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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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1271994 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
- B- T. `$ G& {; {0 ?NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 5 u' s/ h+ \6 ~8 I7 R; g9 e7 _: Y
+ Author Affiliations1 q. w4 i8 p' y, W  E. i( p

4 \( i' O8 f! J) y% E4 U1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 9 A% S+ N& @* r  Y
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 1 _" @) X7 A% _2 F+ S1 Z7 R6 u/ S* O
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ! V  q# w( I9 y/ G1 Z
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan / I1 B2 U2 T/ s5 a$ e$ l& V
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
: }8 H+ i3 H+ H# v6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
1 j6 P/ c  E$ b2 ]7Kinki University School of Medicine, Osaka 589-8511, Japan
* i6 V. g$ e5 {2 ]8 J6 S8Izumi Municipal Hospital, Osaka 594-0071, Japan 9 k( ?1 R& G* t9 n0 ^
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 4 B5 w0 M3 R/ q) A+ o7 r) |
Correspondence 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 : t3 P+ S: S. C+ ?; j) f. J  \- x7 R
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 t+ ?' y5 |* [" U3 G
9 W+ c; R/ }* z3 ]- \; 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 & d, e" J) ~8 O8 `

; b+ I5 G% v% k4 O. ^. R% n, F: BAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
4 j+ W) {, Z8 I/ P
  I# d. V$ H& J# HAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
8 A8 `  l/ {$ i- }6 C; v5 U" O$ h# V; @, u
Published online on: Thursday, December 1, 2011
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$ v* s* I- B$ E8 q  gDoi: 10.3892/ol.2011.507
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  V6 B8 @8 L( h" W  O" j$ K) |) |Pages: 405-410
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% u5 g4 ~! r) _% {+ h3 HAbstract:
4 L  Z# h; Q7 c5 ^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." r" s8 f% R/ o3 l( X- [0 I3 k

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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
! W  i1 [0 ~7 {F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
  _5 I- Z- K7 U+ Author Affiliations
/ Y  |/ ?, Y9 S* [1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
* i$ i3 e: t- d" W( y9 J2 H. }2Department of Thoracic Surgery, Kyoto University, Kyoto : _5 N5 K$ h3 ~
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 6 ?+ t' Z, ?' S$ [$ o- x$ F
&#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 `% m$ ?' e0 f& C8 q# B! H4 [& ]
Received September 3, 2010. . M; h: t$ K) U1 d
Revision received November 11, 2010.
. O1 W( Z* A$ \5 W' \. g. ]; \Accepted November 17, 2010.
' L2 \6 U/ Z  Q5 U+ VAbstract9 g: z, K0 W: F, I
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. G! ?# p' D: Q
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.
5 {  M" \6 x. M& V* d  J  P. 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.
8 P* Z: y* y! S, n( h0 q: DConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.   C- y9 u3 a2 ^! D& @5 m" w9 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。+ C% R4 \3 @" Z1 o) d
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?0 v8 r; e% R( w3 H
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
- K; O+ T; d$ f( Jhttp://clinicaltrials.gov/ct2/show/NCT015235873 Q+ m# g* H: P& o+ _/ H* M

- ~! l: Y$ O" xBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC! x/ }' u4 ^0 K( C; n3 ]  E  [3 q0 C
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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. W) `' e! Y+ T# B# q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。( q5 ?! ^) R) H$ W2 k1 n6 m: _9 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 . j! z. }* s1 }0 @% P  W; O% ]
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。
- }( M/ F- F0 u" u; g, M) @$ L至今为止,未出 ...

2 I2 z  L0 Q$ {: L6 ]# h4 p5 t没有副作用是第一追求,效果显著是第二追求。
2 _; z& C$ Z& d不错。

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