4.7 Article

Phase 2 study for nonmetastatic extremity high-grade osteosarcoma in pediatric and adolescent and young adult patients with a risk-adapted strategy based on ABCB1/P-glycoprotein expression: An Italian Sarcoma Group trial (ISG/OS-2)

Journal

CANCER
Volume 128, Issue 10, Pages 1958-1966

Publisher

WILEY
DOI: 10.1002/cncr.34131

Keywords

adolescents and young adults (AYAs); ATP binding cassette subfamily B member 1 (ABCB1); chemotherapy; high-grade bone sarcoma; mifamurtide; osteosarcoma; pediatric bone tumors; P-glycoprotein

Categories

Funding

  1. Italian Sarcoma Group
  2. Associazione Onlus il Pensatore: Matteo Amitrano
  3. Associazione Mario Campanacci
  4. Carisbo Foundation Call for Translational and Clinical Medical Research
  5. 5xMille contributions

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This study aimed to evaluate the effectiveness of risk-adapted treatment strategy in Pgp+ patients and showed that adjuvant mifamurtide combined with HDIFO could improve EFS.
Background According to retrospective osteosarcoma series, ABCB1/P-glycoprotein (Pgp) overexpression predicts for poor outcomes. A prospective trial to assess a risk-adapted treatment strategy using mifamurtide in Pgp+ patients was performed. Methods This was a phase 2, multicenter, uncontrolled trial including patients 40 years old or younger with nonmetastatic extremity high-grade osteosarcoma stratified according to Pgp expression. All patients received high-dose methotrexate, doxorubicin, and cisplatin (MAP) preoperatively. In Pgp+ patients, mifamurtide was added postoperatively and combined with MAP for a good histologic response (necrosis >= 90%; good responders [GRs]) or with high-dose ifosfamide (HDIFO) at 3 g/m(2)/d on days 1 to 5 for a histologic response < 90% (poor responders [PRs]). Pgp- patients received MAP postoperatively. After an amendment, the cumulative dose of methotrexate was increased from 60 to 120 g/m(2) (from 5 to 10 courses). The primary end point was event-free survival (EFS). A postamendment analysis was performed. Results In all, 279 patients were recruited, and 194 were included in the postamendment analysis: 70 (36%) were Pgp-, and 124 (64%) were Pgp+. The median follow-up was 51 months. For Pgp+ patients, 5-year EFS after definitive surgery (null hypothesis, 40%) was 69.8% (90% confidence interval [CI], 62.2%-76.2%): 59.8% in PRs and 83.7% in GRs. For Pgp- patients, the 5-year EFS rate was 66.4% (90% CI, 55.6%-75.1%). Conclusions This study showed that adjuvant mifamurtide, combined with HDIFO for a poor response to induction chemotherapy, could improve EFS in Pgp+ patients. Overall, the outcomes compared favorably with previous series. Mifamurtide and HDIFO as salvage chemotherapy are worth further study.

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