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我父亲肺鳞癌的治疗贴(2014年3月1日驾鹤西去)

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1250937 1620 老马 发表于 2011-10-27 08:05:18 | 置顶 |
老马  博士一年级 发表于 2012-4-27 18:50:42 | 显示全部楼层 来自: 浙江温州
Pooled Analysis of S-1 Trials in Non-Small Cell Lung Cancer According to Histological Type
! t5 p3 Y. N% a5 y* L2 |NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 ( c/ t' A7 c% i9 Q# ~
+ Author Affiliations
% Y( I( i0 u) n4 j7 T/ |6 I& R! j) ~* K6 p5 E  G5 E
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan # m0 q$ i0 U6 S* I
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
: s/ Z0 \+ k( U3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
9 }( v0 V0 T2 r7 I2 m4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 0 Y0 T7 ~4 w  T
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
3 Z+ b& p( Z5 g8 [" S, U6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan , y6 O" j7 u8 j( v
7Kinki University School of Medicine, Osaka 589-8511, Japan   O; f2 E  ?& e( s4 h
8Izumi Municipal Hospital, Osaka 594-0071, Japan . T9 [: {1 @- o, S
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
/ s# L. ?2 w0 V  J8 K  y7 ACorrespondence to: Nobuyuki Yamamoto, Division of Thoracic Oncology, Shizuoka Cancer Center, 1007 Shimonagakubo, Nagaizumi-cho, Sunto-gun, Shizuoka 411-8777, Japan. Tel: +81 559895222, Fax: +81 559895783, e-mail: n.yamamoto@scchr.jp / A3 A1 _) x4 {4 p* h! m& V  R& V
AbstractBackground: The antimetabolic agent S-1 inhibits thymidylate synthase similar to pemetrexed, but through a different mechanism of action. Whether the antitumour activity of S-1 depends on histological type remains unclear. We analysed pooled data from 2 phase II clinical studies of cisplatin and S-1 in patients with previously untreated advanced non-small cell lung cancer. Patients and Methods: We comprised 110 patients with stage IIIB or IV non–small cell lung cancer. Univariate and multivariate analyses were performed to determine the effects of histological type on progression-free survival and response rates. Results: On pooled analysis of the data, according to histological type, median progression-free survival was 3.8 months in patients with squamous cell carcinoma and 4.4 months in those with non-squamous cell carcinoma. Both analyses showed that progression-free survival and response rate did not differ significantly. Conclusion: Unlike molecular targeted agents and pemetrexed, a combination of cisplatin and S-1 may be no difference in response according to histological type.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:52:43 | 显示全部楼层 来自: 浙江温州
S-1 monotherapy for previously treated non-small cell lung cancer: A retrospective analysis by age and histopathological type , z) B% B  W6 J4 s" C8 b

& p; r/ e1 l$ y0 dAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
; z; D4 h' v' s5 B# _0 h+ x) _9 P8 @* i; L: b* u
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  . \+ q! h8 R8 I" p4 Q( o1 \/ J

