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DNA and RNA flow cytometric study in multiple myeloma. Clinical correlations
Author(s) -
Tafuri Agostino,
Meyers Jane,
Lee Burton J.,
Andreeff Michael
Publication year - 1991
Publication title -
cancer
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.052
H-Index - 304
eISSN - 1097-0142
pISSN - 0008-543X
DOI - 10.1002/1097-0142(19910115)67:2<449::aid-cncr2820670222>3.0.co;2-e
Subject(s) - biopsy , rna , multiple myeloma , dna , medicine , acridine orange , pathology , bone marrow , flow cytometry , vincristine , aneuploidy , gastroenterology , chemotherapy , immunology , biology , staining , cyclophosphamide , gene , chromosome , genetics
Flow cytometric studies of cellular DNA and RNA content using the acridineorange technique were conducted in 81 patients with multiple myeloma (MM). All patients were treated with the M‐2 protocol and clinical response was evaluated according to the criteria of the Chronic Leukemia‐Myeloma Task Force. Aneuploid DNA stemlines were found in 38.2% of untreated patients with a median DNA index (DNA‐I) of 1.15 in marrow aspirates and 1.22 in biopsy specimens. The median percentage of cells with abnormal DNA content was 31.5 (aspirates) and 35 (biopsy specimens) and a positive correlation with the percentage of bone marrow plasma cells was observed. Significantly higher proliferation (S‐phase) was found in marrow biopsy specimens as compared with marrow aspirates. Significantly higher RNA content (RNA index [RNA‐I]) was observed in aneuploid versus diploid patients in biopsy material. There was no difference in response to the Memorial Hospital M‐2 protocol between diploid and aneuploid patients. In patients with DNA‐I > 1.15 remission duration was shorter as compared with DNA‐I ≦ 1.15. Furthermore, no difference in cellular RNA content was noted between responders and nonresponders. This study demonstrates no correlation between cellular RNA content and response, as previously described for patients treated with vincristine, Adriamycin, and dexamethasone (VAD), but DNA aneuploidy appears to be an adverse prognostic factor in MM patients treated with the M‐2 protocol. It also demonstrates that prognostic models for MM are not universal but depend on the chemotherapeutic regimen used.