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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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1247402 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
7 `5 h6 E$ H" y" s8 {NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 . A# Y( p7 |, I& K- ?
+ Author Affiliations
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1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
/ |* Y, r9 B2 W6 [- d2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 8 m9 ]; n5 |, a% S
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 6 F: W5 |6 F2 o5 T
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
* N) Q  o- e6 B) [3 a2 W" p2 ?: e5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
: z9 {8 X1 ?, s* @6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
- k: B& Z& w' x0 [; [7Kinki University School of Medicine, Osaka 589-8511, Japan
1 N. G0 a3 Q1 ?) s( j* b$ ^; ^4 E8Izumi Municipal Hospital, Osaka 594-0071, Japan " Z, c) X' @. q% v% c7 t* @5 B1 B
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
# z9 s& u7 U4 W# p7 c( K! J* zCorrespondence 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 " o' ^. K8 m: ^# x$ f/ B
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
9 A* [7 t( v" L. W
. B5 d% ^0 j  {+ Y% M8 FAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato & z& [7 _8 a6 M8 f. {

( V! k% J: M, e' U. ~; U( ZAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  ) U- C9 d- b' ^

9 K$ C  }$ V0 v& g1 ]Published online on: Thursday, December 1, 2011 ' D9 m: J6 d3 v/ X$ ?! b

0 K# z: Z, y1 X+ |1 VDoi: 10.3892/ol.2011.507 ' `2 b3 U+ [1 ?: S& J( ~$ A' @

3 v# q5 _- Y8 C5 p! tPages: 405-410
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( V0 c3 b; e0 N) S/ b7 Q5 Z& l/ E! tAbstract:6 F( V) O! h0 [' z
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.
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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! c6 \& W8 c7 i% O
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 ; c# v3 d% L" V8 X& z# ~
+ Author Affiliations8 }) t  i  j- }  s; R9 d
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
* E  {# {( q) ]7 ]5 }0 [, W3 s2Department of Thoracic Surgery, Kyoto University, Kyoto   R: A$ [9 k  g) _2 _# W# ^
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 3 s  y( L# E* `, 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 ) i4 b/ w" I4 p$ v' J: ~# \
Received September 3, 2010.
' e. J: g( r5 n" b# W1 d* _Revision received November 11, 2010. 8 p2 [- K9 g- n' q0 s# ?# j# J
Accepted November 17, 2010. 8 \) r$ t! R9 A& x+ L; w5 q9 Z
Abstract6 i! N- J2 s: X9 t# s3 ~
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. : G3 V$ Z1 S% O2 t) G/ @% U
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.
% Q7 c6 z. N4 z& a2 M$ fResults: 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. 6 U7 Y/ D* z. z$ I
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study.
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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。. }3 w1 \9 F: G3 E
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?3 W( D1 d" g+ E- D7 x1 n& `
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 Chemotherapy4 _% q+ g9 [5 S- w" O5 k. w
http://clinicaltrials.gov/ct2/show/NCT01523587; x! X0 }1 ?0 D' \# C; |! m

6 _+ r# \$ b: U& A# y  T) D6 r  T! `BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC( ^3 s! G3 i. N6 O! m! R
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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" e( z( k5 ^. K% M( z7 b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。% {9 H& h8 A: E  E7 x+ K" G7 a
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
! s7 Q& Q/ r) C0 \; b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。( L+ ]5 b" N* A, f8 p
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。
5 C6 T9 U, V  r8 n8 \9 G不错。

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