; @0 v2 r3 u( K; mPublished online on: Thursday, December 1, 2011
3 L% X; b& i; V& Z
& n1 u4 p+ ?# O. n3 j2 `) p/ I; Y+ ^" bDoi: 10.3892/ol.2011.507 ( H/ [1 R! \* I) S
- S0 {6 {) W# E" Z8 [8 y% T
Pages: 405-410
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: N$ D4 H( X, v( r& l8 AAbstract:
# g- E- }4 Y4 ^6 _3 w, B# N% W# rS-1, an oral fluoropyrimidine derivative, has been approved for the treatment of non-small cell lung cancer (NSCLC) in Japan. In the present study, the efficacy and safety of S-1 monotherapy for elderly patients with previously treated NSCLC were retrospectively evaluated, and the efficacy of S-1 monotherapy was compared by histopathological type. This retrospective study included 54 patients with advanced or recurrent NSCLC who had received S-1 monotherapy following the failure of previous chemotherapy regimens at our institutes. Patient outcomes were compared based on their age and histopathological type. S-1 was administered orally, twice daily, while the duration and interval were modified according to the medical condition of each patient. The default delivery schedule, the mean number of S-1 cycles, did not differ significantly between the two age groups (<70 and ≥70 years). The rate of therapy discontinuation, schedule modification or dose reduction due to intolerable toxicities or patient refusal was relatively frequent in the older group (40.7 and 55.6% for ages <70 and ≥70 years, respectively; p=0.414), and the incidence of grade 3 anemia was relatively high in the older group (3.7 and 18.5%, respectively; p=0.192). The response rates (13.0 and 4.8%, respectively; p=0.609) and disease control rates (39.1 and 33.3%, respectively; p=0.761) did not differ significantly between the two age groups. According to histopathological type, the disease control rate was significantly higher in adenocarcinoma (57.9%) compared to non-adenocarcinoma (20.0%, p=0.013). Thus, S-1 monotherapy may be equally effective and tolerated in patients <70 years and those ≥70 years. Additionally, adenocarcinoma may have a higher disease control rate than non-adenocarcinoma.
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个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-27 18:57:27 | 显示全部楼层 来自: 浙江温州
Thymidylate synthase (TS) gene expression in primary lung cancer patients: a large-scale study in Japanese population3 m' L" [7 }) Y
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
  g! w. n9 l7 l8 C1 Q: `+ Author Affiliations6 N" j1 o* ^; v0 `5 J9 x
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
% Z% b: q9 v# w8 K2Department of Thoracic Surgery, Kyoto University, Kyoto
- `5 x; v/ ?, \3 _3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan # {$ x5 S. ?8 z) k- {" i5 W
&#8629;*Correspondence to: Dr F. Tanaka, Second Department of Surgery, University of Environmental and Occupational Health, 1-1 Isegaoka, Yahata-nishi, Kitakakyushu, 807-8555, Japan. Tel: +81-93-891-7442; Fax: +81-93-692-4004; E-mail: ftanaka@med.uoeh-u.ac.jp . f9 G( W3 }' t
Received September 3, 2010. 2 f0 q& n9 a, \$ h: s
Revision received November 11, 2010. * |6 u& l1 a* `1 w( t
Accepted November 17, 2010.
* V6 D+ g1 N6 GAbstract
* }5 l% c/ Z6 zBackground: Previous small-sized studies showed lower thymidylate synthase (TS) expression in adenocarcinoma of the lung, which may explain higher antitumor activity of TS-inhibiting agents such as pemetrexed. ' K" e. r/ `, T" `% B% X5 {
Patients and methods: To quantitatively measure TS gene expression in a large-scale Japanese population (n = 2621) with primary lung cancer, laser-captured microdissected sections were cut from primary tumors, surrounding normal lung tissues and involved nodes.
& e- c5 f6 g5 N7 m' MResults: TS gene expression level in primary tumor was significantly higher than that in normal lung tissue (mean TS/β-actin, 3.4 and 1.0, respectively; P < 0.01), and TS gene expression level was further higher in involved node (mean TS/β-actin, 7.7; P < 0.01). Analyses of TS gene expression levels in primary tumor according to histologic cell type revealed that small-cell carcinoma showed highest TS expression (mean TS/β-actin, 13.8) and that squamous cell carcinoma showed higher TS expression as compared with adenocarcinoma (mean TS/β-actin, 4.3 and 2.3, respectively; P < 0.01); TS gene expression was significantly increased along with a decrease in the grade of tumor cell differentiation. There was no significant difference in TS gene expression according to any other patient characteristics including tumor progression. * C/ b% k' v' D6 m0 b
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 0 J, b% T* s4 o9 v: z: z4 a, t
个人公众号:treeofhope
走在异乡  高中一年级 发表于 2012-4-28 00:30:22 | 显示全部楼层 来自: 四川成都
一直关注老马的帖子,前方的指明灯。祝福你爸好疗效
累计签到:1 天
连续签到:1 天
[LV.1]初来乍到
baiselianyi  初中二年级 发表于 2012-4-28 10:24:44 | 显示全部楼层 来自: 浙江台州
一直得到老马帮助,祝福老马爸爸
老马  博士一年级 发表于 2012-4-28 18:00:37 | 显示全部楼层 来自: 浙江温州
26日吃了12片地米(0.75mg一片),27日吃了22片地米(0.75mg 一片),28日吃了12片地米(0.75mg一片),都分二次吃。- o0 t7 \+ h4 t' L: h5 x' W
今天为止没有任何反应,每天吃VC,VB2,还有漱口水,就怕口腔溃疡。
个人公众号:treeofhope
bishop_cn  大学一年级 发表于 2012-4-28 23:16:11 | 显示全部楼层 来自: 中国
副作用如何,单药反应很小吧?4 h8 s2 \6 r5 ~0 s' @
老马  博士一年级 发表于 2012-4-29 00:20:00 | 显示全部楼层 来自: 浙江温州
LUX-Lung 8: A Phase III Trial of Afatinib (BIBW 2992) Versus Erlotinib for the Treatment of Squamous Cell Lung Cancer After at Least One Prior Platinum Based Chemotherapy
5 a  Z; B9 C9 P, Q: h. D4 B; Rhttp://clinicaltrials.gov/ct2/show/NCT01523587/ K, Z& `4 ~( J( O" _

2 C% M0 G8 `4 N! X' J' W  kBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
. U# \& o* X$ T  t; O& i5 vhttp://clinicaltrials.gov/ct2/show/NCT01156545
个人公众号:treeofhope
老马  博士一年级 发表于 2012-4-29 20:53:58 | 显示全部楼层 来自: 浙江温州
本帖最后由 老马 于 2012-4-30 09:33 编辑
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  t# b" x3 C, R8 M; R, v+ D! s从4月24日开始到4月28日,打了5天的舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。
0 M7 ~3 s8 C( ~8 T7 h, R  |至今为止,未出现化疗副作用。
个人公众号:treeofhope
英雄武松  大学四年级 发表于 2012-4-30 01:37:05 | 显示全部楼层 来自: 哈萨克斯坦
老马 发表于 2012-4-29 20:53 # w$ h4 O# K0 P- R; V+ v& Q) [6 g
从4月24日开始到4月28日,打了5天的打了5天舒普深(注射用头孢哌酮钠舒巴坦钠),效果非常好。$ h# X- P7 f% C$ j3 \$ J/ u5 r
至今为止,未出 ...

( _) b# g, I' y1 g1 l6 Y6 w没有副作用是第一追求,效果显著是第二追求。  c1 [7 R: t9 u: @  I6 ^
不错。

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