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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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1131311 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% N1 j" N7 U5 @& s4 ]/ ^& |
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9
  u. e, {+ j+ ^9 q  O" E+ Author Affiliations
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" `4 V6 e; @5 V' a2 Q! D- b& c4 x- _1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan & A2 X4 a" |! _) b: L0 ]( g
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
5 V  I/ q9 B2 J( S7 z* i" T' z3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan ; x8 G* J) Q& P6 @
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
7 F+ T0 E- \: H! a. E5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan - u9 I( u3 U, s4 I6 Q
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan , Q3 h3 ]  j" P# S0 p
7Kinki University School of Medicine, Osaka 589-8511, Japan
! n5 t% m8 P, y9 D: n8Izumi Municipal Hospital, Osaka 594-0071, Japan 2 B4 V8 z4 U  ~; W) k* _
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan 5 Z& Y! m# Y; h: ~$ Z# z0 J0 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 & `3 z9 K" J0 y+ R+ G6 Q5 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
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: L% B, d7 }; x0 `Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato % L$ c3 H; l, @) C& R6 C  c6 o
2 a1 t8 K  t: Y- c
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  % U" W7 R  l8 q, y+ \. ^
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Published online on: Thursday, December 1, 2011
% M1 w0 w8 v: O* w1 Z: i$ h* U2 }: b0 _, W3 z6 m1 X6 r
Doi: 10.3892/ol.2011.507
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Pages: 405-410 5 t2 |; G( G, |' _4 q: Y
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Abstract:* I, `5 p' a: ]. ~
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." U, ~& j0 g3 F
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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
% i9 k4 ], D5 n% C: o8 k& KF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 2 }( \' o# L8 ~& Z, X
+ Author Affiliations# }6 `$ v7 A! t# y! O* ?5 w7 C
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
  h. y# o5 j0 s" @: c" {2Department of Thoracic Surgery, Kyoto University, Kyoto
+ t4 `8 \' H& N9 w; k3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
' \# e: Y6 T9 W5 Q! T, N&#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 7 [5 Z9 P) L" b; z
Received September 3, 2010. ( w4 e9 U0 P' ]2 \5 A7 V2 M+ r  L
Revision received November 11, 2010.
* M" g0 S; S! O* e- pAccepted November 17, 2010.
  v! @' d# }: ]- M7 ^9 QAbstract
$ i6 ]7 U0 @( K2 Y- l+ {" I$ p- n% gBackground: 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.
! D: Y! E5 U/ w' t/ ?6 gPatients 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.
8 Z6 E8 f4 a9 M" t' R0 oResults: 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. % O; g$ E  Z) o, ]  Q8 s: z
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。
2 L2 A6 |+ l% I; a' a: Y+ |4 S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?6 q& ~  a! [0 a& T4 J
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
/ a# h+ L' G+ o% rhttp://clinicaltrials.gov/ct2/show/NCT01523587
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BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC2 x9 F% Y& h1 e5 z
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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- o+ O9 j9 {  [  l3 t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。
! o9 l( z* h: g5 X+ d7 ^0 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
5 ]; [4 m4 B2 ^5 N& r1 @% c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。
- C# I# Y0 k( ?0 H; E0 C: 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。
$ C  J8 ^1 |& C* }不错。

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