-
Je něco špatně v tomto záznamu ?
Prognostic factors in follicular lymphoma in the rituximab era: how to identify a high-risk patient?
Vit Prochazka, Tomas Papajik, Marie Jarosova, Karel Indrak
Jazyk angličtina Země Česko
Typ dokumentu práce podpořená grantem, přehledy
NLK
Directory of Open Access Journals
od 2001
Free Medical Journals
od 1998
Medline Complete (EBSCOhost)
od 2007-06-01
ROAD: Directory of Open Access Scholarly Resources
od 2001
- MeSH
- folikulární lymfom farmakoterapie imunologie mortalita patologie MeSH
- hodnocení rizik MeSH
- lidé MeSH
- míra přežití MeSH
- myší monoklonální protilátky terapeutické užití MeSH
- přežití bez známek nemoci MeSH
- prognóza MeSH
- protinádorové látky terapeutické užití MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- práce podpořená grantem MeSH
- přehledy MeSH
Background. Follicular lymphoma accounts for about 20–30% of non-Hodgkin's lymphomas. Clinical behaviour and overall prognosis are highly variable, ranging from indolent forms with occasional spontaneous remissions to rapidly progressive disease. Methods and Results. Modern treatment strategies have shifted from a primarily “palliative” approach to more intensive risk-adapted therapy with the intention of achieving complete long-term remission. New targeted treatment with monoclonal antibodies (MoAb) and radioimmunoconjugates (RIT) has resulted in unprecedented improvements in treatment outcome. At the same time, a large amount of information is now available on lymphomagenesis, the role of the microenvironment of lymphomatous follicles and cytogenetic abnormalities. We can better understand the role of the patient's innate anti-lymphoma immunity. Although no standard front-line therapy has been established, increasingly more data show that risk-adapted treatment strategy have survival benefits for high-risk patients. For this reason, accurate prognostic indices are urgently needed to find optimal therapies for particular lymphoma patients. Whereas the currently used FLIPI index was established in the pre-rituximab era, the newly designed FLIPI 2 index still needs to be confirmed in prospective trials. Conclusion. New therapeutic approaches with MoAb, RIT and other biological agents allow the population to be divided into increasing numbers of groups with different outcomes. All in all, in the near future, we will probably not use only one basic prognostic index for all populations of FL patients. New prognostic schemes should analyze patients separately and include both disease- and patient/host-related parameters.
Citace poskytuje Crossref.org
Lit.: 90
- 000
- 00000naa 2200000 a 4500
- 001
- bmc11036796
- 003
- CZ-PrNML
- 005
- 20120423092619.0
- 008
- 111011s2011 xr e eng||
- 009
- AR
- 024 7_
- $a 10.5507/bp.2011.015 $2 doi
- 040 __
- $a ABA008 $b cze $c ABA008 $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xr
- 100 1_
- $a Procházka, Vít $7 xx0143822
- 245 10
- $a Prognostic factors in follicular lymphoma in the rituximab era: how to identify a high-risk patient? / $c Vit Prochazka, Tomas Papajik, Marie Jarosova, Karel Indrak
- 314 __
- $a Department of Hemato-Oncology, University Hospital Olomouc, Czech Republic
- 504 __
- $a Lit.: 90
- 520 9_
- $a Background. Follicular lymphoma accounts for about 20–30% of non-Hodgkin's lymphomas. Clinical behaviour and overall prognosis are highly variable, ranging from indolent forms with occasional spontaneous remissions to rapidly progressive disease. Methods and Results. Modern treatment strategies have shifted from a primarily “palliative” approach to more intensive risk-adapted therapy with the intention of achieving complete long-term remission. New targeted treatment with monoclonal antibodies (MoAb) and radioimmunoconjugates (RIT) has resulted in unprecedented improvements in treatment outcome. At the same time, a large amount of information is now available on lymphomagenesis, the role of the microenvironment of lymphomatous follicles and cytogenetic abnormalities. We can better understand the role of the patient's innate anti-lymphoma immunity. Although no standard front-line therapy has been established, increasingly more data show that risk-adapted treatment strategy have survival benefits for high-risk patients. For this reason, accurate prognostic indices are urgently needed to find optimal therapies for particular lymphoma patients. Whereas the currently used FLIPI index was established in the pre-rituximab era, the newly designed FLIPI 2 index still needs to be confirmed in prospective trials. Conclusion. New therapeutic approaches with MoAb, RIT and other biological agents allow the population to be divided into increasing numbers of groups with different outcomes. All in all, in the near future, we will probably not use only one basic prognostic index for all populations of FL patients. New prognostic schemes should analyze patients separately and include both disease- and patient/host-related parameters.
- 650 _2
- $a myší monoklonální protilátky $x terapeutické užití $7 D058846
- 650 _2
- $a protinádorové látky $x terapeutické užití $7 D000970
- 650 _2
- $a přežití bez známek nemoci $7 D018572
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a folikulární lymfom $x farmakoterapie $x imunologie $x mortalita $x patologie $7 D008224
- 650 _2
- $a prognóza $7 D011379
- 650 _2
- $a hodnocení rizik $7 D018570
- 650 _2
- $a míra přežití $7 D015996
- 655 _2
- $a práce podpořená grantem $7 D013485
- 655 _2
- $a přehledy $7 D016454
- 700 1_
- $a Papajík, Tomáš, $d 1967- $7 xx0060566
- 700 1_
- $a Jarošová, Marie, $d 1950- $7 xx0053403
- 700 1_
- $a Indrák, Karel, $d 1947- $7 jn20000401162
- 773 0_
- $w MED00012606 $t Biomedical papers $g Roč. 155, č. 2 (2011), s. 99-108 $x 1213-8118
- 856 41
- $u http://biomed.papers.upol.cz/pdfs/bio/2011/02/01.pdf $y plný text volně přístupný
- 910 __
- $a ABA008 $b A 1502 $c 958 $y 2
- 990 __
- $a 20111011121959 $b ABA008
- 991 __
- $a 20120423092556 $b ABA008
- 999 __
- $a ok $b bmc $g 882724 $s 746958
- BAS __
- $a 3
- BMC __
- $a 2011 $b 155 $c 2 $d 99-108 $m Biomedical papers of the Medical Faculty of the University Palacký, Olomouc Czech Republic $x MED00012606
- LZP __
- $a 2011-52/vtme