-
Je něco špatně v tomto záznamu ?
Increased efficacy of a dose-dense regimen of neoadjuvant chemotherapy in breast carcinoma: a retrospective analysis
Bohuslav Melichar, Helena Hornychová, Hana Kalábová, Hana Bašová, Jindřiška Mergancová, Hana Urminská, Pavel Jandík, Vladimír Červinka, Jan Laco, Aleš Ryška
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NS10286
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Plný text - Článek
Zdroj
NLK
ProQuest Central
od 1997-03-01 do Před 1 rokem
Health & Medicine (ProQuest)
od 1997-03-01 do Před 1 rokem
- MeSH
- dospělí MeSH
- imunohistochemie MeSH
- lidé středního věku MeSH
- lidé MeSH
- nádory prsu chemie farmakoterapie mortalita patologie MeSH
- neoadjuvantní terapie MeSH
- protokoly protinádorové kombinované chemoterapie terapeutické užití MeSH
- receptor erbB-2 analýza MeSH
- receptory pro estrogeny analýza MeSH
- receptory progesteronu analýza MeSH
- retrospektivní studie MeSH
- senioři MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Neoadjuvant chemotherapy is being increasingly used in the treatment of breast carcinoma. We performed a single-center retrospective analysis of the results of neoadjuvant therapy in 376 breast carcinoma patients treated with three different regimens combining doxorubicin and paclitaxel (AT), dose-dense doxorubicin and cyclophosphamide with sequential weekly paclitaxel (DD AC-P), or the combination of trastuzumab with chemotherapy (DD AC-PT). The expression of estrogen receptors (ER), progesterone receptors (PR) and human epidermal growth factor receptor (HER)-2 was determined immunohistochemically. Pathological response was determined in 318 patients. Pathological complete response (pCR) was observed in 18% of patients. The pCR rate was significantly higher in patients treated with DD regimen (22 vs. 13%) and younger than 55 years (23 vs. 13%). The pCR rate was higher in patients with triple negative (TN) tumors (43%) and tumors over-expressing HER-2 (HER-2+; 28%) compared to patients with ER- or PR-positive tumors not expressing HER-2 (ER/PR+HER-2-; 6%). In patients with TN tumors pCR rate was significantly higher after treatment with DD AC-P compared to AT (61 vs. 22%, p=0.005). pCR was associated with significantly improved relapse-free survival (RFS) and overall survival (OS), but when analysis was performed based on tumor phenotype, the difference was significant only in patients with TN tumors. In multivariate analysis, pCR, stage, and ER expression were significant predictors of RFS, while pCR, stage, ER and DD regimen were significant predictors of OS. In conclusion, present data indicate superiority of a DD regimen in obtaining pCR in patients with breast carcinoma treated with neoadjuvant chemotherapy. The difference in efficacy is due mostly to markedly higher pCR rate in patients with TN tumors.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc13031934
- 003
- CZ-PrNML
- 005
- 20141114124235.0
- 007
- ta
- 008
- 131002s2012 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1007/s12032-012-0195-y $2 doi
- 035 __
- $a (PubMed)22392196
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Melichar, Bohuslav $u Department of Oncology, Palacký University Medical School and Teaching Hospital, Olomouc, Czech Republic; Department of Oncology and Radiotherapy, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic. bohuslav.melichar@fnol.cz
- 245 10
- $a Increased efficacy of a dose-dense regimen of neoadjuvant chemotherapy in breast carcinoma: a retrospective analysis / $c Bohuslav Melichar, Helena Hornychová, Hana Kalábová, Hana Bašová, Jindřiška Mergancová, Hana Urminská, Pavel Jandík, Vladimír Červinka, Jan Laco, Aleš Ryška
- 520 9_
