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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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1465610 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/ |& O0 o5 ?5 `- R' \NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 5 {, j' }0 M: G' |
+ Author Affiliations6 [6 d9 [& W/ e! n

3 a2 i; I! ]. G- F1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ; }$ K; m: V! X& x# s# a, X  p
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 8 L- p6 u: {1 k3 A% O' }5 H5 m
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
1 `# m5 a& b! g- g9 Q4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan ' o6 f* }9 ?3 J2 f" k5 k/ H4 t
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan * O9 f- S# j7 W2 e/ _8 d
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan 5 h/ c4 A2 g, |9 E8 x+ Z* X
7Kinki University School of Medicine, Osaka 589-8511, Japan
! [/ d2 j+ H; y" i& E0 `8 q8Izumi Municipal Hospital, Osaka 594-0071, Japan 5 X. W" R8 V8 A) `* t& m. o( T2 h
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan . l% @& T/ p* }9 g: t! Z. h6 ^
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 * L* k0 w9 p4 @4 o3 ?' J; m$ G
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 7 A# J+ @) t0 i. d
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Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato 3 j' d) W7 ]  B* [* e

, @# w# j% q& m1 S2 RAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
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0 Y3 y0 k6 E. @( a' q% V  @Published online on: Thursday, December 1, 2011
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) z2 |! x2 `0 I2 }. uDoi: 10.3892/ol.2011.507
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Pages: 405-410 0 Z; O* u1 f' p3 O* U

* h6 i7 P2 ?0 g* m5 kAbstract:
5 _, K( X& H0 b' T  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.' c/ z& s' d+ Z, @
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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
/ |! D! E0 S$ N1 d, O+ `- OF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
% Y0 u7 q+ ?1 w; Z, k, ~5 Y+ Author Affiliations* ^0 q8 R7 H9 w8 x# S' G
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
. R& g; `% O& q* i* q2Department of Thoracic Surgery, Kyoto University, Kyoto   M+ m) j0 L+ m2 E0 Z
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan # F/ I: ^( O' }; F! F8 P& p
&#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
6 _% `0 s# I  OReceived September 3, 2010.
1 E7 y3 O5 {; u- ]Revision received November 11, 2010. 9 b$ u1 C/ @% h8 o& d
Accepted November 17, 2010.
: c# v+ ?6 k, m4 w/ e3 l, e  \Abstract7 L. S7 y1 K0 Z- v1 L
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.
4 |) ]0 t) r; }$ e* B- G2 `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. ) {, l/ Y& _' ~8 ^9 f
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. 8 g: E# e, z. _3 N9 E
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。
5 ?* ~4 X4 {) I1 R6 w8 a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?. ^5 ~- F5 W/ U; W4 D. [! q
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
& ^, p7 L: ~. C! |& c- ^% r8 Thttp://clinicaltrials.gov/ct2/show/NCT01523587
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: z1 x- L$ ~3 v' f" o- i5 y. J/ NBIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC
9 w. q9 z: t/ {' d+ a1 Vhttp://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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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。
! K  S% X6 \, f; X  R; N- o$ X+ K% J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 ( z- b' K+ R1 v+ Z. Y) b: K
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。$ Q& k" s, ]7 W0 ?, Y! F
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。, N& Y* R- P9 E  Y# M& L! Z7 c
不错。

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