JP5314600B2 - 造血器癌および増殖性疾患の治療のための固定した薬物比 - Google Patents
造血器癌および増殖性疾患の治療のための固定した薬物比 Download PDFInfo
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Description
本出願は2007年2月16日に出願された米国出願番号第60/901,772号、および2007年8月17日に出願された米国出願番号第60/965,196号の利益を主張し、それらのそれぞれはそのまま参照として本明細書に援用される。
[1]対象の癌または血液増殖性疾患を治療するための方法における固定した、非拮抗モル比のシタラビンとアントラサイクリンを含む医薬組成物の使用であって、
該方法は12時間以下の期間にわたり該組成物を静脈内投与することを含み、
固定した比は少なくとも4時間血漿中で維持され、そして
固定した、非拮抗モル比のシタラビンとアントラサイクリンはリポソーム内に被包される、前記使用。
[2]組成物が8時間以下で投与される、[1]に記載の使用。
[3]組成物が3時間以下で投与される、[2]に記載の使用。
[4]前記組成物が90分間以下で投与される、[3]に記載の使用。
[5]シタラビン対アントラサイクリンの前記の固定した非拮抗モル比が約1:1〜25:1の間である、[1]〜[4]のいずれかに記載の使用。
[6]前記の固定した、非拮抗モル比が約5:1である、[5]に記載の使用。
[7]シタラビンが250mg/m 2 以下の用量で投与される、[1]〜[4]のいずれかに記載の使用。
[8]前記リポソームがDSPC、DSPGおよびコレステロールを含む、[1]〜[4]のいずれかに記載の使用。
[9]前記リポソームが7:2:1のモル比でDSPC:DSPG:コレステロールを含む、[8に記載の使用。
[10]アントラサイクリンがダウノルビシンである、[1]〜[4]のいずれかに記載の使用。
[11]前記組成物の用量が32〜134ユニット/m 2 であり、1ユニットが1mgシタラビンおよび0.44mgダウノルビシンである、[10]のいずれかに記載の使用。
[12]前記投与がIVドリップによるものである、[1]〜[4]のいずれかに記載の使用。
[13]癌または血液増殖性疾患が、急性リンパ性白血病(ALL)、急性骨髄性白血病(AML)および急性前骨髄球白血病(APL)から選択される進行した血液癌であり、そして前記血液増殖性疾患が骨髄異形成症候群(MDS)である、[1]〜[4]のいずれかに記載の使用。
[14]前記対象が少なくとも1種の抗癌投薬計画を以前に受けている、および/または以前に寛解を経験している、[1]〜[4]のいずれかに記載の使用。
[15]前記対象が前記抗癌投薬計画後18ヶ月以内に再発を経験している、[14]に記載の使用。
[16]前記対象が前記抗癌投薬計画後6ヶ月以内に再発を経験している、[15]に記載の使用。
[17]完全寛解率の増加の関数として、および/または完全寛解継続期間の延長および/または進行までの時間の延長および/または生存の延長の関数として治療効果を測定することをさらに含む、[1]〜[4]のいずれかに記載の使用。
[18]前記治療効果が、シタラビンとアントラサイクリンが標準治療プロトコルで投与される場合に得られるものより大きい、[17]に記載の使用。
[19]非造血毒性の減少としての改善された安全性結果を測定することをさらに含む、[1]〜[4]のいずれかに記載の使用。
[20]非造血毒性が粘膜炎および/または脱毛である、[19]に記載の使用。
[21]安全性結果が、シタラビンとアントラサイクリンが標準治療プロトコルで投与される場合に得られるものより大きい、[19]に記載の使用。
一側面では、対象における癌または血液増殖性疾患を治療するための方法が本明細書に提供され、該方法は固定した、非拮抗モル比のシタラビンと、ダウノルビシンのようなアントラサイクリンを含む医薬組成物を該対象に投与することを含み、ここでシタラビン:アントラサイクリンの比は少なくとも約4時間、血漿中において非拮抗比で維持される。別の態様では、固定した、非拮抗モル比は少なくとも約8時間、少なくとも約16時間、または少なくとも約24時間維持される。アントラサイクリンはダウノルビシンまたはミトキサントロンでありうる。特定の態様では、アントラサイクリンはダウノルビシンである。典型的には、シタラビンとアントラサイクリンは1以上の送達ベヒクルと安定的に結合している。送達ベヒクル中の被包は調和した様式で疾患部位に2以上の薬剤が送達されることを可能にし、それによって薬剤が非拮抗比で疾患部位に存在することを確実にする。この結果は、薬剤が送達ベヒクル内に一緒に被包されるか、または非拮抗比が疾患部位で維持されるように投与される送達ベヒクル内に別個に被包されるかのいずれでも達成されることになる。(送達システムの薬物動態学(PK)が同程度の場合)調和した送達が達成されるように、PKは送達ベヒクル自体によって制御される。一態様では、送達ベヒクルはリポソームである。
シタラビンとアントラサイクリンの場合、in vitroでの非拮抗モル比は25:1〜約1:1の間であり、ここで5:1のモル比が最適であることが見いだされた。適切なアントラサイクリンはどれも使用することができる。アントラサイクリンは、ダウノルビシン、イダルビシンまたはミトキサントロンでありうる。特定の態様では、アントラサイクリンはダウノルビシンである。
開示された方法はまた、再発した癌を治療することにおいて治療的に有効である。“再発した癌”は以前の治療に反応して、以前に完全に、または部分的に寛解した後に再発した癌を表す。再発は、臨床的、放射線的、もしくは生化学的アッセイによって、または癌マーカーの増大したレベルによって検出されるような腫瘍細胞の再出現または再成長を含む、任意のやり方で定義することができる。先行治療には、化学療法、生物学的またはホルモン療法、放射線療法、および骨髄移植を挙げることができるが、それらに限定されない。
