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小児急性リンパ性白血病の後に最初のイベントとして二次性腫瘍の累積的発生率
Nobuko Hijiya1, Melissa M Hudson, Shelly Lensing
1Department of Oncology, St Jude Children's Research Hospital, Memphis, TN 38105-2794, USA. nobuko.hijiya@stjude.org
JAMA
|March 22, 2007
まとめ
幼児期急性リンパ性白血病の生存者における二次がんのリスクは,30年以上にわたって大幅に増加し,攻撃的な腫瘍の有意な増加があります. 生存者にとって,生涯の監視は極めて重要です.
科学分野:
- 小児腫瘍学 小児腫瘍学
- 癌の流行病学について
- 長期的ながん生存率
背景:
- 幼児の急性リンパ性白血病 (ALL) の治療後の15〜20年以上の二次がん発生に関するデータは限られている.
- 長期的なリスクを理解することは,すべての生存者の結果を改善するために不可欠です.
研究 の 目的:
- 30年以上の小児ALL患者における二次性腫瘍の累積的発生率を決定する.
- このコホートにおける遅発腫瘍の種類とパターンを特徴付ける.
主な方法:
- 1962年から1998年の間にALL治療を受けた2,169人の小児患者の遡及的分析.
- 追跡期間の中央値は18.7年 (範囲は2.4~41.3年) でした.
- 一般人口と比較した累積発生率と標準発生率の計算.
主要な成果:
- ALL治療の30年後の二次性腫瘍の累積発生率は10.85%に達しました.
- 髄膜腫と基礎細胞癌を除くと,30年間の罹患率は6.27%で,一般人口より13.5倍増加しました.
- 骨髄性悪性腫瘍,脳腫瘍,癌の有意な増加が観察され,攻撃的な腫瘍は予想以上に頻繁に発生しました.
結論:
- 2次性腫瘍の発生率は,小児ALL治療の30年後に着実に上昇しています.
- 攻撃的な悪性腫瘍を含む遅発の腫瘍は,実質的な長期的なリスクをもたらす.
- ALLの生存者は,二次がんの発症をモニタリングし管理するために,生涯の追跡が推奨されます.
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