Irinotecan and temozolomide in recurrent Ewing sarcoma: an analysis in 51 adult and pediatric patients

Authors

  • E. Palmerini Istituto Ortopedico Rizzoli, Bologna, Italy
  • R. L. Jones Royal Marsden Hospital and Institute of Cancer Research, London, UK
  • E. Setola Istituto Ortopedico Rizzoli, Bologna, Italy
  • P. Picci Istituto Ortopedico Rizzoli, Bologna, Italy
  • E. Marchesi Istituto Ortopedico Rizzoli, Bologna, Italy
  • R. Luksch Istituto Nazionale Tumori, Milan, Italy
  • G. Grignani Candiolo Cancer Institute – FPO, IRCCS, Torino, Italy
  • M. Cesari Istituto Ortopedico Rizzoli, Bologna, Italy
  • A. Longhi Istituto Ortopedico Rizzoli, Bologna, Italy
  • M. E. Abate Istituto Ortopedico Rizzoli, Bologna, Italy
  • A. Paioli Istituto Ortopedico Rizzoli, Bologna, Italy
  • Z. Szucs Royal Marsden Hospital and Institute of Cancer Research, London, UK
  • L. D’ambrosio Candiolo Cancer Institute – FPO, IRCCS, Torino, Italy
  • K. Scotlandi Istituto Ortopedico Rizzoli, Bologna, Italy
  • F. Fagioli OIRM, Torino, Italy
  • S. Asaftei OIRM, Torino, Italy
  • S. Ferrari Istituto Ortopedico Rizzoli, Bologna, Italy

DOI:

https://doi.org/10.1080/0284186X.2018.1449250

Abstract

Background: Data on temozolomide (TEM) and irinotecan (IRI) activity in recurrent Ewing sarcoma (EWS), especially in adult patients, are limited.

Methods: Patients receiving TEM 100 mg/m2/day oral, and IRI 40 mg/m2/day intravenous, days 1–5, every 21 days, were included in this multi-institutional retrospective study. Disease control rate (DCR) [overall response rate (ORR) [complete response (CR) + partial response (PR)] + stable disease (SD)], 6-months progression-free survival (6-mos PFS) and 1-year overall survival (OS) were assessed.

Results: The median age of the 51 patients was 21 years (range 3–65 years): 34 patients (66%) were adults (≥18 years of age), 24 (48%) had ECOG 1 and 35 (69%) were presented with multiple site recurrence. TEMIRI was used at first relapse/progression in 13 (25%) patients, while the remainder received TEMIRI for second or greater relapse/progression. Fourteen (27%) patients had received prior myeloablative therapy with busulfan and melphalan. We observed five (10%) CR, 12 (24%) PR and 19 (37%) SD, with a DCR of 71%. 6-mos PFS was 49% (95% CI 35–63) and it was significantly influenced by ECOG (6-mos PFS 64% [95% CI 45–83] for ECOG 0, 34% [95% CI 14–54] for ECOG ≥1; p = .006) and LDH (6-mos PFS 62% [95% CI 44–79] for normal LDH, 22% [95% CI 3–42] for high LDH; p = .02), with no difference according to line of treatment, age and metastatic pattern. One-year OS was 55% (95% CI 39–70), with RECIST response (p = .001) and ECOG (p = .0002) independently associated with outcome. Grade 3 and 4 toxicity included neutropenia in 12% of patients, thrombocytopenia in 4%, diarrhea in 4%.

Conclusions: This series confirms the activity of TEMIRI in both adults and pediatric patients. This schedule offers a 71% DCR, independently of the line of chemotherapy. Predictive factors of response are ECOG and LDH.

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Published

2018-07-03

How to Cite

Palmerini, E., Jones, R. L., Setola, E., Picci, P., Marchesi, E., Luksch, R., … Ferrari, S. (2018). Irinotecan and temozolomide in recurrent Ewing sarcoma: an analysis in 51 adult and pediatric patients. Acta Oncologica, 57(7), 958–964. https://doi.org/10.1080/0284186X.2018.1449250