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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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1398255 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
! ~2 i! l* T0 DNOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 3 L" I* ~5 W' c: f+ D4 I
+ Author Affiliations0 x' m6 _) k3 l! j+ o8 @

: k0 V/ ?2 S* Y! ]: t% {1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan . A1 K' l, Y  d- j) Q# t, B) D. f
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
2 Q/ R4 A; }9 D: k2 O" g0 x; f  C3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
. v( A$ y/ h- ~4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan 0 l. `9 ]% K5 D
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
3 L9 m# k* z, g: R1 i6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
. K! P9 B. @. g0 x7Kinki University School of Medicine, Osaka 589-8511, Japan
, N! H5 R: R6 s7 J" e4 J8Izumi Municipal Hospital, Osaka 594-0071, Japan , n  w3 F- F( ~7 I4 n. B
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
4 o- n' R4 c8 _+ yCorrespondence 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
2 w# v2 @. d8 S; l- @# [/ p9 F) WAbstractBackground: 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. , U6 m! j) u; K9 l* s) p7 A, d

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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
% C- q8 a  [/ o: z2 r% w) J9 ^1 ~+ h6 H; q
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato . [7 _- C6 s+ z; f; K( z( m3 b

" r9 e* l- c  X3 FAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  2 R, x( L  ?. X5 u5 C7 v

8 |) f( e+ q+ X3 I7 Z0 J1 VPublished online on: Thursday, December 1, 2011
' t: ?2 |% H2 K, i& M* b7 K1 i; {% f; R
Doi: 10.3892/ol.2011.507
' U+ c# ^1 @: C% ]8 J/ T+ M" N; U: ~1 d& I
Pages: 405-410
2 c5 R& A' ~* f9 l2 x9 S6 c* L2 r
$ Q3 Z/ `" h" f; uAbstract:
# e/ e- t( t' Z/ X9 OS-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.% y. ]* B, ]% ~4 P' d6 p$ [

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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# w! t* v5 q5 F3 ?
F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 1 r/ m8 u4 f1 {8 G  Q+ z6 a6 M' N
+ Author Affiliations- g# r, Q, |4 Y! g* [* ]3 T
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
9 G3 `8 L2 J1 m: S: k2Department of Thoracic Surgery, Kyoto University, Kyoto 8 Z! A% h4 m, h9 _3 ^8 c
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan . ?/ U2 M5 E. ]' ]
&#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 Q4 n4 R9 F+ T  C- WReceived September 3, 2010. 3 R& ~. ^  A& X5 Z, z. h+ h3 l
Revision received November 11, 2010.
# G$ G5 j+ _1 w8 O" G$ pAccepted November 17, 2010. 9 t. w* `$ L2 P* T4 {
Abstract0 A0 X: k  a4 T% t- _  T
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.
, Z$ T/ Q' d2 S, \! v$ h, H/ q, l9 EPatients 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. " v) D- K: X2 S1 M1 O1 d" `
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 }0 e6 s2 J+ D. J: k3 }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。
7 @% Q2 E! A5 x* ^8 K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?7 u6 h( s9 B5 A; 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 Chemotherapy
0 [5 l: _2 J0 h+ X5 Ehttp://clinicaltrials.gov/ct2/show/NCT01523587$ a( B/ r/ h6 i) g# l# e$ z
. V9 J+ n2 R! r/ A5 o
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC8 D" a& A' L5 n& W) m- A1 b' x
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 ; B- |* |* C) A4 j( e, \( f

6 z3 i) O0 ^; ]+ D: ^! w% A3 G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 m3 T, |  l/ a1 x
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

2 S7 ~" v1 a; U4 T3 o没有副作用是第一追求,效果显著是第二追求。) ?5 K& [; _8 F1 s( U- S
不错。

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