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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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1273674 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 w' j/ y% \. u$ ^) V  i; aNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
+ U2 g: F# p! O+ T+ Author Affiliations# w( b5 j% \, h" X3 y' d9 I& o6 U
6 V4 X2 r9 y; @9 B, E, K
1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ' F. ?/ Z% \8 @  a
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
* l! o8 _2 @7 I) P; @3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
+ z: F  Q. K9 N% F* D' D: W4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan   b) P! c2 G2 ?
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
0 D$ H& J, F; A8 o+ P, G! C5 H3 g6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
* [: ?$ w3 s- a) }7Kinki University School of Medicine, Osaka 589-8511, Japan
. S& M  p: p' q, c2 u; f& n' O8Izumi Municipal Hospital, Osaka 594-0071, Japan # }- B' F- e! c5 ^1 Q' Y# i
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan & C+ Q5 z1 o% D
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
$ Q( A2 Z9 \* AAbstractBackground: 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 6 N2 J! Y) b  ?$ a% S& p* w, _! r" B

! J, d; }: Y( K( LAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
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( y+ }+ k# R' {Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  # r6 N% _% Y9 Q3 Z* b$ l; G5 O
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Published online on: Thursday, December 1, 2011
8 O" g* S8 C5 S% f  c. \3 |: {8 E. x8 E; n
Doi: 10.3892/ol.2011.507 0 a' \" U& }5 X( i

6 O/ ]4 h/ Y# x3 F# D$ PPages: 405-410
3 [' t( F8 g! N" h: f% N$ l% a5 l; W5 r& |. @; z7 w9 X& o) [: X1 Y
Abstract:
: b: ~, {& F8 g& e" RS-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
! a) E/ B- o# X" c8 wF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
: d7 O: v+ M4 v1 M+ Author Affiliations
( i2 ~' |7 ^0 h9 q) q1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
; H! V  i+ [3 s& J. L2 A/ m- j* ~2Department of Thoracic Surgery, Kyoto University, Kyoto , |% l  z3 w2 u8 j8 {6 j, U
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan # j  f! G; e5 O3 U8 k) @7 O
&#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 E$ t2 H0 T$ O8 A% c; G3 d! cReceived September 3, 2010.
( k! J6 Y# s5 u- i( zRevision received November 11, 2010. - H+ H9 ?2 T6 W  M& n
Accepted November 17, 2010.
0 B. |5 i9 D! `$ t% gAbstract
8 o0 `$ A( I8 V/ P9 J4 `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.
1 E. K" c* ~7 M- D/ xPatients 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. ( ?2 [  Q/ h- P* ?) [& R! i
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.
6 O1 J: g& |! A/ lConclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. & Y( |' @, P3 c. q
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。; w( C, o4 g( Q- B4 i
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* u& d1 b0 M$ @1 m; n
http://clinicaltrials.gov/ct2/show/NCT01523587' e6 J& Y* p6 l+ c" c- M: A0 O
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC' J  B: L  c$ Q3 |7 F
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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# R, C$ N& z$ t0 X+ a! U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。
4 J% o( r% C* 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

1 R* n& F& w' o! |% B3 m没有副作用是第一追求,效果显著是第二追求。
- k; Q; r# x; W/ z不错。

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