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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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1220271 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
# o' [# t2 R# O* e% W/ X+ PNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9   x# ^' ~7 D& W
+ Author Affiliations% I8 B5 n, V  A) R# L" s

, f6 x, i& [) `& x. t, ], o$ U6 [1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan : q+ l% I: l9 n  ?6 b
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan # E" |! j* U4 {
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
2 @; |  e1 c  u; z: @2 t4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 5 ~# Q. L# {) g* C' `
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 2 \0 r+ V! J( a" @( ~* T+ j
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 4 |; c( j. N1 t$ X' K
7Kinki University School of Medicine, Osaka 589-8511, Japan
3 R2 }* G4 o5 ^* [  |5 r3 T' J8Izumi Municipal Hospital, Osaka 594-0071, Japan
1 ]2 i6 Q9 [+ \. H9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan # \; _  s5 K' O: [% V- T
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 ! F  E" C7 d6 T& Z
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.
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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
1 |$ a' h7 D6 M5 \3 O( F+ m
6 O) K! B0 n) wAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
, T7 F+ }, _. ]1 u: m# I) Y  G
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  % o* K2 Y- J' e" B
! e% [2 V2 k: w  X5 y
Published online on: Thursday, December 1, 2011
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1 a$ g9 B7 D. RDoi: 10.3892/ol.2011.507 & W9 |' X; U1 U$ g5 D
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Pages: 405-410 0 {2 P" r" }+ P/ d7 d8 G9 A

  V6 h6 r2 z. @  z# H  ]3 \6 S! W) q! \Abstract:
  ~( M) F6 s+ n) d- H! y) hS-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.
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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& {3 `  t( ?- V" ~$ S) P) b) B
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
+ z# R# [4 M) ?* a8 W5 W) n! y& H+ Author Affiliations
9 p# i1 f9 [- x! G9 m1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ! _% t; Y' F0 ~8 x- T" A
2Department of Thoracic Surgery, Kyoto University, Kyoto
; H! t$ [" Q: c8 R5 {7 w3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
* }7 r( d+ g+ f* J( T&#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 - Q: m% n# Z. `! w
Received September 3, 2010.
, h- z! @3 @* a7 o. b: N0 x# i" }Revision received November 11, 2010. + |* T8 F5 C9 c
Accepted November 17, 2010. ! b6 Y% u8 w. F
Abstract
% X5 H( g4 A' c6 j& ~  f9 VBackground: 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.
* ^4 ~" T6 M# s+ y7 nPatients 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.
0 i+ N; R8 H' b) W3 }. x5 F* ]# t( h8 J6 SResults: 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 Q( A* N7 ~/ WConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. , {, [& ~+ d6 y2 r- ^9 E
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 `  j% @! J5 j5 a% @* g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
- O1 j& k+ H# Y: k  _' a; ihttp://clinicaltrials.gov/ct2/show/NCT015235875 q" g; j3 J+ p* ?+ ?
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC; o+ f8 [/ i' A6 |5 t
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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: |0 I; E% `3 N7 Q' L+ \" F2 f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。7 `# H! }8 U2 a3 _
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

, _: Z# Z/ [8 e2 f3 L1 j3 R没有副作用是第一追求,效果显著是第二追求。. ?. t) d; r6 f; v( X
不错。

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