JP2013522237A5 - - Google Patents
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- JP2013522237A5 JP2013522237A5 JP2012557285A JP2012557285A JP2013522237A5 JP 2013522237 A5 JP2013522237 A5 JP 2013522237A5 JP 2012557285 A JP2012557285 A JP 2012557285A JP 2012557285 A JP2012557285 A JP 2012557285A JP 2013522237 A5 JP2013522237 A5 JP 2013522237A5
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- 239000003112 inhibitor Substances 0.000 claims 21
- 230000002401 inhibitory effect Effects 0.000 claims 21
- 108090001123 antibodies Proteins 0.000 claims 13
- 102000004965 antibodies Human genes 0.000 claims 13
- 239000002246 antineoplastic agent Substances 0.000 claims 6
- 208000003721 Triple Negative Breast Neoplasms Diseases 0.000 claims 4
- 206010028980 Neoplasm Diseases 0.000 claims 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 102000015694 estrogen receptors Human genes 0.000 claims 2
- 108010038795 estrogen receptors Proteins 0.000 claims 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical group [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 claims 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 2
- 210000004881 tumor cells Anatomy 0.000 claims 2
- XRYJULCDUUATMC-CYBMUJFWSA-N 4-[4-[[(1R)-1-phenylethyl]amino]-7H-pyrrolo[2,3-d]pyrimidin-6-yl]phenol Chemical compound N([C@H](C)C=1C=CC=CC=1)C(C=1C=2)=NC=NC=1NC=2C1=CC=C(O)C=C1 XRYJULCDUUATMC-CYBMUJFWSA-N 0.000 claims 1
- 108010005144 Bevacizumab Proteins 0.000 claims 1
- 239000005461 Canertinib Substances 0.000 claims 1
- 229950002826 Canertinib Drugs 0.000 claims 1
- OMZCMEYTWSXEPZ-UHFFFAOYSA-N Canertinib Chemical compound C1=C(Cl)C(F)=CC=C1NC1=NC=NC2=CC(OCCCN3CCOCC3)=C(NC(=O)C=C)C=C12 OMZCMEYTWSXEPZ-UHFFFAOYSA-N 0.000 claims 1
- 108010022830 Cetuximab Proteins 0.000 claims 1
- 230000004544 DNA amplification Effects 0.000 claims 1
- 229940121647 EGFR inhibitors Drugs 0.000 claims 1
- 102100016662 ERBB2 Human genes 0.000 claims 1
- 101700025368 ERBB2 Proteins 0.000 claims 1
- 229960001433 Erlotinib Drugs 0.000 claims 1
- AAKJLRGGTJKAMG-UHFFFAOYSA-N Erlotinib Chemical compound C=12C=C(OCCOC)C(OCCOC)=CC2=NC=NC=1NC1=CC=CC(C#C)=C1 AAKJLRGGTJKAMG-UHFFFAOYSA-N 0.000 claims 1
- XGALLCVXEZPNRQ-UHFFFAOYSA-N Gefitinib Chemical group C=12C=C(OCCCN3CCOCC3)C(OC)=CC2=NC=NC=1NC1=CC=C(F)C(Cl)=C1 XGALLCVXEZPNRQ-UHFFFAOYSA-N 0.000 claims 1
- RCINICONZNJXQF-MZXODVADSA-N Intaxel Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 claims 1
- 239000005411 L01XE02 - Gefitinib Substances 0.000 claims 1
- 239000002136 L01XE07 - Lapatinib Substances 0.000 claims 1
