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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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1397126 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 Type9 p/ r" M7 a( b8 L5 P+ {" q
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 + U# n8 u* X8 h; b
+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan * M: C' R  S( E! ], H% R! a
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 7 m5 u/ b+ ^5 _% k' b
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
$ E! B  }& \/ N8 ~4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
9 O, v" E; ^/ B, o8 d3 Y( }6 ?% t* n5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan # J# g$ |: C- J! O8 h" q. X8 x! @
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
1 s' R$ m& v3 p% g7Kinki University School of Medicine, Osaka 589-8511, Japan
+ a9 Q# v" V  ^9 R% Y8Izumi Municipal Hospital, Osaka 594-0071, Japan
, A0 s& y# I5 x, [9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
5 @0 I2 z1 Y" `0 s; T( mCorrespondence 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 7 A- \+ X5 A# \; f$ c
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. . H- P9 f$ B6 ?3 [
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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 / p, P- ]" d( J$ o' ~/ Q

  Z5 o5 ~( m- X! g# q: o: F- qAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
! E/ X, b$ J2 I9 n9 T6 h3 L! l8 l4 [8 V8 @+ k" y* ~
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  , y9 e/ x3 h( Z8 J, r
, J" l& T* U4 L1 S
Published online on: Thursday, December 1, 2011 + ~) E# g% j  J6 s% g

* y7 m+ q2 a5 IDoi: 10.3892/ol.2011.507 $ F1 c  l2 c1 e8 p/ O5 q% _) l2 @3 L
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Pages: 405-410
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4 Q; c& i0 B$ x* \8 `: ?: TAbstract:9 Y- u) }9 J1 P+ D! C; p
S-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 population
- e' u* Z& a! O! j5 [+ k3 S' nF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 3 _) y2 Z7 m# P3 v
+ Author Affiliations
/ e/ V3 e3 E" O, ^6 S& U9 K1 M1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ' h2 r% M( G9 D
2Department of Thoracic Surgery, Kyoto University, Kyoto
2 S: m% }# D4 [% \, d- m3 K3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
) c  F* c5 B8 F6 x&#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 ! R0 _: ^. X; {4 @6 E
Received September 3, 2010. ; C, N2 z) r; l- O
Revision received November 11, 2010.
; Z" o4 o; j3 s: s2 ?( q9 a4 w$ l. p5 WAccepted November 17, 2010.
: F5 L* d1 X4 Y# gAbstract
* f; k# L( t$ M& Y4 ]/ LBackground: 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.
# y1 f" s! q- z$ ?3 ]  _% l8 F# _, e  bPatients 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. - G4 |. ~, T2 A+ h5 Q1 {5 f7 ^0 S
Results: 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.
9 }% F9 a5 R* }6 K/ @( L+ ?Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ( v9 a$ i1 v8 z0 x
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。
) d! g7 W2 G0 f" Z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?& y4 I4 [1 @2 O  |% F
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
3 y: \! A! n3 {http://clinicaltrials.gov/ct2/show/NCT015235877 w; H" q# ^& Z0 Y" F) c

; a: ^% P4 V/ w. X# ?; U9 Q! M8 L( l& qBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
$ |8 V1 D( J6 D/ Ghttp://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 0 x$ Z( h1 [# G- `* X; E" R
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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。. @# i2 I# [7 L; ]
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
3 N2 z( E( j* j' M4 n$ ?" t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。
6 S( X6 z1 V# p- y至今为止,未出 ...
% {" M, i* V+ B' |0 L  F
没有副作用是第一追求,效果显著是第二追求。
% }3 o) |* M6 n5 g# a8 l不错。

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