sapporo/JP
  • 18 18. division Of Pulmonary Medicine, Allergy, And Rheumatology, Iwate Medical University, Morioka/JP
  • 19 19. department Of Palliative Medicine, Tohoku University School of Medicine, Sendai/JP

Resources

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Abstract 521P

Background

Cisplatin plus irinotecan (PI) regimen is used for patients with extensive disease (ED)-SCLC. Amrubicin is mainly used for relapsed SCLC. HOT1401/NJLCG1401 trial, open-label randomized phase II trials was designed to assess the benefit of maintenance therapy in patients with ED-SCLC who responded induction therapy.

Methods

Eligible patients were aged 20-74 years; had histologically or cytologically confirmed, ED-SCLC. After induction therapy PI (P: 60mg/m2 on day 1, I: 60mg/m2 on days 1, 8, 15, every 4 weeks for 4 cycles), patients who attained CR, PR and SD were randomized to either maintenance irinotecan (I: 60mg/m2 on days 1, 8, every 3 weeks) or amrubicin (A: 35 mg/m2 on days 1-3 every 3 weeks). The primary endpoint is 6-months PFS rate.

Results

A total of 34 patients were enrolled from 2014 to 2017. Twenty patients had disease progression or incomplete of induction chemotherapy, finally 14 (41.1%) patients were randomly assigned to receive irinotecan (n = 7) and amrubicin (n = 7). This study was terminated prematurely because of low patient accrual. Of the evaluable patients (n = 34) the overall objective response rate was 73%, median progression free survival was 5.7 months (95% CI: 3.6 -11.8), and median overall survival was 20.1 months (95% CI: 13.7-NR). Six months PFS rate was 47 % (95%CI: 31.4-63.2). Sub group analysis showed the patients receive maintenance group showed longer PFS and OS than those without (15.8 months and 3.5 months, respectively p < 0.001), (15.4 months and NR months, respectively p = 0.0016). There was no difference in median PFS between the patients treated with irinotecan and those with amrubicin (7.4 months and 21.1 months, respectively p = 0.63). The most common adverse events were neutropenia, anemia during maintenance therapy. Grade 3 or higher hematological toxicity was observed more frequently in amrubicin arm. Treatment related death was not observed in this study.

Conclusions

Maintenance therapy of irinotecan or amrubicin after induction therapy was well tolerated. Some patients might be effective for maintenance therapy.

Clinical trial identification

UMIN 000013882.

Editorial acknowledgement

Legal entity responsible for the study

HOT/NJLCG.

Funding

Has not received any funding.

Disclosure

All authors have declared no conflicts of interest.

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