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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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1245846 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( M/ q. R9 g) H! B( R
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
# E' A$ K/ p9 c- L: Z& ?9 t# e" q+ Author Affiliations: b) c: S. `3 T( l, h7 m
1 l  N7 b& ^# g
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
/ Z5 J4 a, g( H2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan * p  ]% K+ S8 k: J
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 7 _+ u, C: E  ^+ `6 l
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
  h9 K( n7 O9 y  J" R$ C5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
6 C$ k) A+ c( U5 p& H8 s3 O! w6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
$ l# [( U  t' J! ?7 s7 ?7Kinki University School of Medicine, Osaka 589-8511, Japan . D% v5 V5 P/ s% b. a" F# s
8Izumi Municipal Hospital, Osaka 594-0071, Japan
# e. D5 p/ D0 E5 f# t9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
* T6 e; b" Z8 P$ h3 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 4 _* P# M% F% s. 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. 0 \, b0 o. y  x' w( j
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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
' x% X/ C3 q. M& X
; n4 y% l( E8 o) `+ WAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
0 X' I2 c1 Z$ M* {9 a/ H
2 v/ }, |* h( oAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  " p& |6 f4 @& X  a0 h! Z

2 |" X0 q  p% w& \9 F* v" kPublished online on: Thursday, December 1, 2011 ) }* [- K& D0 ~. \5 o

2 E* k  z+ ?' v5 P% R3 yDoi: 10.3892/ol.2011.507 5 Y3 P+ M. X. C  g) z) {
$ M5 M, P( T- }% w! Z! x
Pages: 405-410 2 R# V4 w, f7 }9 N: k
5 M& x) S0 Q+ Q, e, Q! ?/ e
Abstract:
2 x) P. O1 f% S& B, @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.0 b# A$ \7 d1 A3 {6 J

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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 R& j% b7 o& D& ]$ ~- u
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
1 [. J" ?# X3 \5 v5 E& h0 Y7 n+ Author Affiliations% D, R! ]: G$ h
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ' @+ ?7 Q2 |4 {! H( R# B
2Department of Thoracic Surgery, Kyoto University, Kyoto
" {; }1 L" g$ q: Y  N, }* ^3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan - y5 T$ f$ [$ `% A; a, S! O6 ^$ I
&#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 7 Y7 }% y, ?# f* q6 A  \1 ]
Received September 3, 2010. ( Z2 P6 m9 Q. O/ m4 D' Z" C) `
Revision received November 11, 2010.
1 e" G0 _& |- y' `Accepted November 17, 2010. - t( W! U. O' }+ P
Abstract; G1 H$ L% }' X& |, o* J2 k
Background: 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. ( L- D/ y% I) @5 B6 q$ P' a) `
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.
/ S0 t( m% B* ^+ [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. ( b+ M8 |' l8 `
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. ) s6 u1 `: @7 G5 z( V! H
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$ S; {. e# A' A3 H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?
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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! w4 h$ f0 i/ {
http://clinicaltrials.gov/ct2/show/NCT015235874 n8 N; ?! d% K/ d) p4 [

5 a4 p# ~0 R5 u& lBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
0 `. I8 Q4 Y4 J. U! Rhttp://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 9 R  {3 I: r9 B5 \1 L; o

$ D6 D7 j7 K: \3 G& g5 u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。& Q6 p' c8 X6 C9 n' ?. A7 `$ C
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
  U$ S) B& r* k# k6 Y. o, X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。
# I3 E6 ?2 i2 P: J2 C( z至今为止,未出 ...
: W$ h' @  K% `& e
没有副作用是第一追求,效果显著是第二追求。, c* ^+ n2 P- W: N: P$ u. A  f
不错。

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