CPX−351によるin vivo研究
CPX−351(シタラビン:ダウノルビシン)リポソーム注入液の毒性は、単回用量および反復(3用量を1日おき、2週間後に繰り返す)用量を与えられたラットおよびイヌにおいて研究されてきた。
第1相治験
物理的、化学的および薬学的情報 CPX−351は抗新生物薬シタラビンおよびダウノルビシンの固定した組み合わせのリポソーム製剤である。2種の薬物は、前臨床研究において非拮抗活性を有することが示された5:1のモル比でリポソームの内側に存在する。リポソーム膜は7:2:1モル比のジステアロイルホスファチジルコリン、ジステアロイルホスファチジルグリセロールおよびコレステロールから構成される。これらのリポソームはおよそ100nmの名目上の直径を有し、スクロース−リン酸−バッファー、pH7.4に懸濁される。滅菌は0.22μmフィルターによる濾過により達成される。
・骨髄の細胞密度減少(>50%減少、芽球の減少を伴う)
および/または
・ことによると、おそらくまたは明確にCPX−351に関連する、非血液学的治療から出現した事象(≧グレード2<DLT)。
結果。この研究は、非ランダム化、オープンラベル、単群、用量エスカレーション第1相治験である。現在までの研究登録期間はおよそ18ヶ月間を要した。すべて以前に治療を受けている33人の対象(男性22人;女性11人)、年齢中央値62歳(24〜81)が10コホートに登録された。初めの10コホートの実態的人口統計および配置は以下の表6に要約される:
・骨髄細胞密度減少(>50%減少、芽球減少を伴う)
および/または
・ことによると、おそらくまたは明確にCPX−351に関連する、非血液学的治療から出現した事象(≧グレード2<DLT)。
CPX−351第1相治験−症例研究
以下は、進行中のCPX−351第1相治験において治療された患者の5例の症例研究である。
CPX−351第1相治験−薬物動態学
研究の薬物動態学(PK)解析の目標
・白血病患者におけるCPX−351投与後のシタラビンおよびダウノルビシンならびに選択された代謝産物(Ara−Uおよびダウノルビシノール)の単回投与および複数回投与の薬物動態学を決定すること。
・癌患者におけるCPX−351の全体的暴露、用量釣り合い、および蓄積に関する予備情報を集めること。
・可能ならば、CPX−351成分への暴露強度と効果(安全性および有効性)間の相関関係を樹立すること。
・1日目の投与前、注入中45分(または注入の中間点)および90分(または注入の終了時)、その後注入開始に対応して2、4、6、8、12、および24時間において。
・3日目の投与前、注入中45および90分において。
・5日目の投与前、注入中45分(または注入の中間点)および90分(または注入の終了時)において、その後注入開始に対応して2、4、6、8、12、24、48、72、96、および168時間において。
Cmax 最大の観察された濃度
Tmax Cmax出現時期
λz 最終相(5日目の投与後だけ)の自然体数(In)に変換された濃度対時間データの直線回帰から得られた排出速度定数
t1/2 最終半減期、In(2)/λzとして計算
AUC(0〜最後) 直線台形法により得られた、0時から最後の投与後の定量可能な血漿中濃度の時間までの血漿中濃度−時間曲線下面積
AUC(0〜無限) 0時から無限時まで外挿した血漿中濃度−時間曲線下面積
CL (研究5日目だけのシタラビンおよびダウノルビシンに対して)用量/AUC(0〜無限)としてコンピュータにより算出された全身クリアランス
また薬物動態学解析のコンパートメント法を利用して、代謝産物配置動態学を評価し、および/または薬物動態学/薬力学モデリングを実施してもよい。
Claims (5)
- ヒトを対象とする白血病を治療するための方法において使用する、シタラビン対ダウノルビシンが5:1の固定したモル比である、シタラビンとダウノルビシンから実質的になる医薬組成物であって、
該方法は、シタラビンが32〜134mg/m2の単回投与で供給され、投与サイクルを通じて96〜402mg/m2の合計量で供給される投与サイクルにおいて、8時間以下の期間にわたり該組成物を単回投与で静脈内投与することから実質的になり、
固定したモル比は少なくとも4時間血漿中で維持され、そして
固定したモル比のシタラビンとダウノルビシンは、7:2:1のモル比であるDSPC:DSPG:コレステロールを含むリポソーム内に被包され、
該投与サイクルは、第1日目の最初の投与、第3日目の2回目の投与および第5日目の3回目の投与からなる、前記組成物。 - 3時間以下で投与される、請求項1に記載の組成物。
- 90分間以下で投与される、請求項2に記載の組成物。
- 白血病が、急性リンパ性白血病(ALL)、急性骨髄性白血病(AML)または急性前骨髄球白血病(APL)である、請求項1〜3のいずれかに記載の組成物。
- 前記対象が少なくとも1種の抗癌投薬計画を以前に受けている、請求項1〜3のいずれかに記載の組成物。
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WO2007076117A2 (en) | 2005-12-22 | 2007-07-05 | Celator Pharmaceuticals, Inc. | Liposomal formulations comprising secondary and tertiary amines and methods for preparing thereof |
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