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RU2018145512A - Биологические маркеры, которые могут быть использованы в иммунотерапии рака - Google Patents

Биологические маркеры, которые могут быть использованы в иммунотерапии рака Download PDF

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RU2018145512A
RU2018145512A RU2018145512A RU2018145512A RU2018145512A RU 2018145512 A RU2018145512 A RU 2018145512A RU 2018145512 A RU2018145512 A RU 2018145512A RU 2018145512 A RU2018145512 A RU 2018145512A RU 2018145512 A RU2018145512 A RU 2018145512A
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Санг Дзае КИМ
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Джемвакс Энд Каэл Ко., Лтд.
Санг Дзае КИМ
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    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
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Claims (23)

1. Способ лечения индивидуума, страдающего от локально-распространенного или метастатического рака поджелудочной железы, включающий:
(a) определение уровня эотаксина (масс./об.) в образце сыворотки индивидуума;
(b) сравнение уровня (a) со средним уровнем эотаксина в сыворотке (масс./об.) в популяции индивидуумов, имеющих локально-распространенный или метастатический рак поджелудочной железы, и если уровень в сыворотке индивидуума по меньшей мере на 10% выше, чем средний уровень в сыворотке,
(c) введение композиции, включающий полипептид, состоящий из SEQ ID NO: 1, индивидууму одновременно с лечением гемцитабином и капецитабином, вследствие чего время выживания увеличивается.
2. Способ по п.1, где капецитабин вводят как 5 фторурацил.
3. Способ по п.1, где композицию вводят в комбинации с гранулоцитарно-макрофагальным колониестимулирующим фактором (GM-CSF).
4. Способ по п.1, где гранулоцитарно-макрофагальный колониестимулирующий фактор (GM-CSF) вводят до введения композиции.
5. Способ по п.1, где композицию вводят парентерально.
6. Способ по п.1, дополнительно включающий измерение уровня CRP (масс./об.) в сыворотке индивидуума после введения, и продолжение введения, если уровень CRP более чем на 10% ниже средней величины в популяции индивидуумов, страдающих от такого же рака.
7. Способ по п.4, где
GM-CSF вводят за 10-15 минут до введения композиции,
GM-CSF и композицию вводят внутрикожно, и
GM-CSF и композицию вводят три раза в течение первой недели лечения, один раз в течение второй, третьей, четвертой, и шестой недель лечения, и один раз каждые четыре недели после этого.
8. Способ лечения индивидуума, страдающего от рака, включающий:
(a) определение уровня эотаксина (масс./об.) в образце сыворотки индивидуума;
(b) сравнение уровня (a) со средним уровнем эотаксина в сыворотке (масс./об.) в популяции индивидуумов, имеющих рак, и если уровень в сыворотке индивидуума по меньшей мере на 10% выше, чем средний уровень в сыворотке,
(c) введение композиции, включающий полипептид, состоящий из SEQ ID NO: 1, индивидууму одновременно с лечением гемцитабином и капецитабином, вследствие чего время выживания повышается.
9. Способ лечения индивидуума, страдающего от локально-распространенного или метастатического рака поджелудочной железы, включающий:
(a) определение уровня эотаксина (масс./об.) в образце сыворотки индивидуума;
(b) определение уровня CRP (масс./об.) в образце сыворотки индивидуума;
(c) сравнение уровня (a) со средним уровнем эотаксина в сыворотке (масс./об.) в популяции индивидуумов, имеющих локально-распространенный или метастатический рак поджелудочной железы;
(d) сравнение уровня (b) со средним уровнем CRP в сыворотке (масс./об.) в популяции индивидуумов, имеющих локально-распространенный или метастатический рак поджелудочной железы; если уровень эотаксина в сыворотке индивидуума по меньшей мере на 10% выше, чем средний уровень сыворотки, и уровень CRP по меньшей мере на 10% ниже чем средний уровень в популяции индивидуумов, страдающих от такого же рака,
(e) введение композиции, включающий полипептид, состоящий из SEQ ID NO: 1, индивидууму одновременно с лечением гемцитабином и капецитабином, вследствие этого время выживания увеличивается.
RU2018145512A 2013-06-07 2014-06-05 Биологические маркеры, которые могут быть использованы в иммунотерапии рака RU2725744C2 (ru)

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