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[Cancer Research 26, 241-244, February 1, 1966]
© 1966 American Association for Cancer Research

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Remission Maintenance in Acute Lymphocytic Leukemia with Hydroxyurea1

Robert C. Storrs, Irving J. Wolman, Bernard D. Gussoff and Juliet Hananian2

Hitchcock Hospital, Dartmouth Medical School, Hanover, New Hampshire (R. C. S.), Children's Hospital of Philadelphia, Philadelphia, Pennsylvania (I. J. W.), Maimonides Hospital of Brooklyn and Long Island Jewish Hospital, New York (B. D. G.), and Roswell Park Memorial Institute, Buffalo, New York (J. H.)

After complete remission had been induced by prednisone and vincristine in children with acute leukemia, hydroxyurea was used in an effort to maintain remission. No significant prolongation of remission occurred despite the appearance of toxicity in over 50% of the high dosage group. An equally significant observation was that the duration of remission produced by prednisone and vincristine was longer in those who had not received vincristine during a prior induced remission.

1 This study was undertaken by the Acute Leukemia Cooperative Group B (Chairman, James F. Holland) and was supported by Public Health Service Research Grants from the National Cancer Institute. Other participating members of the Group are: Mount Sinai Hospital, New York, New York; Bowman Gray School of Medicine, Winston-Salem, North Carolina; University of Miami Medical School, Miami, Florida; Rhode Island Hospital, Providence, Rhode Island; and Mayo Clinic, Rochester, Minnesota.

2 This work was supported by Grant CA-04326 (R.C.S.), Grant CA-04737 (I.J.W.), Grant CA-05923 (B.D.G.), and Grant CA-07918 (J.H.).

Received 3/19/65. Revised 8/18/65.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1966 by the American Association for Cancer Research.