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JPWO2021187615A5 - - Google Patents

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Publication number
JPWO2021187615A5
JPWO2021187615A5 JP2022548860A JP2022548860A JPWO2021187615A5 JP WO2021187615 A5 JPWO2021187615 A5 JP WO2021187615A5 JP 2022548860 A JP2022548860 A JP 2022548860A JP 2022548860 A JP2022548860 A JP 2022548860A JP WO2021187615 A5 JPWO2021187615 A5 JP WO2021187615A5
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JP
Japan
Prior art keywords
marker
chemokine
cxcl11
cxcl9
cxcl10
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Pending
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JP2022548860A
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Japanese (ja)
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JP2023517487A (en
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Priority claimed from PCT/JP2021/011302 external-priority patent/WO2021187615A1/en
Publication of JP2023517487A publication Critical patent/JP2023517487A/en
Publication of JPWO2021187615A5 publication Critical patent/JPWO2021187615A5/ja
Pending legal-status Critical Current

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Claims (14)

有効量のPD-1/PD-L1阻害剤の投与を含む治療法に応答性であるがんを有しているかまたは有していると疑われる患者に対する、前記PD-1/PD-L1阻害剤の治療的効果予測する方法であって、以下の段階を含む、方法:
患者に由来する試料中の以下の(i)および(ii)を検出する段階:
(i)CD8陽性T細胞に対してクロスプレゼンテーション能力を有する樹状細胞(DC)の、腫瘍内の量を推定するための、少なくとも1つのマーカー;および
(ii)腫瘍内でエフェクターT細胞を集積させる、少なくとも1つのケモカイン。
PD-1/PD-L1 inhibition in patients having or suspected of having cancer that is responsive to a therapy comprising administration of an effective amount of a PD-1/PD-L1 inhibitor. A method of predicting the therapeutic effect of an agent , the method comprising the steps of:
Detecting (i) and (ii) of the following in a sample derived from a patient:
(i) at least one marker for estimating the amount within the tumor of dendritic cells (DC) capable of cross-presenting to CD8+ T cells; and
(ii) at least one chemokine that recruits effector T cells within the tumor;
治療法が、有効量の抗PD-L1抗体の投与を含む、請求項1記載の方法。 2. The method of claim 1, wherein the treatment method comprises administering an effective amount of an anti-PD-L1 antibody. 治療法が、有効量のアテゾリズマブの投与を含む、請求項1または2記載の方法。 3. The method of claim 1 or 2, wherein the treatment method comprises administering an effective amount of atezolizumab. がんが非小細胞肺癌である、請求項1~3のいずれか一項記載の方法。 4. The method according to any one of claims 1 to 3, wherein the cancer is non-small cell lung cancer. 各マーカーが、T細胞活性化マーカーではない、請求項1~4のいずれか一項記載の方法。 5. The method of any one of claims 1-4, wherein each marker is not a T cell activation marker. 前記少なくとも1つのマーカーが、XCR1、Clec9、Irf8、Batf3、CD205、CD103、およびCD141のうちの1つ、2つ、3つ、4つ、5つ、6つ、またはすべてである、請求項1~5のいずれか一項記載の方法。 1 . The at least one marker is one, two, three, four, five, six, or all of XCR1, Clec9, Irf8, Batf3, CD205, CD103, and CD141. The method described in any one of ~5. 前記少なくとも1つのマーカーがXCR1である、請求項1~6のいずれか一項記載の方法。 7. The method according to any one of claims 1 to 6, wherein said at least one marker is XCR1. 前記少なくとも1つのケモカインがCXCR3リガンドである、請求項1~7のいずれか一項記載の方法。 8. The method of any one of claims 1 to 7, wherein said at least one chemokine is a CXCR3 ligand. 前記少なくとも1つのケモカインが、CXCL9、CXCL10、およびCXCL11のうちの1つ、2つ、またはすべてである、請求項1~8のいずれか一項記載の方法。 9. The method of any one of claims 1-8, wherein the at least one chemokine is one, two, or all of CXCL9, CXCL10, and CXCL11. 前記少なくとも1つのケモカインが、CXCL9、CXCL10、およびCXCL11のすべてである、請求項1~9のいずれか一項記載の方法。 10. The method of any one of claims 1-9, wherein the at least one chemokine is all CXCL9, CXCL10, and CXCL11. (i)を検出する段階が、マーカーのmRNA発現レベルを測定することであり、
(ii)を検出する段階が、ケモカインのmRNA発現レベルを測定することである、
請求項1~10のいずれか一項記載の方法。
The step of detecting (i) is to measure the mRNA expression level of the marker,
(ii) the step of detecting is measuring the mRNA expression level of the chemokine;
The method according to any one of claims 1 to 10.
(i)および(ii)を検出する段階が、マーカーおよび1つまたは複数のケモカインのmRNA発現レベルを測定することである、請求項1~11のいずれか一項記載の方法。 12. The method of any one of claims 1 to 11, wherein the step of detecting (i) and (ii) is measuring the mRNA expression level of the marker and one or more chemokines. マーカーがXCR1であり、1つまたは複数のケモカインが、CXCL9、CXCL10、およびCXCL11より選択される、請求項12記載の方法。 13. The method of claim 12, wherein the marker is XCR1 and the one or more chemokines are selected from CXCL9, CXCL10, and CXCL11. ケモカインが、CXCL9、CXCL10、およびCXCL11のすべてである、請求項13記載の方法。 14. The method of claim 13, wherein the chemokines are all CXCL9, CXCL10, and CXCL11.
JP2022548860A 2020-03-19 2021-03-19 Biomarkers for predicting response to checkpoint inhibitors Pending JP2023517487A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2020048845 2020-03-19
JP2020048845 2020-03-19
PCT/JP2021/011302 WO2021187615A1 (en) 2020-03-19 2021-03-19 Biomarkers for predicting the response to checkpoint inhibitors

