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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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1151485 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( n5 L! T8 G0 q4 h- q" [
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 2 o: A+ f$ Z3 t6 Y0 ^. V5 |& {
+ Author Affiliations
! j) h9 v! s, e. }/ j! r4 f5 T( X
8 c1 f/ c/ L- J2 Q4 O7 d1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan ! h9 j7 |  T, h! B4 a2 v
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
4 L# i+ a6 u# s: _3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan
" U+ s( S3 w1 @6 Y7 k$ Q; x4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan
- x8 d* n" j. n9 H4 c& B/ {7 F5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan
" D9 E' u) |1 o9 }6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan % V  |, ~7 L3 d$ t% \# }4 z
7Kinki University School of Medicine, Osaka 589-8511, Japan ; ]$ r$ ~' T% x& v
8Izumi Municipal Hospital, Osaka 594-0071, Japan 1 w9 j. t6 }5 p, t' g
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
# h0 }: C" c8 pCorrespondence 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
. n6 E  k, Q: j5 ]$ qAbstractBackground: 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. / x* ^) ^* c: P% M5 J
; {7 v' \# H+ a# X6 H. Z/ ?
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 ' P. L8 m8 x9 z) Z" K3 d& t, S- H

2 M6 ?+ t( C6 I, ^* ]& ?Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
% U. _$ o* o, [- G( q. q% D' R, g! |6 b& Z' h9 _5 |, J, S
Affiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  
" t( b$ P: \' `+ D5 ^
: G/ d; \% B& n& s+ FPublished online on: Thursday, December 1, 2011 ! X4 ], {! G$ M4 K

* ]& n, B, ^& E2 j5 H' N( V  D. XDoi: 10.3892/ol.2011.507
* X, B$ Y, t* [
* ^& s9 |; y0 |- \- }Pages: 405-410
# \2 E2 r& I7 c: G0 M' N/ [
7 q+ j; D( e3 G+ T+ ^Abstract:/ S9 a% Z, n" o% M6 Q0 ^- W
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.4 }& h; J3 z* l6 r( R

2 Q( ]- ^" {# D" H
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
, c3 e$ f4 B" _F. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3 6 [7 l! T6 ?. _5 I( p0 m
+ Author Affiliations
; f5 W2 E! m% D# w3 {3 M8 h5 v5 e; c1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu ' [8 s1 C* U8 Q+ w2 v
2Department of Thoracic Surgery, Kyoto University, Kyoto
4 X! E7 T9 e1 {3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
, [( G9 ?. x! F2 r' h2 V&#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
* a+ X/ [0 A2 x) D6 pReceived September 3, 2010.
9 m. G6 M8 R. K/ V- B* W7 G8 l9 a! gRevision received November 11, 2010.
6 a, i  _. P& j7 E: [6 MAccepted November 17, 2010.
0 {9 o& _/ G7 I  Z4 XAbstract
. J: K0 N; v' ~# V1 t0 f  ?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.
+ o* O* [* t$ n5 yPatients 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. * Z, P  ~/ B( m9 [
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. ( p' r. j5 i9 k6 F2 G0 y" `' q
Conclusion: Lower TS expression in adenocarcinoma of the lung was confirmed in a large-scale study. 4 c. M& R9 ^3 v( |7 y9 i$ L. V
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。
' c: d7 h8 \, E+ ^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 N2 E% J1 A/ E  z# g
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. b- S$ ?* Z5 R8 F5 r$ _http://clinicaltrials.gov/ct2/show/NCT015235871 n, X6 B4 n% k0 `
* I" w3 O2 v' C$ ~" U# Q& b
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC5 ]' w2 w- ]* C: Y$ m
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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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。
2 ?" @1 H* k/ T  E8 L: G8 p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
' M' x6 T% F3 C" T$ q# S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。
: ]+ v5 S7 i/ m9 l至今为止,未出 ...
% D( j8 q7 @+ B3 Q) }3 y9 O6 H
没有副作用是第一追求,效果显著是第二追求。# c2 J3 o- W9 T# a3 t" c2 _
不错。

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