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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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1138288 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
+ i8 g, D' Y- nNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
- A' [' B: M, g+ e+ Author Affiliations
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' b- R; E' v+ a. w2 v4 o8 y: L( D/ V1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan
+ L* u$ ?6 h* @# j* t9 ?2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan , K( Y% U8 q6 |6 Y/ {
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
" ~/ g: i3 c% _3 V* {4 |1 S4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan * j0 k/ J8 o$ z# p' Q  v! K6 x+ ^
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 0 P( A+ `* x$ t1 y4 e3 |
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan , R- r, V. r2 ?# L7 J+ u2 O
7Kinki University School of Medicine, Osaka 589-8511, Japan
9 p. j2 L& _) d3 S6 @$ O0 [. V8Izumi Municipal Hospital, Osaka 594-0071, Japan - [; n$ Y4 n# e6 z9 F2 n
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
. w8 g; C( @5 L. q" r+ qCorrespondence 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 0 `8 X5 D& D' ~7 b$ t
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. 1 [3 U9 U1 p% r) }5 t

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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 ( z2 R& X( X! P9 k3 Q

4 [# K$ I# k: N8 I) U0 N: Y2 OAuthors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato & w3 c( g& v* y  h

! S2 f6 f# @9 Q* b- }3 G( BAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan    a' r; Y" K4 _8 a; Q
$ H* P/ y% N+ U* l) j) u. L
Published online on: Thursday, December 1, 2011
5 Q2 F0 H3 M( ~8 [# }4 ?1 B; H8 b) K+ r7 f2 |2 h" c7 E
Doi: 10.3892/ol.2011.507 4 U! P, q$ a% i1 w; W

- i! u( v8 ~4 x" K4 Z' CPages: 405-410
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6 N5 P; ?! v* b/ _9 G8 J7 q0 o: F) lAbstract:+ u2 V" o' _: M2 C% r
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.0 C( d3 t6 _% J- H- K2 T1 b; U4 O
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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$ H* x/ F' P4 q  N4 r) t
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
; E4 p% a3 _0 c9 y/ |. Z+ Author Affiliations0 b% }2 J* E9 I$ U
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu & A. x* K; `* x; o1 p
2Department of Thoracic Surgery, Kyoto University, Kyoto
1 K/ F0 H* [6 K% Q; c9 X$ M& @3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan 3 F6 {) O1 B4 c. k, F- q
&#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
4 i" q' x( V8 _. _, {( QReceived September 3, 2010.
2 Q. l8 k7 T. v& ~% FRevision received November 11, 2010.
' a) W2 p& Q  C8 D* n: d; ^Accepted November 17, 2010. - l$ ^7 i% ~. i& U
Abstract
& E: s8 j. |% N" S% `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.
6 p8 r. d( V- b/ B5 ZPatients 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.
' S8 M" n* x8 QResults: 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. % ^% w. l6 @! {8 ]( u# G/ i8 ?
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 5 M. y  F* r  ~5 Y
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。$ k0 O9 i) Z* a# e; F9 _( e( R1 U
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?$ G2 Z4 q" F+ a, g! V6 E# {
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# V" f* _  o+ w: N8 ?+ W0 a. y% r
http://clinicaltrials.gov/ct2/show/NCT015235870 A! B# \/ J/ b% e9 M; B7 \2 A" {' F

2 r7 w* z1 u  j9 ]BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC7 _7 N* b5 _7 P' R; P
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 & i) l. z  z& g
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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。
! i$ J& |4 s$ F$ G2 C9 T  Q3 D; `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 0 W* w) ^* n9 M$ [9 }& m
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。
* e8 d! N( a" j# S至今为止,未出 ...

" V6 F. I0 I; f  f没有副作用是第一追求,效果显著是第二追求。
6 G( q# \. ?/ @& q" U, j$ u不错。

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