Skip to main content

Advertisement

Log in

Lower optimal dose of amrubicin for relapsed small-cell lung cancer: a retrospective study

  • Original Article
  • Published:
International Journal of Clinical Oncology Aims and scope Submit manuscript

Abstract

Background

Amrubicin (AMR) is one of the most active agents for small-cell lung cancer (SCLC). However, hematologic toxicity and infection at a commonly used dose (40 mg/m2) is problematic; the optimal dose remains undetermined.

Patients and methods

To evaluate the optimal dose of AMR in terms of efficacy and safety, we reviewed consecutive data on patients with relapsed SCLC who received AMR at doses of 40, 35, and 30 mg/m2 (on days 1–3) at Nippon Medical School Hospital between October 2010 and November 2021.

Results

We reviewed the data of 86 patients (20, 45, 27 who received AMR doses of 40, 35, 30 mg/m2, respectively) according to our study criteria. For patients  ≥ 75 years, the proportion who received second-line treatment tended to be higher in the 30–35 mg/m2 group. Objective response rates were 37/46/35%, median progression-free survival (PFS) were 3.0/4.7/3.2 months, and median overall survival (OS) were 7.8/16.3/8.0 months, respectively. Grade 4 neutropenia occurred in 58/39/31% of patients, which was higher for the 40 mg/m2 group. The incidence of febrile neutropenia did not differ between groups. Multivariate analysis identified the AMR dose was not associated with longer PFS and OS.

Conclusion

Treatment with AMR between 30 and 35 mg/m2 showed relatively mild hematologic toxicity compared with AMR at 40 mg/m2, without any significant difference in efficacy. Lower dose of AMR for relapsed SCLC could be a promising treatment option.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1

Similar content being viewed by others

References

  1. Siegel RL, Miller KD, Jemal A (2020) Cancer statistics, 2020. CA Cancer J Clin 70:7–30

    Article  PubMed  Google Scholar 

  2. Das M, Padda SK, Weiss J et al (2021) Advances in treatment of recurrent Small Cell Lung Cancer (SCLC): insights for optimizing patient outcomes from an expert roundtable discussion. Adv Ther 38:5431–5451

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  3. Hanada M, Mizuno S, Fukushima A et al (1998) A new antitumor agent amrubicin induces cell growth inhibition by stabilizing topoisomerase II-DNA complex. Jpn J Cancer Res 89:1229–1238

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Sekine I, Okamoto H, Horai T et al (2014) A randomized phase III study of single-agent amrubicin vs. carboplatin/etoposide in elderly patients with extensive-disease small-cell lung cancer. Clin Lung Cancer 15:96–102

    Article  CAS  PubMed  Google Scholar 

  5. von Pawel J, Jotte R, Spigel DR et al (2014) Randomized phase III trial of amrubicin versus topotecan as second-line treatment for patients with small-cell lung cancer. J Clin Oncol 32:4012–4019

    Article  Google Scholar 

  6. Eisenhauer EA, Therasse P, Bogaerts J et al (2009) New response evaluation criteria in solid tumours: revised RECIST guideline (version 1.1). Eur J Cancer 45:228–247

    Article  CAS  PubMed  Google Scholar 

  7. Kaira K, Sunaga N, Tomizawa Y et al (2010) A phase II study of amrubicin, a synthetic 9-aminoanthracycline, in patients with previously treated lung cancer. Lung Cancer 69:99–104

    Article  PubMed  Google Scholar 

  8. Asai N, Ohkuni Y, Matsunuma R et al (2012) Efficacy and safety of amurubicin for the elderly patients with refractory relapsed small cell lung cancer as third-line chemotherapy. J Cancer Res Ther 8:266–271

    Article  CAS  PubMed  Google Scholar 

  9. Shimokawa T, Shibuya M, Kitamura K et al (2009) Retrospective analysis of efficacy and safety of amrubicin in refractory and relapsed small-cell lung cancer. Int J Clin Oncol 14:63–69

    Article  CAS  PubMed  Google Scholar 

  10. Foster NR, Mandrekar SJ, Schild SE et al (2009) Prognostic factors differ by tumor stage for small cell lung cancer: a pooled analysis of North Central Cancer Treatment Group trials. Cancer 115:2721–2731

    Article  CAS  PubMed  Google Scholar 

  11. Albain KS, Crowley JJ, LeBlanc M et al (1990) Determinants of improved outcome in small-cell lung cancer: an analysis of the 2,580-patient Southwest Oncology Group data base. J Clin Oncol 8:1563–1574

    Article  CAS  PubMed  Google Scholar 

  12. Horn L, Mansfield AS, Szczęsna A et al (2018) First-line atezolizumab plus chemotherapy in extensive-stage small-cell lung cancer. N Engl J Med 379:2220–2229

    Article  CAS  PubMed  Google Scholar 

  13. Paz-Ares L, Dvorkin M, Chen Y et al (2019) Durvalumab plus platinum-etoposide versus platinum-etoposide in first- line treatment of extensive-stage small-cell lung can- cer (CASPIAN): a randomised, controlled, open-label, phase 3 trial. Lancet 394:1929–1939

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgements

The authors thank the study participants, who provided clinicopathological data for our analysis.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Shinji Nakamichi.

Ethics declarations

Conflict of interest

Dr. Kubota received research fund from Nihon Kayaku, AstraZeneca and payment or honoraria for lectures and presentations from Chugai Pharmaceutical. Dr. Seike received payment or honoraria for lectures and presentations from AstraZeneca, Chugai Pharmaceutical, Taiho Pharmaceutical, MSD, Ono Pharmaceutical, Bristol–Myers Squibb, Eli Lilly Japan, Takeda Pharmaceutical, Nihon Kayaku, Nippon Boehringer Ingelheim, Pfizer, Kyowa–Hakko Kirin, and Novartis. No other disclosures were reported.

Ethics statement

The protocol of this study was approved by the Institutional Review Board of Nippon Medical School Hospital (B-2022-538).

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Nakamichi, S., Kubota, K., Zou, F. et al. Lower optimal dose of amrubicin for relapsed small-cell lung cancer: a retrospective study. Int J Clin Oncol 28, 872–879 (2023). https://doi.org/10.1007/s10147-023-02343-9

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10147-023-02343-9

Keywords

Navigation