- BCFGMOOMADDAQU-UHFFFAOYSA-N Lapatinib Chemical compound O1C(CNCCS(=O)(=O)C)=CC=C1C1=CC=C(N=CN=C2NC=3C=C(Cl)C(OCC=4C=C(F)C=CC=4)=CC=3)C2=C1 BCFGMOOMADDAQU-UHFFFAOYSA-N 0.000 claims 1
- 229950008001 Matuzumab Drugs 0.000 claims 1
- 229950010203 Nimotuzumab Drugs 0.000 claims 1
- 229960001592 Paclitaxel Drugs 0.000 claims 1
- 108010061219 Panitumumab Proteins 0.000 claims 1
- 101710037934 QRSL1 Proteins 0.000 claims 1
- 229940045698 antineoplastic Taxanes Drugs 0.000 claims 1
- 229960000397 bevacizumab Drugs 0.000 claims 1
- 238000004166 bioassay Methods 0.000 claims 1
- 229960005395 cetuximab Drugs 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 102000017256 epidermal growth factor-activated receptor activity proteins Human genes 0.000 claims 1
- 108040009258 epidermal growth factor-activated receptor activity proteins Proteins 0.000 claims 1
- 229960002584 gefitinib Drugs 0.000 claims 1
- 230000002055 immunohistochemical Effects 0.000 claims 1
- 229960004891 lapatinib Drugs 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- 108010029633 matuzumab Proteins 0.000 claims 1
- 108010001830 monoclonal antibody 806 Proteins 0.000 claims 1
- 108010043585 nimotuzumab Proteins 0.000 claims 1
- 229960001972 panitumumab Drugs 0.000 claims 1
- 229910052697 platinum Inorganic materials 0.000 claims 1
- 102000003998 progesterone receptors Human genes 0.000 claims 1
- 108090000468 progesterone receptors Proteins 0.000 claims 1
- 230000011664 signaling Effects 0.000 claims 1
- 150000003384 small molecules Chemical class 0.000 claims 1
- 229930003347 taxol Natural products 0.000 claims 1
- 239000005483 tyrosine kinase inhibitor Substances 0.000 claims 1
- 229940121358 tyrosine kinase inhibitors Drugs 0.000 claims 1
- 239000002525 vasculotropin inhibitor Substances 0.000 claims 1
Claims (15)
- トリプルネガティブ乳癌の治療の方法において使用するためのＥｒｂＢ３阻害剤であって、抗ＥｒｂＢ３抗体である、ＥｒｂＢ３阻害剤。
- 前記抗ＥｒｂＢ３抗体が、
アミノ末端からカルボキシ末端の順で、
配列番号３に示されるＶＨ ＣＤＲ１の配列、
配列番号４に示されるＶ Ｈ ＣＤＲ２の配列、および
配列番号５に示されるＶ Ｈ ＣＤＲ３の配列、ならびに
アミノ末端からカルボキシ末端の順で、
配列番号６に示されるＶＬ ＣＤＲ１の配列、
配列番号７に示されるＶ Ｌ ＣＤＲ２の配列、および
配列番号８に示されるＶ Ｌ ＣＤＲ３の配列
を含む、請求項１に記載の使用のための請求項１に記載の阻害剤。 - 前記抗ＥｒｂＢ３抗体が以下：
(ａ)配列番号１に示されるＶ Ｈ 配列と配列番号２に示されるＶ Ｌ 配列とを含む抗体；
(ｂ)配列番号９に示されるＶ Ｈ 配列と配列番号１０に示されるＶ Ｌ 配列とを含む抗体；
(ｃ)配列番号１７に示されるＶ Ｈ 配列と配列番号１８に示されるＶ Ｌ 配列とを含む抗体；および
(ｄ)配列番号２５に示されるＶ Ｈ 配列と配列番号２６に示されるＶ Ｌ 配列とを含む抗体
より選択される、請求項１に記載の使用のための請求項１に記載の阻害剤。 - 前記トリプルネガティブ乳癌腫瘍が以下：
（ｉ）基底様発現型；または
（ｉｉ）基底様以外の発現型
を有すると病理組織学的に特徴付けられる、請求項１〜３のいずれか一項に記載の使用のための請求項１〜３のいずれか一項に記載の阻害剤。 - 前記方法が、少なくとも１つの追加の抗癌剤を投与する工程をさらに含む、請求項１〜４のいずれか一項に記載の使用のための請求項１〜４のいずれか一項に記載の阻害剤。
- 前記追加の抗癌剤が、ＥｒｂＢ３阻害剤ではない、請求項５に記載の使用のための請求項５に記載の阻害剤。
