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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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1114688 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; m0 l* ?6 D" M/ N6 B
NOBUYUKI YAMAMOTO1, TAKEHARU YAMANAKA2, YUKITO ICHINOSE3, KAORU KUBOTA4, HIROSHI SAKAI5, AKIHIKO GEMMA6, NAGAHIRO SAIJO7, MASAHIRO FUKUOKA8 and HISANOBU NIITANI9 7 V, `# h9 U* j3 x
+ Author Affiliations# Z. p3 z9 }3 u$ K) |

+ g) |, ~% Z) W1Division of Thoracic Oncology, Shizuoka Cancer Center, Shizuoka 411-8777, Japan 0 P1 n4 K9 n. T0 N* R
2Cancer Biostatistics Laboratory, Institute for Clinical Research, National Kyushu Cancer Center, Fukuoka 811-1395, Japan 9 J  X: `- [# R- J
3Department of Thoracic Oncology, National Kyushu Cancer Center, Fukuoka 811-1395, Japan   K7 p; @" r) A  q
4Division of Thoracic Oncology, National Cancer Center Hospital, Tokyo 104-0045, Japan " [  c: i1 K5 h; W
5Division of Thoracic Oncology, Saitama Cancer Center, Saitama 362-0806, Japan 9 g$ N! X; S6 [( C$ ]  o2 d
6Division of Pulmonary Medicine, Infectious Diseases, and Oncology Department of Internal Medicine, Nippon Medical School, Tokyo 113-8603, Japan
: w( U3 g( m* L' c0 R5 a# D7Kinki University School of Medicine, Osaka 589-8511, Japan
  A" M- B* W  N" c4 c1 {8Izumi Municipal Hospital, Osaka 594-0071, Japan " ~# V3 A# f) S% j
9Tokyo Cooperative Oncology Group, Tokyo 105-0013, Japan
5 y# |& E( E2 B: F* l$ b' u, NCorrespondence 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 & V& z/ d! z5 u+ M- N5 z: Q
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. 6 R6 n% w$ X* t3 ~& v7 ~
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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
, F; p0 a/ `% G9 r! G& D* d& Z. X+ ]
Authors: Yuki Tomita, Tetsuya Oguri, Osamu Takakuwa, Makoto Nakao, Eiji Kunii, Takehiro  Uemura, Hiroaki Ozasa, Mikinori Miyazaki, Ken Maeno, Shigeki Sato
+ @- Z1 f% v) w: N9 o
# {5 B3 N7 x: C! a' t- ^; WAffiliations: Department of Medical Oncology and Immunology, Nagoya City University Graduate School of Medical Sciences, Mizuho-cho, Mizuho-ku, Nagoya, Aichi 467-8601, Japan  . O; w! ?" l( c. u& L" ~0 c/ z

+ F1 y6 V, P7 ?- ?Published online on: Thursday, December 1, 2011 ) W) e( w5 A1 F* ?; H0 |$ [2 u( g
1 V! {# x1 ?! L/ W' f6 ]& F9 C
Doi: 10.3892/ol.2011.507
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# e$ d, ?: y3 S  m. n5 I( N" APages: 405-410
+ m: @  O2 ?( {6 @% o! f0 R+ o9 G+ l+ e. H1 W6 {. u
Abstract:7 J$ E& N6 F( r1 b
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.1 f9 f1 p" j1 d/ n: ~& \

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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
; X" w% X  m+ S7 KF. Tanaka1,*, H. Wada2, Y. Fukui3 and M. Fukushima3
9 a4 Q/ s  u# D3 ?; `: R) H+ Author Affiliations/ _. n% n' _$ b( g
1Second Department of Surgery, University of Environmental and Occupational Health, Kitakakyushu
# V0 I8 G2 N, ~" N' m: z8 O/ P! Y8 u2Department of Thoracic Surgery, Kyoto University, Kyoto & B! Z) @2 v2 U) K
3Tokushima Research Center, Taiho Pharmaceutical Co. Ltd, Tokushima, Japan
, ]1 L' P  \- c&#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
/ G4 @: o" l% z, p* mReceived September 3, 2010.
+ [% h. K0 X, n+ v% rRevision received November 11, 2010.
! V& B! U2 m2 J; ]1 r1 C2 [! FAccepted November 17, 2010. ' D, k3 S4 h* P
Abstract
; p; L% L: w* ~0 M0 O: m, F. RBackground: 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.
! _+ d0 L" v& G! {' h* ~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.
  b% @2 g: i" s6 r4 W/ k: 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. + L) t4 [& |- _, q! i/ K0 x7 [+ u
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。
* H3 x8 g/ _& ^, C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?
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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 Chemotherapy8 n  {, M0 d% a2 C9 i+ P5 m4 y+ c3 v
http://clinicaltrials.gov/ct2/show/NCT01523587& k  {+ _/ W  @5 q9 Y  T) b
" ?2 j4 @2 `2 x. W/ b9 W+ ~
BIBW 2992 Plus Simvastatin vs. BIBW 2992 in Previously Treated Patients With Advanced Non-adenocarcinomatous NSCLC* v% Q2 Z5 M' O8 E; k
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 * q( c! h) }1 y3 }7 W. p, \, F/ o

2 v: q$ K! w. Q' F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。1 [- M) ~( ?) w0 y+ Q5 ]" 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 " J- ~  ?. k' V3 I
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。
  A! y2 f% E( g3 N6 m- I7 g至今为止,未出 ...

/ F% O0 `) Q2 f4 o$ t没有副作用是第一追求,效果显著是第二追求。  v- \: c" V- {3 Y( D* j! z
不错。

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