Clinical outcomes for patients with thymoma and thymic carcinoma after undergoing different front-line chemotherapy regimens

Cancer Med. 2022 Sep;11(18):3445-3456. doi: 10.1002/cam4.4711. Epub 2022 Mar 29.

Abstract

Background: Front-line platinum-base chemotherapy for advanced thymoma and thymic carcinoma (TC) improves resectability and prolongs patients' overall survival (OS). In this study, we evaluated patients' outcomes given different front-line regimens: cisplatin, doxorubicin, and cyclophosphamide (CAP); cisplatin and etoposide (EP); or cisplatin and paclitaxel (TP).

Materials and methods: We retrospectively evaluated the medical records of patients with advanced thymoma and TC who were treated at our medical center between 2005 and 2015. We investigated objective response rates (ORRs), progression-free survival (PFS), and OS after undergoing different front-line regimens.

Results: Among the 108 enrolled patients, 37 (34%) had thymoma and 71 (66%) had TC; 45 received CAP, 36 received EP, and 27 received TP regimens. The ORRs of patients receiving CAP, EP, and TP were 51%, 50%, and 41%, respectively. For patients with stage III and IVA disease, the median PFS after CAP, EP, and TP were 34.5, 26.4, and 18.0 months (p = 0.424), respectively, and the 5-year OS rates were 84.9%, 70.6%, and 60.0% (p = 0.509). In patients with stage IVB disease, the median PFS were 9.4, 8.2, and 11.6 months after undergoing CAP, EP, and TP (p = 0.173), respectively, and the 5-year OS rates were 41.1%, 39.1%, and 14.3% (p = 0.788). TC pathology subtype and liver metastasis were associated with poor OS. Three patients with stage IVB TC had an OS of more than 5 years.

Conclusion: Different front-line chemotherapy regimens may provide similar long-term PFS and OS in patients with advanced thymoma and TC. In addition to TC and liver metastasis were associated with poor OS, other potential prognostic factors are warranted for studying.

Keywords: front-line chemotherapy; overall survival; thymic carcinoma; thymoma.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Cisplatin / therapeutic use
  • Cyclophosphamide
  • Doxorubicin / therapeutic use
  • Etoposide / therapeutic use
  • Humans
  • Liver Neoplasms* / drug therapy
  • Paclitaxel
  • Platinum / therapeutic use
  • Retrospective Studies
  • Thymoma* / drug therapy
  • Thymus Neoplasms*

Substances

  • Platinum
  • Etoposide
  • Doxorubicin
  • Cyclophosphamide
  • Paclitaxel
  • Cisplatin