PMID- 22422736 OWN - NLM STAT- MEDLINE DCOM- 20121015 LR - 20211021 IS - 1545-5017 (Electronic) IS - 1545-5009 (Print) IS - 1545-5009 (Linking) VI - 59 IP - 4 DP - 2012 Oct TI - Clinical significance of pulmonary nodules detected by CT and Not CXR in patients treated for favorable histology Wilms tumor on national Wilms tumor studies-4 and -5: a report from the Children's Oncology Group. PG - 631-5 LID - 10.1002/pbc.24123 [doi] AB - BACKGROUND: Metastatic lung disease in Wilms tumor (WT) patients was traditionally identified by chest radiograph (CXR). It is unclear whether patients with small lesions, detectable only by computed tomography ("CT-only" lesions), require the more intensive therapy, including doxorubicin and lung irradiation, given to patients with metastases detectable by CXR. PROCEDURES: This study involved 417 patients with favorable histology WT and isolated lung metastases (detected by CXR or CT) who were registered on National Wilms tumor Study (NWTS)-4 or -5. Outcomes by method of detection (CXR vs. CT-only), use of lung radiation, and 2- or 3-drug chemotherapy (dactinomycin and vincristine +/- doxorubicin) were determined and compared using the log-rank test. RESULTS: There were 231 patients with lung lesions detected by CXR and 186 by CT-only. Of the patients with CT-only nodules, 37 received only 2 drugs and 101 did not receive lung radiation. Five-year event-free survival (EFS) was greater for patients receiving three drugs (including doxorubicin) with or without lung radiation than for those receiving two drugs (80% vs. 56%; P = 0.004). There was no difference seen in 5-year overall survival (OS) between the 3- and 2-drug subsets (87% vs. 86%; P = 0.91). There were no significant differences in EFS (82% vs. 72%; P = 0.13) or OS (91% vs. 83%; P = 0.46) for patients with CT-only nodules whether they received lung radiation or not. CONCLUSIONS: Our results suggest that patients with CT-only lung lesions may have improved EFS but not OS from the addition of doxorubicin but do not appear to benefit from pulmonary radiation. CI - Copyright (c) 2012 Wiley Periodicals, Inc. FAU - Grundy, Paul E AU - Grundy PE AD - Department of Pediatrics and Oncology, University of Alberta, Edmonton Canada. paul.grundy@albertahealthservices.ca FAU - Green, Daniel M AU - Green DM FAU - Dirks, Astrid C AU - Dirks AC FAU - Berendt, Andrea E AU - Berendt AE FAU - Breslow, Norman E AU - Breslow NE FAU - Anderson, James R AU - Anderson JR FAU - Dome, Jeffrey S AU - Dome JS LA - eng GR - CA98543/CA/NCI NIH HHS/United States GR - U10 CA042326-18S1/CA/NCI NIH HHS/United States GR - R01 CA054498/CA/NCI NIH HHS/United States GR - U10 CA098543/CA/NCI NIH HHS/United States GR - U10 CA098543-01/CA/NCI NIH HHS/United States GR - CA42326/CA/NCI NIH HHS/United States PT - Journal Article PT - Multicenter Study PT - Randomized Controlled Trial PT - Research Support, N.I.H., Extramural DEP - 20120315 PL - United States TA - Pediatr Blood Cancer JT - Pediatric blood & cancer JID - 101186624 RN - 0 (Antineoplastic Agents) SB - IM MH - Antineoplastic Agents/therapeutic use MH - Child MH - Child, Preschool MH - Combined Modality Therapy MH - Disease-Free Survival MH - Female MH - Humans MH - Kidney Neoplasms/*pathology/therapy MH - Lung Neoplasms/*diagnostic imaging/*secondary MH - Male MH - Nephrectomy MH - *Radiography, Thoracic MH - *Tomography, X-Ray Computed MH - Wilms Tumor/*diagnostic imaging/*secondary/therapy PMC - PMC3397278 MID - NIHMS356503 COIS- Authors' Disclosures of Potential Conflicts of Interest The authors do not disclose any conflicts of interest. EDAT- 2012/03/17 06:00 MHDA- 2012/10/16 06:00 PMCR- 2013/10/01 CRDT- 2012/03/17 06:00 PHST- 2011/10/06 00:00 [received] PHST- 2012/02/08 00:00 [accepted] PHST- 2012/03/17 06:00 [entrez] PHST- 2012/03/17 06:00 [pubmed] PHST- 2012/10/16 06:00 [medline] PHST- 2013/10/01 00:00 [pmc-release] AID - 10.1002/pbc.24123 [doi] PST - ppublish SO - Pediatr Blood Cancer. 2012 Oct;59(4):631-5. doi: 10.1002/pbc.24123. Epub 2012 Mar 15.