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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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1377241 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
3 N2 {3 G4 u& K$ jNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 " e$ x6 K8 O7 F9 z* V
+ Author Affiliations& y/ X/ p/ j# F6 j& c

& |+ P. k# S+ @# ~9 U9 m1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
' ^; J4 l! p8 \* q1 P. i% s# a2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan $ y$ ]% p" T' E8 y$ k2 k+ N, |6 y2 }# }
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
% }4 Y  O5 `% G6 z: q4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
  F8 L' ?  T+ S3 X  q% Y5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
. V) @& F& p4 c  A7 a* \+ h6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 7 w8 w, S. K8 n6 r; Y
7Kinki University School of Medicine, Osaka 589-8511, Japan ' v9 P, l7 e) P
8Izumi Municipal Hospital, Osaka 594-0071, Japan
  J: t: L2 y# x+ Z9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan ; r( s+ Q9 |/ D" s3 u
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 ' c/ t, x# r" ^# z& 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. , j. @- d& @2 f2 A9 o4 ^+ k  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 8 l. s' {; a5 O7 Z. p

% R' ^7 S+ o& K2 R$ ~( CAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 4 |3 ~1 u. |+ d( ^3 _' y' B
8 F3 y5 f- l- v# y- e
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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1 s& b6 \8 S) U8 h8 `9 }5 L6 H9 [Published online on: Thursday, December 1, 2011 # p" A! h! d9 g1 d) Y" b* K) W

7 S4 T' ~% P: T6 NDoi: 10.3892/ol.2011.507
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Pages: 405-410 " u2 Y+ x2 A/ E
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Abstract:, B5 i- Z" |) h8 [0 v) U
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; V+ {6 X1 R9 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( b1 q6 M* l% w0 L, I7 k! y  X
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ( H7 f! C- O2 W$ A6 V
+ Author Affiliations3 \4 b+ X; W4 d2 z3 }
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu : I/ w" B1 ~" F9 [! `
2Department of Thoracic Surgery, Kyoto University, Kyoto ) M+ k- o& K( Z. \, x' ~
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan " t5 v$ h* Q9 K" ]$ s( J+ X/ j
&#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 / w2 R) g3 A8 R. x4 X5 q
Received September 3, 2010. . r1 S1 S4 W% `: t
Revision received November 11, 2010. , P1 X8 U: N3 C) R+ i1 x( ?
Accepted November 17, 2010.
' v2 N+ b* D) ~: `* t2 v0 v% C/ hAbstract6 N7 K, N' F- f  `" |0 x" f4 P4 }
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.
3 L1 _3 ?2 x1 z2 R0 q# o" z7 uPatients 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.
4 O1 a6 P. X  AResults: 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.
1 ^4 m3 e5 |& C& m' o1 `Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. $ T/ D4 r4 n/ c- B% j0 N" i  [
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。* n) M1 C' q" [# V! V* M" O
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
; M( n6 a& g9 }+ d4 `http://clinicaltrials.gov/ct2/show/NCT01523587
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6 i( q" w9 v  ?5 ^' C. ?: f0 HBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC& E3 Q4 x! D, ]2 A7 N+ S  G
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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: A  M# r  Y) ^4 d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 z) h7 T' H  Q3 S  x" _9 U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 w7 K4 j  c' \3 q; b' G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。
" ?  j& T/ o8 ]+ C7 K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。
3 F" i' I' O, s, E/ G$ q不错。

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