- $a Neoadjuvant chemotherapy is being increasingly used in the treatment of breast carcinoma. We performed a single-center retrospective analysis of the results of neoadjuvant therapy in 376 breast carcinoma patients treated with three different regimens combining doxorubicin and paclitaxel (AT), dose-dense doxorubicin and cyclophosphamide with sequential weekly paclitaxel (DD AC-P), or the combination of trastuzumab with chemotherapy (DD AC-PT). The expression of estrogen receptors (ER), progesterone receptors (PR) and human epidermal growth factor receptor (HER)-2 was determined immunohistochemically. Pathological response was determined in 318 patients. Pathological complete response (pCR) was observed in 18% of patients. The pCR rate was significantly higher in patients treated with DD regimen (22 vs. 13%) and younger than 55 years (23 vs. 13%). The pCR rate was higher in patients with triple negative (TN) tumors (43%) and tumors over-expressing HER-2 (HER-2+; 28%) compared to patients with ER- or PR-positive tumors not expressing HER-2 (ER/PR+HER-2-; 6%). In patients with TN tumors pCR rate was significantly higher after treatment with DD AC-P compared to AT (61 vs. 22%, p=0.005). pCR was associated with significantly improved relapse-free survival (RFS) and overall survival (OS), but when analysis was performed based on tumor phenotype, the difference was significant only in patients with TN tumors. In multivariate analysis, pCR, stage, and ER expression were significant predictors of RFS, while pCR, stage, ER and DD regimen were significant predictors of OS. In conclusion, present data indicate superiority of a DD regimen in obtaining pCR in patients with breast carcinoma treated with neoadjuvant chemotherapy. The difference in efficacy is due mostly to markedly higher pCR rate in patients with TN tumors.
- 650 _2
- $a dospělí $7 D000328
- 650 _2
- $a senioři $7 D000368
- 650 _2
- $a protokoly protinádorové kombinované chemoterapie $x terapeutické užití $7 D000971
- 650 _2
- $a nádory prsu $x chemie $x farmakoterapie $x mortalita $x patologie $7 D001943
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 _2
- $a lidé $7 D006801
- 650 _2
- $a imunohistochemie $7 D007150
- 650 _2
- $a lidé středního věku $7 D008875
- 650 _2
- $a neoadjuvantní terapie $7 D020360
- 650 _2
- $a receptor erbB-2 $x analýza $7 D018719
- 650 _2
- $a receptory pro estrogeny $x analýza $7 D011960
- 650 _2
- $a receptory progesteronu $x analýza $7 D011980
- 650 _2
- $a retrospektivní studie $7 D012189
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Hornychová, Helena $u Department of Pathology, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic
- 700 1_
- $a Kalábová, Hana $u Department of Oncology, Palacký University Medical School and Teaching Hospital, Olomouc, Czech Republic
- 700 1_
- $a Bašová, Hana $u Department of Oncology and Radiotherapy, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic
- 700 1_
- $a Mergancová, Jindřiška $u Department of Surgery, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic
- 700 1_
- $a Urminská, Hana $u Department of Radiology, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic
- 700 1_
- $a Jandík, Pavel $u Department of Surgery, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic
- 700 1_
- $a Cervinka, Vladimír $u Department of Pathology, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic
- 700 1_
- $a Laco, Jan $u Department of Pathology, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic
- 700 1_
- $a Ryška, Aleš $u Department of Pathology, Charles University Medical School and Teaching Hospital, Hradec Kralove, Czech Republic
- 773 0_
- $w MED00012126 $t Medical oncology (Northwood, London, England) $x 1559-131X $g Roč. 29, č. 4 (2012), s. 2577-2585
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/22392196 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20131002 $b ABA008
- 991 __
- $a 20141114124250 $b ABA008
- 999 __
- $a ok $b bmc $g 996021 $s 830379
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2012 $b 29 $c 4 $d 2577-2585 $i 1559-131X $m Medical oncology $n Med Oncol $x MED00012126
- GRA __
- $a NS10286 $p MZ0
- LZP __
- $a Pubmed-20131002