Publications (2)

Publication Number Publication Date
JP2023517487A JP2023517487A (en) 2023-04-26
JPWO2021187615A5 true JPWO2021187615A5 (en) 2024-02-29

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US (1) US20230146730A1 (en)
EP (1) EP4121769A4 (en)
JP (1) JP2023517487A (en)
KR (1) KR20220156855A (en)
CN (1) CN115485559A (en)
AU (1) AU2021239667A1 (en)
CA (1) CA3168951A1 (en)
IL (1) IL296431A (en)
MX (1) MX2022011068A (en)
TW (1) TW202140568A (en)
WO (1) WO2021187615A1 (en)

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR095363A1 (en) 2013-03-15 2015-10-14 Genentech Inc BIOMARKERS AND METHODS FOR THE TREATMENT OF CONDITIONS RELATED TO PD-1 AND PD-L1
WO2015120382A1 (en) 2014-02-07 2015-08-13 The Johns Hopkins University Predicting response to epigenetic drug therapy
US11326211B2 (en) 2015-04-17 2022-05-10 Merck Sharp & Dohme Corp. Blood-based biomarkers of tumor sensitivity to PD-1 antagonists
GB201512869D0 (en) 2015-07-21 2015-09-02 Almac Diagnostics Ltd Gene signature for minute therapies
JP7034080B2 (en) * 2016-02-25 2022-03-11 メモリアル スローン ケタリング キャンサー センター Recombinant MVA or MVAΔE3L expressing human FLT3L and their use as immunotherapeutic agents against solid tumors
WO2017176925A1 (en) 2016-04-05 2017-10-12 Bristol-Myers Squibb Company Cytokine profiling analysis for predicting prognosis of a patient in need of an anti-cancer treatment
WO2017190074A1 (en) * 2016-04-28 2017-11-02 The University Of Chicago Lymphangiogenesis for therapeutic immunomodulation
EP3516396B1 (en) 2016-09-26 2024-11-13 F. Hoffmann-La Roche AG Predicting response to pd-1 axis inhibitors
MX2019012192A (en) * 2017-04-14 2020-01-21 Genentech Inc Diagnostic and therapeutic methods for cancer.
WO2018209324A2 (en) 2017-05-11 2018-11-15 The Broad Institute, Inc. Methods and compositions of use of cd8+ tumor infiltrating lymphocyte subtypes and gene signatures thereof
CA3066054A1 (en) 2017-06-04 2018-12-13 Rappaport Family Institute For Research In The Medical Sciences Method of predicting personalized response to cancer therapy and kit therefor
GB202209539D0 (en) 2017-06-13 2022-08-10 Bostongene Corp Systems and methods for identifying cancer treatments from normalized biomarker scores
CA3105988A1 (en) * 2018-07-11 2020-01-16 Abhishek Datta High-affinity, isoform-selective tgf.beta.1 inhibitors and use thereof

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