Serial Monitoring of Circulating Melanoma Cells During Neoadjuvant Biochemotherapy for Stage III Melanoma: Outcome Prediction in a Multicenter Trial

Author:

Koyanagi Kazuo1,O'Day Steven J.1,Gonzalez Rene1,Lewis Karl1,Robinson William A.1,Amatruda Thomas T.1,Wang He-Jing1,Elashoff Robert M.1,Takeuchi Hiroya1,Umetani Naoyuki1,Hoon Dave S.B.1

Affiliation:

1. From the Department of Molecular Oncology, John Wayne Cancer Institute at Saint John's Health Center; Angeles Clinic and Research Institute, Santa Monica; Department of Biostatistics, University of California, Los Angeles School of Medicine, Los Angeles, CA; University of Colorado Cancer Center, Aurora, CO; and North Memorial Health Care, Hubert H. Humphrey Cancer Center, Robbinsdale, MN

Abstract

PurposeCirculating tumor cells (CTCs) in blood may be important in assessing tumor progression and treatment response. We hypothesized that quantitative real-time reverse transcriptase polymerase chain reaction using multimarker mRNA assays could detect CTCs and be used as a surrogate predictor of outcome in patients receiving neoadjuvant biochemotherapy (BC) for melanoma.Patients and MethodsBlood specimens were collected at four sampling points from 63 patients enrolled on a prospective multicenter phase II trial of BC before and after surgical treatment of American Joint Committee on Cancer stage III melanoma. Each specimen was assessed by quantitative real-time reverse transcriptase polymerase chain reaction for expression of four melanoma-associated markers: melanoma antigen recognized by T cells 1; β1 → 4-N-acetylgalactosaminyltransferase; paired box homeotic gene transcription factor 3; and melanoma antigen gene-A3 family, and the changes of CTCs during treatment and prognostic effect of CTCs after overall treatment on recurrence and survival were investigated.ResultsAt a median postoperative follow-up time of 30.4 months, 44 (70%) patients were clinically disease free. In relapse-free patients, the number of detected markers significantly decreased during preoperative BC (P = .036), during postoperative BC (P = .002), and during overall treatment (P < .0001). Marker detection after overall treatment was associated with significant decreases in relapse-free and overall survival (P < .0001). By multivariate analysis using a Cox proportional-hazards model, the number of markers detected after overall treatment was a significant independent prognostic factor for overall survival (risk ratio, 12.6; 95% CI, 3.16 to 50.5; P = .0003).ConclusionSerial monitoring of CTCs in blood may be useful for indicating systemic subclinical disease and predicting outcome of patients receiving neoadjuvant BC for metastatic melanoma.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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