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Lack of complete response pretransplant is not associated with inferior overall survival for stage 4a metastatic retinoblastoma.

Authors :
Farouk Sait S
Bernot MR
Klein E
Abramson DH
Francis JH
Gilheeney S
Karajannis MA
Spitzer B
Wolden S
Dunkel IJ
Kernan NA
Source :
Pediatric blood & cancer [Pediatr Blood Cancer] 2023 Jan; Vol. 70 (1), pp. e29921. Date of Electronic Publication: 2022 Aug 08.
Publication Year :
2023

Abstract

Background: Stage 4a metastatic retinoblastoma (RB) is curable with intensive multimodality therapy including myeloablative chemotherapy with autologous stem cell transplant (HDC-ASCT) and involved field radiation therapy (IFRT). To our knowledge, no data exist on the impact of (a) pre-ASCT disease status, and (b) IFRT to sites of metastatic disease post ASCT on survival.<br />Procedure: We retrospectively reviewed patients with stage 4a metastatic RB who underwent induction chemotherapy followed by HDC-ASCT, with or without IFRT, to residual tumor sites at Memorial Sloan Kettering Cancer Center (MSKCC) (n = 24).<br />Results: The degree of postinduction response prior to ASCT did not affect outcome, with 5-year overall survival (OS) of 68% and 86% in patients who achieved complete response (CR) and very good partial response (VGPR)/partial response (PR) prior to ASCT, respectively. IFRT administered post ASCT in patients with possible residual bony metastatic disease increases the likelihood of developing osteosarcoma in the radiation field.<br />Conclusion: OS for patients with stage 4a metastatic RB treated with ASCT with VGPR or PR to pretransplant chemotherapy was not significantly different from patients with CR. In addition, IFRT does not seem to be required for bony disease control and increased the likelihood of developing osteosarcoma.<br /> (© 2022 Wiley Periodicals LLC.)

Details

Language :
English
ISSN :
1545-5017
Volume :
70
Issue :
1
Database :
MEDLINE
Journal :
Pediatric blood & cancer
Publication Type :
Academic Journal
Accession number :
35934994
Full Text :
https://doi.org/10.1002/pbc.29921