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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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1289209 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 Type6 X$ k. I$ l  z# _' {
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
5 Q! `! K  z" p; ?6 O1 J1 y& B1 z+ Author Affiliations7 B4 w8 n& ?* F2 k: n) G

) `3 D/ k9 I2 ?1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
6 C8 R8 n8 M7 t2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
, p; @6 D3 k- J4 d% a3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
5 r# C3 O! Q- p1 B4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan . |* i4 w+ k% @
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan ; `$ t# i7 s% B" Z) j) {$ i. N
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
5 j1 D8 _/ Y! g7Kinki University School of Medicine, Osaka 589-8511, Japan 9 p2 t( i8 W2 Z5 J
8Izumi Municipal Hospital, Osaka 594-0071, Japan 0 l6 ?/ _. n; H: H* ~2 {
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
5 F- W+ z1 ^& X% WCorrespondence 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
; H, \; u0 B1 r1 DAbstractBackground: 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. 5 B" q3 c8 A9 x
& T* d; x4 x1 `3 e8 M
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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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
2 U: d9 ^% i2 K; z) o3 U, i4 A
. P( h$ A5 S7 r# M: \% g0 bAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
) ]' r" d; P; a8 A- k& [+ I. P( i
8 J8 p: ]3 d. l6 \* J  O' f6 ?Published online on: Thursday, December 1, 2011 8 _; l5 b: c; e/ K3 {& A4 Y

. J/ u, Y8 F. m; f/ U8 A$ t% o$ vDoi: 10.3892/ol.2011.507
5 j/ @1 v) j6 E( l  q( a6 H! e# y7 \
Pages: 405-410 0 |5 w: I1 l5 _# C2 K4 n* u+ O

) P. F; W6 f3 uAbstract:6 A" m7 C' j7 V0 z- e  L( I
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.
4 t* G+ v& e: I  I. u % x5 L7 E( Q- U7 U" ?$ X' ?' a
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( r( c8 k7 E- M' ~* _
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 6 g' s, I' \7 ~' {& i
+ Author Affiliations
7 R: R' S! l3 u2 h$ h1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ; ?* d" _( C$ G4 n# {7 _; M( E& G
2Department of Thoracic Surgery, Kyoto University, Kyoto
3 C- j1 c% Q0 y% P3 y; O0 v3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan : _: S) p$ ]' g" F/ n
&#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
1 b; @& c9 S6 W- ~2 QReceived September 3, 2010.
" G& u( ^- p0 u0 i2 e: c) s) ^  wRevision received November 11, 2010.
7 ]) P2 Y: L; \8 U. t" g1 T+ AAccepted November 17, 2010.
  @* q$ m; [' m$ BAbstract& ?- |2 @$ s: O: E# |
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. 2 V- e* s3 E3 ^0 B- t
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. ' X3 A: ^; [, @5 [
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. # a2 F; t( B* v* ^
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 4 b, S* P/ y- V# H8 R
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。
4 k8 V7 w) u) f' U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?+ I- I7 A9 R' y& K/ [4 `+ Q
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 Chemotherapy6 j5 n/ F1 ^) A7 e& L0 q/ a% Y" W
http://clinicaltrials.gov/ct2/show/NCT01523587
% R$ z! b9 w. S( d) _
( t% v* w  c; n$ T& K8 MBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC2 G2 w# e- R* U7 I
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。
1 u2 q: h' [$ g. H% o! K' 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 T3 O$ U2 D' l  T( H9 [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。( J5 [& {# h, y( i7 d# S
至今为止,未出 ...

) h. h3 j, e) n' a0 o; N% q没有副作用是第一追求,效果显著是第二追求。
- V* R5 z7 F& s% |4 i" l, k不错。

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