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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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1214089 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$ B3 O  E. ^" z' L+ l2 M: v0 W
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 4 T, k- w/ C' W0 Z8 o6 K2 ]
+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
# h2 ]: {8 j' a) x2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan / b' n2 q" N! O8 d, G; K
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan , U& h; W- a4 b+ u
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
8 j+ {. h3 R- p" d: Y5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
# f4 F' A+ {: a# ?) i6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
0 Z1 u; |& F& Z& |# d) [0 y7Kinki University School of Medicine, Osaka 589-8511, Japan
# ?) C4 \1 Y. p) {  k8Izumi Municipal Hospital, Osaka 594-0071, Japan 6 y$ c( \8 _3 G4 {. M9 A
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
2 T3 d8 z0 I% i6 tCorrespondence 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
  ?" b! M% H* a" i+ \& H9 CAbstractBackground: 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
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0 u( @/ `& m. I$ u, Z" n! ~, AAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
, K: t3 h4 W' m3 T! v
9 j; h) d9 ~/ Y. cAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
' o) s; _; Y& _$ n$ _: z3 v) n2 \$ E) [: M# R2 \; Y. l% w! Z
Published online on: Thursday, December 1, 2011 . T$ o* P8 B' g9 T' G+ F
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Doi: 10.3892/ol.2011.507 8 J/ v, m7 c1 Z
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Pages: 405-410
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9 w6 i+ O0 y, R& p8 S* qAbstract:
8 E& w1 N/ f6 K- H) 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.9 j2 ]1 J; e$ k# S$ {9 Q

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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
5 P; Q- j1 p# I% g) ]5 MF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
, J: o: ^' r( [% [# \7 b0 \" B6 A% V+ Author Affiliations
; `: F  E; \* P7 i1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
! @$ W; C9 \; ^; X/ z2Department of Thoracic Surgery, Kyoto University, Kyoto & X( ^) |& p" x! Y' E  {+ Z* q
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
5 |* D) ~$ B& v& 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
/ e$ Q7 h3 j, @7 Z$ oReceived September 3, 2010. " W) e0 s8 ~% v0 {4 p
Revision received November 11, 2010.
2 ^1 I) D" L' T7 m: yAccepted November 17, 2010. & l* ^# S" g6 _2 X: Z+ E
Abstract
$ s5 g7 \; c3 P3 \; q! x) \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. ; W& z! \" |1 S$ `
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. / |# N1 Y* T3 v9 P) C' y* J) ]
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.
7 |. z/ N7 T1 DConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 0 @; O0 Z5 ~0 u( ^- ~8 K+ Z
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。
2 ~: Q- }0 A, H1 t) N8 _. _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
+ y: m1 `3 w# ~http://clinicaltrials.gov/ct2/show/NCT015235878 r: u' ]+ [. m2 N: z

( m9 X* X* r- @& v( F  f, u! I2 ^BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
7 a7 o- a+ v' V/ I5 f9 N$ ~http://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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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 Z. t+ b. \& t$ u' l) B: 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 1 z! e5 b# @5 n' M3 O4 b8 I
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。# d4 w, b+ Q! |5 D2 p/ x
至今为止,未出 ...
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没有副作用是第一追求,效果显著是第二追求。. N) S; b7 a& I; s" n( _
不错。

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