- 前記少なくとも１つの追加の抗癌剤が、白金系化学療法薬、タキサン、チロシンキナーゼ阻害剤、抗ＥＧＦＲ抗体、抗ＥｒｂＢ２抗体、それらの組み合わせ、ＥＧＦＲ阻害剤、およびＶＥＧＦ阻害剤から選択される、請求項５または６に記載の使用のための請求項５または６に記載の阻害剤。
- 前記少なくとも１つの追加の抗癌剤が、パクリタキセルである、請求項７に記載の使用のための請求項７に記載の阻害剤。
- 前記少なくとも１つの追加の抗癌剤が、抗ＥＧＦＲ抗体である、請求項７に記載の使用のための請求項７に記載の阻害剤。
- 前記抗ＥＧＦＲ抗体が、セツキシマブ、マツズマブ、パニツムマブ、ニモツズマブ、およびｍＡｂ８０６から選択される、請求項９に記載の使用のための請求項９に記載の阻害剤。
- 前記ＥＧＦＲ阻害剤が、ゲフィチニブ、ラパチニブ、カネルチニブ、ペリチニブ、エルロチニブＨＣＬ、ＰＫＩ−１６６、ＰＤ１５８７８０、およびＡＧ１４７８から選択されるＥＧＦＲシグナル伝達の小分子阻害剤である、請求項７に記載の使用のための請求項７に記載の阻害剤。
- 前記ＶＥＧＦ阻害剤が、ベバシズマブを含む、請求項７に記載の使用のための請求項７に記載の阻害剤。
- 前記トリプルネガティブ乳癌腫瘍は、
腫瘍細胞が、エストロゲン受容体（ＥＲ）およびプロゲステロン受容体に関してマイナスの得点を取り、多クローン性抗ＨＥＲ２一次抗体を使用する半定量的免疫組織化学的アッセイを使用して、０、１＋、または２＋の試験結果を得る腫瘍
である、請求項１〜３のいずれか一項に記載の使用のための請求項１〜３のいずれか一項に記載の阻害剤。 - 前記腫瘍細胞が、ＨＥＲ２遺伝子増幅に関してＦＩＳＨネガティブである、請求項１３に記載の使用のための請求項１３に記載の阻害剤。
- トリプルネガティブ乳癌の治療のための薬剤を製造するためのＥｒｂＢ３阻害剤の使用であって、該阻害剤がＥｒｂＢ３抗体である、ＥｒｂＢ３阻害剤の使用。
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US31289510P | 2010-03-11 | 2010-03-11 | |
| US61/312,895 | 2010-03-11 | ||
| PCT/US2011/028129 WO2011112953A2 (en) | 2010-03-11 | 2011-03-11 | Use of erbb3 inhibitors in the treatment of triple negative and basal-like breast cancers |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016045111A Division JP6185102B2 (ja) | 2010-03-11 | 2016-03-09 | トリプルネガティブおよび基底様乳癌の治療におけるｅｒｂｂ３阻害剤の使用 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2013522237A JP2013522237A (ja) | 2013-06-13 |
| JP2013522237A5 true JP2013522237A5 (ja) | 2014-04-24 |
Family
ID=44513103
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2012557285A Pending JP2013522237A (ja) | 2010-03-11 | 2011-03-11 | トリプルネガティブおよび基底様乳癌の治療におけるｅｒｂｂ３阻害剤の使用 |
| JP2016045111A Expired - Fee Related JP6185102B2 (ja) | 2010-03-11 | 2016-03-09 | トリプルネガティブおよび基底様乳癌の治療におけるｅｒｂｂ３阻害剤の使用 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016045111A Expired - Fee Related JP6185102B2 (ja) | 2010-03-11 | 2016-03-09 | トリプルネガティブおよび基底様乳癌の治療におけるｅｒｂｂ３阻害剤の使用 |
Country Status (21)
| Country | Link |
|---|---|
| US (4) | US8895001B2 (ja) |
| EP (2) | EP2544680B1 (ja) |
| JP (2) | JP2013522237A (ja) |
| KR (1) | KR101798679B1 (ja) |
| CN (1) | CN102858335B (ja) |
| AU (1) | AU2011224186C1 (ja) |
| BR (1) | BR112012022802A2 (ja) |
| CA (1) | CA2792327C (ja) |
| DK (1) | DK2544680T3 (ja) |
| EA (1) | EA201201186A1 (ja) |
| ES (1) | ES2535503T3 (ja) |
| HK (1) | HK1174254A1 (ja) |
| IL (1) | IL221693A (ja) |
| MX (1) | MX344355B (ja) |
| NZ (1) | NZ602084A (ja) |
| PL (1) | PL2544680T3 (ja) |
| PT (1) | PT2544680E (ja) |
| SG (1) | SG183532A1 (ja) |
| UA (1) | UA111149C2 (ja) |
| WO (1) | WO2011112953A2 (ja) |
| ZA (1) | ZA201206425B (ja) |
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